Related Articles Results

Tuesday Apr 06, 2010
Long-Term Methotrexate Use Does Not Reduce Relapse Rates for Juvenile Arthritis
Children with juvenile idiopathic arthritis do not have their relapse rates reduced by a longer treatment course with the drug methotrexate...

Wednesday Feb 17, 2010
AstraZeneca to Enter the RA Market
AstraZeneca is entering the rheumatoid arthritis (RA) market by gaining rights to Rigel’s RA drug...

Monday Feb 01, 2010
CP-690,550, Pfizer's Oral JAK Inhibitor, Demonstrates Response in Patients with Active Rheumatoid Arthritis
Pfizer’s oral JAK Inhibitor CP-690,550 shows efficacy at improving the pain, function, and health status of RA patients...

Wednesday Dec 02, 2009
OxyPharma's New RA Drug Shows Positive Phase II Results
Rabeximod, an orally-administered DMARD, showed promise as a new RA treatment during a 16-week study...

Thursday Nov 12, 2009
TNF Inhibitors Do Not Raise Cancer Risk
No increased cancer risk was seen during the first 6 years of anti-TNF therapy for rheumatoid arthritis...

Thursday Oct 22, 2009
For Early RA, Start with Six Months of MTX, then Add Two More DMARDs
ACR researchers report that initial treatment with methotrexate followed by step-up to two more DMARDs if needed at 6 months is as good as adding a TNF inhibitor...

Wednesday Oct 21, 2009
Phase 2 Data Support Pfizer's JAK Inhibitor for RA
Two Phase 2 trials reported at ACR show efficacy of JAK inhibitor now in Phase 3...

Tuesday Oct 20, 2009
Infliximab Plus MTX for JIA
Infliximab plus methotrexate (MTX) bests combinations of traditional disease modifying drugs and/or MTX alone for the treatment of polyarticular juvenile idiopathic arthritis...

Tuesday Oct 06, 2009
Simponi Scores EU OK for RA, PsA, AS
Simponi (golimumab) anti-TNF is the first monthly anti-TNF injectable to gain broad EU approval...

Tuesday Sep 08, 2009
RA Drug Array ARRY-162 Fails in Phase 2
A new rheumatoid drug from Array BioPharma that modulates the MEK pathway did not meet Phase 2 efficacy goals...

Thursday Aug 27, 2009
Lexicon Moves LX2931 Into RA Phase 2
Lexicon's LX2931 S1P lyase blocker is in Phase 2 trials in rheumatoid arthritis...

Wednesday Aug 05, 2009
Psoriasis: Not Just Skin Deep
Mark G. Lebwohl, MD says psoriasis affects the heart and other vital organs, and treatment with TNF-blockers may reduce the risk of these comorbidities...

Monday Jun 22, 2009
EULAR Studies Show New Picture of B-Cell Depletion in RA
A group of studies reported at EULAR show that B-cell depletion is a relatively safe and effective treatment option for patients with rheumatoid arthritis (RA)...

Wednesday Jun 17, 2009
EULAR Report Shows Tocilizumab Protects Joints in RA
Actemra^® maintained structure and function in a wide range of RA patients in the LITHE study, with response durations of 2 years in interim analyses...

Tuesday Jun 16, 2009
Infliximab Still Going Strong At 7 Years for RA Treatment
Infliximab efficacy and safety are maintained through at least 7 years of use for rheumatoid arthritis treatment...

Wednesday May 20, 2009
X-ray Stability Lags RA Remission by Months
Radiographic joint damage grinds to a halt only after at least 9 months of sustained disease remission...

Thursday May 14, 2009
FDA OKs UCB's Cimzia for Moderate to Severe RA
Cimzia^® (certolizumab pegol), the only pegylated anti-TNF, has been approved for use in the US...

Thursday May 07, 2009
Half of Early RA Patients Treated With Combo DMARDs Have No Disability After 11 Years
Treating early RA with 3 conventional DMARDs leads to more sustained remissions and better outcomes than starting with a single DMARD, regardless of what regimen is used after year 2...

Wednesday Apr 29, 2009
Simponi Approved in US for RA, PsA, AS
The US Food and Drug Administration this week joined Canada's drugs agency in approving Simponi (golimumab) for moderate to severe RA, active PsA, and active ankylosing spondylitis...

Tuesday Apr 14, 2009
Golimumab Gets Canadian OK for RA, PsA, AS
Health Canada has approved Centocor's Simponi (golimumab) for treatment of moderately to severely active rheumatoid arthritis (RA), active psoriatic arthritis (PsA), and active ankylosing spondylitis (AS)...

Wednesday Mar 25, 2009
Licorice Reduces Cyclosporine, Raises Methotrexate Levels
Licorice, often used in candies and food flavorings, significantly reduces absorption of cyclosporine, leading to lower than expected blood levels, but prolongs methotrexate clearance...

Wednesday Feb 18, 2009
Ustekinumab Reduces Psoriatic Arthritis Pain, Clears Lesions
Ustekinumab (CNTO 1275), a new monoclonal antibody that blocks interleukin (IL)-12 and IL-23 (IL-23), may help thwart the pain, swelling and lesions of psoriatic arthritis...

Monday Feb 02, 2009
Rituximab B-Cell Depletion Stops JIA
Systemic onset JIA responded dramatically to B-cell depletion with rituximab...

Thursday Dec 04, 2008
RA Improving Due to Better Management, Not New Drugs
Better monitoring and more aggressive use of old drugs, especially methotrexate, have contributed more to recent improvements in RA outcomes in Spain than the arrival of new drugs such as TNF inhibitors...

Tuesday Nov 25, 2008
Who Stays in RA Remission After TNF Blockade Stops?
Patients who start treatment soon after RA symptoms appear, and who have increased functional T-cells, higher levels of interleukin-10, and lower levels of interleukin-12 maintain sustained remission even after stopping TNF-blockers...

Wednesday Nov 05, 2008
Study Establishes Safety of Long-Term Juvenile Arthritis Treatments
Three-year data reported at ACR show that long-term etanercept, with or without MTX, is safe and effective in juvenile rheumatoid arthritis...

Tuesday Nov 04, 2008
Genentech, Biogen Idec Rituxan Phase III Data in RA Patients Showed Patients who Received Fixed Interval Re-Treatment Maintained Treatment Response; Positive Phase III Data Also Reported for Rituxan plus MTX in Biologic-Naïve RA Patients, Immune Response in Rituxan-Treated Patients Yielded Mixed Results in Phase II Study
Rituxan, in combination with MTX, is indicated to reduce signs and symptoms and to slow the progression of structural damage in adult patients with moderately-to-severely active RA who have had an inadequate response to one or more TNF antagonist therapies...

Thursday Oct 30, 2008
Old Malaria Drug Reduces Diabetes Risk in RA, Protects Kidneys in Lupus
The inexpensive old drug hydroxychloroquine (HCQ) shows remarkable protective ability against diabetes in patients with rheumatoid arthritis and against renal disease in patients with lupus...

Wednesday Oct 29, 2008
Denosumab Bests Alendronate for Increasing Bone Mass
One year of denosumab was more likely to produce a 3% gain in hip or spine bone mass than one year of alendronate...

Tuesday Oct 28, 2008
Syk Kinase Inhibitor R788 (Tamatinib fosdium) Achieves  ACR20 Response Rates Over 60% in Phase II Trial
The oral Syk kinase inhibitor R788 achieved impressive efficacy in a phase II RA trial...

Wednesday Oct 22, 2008
Biogen Idec Reports Top-Line Results From Phase II Clinical Trial of Baminercept in RA; Will Discontinue Development in RA
The phase II trial of baminercept in RA patients who have had an inadequate response to conventional therapy with a disease-modifying antirheumatic drug did not meet its primary endpoint...

Tuesday Oct 21, 2008
Centocor Reports Efficacy of Remicade^® vs Azathioprine in Treatment of Crohn’s Disease
Azathioprine is not approved in the US for the treatment of CD but is approved in some countries outside the US and is widely used by gastroenterologists and other physicians in the US to treat CD patients...

Wednesday Oct 01, 2008
Roche Says US FDA Issues Complete Response Letter for Actemra^® Biologics License Application; No New Clinical Studies Requested
Actemra^® (tocilizumab) is the first humanized interleukin-6 (IL-6) receptor-inhibiting monoclonal antibody studied for the treatment of adults with moderate-to-severe rheumatoid arthritis...

Friday Sep 12, 2008
Breaking News: FDA Warns About Fatal PML in RA Patient Taking Rituxan^®
FDA issued a MedWatch warning reporting the first fatal PML case in a patient taking Rituxan for RA...

Tuesday Sep 09, 2008
Can-Fite Reports that Seikagaku Corp, Exclusive Licensee of CF101 in Japan, is to Initiate Phase I Trial in Japan to Treat RA; Can-Fite to Receive $1 Million USD
CF101, Can-Fite’s lead compound, is an oral drug that has been successfully used in animal models and human phase IIa RA trials to test the concept of targeting A(3)AR for the treatment of inflammatory diseases...

Wednesday Aug 27, 2008
Pivotal Humira Trial Shows Durable Benefit in Juvenile Rheumatoid Arthritis
The pivotal trial of adalimumab (Humira^®) shows durable, safe efficacy for up to 2 years for children with polyarticular JRA and positions the TNF-inhibitor as the reasonable second-line drug to add if methotrexate does not provide sufficient disease control...

Friday Aug 22, 2008
While Olympians Chase Medals, Chicken Collagen Advances as RA Immunotherapy
Inducing oral tolerance with chicken type II collagen (CCII) may help alleviate the signs and symptoms of rheumatoid arthritis (RA) with fewer side effects than methotrexate (MTX), Chinese researchers say…

Monday Aug 11, 2008
Hollis-Eden Initiates Phase I/II Clinical Trial With TRIOLEX™ (HE3286) in RA
Hollis-Eden's investigational, nonimmunosuppressive oral drug candidate Triolex™ (HE3286), a stabilized, synthetic analog of a naturally occurring molecule metabolized by the body, is being tested in patients diagnosed with RA who are receiving a stable dose of MTX...

Friday Aug 01, 2008
Roche Reports US FDA Advisory Committee Recommends Approval of Actemra^®; if Approved, Would Be First IL-6 Inhibitor for the Treatment of RA
Hoffmann-La Roche announced that the Arthritis Advisory Committee of the US FDA recommended approval of Actemra^® (tocilizumab), a novel interleukin-6 (IL-6) receptor-inhibiting humanized monoclonal antibody...

Monday Jul 28, 2008
Chelsea Therapeutics Granted UK MHRA Approval to Begin Phase II Trial of Droxidopa, a Prodrug of Norepinephrine, in Fibromyalgia
Droxidopa, an orally active synthetic amino acid precursor of norepinephrine (NE), is converted by the body into norepinephrine and as a prodrug of NE, provides replacement therapy for NE deficiency...

Thursday Jul 24, 2008
Adenosine Receptor Variant Might Be Pharmacogenetic Marker for RA Methotrexate Toxicity Risk
The discovery that variants of the adenosine receptor 2a gene (ADORA2a) are associated with methotrexate toxicity may help identify rheumatoid arthritis (RA) patients who should be treated with something else...

Tuesday Jul 15, 2008
Wyeth Reports European Commission Announces Marketing Authorization for 50 mg Once-Weekly Enbrel^® (etanercept) for Patients With Moderate-to-Severe Psoriasis
The European Commission announced a new 50 mg Enbrel^® (etanercept) once-weekly dosage regimen as an alternative to the currently approved 25 mg Enbrel twice-weekly regimen for the treatment of moderate-to-severe plaque psoriasis...

Friday Jul 11, 2008
MediGene Puts Phase I Trial Hold on Due to Patient Death in Study of RhuDex^® in a New Formulation; Reports Positive Results With RhuDex in Phase IIa Pilot Trial in RA
One study participant suffered a heart problem some days after a scheduled treatment of RhuDex^®, an orally administered candidate for the treatment of RA; it is currently unclear whether there is any correlation between the death and the drug administration...

Thursday Jul 10, 2008
Merck Serono Reports EMEA Confirms Positive Benefit-Risk Balance With Raptiva^® for the Treatment of Psoriasis; European Commission Approved Product Information Update to Include Data on Up to 3 Years of Treatment
The European Commission has approved an update of the Summary of Product Characteristics (SPC) for Raptiva^® (efalizumab) in the treatment of moderate-to-severe chronic plaque psoriasis...

Monday Jul 07, 2008
UCB’s Cimzia^® Filed With EMEA for Treatment of RA: if Approved, Would be First and Only PEGylated, Fc-Free Anti-TNFα Biologic
UCB has submitted an MMA for approval of Cimzia^® (certolizumab pegol) as a subcutaneous treatment for adults with moderate-to-severe active rheumatoid arthritis...

Thursday Jun 26, 2008
New ACR Guidelines Help Clinicians Incorporate Biologics Into RA Treatment Plans
The new American College of Rheumatology guidelines help rheumatologists to choose the right drugs and to monitor RA patients for untoward effects, but the guidelines should not replace sound clinical judgment…

Wednesday Jun 25, 2008
Genmab, GSK to Initiate Phase I/II Clinical Trial of Ofatumumab in Subcutaneous Study in RA
A phase I/II study will be initiated soon to evaluate a subcutaneous route of administration of ofatumumab (HuMax-CD20^®) in rheumatoid arthritis (RA) patients, stable on methotrexate (MTX)...

Tuesday Jun 24, 2008
Nearly Half of Undifferentiated Arthritis Patients Can Achieve Drug-Free Remission After 1 Year of MTX
The chance of achieving drug-free arthritis remission after 1 year of MTX therapy is 46% and is predicted by a negative ACPA status, no or low radiographic damage at baseline, increased age, and shorter disease duration…

Thursday Jun 19, 2008
Infliximab (Remicade^®) Plus Combination DMARD Therapy for Early RA Increases Remission Rate, Slows Radiological Progression
Adding infliximab (INF) to effective combination DMARD therapy for patients with early RA both increases the remission and slows progression of joint damage...

Wednesday Jun 18, 2008
Rigel Launches Two Global Phase IIb Clinical Trials of Syk Inhibitor, R788 (fostamatinib disodium), in RA
Rigel currently has small-molecule product development programs in inflammatory/autoimmune diseases such as rheumatoid arthritis, thrombocytopenia, and asthma...

Tuesday Jun 17, 2008
Tocilizumab Plus Methotrexate Shows Efficacy for Anti-TNF Refractory Rheumatoid Arthritis
Tocilizumab plus methotrexate (MTX) looks to be an effective alternative for rheumatoid arthritis (RA) patients with inadequate response to TNF inhibitors...

Monday Jun 16, 2008
Phase III Data Show Golimumab Efficacy in MTX-Resistant, TNF-Pretreated, Untreated RA
Data from the phase III GO-FORWARD and GO-BEFORE studies show that subcutaneous golimumab improves symptoms, function in RA patients after MTX, anti-TNF failure...

Friday Jun 13, 2008
Clinical, X-ray, and Functional Remission Possible in Early RA With MTX-ETN Combo
Etanercept (ETN) in combination with methotrexate (MTX) was superior to MTX alone in allowing RA patients to achieve clinical remission, radiographic nonprogression, and normalized function... 

Thursday Jun 12, 2008
Increased Melanoma Risk Seen in RA Patients Taking MTX
Rheumatoid arthritis (RA) patients taking methotrexate (MTX) may be at a 3-fold increased risk for developing potentially fatal melanoma…

Thursday Jun 12, 2008
Step-Up, Tight Control Abates Early RA in 50% of Patients by 36 Weeks
As many as half of all early rheumatoid arthritis patients may achieve remission within 36 weeks following step-up therapy coupled with tight control...

Wednesday Jun 11, 2008
How to Tell If an RA Patient is Likely to Achieve DMARD-Free Remission Without Biologics
A number of factors identify rheumatoid arthritis patients whose disease is likely to respond to conventional DMARD treatment with sustained, drug-free remission...

Monday Jun 09, 2008
FDA Launches Major Investigation of Cancer Risk in Children Taking TNF Blockers
The FDA is investigating a possible link between TNF blockers and cancer in children and young adults...

Wednesday Jun 04, 2008
Case Series Adds Support for Routine PET in Polymyalgia Rheumatica
Routine PET might be a useful option in patients with steroid-resistant polymyalgia rheumatica (PMR)...

Thursday May 29, 2008
Medarex Initiates Phase II Proof-of-Concept Trials for MDX-1100, a Fully Human Anti-CXCL10 Monoclonal Antibody, in UC and RA
Medarex announced that it has initiated two phase II clinical development programs of MDX-1100, a fully human monoclonal antibody that targets CXCL10 (also known as IP-10), in ulcerative colitis and rheumatoid arthritis...

Friday May 16, 2008
Centocor Alerts Authorized Distributors and Prescribing Physicians About Stolen Infliximab (Remicade^®)
A transport trailer carrying infliximab (Remicade^®) was stolen en route to a specialty distributor on May 6, 2008...

Wednesday May 14, 2008
Roche’s Fifth Phase III Study for Actemra^® Inhibits Joint Damage and Improves Physical Function of Patients With RA
Roche's Actemra^® (tocilizumab), a humanized interleukin-6 receptor-inhibiting monoclonal antibody, can significantly inhibit structural damage to joints in patients with RA...

Wednesday May 14, 2008
8-Year Data Confirm Etanercept Safety, Efficacy in Juvenile Rheumatoid Arthritis
Long-term open-label data show that etanercept (Enbrel^®) is safe and effective over 8 years of continuous treatment of children with JRA...

Monday May 12, 2008
Rituximab OK Following Anti-TNF-Associated TB
Rituximab is both safe and effective in rheumatoid arthritis (RA) patients who have had active TB while being treated with a TNF-α inhibitor...

Friday May 09, 2008
Treating Early RA With Intensive Step-Up Triple-DMARDs is as Good Starting 3 At Once—Perhaps as Effective as Biologics
Intensive triple therapy with conventional DMARDs in early active RA is as effective as a step-up regimen and is as effective as when all 3 drugs are started together, and both approaches can achieve response rates as high as those seen with biologics…

Thursday May 08, 2008
Trubion Initiates Phase IIb Study of TRU-015, a CD20-directed Drug Candidate, Plus MTX for the Treatment of RA
Trubion's partner Wyeth Pharmaceuticals has commenced patient dosing in a multicenter, phase IIb clinical trial of TRU-015; previously reported data demonstrated TRU-015's ability to significantly improve RA signs and symptoms...

Thursday May 01, 2008
Genentech, Biogen Idec Report Phase II/III Trial of Rituxan^® Fails to Meet Primary or Secondary Endpoints in Lupus
A randomized, double-blind, placebo-controlled, multicenter phase II/III study of Rituxan^® (rituximab) for systemic lupus erythematosus (SLE) did not meet its primary endpoint or any of the six secondary endpoints...

Monday Apr 14, 2008
Orencia Gets FDA Okay for JIA
Pediatric rheumatologists gained a new tool for use in treating juvenile idiopathic arthritis (JIA) with the US Food and Drug Administration’s approval of Orencia^® (abatacept)...

Tuesday Apr 01, 2008
Trubion Announces SBI-087, a Fully Humanized CD20-directed Compound, as Next-Generation Product Candidate for RA and SLE; TRU-015 to Enter Phase IIb RA Clinical Trial
Trubion Pharmaceuticals, Inc announced that its collaboration partner Wyeth Pharmaceuticals has filed an investigational new drug (IND) application for SBI-087 for rheumatoid arthritis (RA), and clinical trial sites are preparing to enroll patients in a phase I study...

Monday Mar 31, 2008
CRP, Anti-CCP, Ultrasound Can Predict Which RA Patients Need Early, Aggressive Treatment to Stave Off Rapid Progression
RA patients with rapidly progressing disease will benefit most from aggressive early treatment with biologics and can be identified using markers such as CRP, anti-CCP, and ultrasound evidence of joint erosion...

Tuesday Mar 25, 2008
New Rheumatoid Arthritis Drug Works for Adults, Children
Two new studies have found tocilizumab to be effective in relieving the symptoms of RA in adults and children…

Thursday Mar 20, 2008
Merrimack Pharmaceuticals Completes Enrollment in a Phase II Study of MM-093, Recombinant AFP, in Patients With RA
Merrimack Pharmaceuticals, Inc's phase II trial to evaluate the safety and efficacy of MM-093, a nonglycosylated, recombinant version of human alpha-fetoprotein (AFP) in patients suffering from rheumatoid arthritis (RA) has completed enrollment...

Tuesday Feb 26, 2008
Abbott Receives FDA Approval for Humira^® (Adalimumab) for Polyarticular Juvenile Idiopathic Arthritis; EOW Dosing
Abbott Laboratories announced it has received US FDA approval to market Humira^® (adalimumab) as a treatment to reduce signs and symptoms of moderately to severely active polyarticular juvenile idiopathic arthritis...

Thursday Feb 14, 2008
Kidney Damage Routinely Overlooked in RA Patients; Serum Cr Not an Adequate Check
Nearly half of RA patients have compromised renal function, half of whom should have their dosage adjusted because of kidney damage...

Wednesday Feb 13, 2008
Hollis-Eden Initiates Phase I/II Clinical Trial With Oral Anti-Inflammatory Drug Candidate Triolexâ„¢ in UC; RA Study Planned in 2Q/08
Hollis-Eden Pharmaceuticals, Inc announced that it has begun a phase I/II clinical trial with Triolexâ„¢ (HE3286), an insulin sensitizer for ulcerative colitis...

Monday Feb 11, 2008
UCB Reports US FDA to Review Cimzia® License Application for Treatment of RA
UCB announced that the US FDA agreed to accept a Biologics License Application for Cimzia® (certolizumab pegol), a PEGylated and Fc-free anti-TNFα antibody-fragment therapeutic, for the treatment of adult patients with active rheumatoid arthritis (RA)...

Friday Feb 08, 2008
TNF Inhibitors, Efalizumab, Alefacept Herald New Era in Psoriasis Treatment
New treatment strategies that include TNF-α inhibitors, efalizumab, and alefacept offer better psoriasis control with less toxicity, but still need to be compared with traditional agents in clinical trials...

Monday Jan 28, 2008
Genentech, Biogen Idec, Roche Report Rituxan® (rituximab, MabThera®) Phase III Trial Meets Study Endpoints in RA; Use as First-Line Biologic Therapy Improves Symptoms 
Genentech, Inc, Biogen Idec, and Roche Pharmaceuticals announced that a pivotal phase III study of rituximab (Rituxan®) met its primary endpoint of greater proportion of biologic-naïve RA patients achieving ACR20 response at week 24, compared with placebo...

Thursday Jan 24, 2008
Bacterial Gastroenteritis Leads to Joint Pain That Seldom Needs Prescription Treatment
Patients who experience gastrointestinal (GI) symptoms after a bacterial outbreak are more likely to report a diagnosis of arthritis in the ensuing 4 years, but they are not likely to report needing prescription drugs for their joint pain...

Thursday Jan 24, 2008
TNFα Inhibitors Can Be Used Again After Treatment of TB Flare
TNFα inhibitors can be safely readministered after either a flare of latent TB or a new TB infection and should be considered an option in patients with otherwise uncontrollable RA...

Wednesday Jan 23, 2008
Abbott's Humira® Approved in US for Treatment of Moderate-to-Severe Chronic Plaque Psoriasis
Abbott Laboratories announced it has received US FDA approval to market Humira® (adalimumab) for adults with moderate-to-severe chronic plaque psoriasis...

Wednesday Jan 16, 2008
Etanercept Clears Plaque Psoriasis in Children and Adolescents
Etanercept (Enbrel®) safely reduces disease severity in children and adolescents with moderate-to-severe plaque psoriasis, and improvements are evident as early as the second week of therapy...

Tuesday Jan 15, 2008
Three More Cases of Significant Neutropenia Lead to Recommendation for Routine CBC Monitoring
Three more cases of significant neutropenia in rheumatoid arthritis (RA) and psoriatic arthritis patients treated with etanercept lead to a recommendation for regular monitoring of complete blood counts (CBC)...

Thursday Jan 10, 2008
SC Beats Oral Methotrexate for RA
Starting treatment with subcutaneous (SC) methotrexate (MTX) is significantly more effective than starting with oral MTX in patients with active, early RA...

Monday Jan 07, 2008
Abbott's Humira® Approved in the EU for Treatment of Moderate-to-Severe Plaque Psoriasis
Abbott announced it has received marketing authorization from the European Commission for the use of the TNF antagonist Humira® (adalimumab) as a treatment for moderate-to-severe plaque psoriasis. Humira is the first fully human, self-injectable biologic for the treatment of psoriasis...

Thursday Jan 03, 2008
Step-Down Therapy With Steroids is Feasible and Effective in Early RA
Step-down therapy for early rheumatoid arthritis (RA) including oral prednisolone is not just feasible in daily practice, it is also more effective than a step-up regimen...

Tuesday Dec 18, 2007
Rigel's Oral Syk Kinase Inhibitor, R788 (tamatinib fosdium), Achieves Statistically Significant ACR-20, -50, -70 in Phase II RA Clinical Study; Achieves Effect As Early As 1 Week
Rigel Pharmaceuticals, Inc announced that its oral syk kinase inhibitor, R788 (tamatinib fosdium), has demonstrated statistically significant results in treating rheumatoid arthritis patients in a recently completed phase II clinical trial...

Friday Dec 14, 2007
New Kid on the Block: Everolimus Looks Promising as Rheumatoid Arthritis Treatment
A "proof-of-concept" study shows that the immunosuppressant everolimus may be an effective addition to MTX for rheumatoid arthritis patients whose disease is only partly MTX-responsive...

Thursday Dec 06, 2007
 Drug Update: Rituximab
Repeat rituximab was notably effective in patients with DMARD-resistant RA, and the B-cell depleting agent is being tested in pediatric SLE and in Sjögren's syndrome...

Monday Dec 03, 2007
Targeted Genetics Announces That US FDA Removed Hold on Phase I/II Clinical Trial of tgAAC94 for Inflammatory Arthritis; Phase II Clinical Trial Protocol Design Underway

Targeted Genetics Corp announced that the US FDA removed the hold on the company's phase I/II clinical trial of tgACC94 for inflammatory arthritis, following the agency's review of the safety data thus far on all 127 subjects and all data from a fatal serious adverse event, which led to the death of a patient...

Friday Nov 30, 2007
Drug Update: Abatacept
Researchers continue to argue for the cost-effectiveness of abatacept in treatment-resistant rheumatoid arthritis, but a real-world analysis raises questions about responses in routine clinical use. Safety data show no increased risk of malignancies or infection...

Monday Nov 26, 2007
Abatacept Wins Plaudits in Refractory JIA
The costimulation blocker abatacept may be a safe and effective option for juvenile idiopathic arthritis patients who have exhausted all other therapies...

Wednesday Nov 21, 2007
Combining MTX or Other DMARD With Biologic Seen as Best Strategy for MTX-Resistant Rheumatoid Arthritis
A systematic review of head-to-head trials and prospective cohort studies found little difference among either conventional DMARDs or anti-tumor necrosis factor (anti-TNF) drugs used as monotherapy, but suggests that adding a conventional DMARD to a biologic may be the best strategy for MTX-resistant RA...

Tuesday Nov 20, 2007
Abbott's Humira® Receives Positive Opinion From EMEA for Treatment of Moderate-to-Severe Plaque Psoriasis 
Abbott Laboratories announced that the Committee for Medicinal Products for Human Use (CHMP), granted Abbott a positive opinion recommending approval of Humira® (adalimumab) for the treatment of moderate-to-severe plaque psoriasis...

Monday Nov 19, 2007
TNF-Blocker Plus MTX Slashes Heart Risk in RA
Combination therapy with a TNF-inhibitor plus MTX slashes heart attack risk by 80% in rheumatoid arthritis (RA) patients...

Friday Nov 16, 2007
Certolizumab Induces Faster Responses in RA
Thirty percent of RA patients treated with certolizumab plus MTX reached ACR20 within the first week of treatment; 50% reached ACR20 within 2 weeks...

Thursday Nov 15, 2007
Response to RA Therapy in First 3 Months Predicts Chance of Remission at 1 Year
Rheumatoid arthritis disease activity during the first 3 months of treatment predicts response at 1 year, and even partial response may "reset the baseline" for subsequent treatment...

Tuesday Nov 13, 2007
Anti-IL-12/23 Monoclonal Produces Dramatic Results in Psoriatic Arthritis
The anti-IL-12/23 monoclonal antibody ustekinumab produced dramatic, durable improvements in psoriatic arthritis, according to phase II data reported at the American College of Rheumatology...

Tuesday Nov 13, 2007
Targeted Genetics Reports Positive Interim Phase I/II Results for tgAAC94 in Inflammatory Arthritis; Tests Indicate tgAAC94 Did Not Contribute to Immunosuppression Leading to Fatal SAE
Targeted Genetics Corp, a clinical-stage biotechnology company, announced that interim data from its phase I/II trial of tgAAC94 for inflammatory arthritis suggest that the investigational therapy showed improvement in patient-reported outcome measures...

Tuesday Nov 13, 2007
Infliximab Adds Little to Combined DMARDs for Early RA--Unless You're Fat
Obesity halves an RA patient's chance of remission with conventional combination DMARD treatment, but adding infliximab can overcome this problem...

Monday Nov 12, 2007
Rheumatologists Optimistic About IL-6 Blocker Tocilizumab
The interleukin-6 (IL-6) blocker tocilizumab is safe, effective, and improves quality of life for rheumatoid arthritis (RA) patients...

Monday Nov 12, 2007
Biogen Idec's Baminercept, the First Lymphotoxin-β Pathway Inhibitor in Development, Shows Promise in Phase IIa Trial in RA Patients; Phase IIb Underway 
Biogen Idec announced results from its phase IIa trial of baminercept, the first dual-mechanism, lymphotoxin-β (LT-β) and LIGHT pathway inhibitor in development for the treatment of autoimmune diseases...

Friday Nov 09, 2007
Efalizumab Suspected of Triggering Arthritis in Subset of Psoriasis Patients
A small subset of patients treated with efalizumab for severe plaque psoriasis developed new-onset psoriatic arthritis...

Thursday Nov 08, 2007
Serum Uric Acid May Be Independent Risk Factor in RA Cardiovascular Disease
Elevated serum uric acid, a potentially modifiable problem, may be an independent risk factor for cardiovascular disease in patients with RA...

Thursday Nov 08, 2007
Half of RA Patients Might Reach Remission With Early, Aggressive Use of Conventional DMARDs
If inflammatory arthritis is detected early and treated vigorously, remission is a possibility for 50% of patients...

Thursday Nov 01, 2007
Few Remissions From Switching to Other DMARDs After MTX Failure
If initial MTX fails to produce remission in RA, adding or switching to other conventional DMARDs is also unlikely to produce remissions...

Tuesday Oct 16, 2007
Combination Therapy is Better for RA Patients Who Partially Responded to Long-term Monotherapy
Many RA patients who have partial responses to long-term etanercept or methotrexate monotherapy can be put into remission by combining these drugs...

Wednesday Sep 12, 2007
Trubion's Preliminary Analysis of Phase IIb Results With Immunotherapeutic TRU-015 Show Improvements in RA Signs and Symptoms Compared With Placebo
Trubion Pharmaceuticals, Inc, a biopharmaceutical company creating product candidates to treat autoimmune disease and cancer, announced preliminary analysis of results from a phase IIb randomized, double-blind, placebo-controlled, multicenter clinical trial of its TRU-015 immunotherapeutic product candidate for rheumatoid arthritis (RA)...

Thursday Aug 23, 2007
Roche Announces NICE Approves MabThera® (rituximab) for Patients With Severe RA
Roche Products Ltd  announced that the independent organization NICE has issued final guidance to the NHS approving the use of MabThera^R (rituximab), in combination with methotrexate, for the treatment of severe active rheumatoid arthritis (RA) in adults...

Wednesday Aug 08, 2007
Bristol-Myers Squibb's Orencia® (abatacept) Supplemental Biologics License Application for JIA Accepted by US FDA for Filing and Review
Bristol-Myers Squibb Co announced that the US FDA has accepted the supplemental biologics license application (sBLA) for filing and review of Orencia® (abatacept) to treat pediatric patients with juvenile idiopathic arthritis (JIA) who have had an inadequate response to one or more disease-modifying antirheumatic drugs (DMARDs) such as methotrexate (MTX) or tumor necrosis factor (TNF) antagonists...

Thursday Aug 02, 2007
TNF Inhibitors May Restore Adrenal Function in RA
TNF inhibitors appear to improve adrenal function in some RA patients, resulting in restoration of stable hormonal homeostasis...

Monday Jul 30, 2007
Long-term MTX or TNF-Inhibitors Do Not Increase EBV Load in RA Patients
The immunosuppressant effects of long-term use of methotrexate or TNF-inhibitors by rheumatoid arthritis (RA) patients do not lead to increased Epstein-Barr virus load...Balandraud N, et al. Arthritis Care Res. 2007;57:762-767.

Monday Jul 23, 2007
Birth Defects Reported After First-Trimester Leflunomide
Leflunomide (Arava^R) has been reported to cause teratogenic effects in animals and is suspected of causing blindness and cerebral palsy in the son of a woman who took the drug through the first 21 weeks of gestation.

Friday Jul 13, 2007
Intensive MTX Therapy Plus Computer Guidance Moves More RA Patients into Remission
Intensive methotrexate (MTX) therapy adjusted with the help of a quantitative computerized decision program may move more early rheumatoid arthritis (RA) patients into remission than conventional MTX treatment…Verstappen SMM, et al. Ann Rheum Dis. 2007; May 22; [Epub ahead of print].

Thursday Jul 12, 2007
Roche's Actemraâ„¢ (tocilizumab) Third Phase III Study Achieves Primary Endpoint in RA Patients Who Failed to Respond to Anti-TNFs; Confirms Findings From Previous Multinational Trials
Hoffmann-La Roche Inc announced that the Actemraâ„¢ RADIATE (RheumAtoiD ArthritIs Study in Anti-TNF FailurEs) trial successfully met its primary endpoint in patients with moderate-to-severe active rheumatoid arthritis (RA) who failed to respond to at least one anti-TNF therapy...

Tuesday Jul 03, 2007
Conventional Drugs Can Beat Back Early RA
Two-year data show that intensive treatment with methotrexate (MTX) and intra-articular corticosteroid can reduce X-ray progression in early RA...

Tuesday Jul 03, 2007
Twenty Percent of Pregnant Women With RA Conceived While Taking Potentially Fetotoxic Drugs
The growing use of combination regimens including methotrexate in early RA warrants increased attention to warning patients about potential risks during the first trimester of pregnancy…

Thursday Jun 21, 2007
Early Data Show That Experimental B-Cell Blocker Passes Muster
Ofatumumab (Humax-CD20^TM), an experimental B-cell depleting agent, may be a safe and effective treatment for RA, but how it compares to rituximab remains to be seen...

Tuesday Jun 19, 2007
Single Dose of Denosumab Reduces Bone Erosion in RA
MRI and X-ray data show that a single dose of denosumab reduces progression of bone erosions in RA patients...

Monday Jun 18, 2007
GSK and Genmab Report Positive Phase II Results With Ofatumumab (HuMax-CD20) in Patients With RA
GlaxoSmithKline (PHILADELPHIA, Pennsylvannia) and Genmab A/S (COPENHAGEN, Denmark) announced positive efficacy data from a phase II study of ofatumumab (HuMax-CD20®), a fully human monoclonal IgG1antibody targeting the CD20 antigen on the surface of B-cells, in patients with rheumatoid arthritis (RA)...

Saturday Jun 16, 2007
Certolizumab, First PEGylated TNF-Blocker, May Surpass Older Drugs in Efficacy, Safety
When used with methotrexate, certolizumab pegol (Cimzia) may move rheumatoid arthritis (RA) patients into remission more quickly than currently available TNF-blockers...

Friday Jun 15, 2007
First Phase III Tocilizumab Data Show Rapid Improvement in RA Disease Activity, Confirming Critical Role of IL-6
Results of the first phase III trial of tocilizumab show that the anti-IL-6 monoclonal combined with methotrexate produces fast, sustained improvements in RA signs and symptoms, including a notable number of DAS28 remissions...

Thursday Jun 14, 2007
Steroids Are DMARDS: MTX Plus Prednisolone Provides Durable Benefit in RA
Study confirms "window of opportunity" in early RA where steroids can reduce structural damage…

Wednesday Jun 13, 2007
Stopping AS May Require Earlier Use of TNF-Inhibitors
Inflammation in AS stops once the subchondral bone is eroded and the bone/cartilage interface disappears, so preventing bone erosion and syndesmophyte formation is likely to require early anti-inflammatory treatment, including TNF-inhibitors...

Monday Jun 11, 2007
Centocor's Remicade® (Infliximab) Receives EU Approval as First and Only Biologic for the Treatment of Pediatric Patients With Severe, Active Crohn's Disease
Centocor, Inc, a wholly owned subsidiary of Johnson & Johnson and Schering-Plough Corp, announced that the European Commission has approved a new indication for Remicade (infliximab) allowing for the treatment of severe, active Crohn's disease (CD) in pediatric patients ages 6 to 17 years, who have not responded to conventional therapy including a corticosteroid, an immunomodulator, and primary nutrition therapy, or who are intolerant to, or have contraindications for such therapies...

Thursday Jun 07, 2007
Leflunomide Trumps MTX for Preventing Relapse in Wegener's Granulomatosis; Side Effects Still a Worry
A head-to-head comparison of leflunomide and MTX for Wegener's granulomatosis was stopped early due to higher relapse rates with MTX...

Wednesday May 30, 2007
Bristol-Myers Squibb Receives European Commission Approval for Orencia® in RA
Bristol-Myers Squibb Co (RUEIL-MALMAISON, France) announced that the European Commission has granted approval for Orencia® (abatacept), the first and only selective costimulation modulator of T-cell activation, for the treatment of rheumatoid arthritis (RA)...

Friday May 25, 2007
Accumulating Evidence Supports Adalimumab for Severe Psoriatic Arthritis
Adalimumab (Humira®) is safe and effective for patients with active psoriatic arthritis (PsA) who showed an inadequate response to disease-modifying antirheumatic drugs (DMARDs)...

Thursday May 03, 2007
FDA Approves Labeling Update for Orencia® (Abatacept) to "Inhibiting" Structural Joint Damage in Adults with Moderate-to-Severe RA
Bristol-Myers Squibb Company announced that the US FDA has approved an update to the product labeling for Orencia® (abatacept) regarding the progression of structural joint damage in rheumatoid arthritis (RA) patients...

Tuesday May 01, 2007
MRI Erosions, Edema in RA  Are Due to Inflammatory Infiltrates in Bone Marrow
Bone erosions and bone marrow edema seen with MRI in joints affected by RA are due to inflammatory infiltrates that have invaded the bone marrow...

Monday Apr 23, 2007
Rigel Provides Clinical Update of R788 Phase II Trials in ITP and RA

Rigel Pharmaceuticals, Inc, a clinical-stage drug development company, provided an update on R788, currently involved in ongoing phase II clinical trials in immune thrombocytopenic purpura (ITP) and rheumatoid arthritis (RA)...

Wednesday Apr 18, 2007
Death Forces Early Termination of Study of Infliximab in Systemic Vasculitis
Adverse events, including one death among nine patients treated, forced early termination of infliximab trial in systemic vasculitis...

Monday Apr 16, 2007
Abbott Seeks US and EU Regulatory Approval for HUMIRA® (Adalimumab) in Psoriasis; Receives US FDA Approval in Crohn's Disease
Abbott Laboratories announced that it has simultaneously submitted a supplemental Biologics License Application (sBLA) with the US FDA and a Type II Variation to the European Medicines Agency (EMEA) seeking approval to market HUMIRA® (adalimumab) as a treatment for moderate-to-severe chronic plaque psoriasis, the fifth autoimmune disease targeted for HUMIRA therapy in both the US and Europe...

Tuesday Apr 10, 2007
Aromatase Inhibitors Linked to Increasing Rate of Arthralgias in Cancer Survivors
Aromatase inhibitors have revolutionized breast cancer treatment, but are also contributing to increased rates of arthralgias in cancer survivors and may uncover underlying RA in some cases...

Wednesday Apr 04, 2007
Repeated B-Cell Depletion Safe, Effective Over 5 Years in RA
B-cell depletion with rituximab was effective for an average of 15 months per cycle and was relatively well tolerated for up to 5 repeat cycles in patients with otherwise refractory RA...

Thursday Mar 22, 2007
6000-Patient Open-Label ReAct Study Shows Adalimumab Safe, Effective Alone or With DMARDs in Hard-to-Treat RA
The largest prospective study to date of the use of a TNF-inhibitor in RA shows that adalimumab (Humira®) is safe and effective alone or in combination with standard disease-modifying antirheumatic drugs (DMARDs)...

Thursday Mar 22, 2007
New Studies Urge Closer Monitoring for JIA-Related Uveitis, TNF-Inhibitors Effective For Difficult Cases

New studies report that uveitis occurs in up to 20% of JIA patients, that TNF-inhibitors may be effective in hard-to-treat cases, and that close monitoring for uveitis should continue even during arthritis remissions...

Tuesday Mar 20, 2007
Two-Year BeSt Data Confirm Benefits of Early Combo DMARDs for Early RA, Highlight Importance of Tight Control and Individualized Treatment
Two-year data from the BeSt trial support initial combination therapy, changed as needed to sustain DAS <2.4, as most effective for preventing progression of early RA...

Tuesday Feb 27, 2007
UCB Reports Significant Reduction in Joint Damage From Phase III Results With Cimzia in Rheumatoid Arthritis; Fc Region Present in Conventional Anti-TNFs Is Not Required for Activity
UCB, a global biopharmaceutical company, announced results of an international, multicenter, placebo-controlled phase III study (RAPID 1) involving nearly 1000 patients that evaluated the investigational agent Cimziaâ„¢ (certolizumab pegol)...

Thursday Feb 08, 2007
Steroids Add 60% to DMARD Efficacy in RA

Cochrane Collaboration reviewers say that steroids should be added to the list of drugs that can change the course of rheumatoid arthritis if used early enough...

Wednesday Jan 31, 2007
New Model Predicts Risk of RA
A newly developed, easy-to-use prediction rule may help rheumatologists determine which patients with undifferentiated arthritis (UA) will progress to rheumatoid arthritis (RA) and require early, aggressive treatment...

Monday Jan 29, 2007
MediGene Initiates Phase IIa Clinical Trial of RhuDex®, an Oral Inhibitor of T-cell Activation, in RA
MediGene AG (MARTINSRIED/MUNICH, Germany), the publicly-held biotechnology company targeting autoimmune diseases and cancer announced the initiation of a phase IIa clinical trial of its drug candidate RhuDex®, a novel, orally bioavailable inhibitor of T-cell costimulation via the CD80-CD28 pathway, in patients with severe rheumatoid arthritis (RA).

Thursday Jan 25, 2007
Anti-Infliximab Antibodies Linked to Nonresponse in AS
New research outlines some drawbacks and limitations in the use of TNF-inhibitors among patients with ankylosing spondylitis (AS) and other forms of spondylarthritis...

Tuesday Jan 16, 2007
Can-Fite Completes Enrollment of 250 Patients in Phase IIb RA Trial of CF101, an A3 Adenosine Receptor Agonist; Receives US$1 Million Payment from Seikagaku Corporation
Can-Fite BioPharma Ltd, a clinical-stage drug development company focused on a portfolio of orally bioavailable, highly selective, small molecule A(3) adenosine receptor (A(3)AR) agonists with potent activities in inflammation and cancer, announced the  completion of patient enrollment in a phase IIb rheumatoid arthritis (RA) clinical trial of CF101, an A(3)AR agonist...

Thursday Jan 11, 2007
Combination DMARD Therapy Leads to Sustained Remission in RA
Treating rheumatoid arthritis (RA) with a combination of disease modifying antirheumatic drugs (DMARDs) plus prednisolone results in sustained remission and blocks the progression of radiographic joint damage in a "remarkable proportion" of patients...

Tuesday Jan 09, 2007
Small Study Highlights Role for Etanercept in Rheumatological Manifestations of HCV
Etanercept seems to be safe and effective for the treatment of rheumatological manifestations associated with hepatitis virus C, but more studies are needed before firm  conclusions can be drawn...

Thursday Dec 21, 2006
ZymoGenetics and Serono Begin Phase II Clinical Trial with Atacicept (TACI-Ig) in RA
ZymoGenetics, Inc and Serono announced the start of a phase II clinical trial of their investigational therapeutic atacicept (formerly TACI-Ig) in patients with rheumatoid arthritis (RA). The randomized, double-blind, placebo-controlled, multicenter, dose-finding study will investigate the efficacy of atacicept in patients with an inadequate disease response to prior treatment with TNF inhibitors.

Thursday Dec 14, 2006
Genmab Sees Positive Interim Data for HuMax-CD20 Phase II in Rheumatoid Arthritis; Starts Planning Phase III Studies
Genmab A/S, a human antibody therapeutics company, announced positive results from an interim analysis of the first 100 patients in the ongoing phase II rheumatoid arthritis (RA) study of HuMAX-CD20 (ofatumumab), a fully human monoclonal IgG1 antibody targeting the CD20 antigen on B-cells and currently in clinical development as a treatment for active RA, as well as for chronic lymphocytic leukemia and follicular non-Hodgkin's lymphoma.

Wednesday Dec 13, 2006
RA Remission Often Accompanied by Silent Synovitis
The majority of rheumatoid arthritis (RA) patients who meet ACR remission criteria still have synovitis detectable on MRI or ultrasound...

Monday Dec 11, 2006
Steroids, Cytotoxics Cause More Heart Damage than Biologics in Treating RA
Biologic immunosuppressive agents used to treat rheumatoid arthritis (RA) carry cardiovascular risks similar to that of methotrexate (MTX), but oral glucocorticoids and other cytotoxic RA drugs are more damaging to the heart...

Wednesday Nov 29, 2006
Millennium Begins Phase II Study of CCR1 Antagonist in Rheumatoid Arthritis 
Millennium Pharmaceuticals, Inc announced the initiation of a randomized, double-blind, placebo-controlled, multicenter phase II study of MLN3897, an orally active, small-molecule antagonist of the chemokine receptor CCR1, in patients with rheumatoid arthritis (RA). 

Wednesday Nov 22, 2006
Sosei Ends Development of AD 452 Following Failure to Achieve Primary and Secondary Endpoints in Phase IIb Clinical Trial for Rheumatoid Arthritis
Sosei Group Corporation, a biopharmaceutical company, announced that AD 452, a novel, small molecule cytokine modulator, disease modifying anti-rheumatic drug (DMARD) being developed for the treatment of rheumatoid arthritis (RA) on a background of methotrexate, failed to meet its primary or secondary efficacy endpoints in a phase IIb clinical trial. As a consequence of these results Sosei has decided to discontinue with the development of this compound for the treatment of RA.

Thursday Nov 16, 2006
Immunomedic, UCB Phase III Trial of Epratuzumab in Lupus Patients No Longer on Clinical Hold
Immunomedics, Inc (MORRIS Plains, New Jersey), a biopharmaceutical company focused on developing therapeutic monoclonal antibodies, announced that their partner, UCB, SA (BRUSSELS, Belgium) has received notification from the US FDA that the clinical hold on existing trials with epratuzumab (a humanized IgG1 monoclonal antibody targeting the B-cell specific surface antigen CD22) in patients with systemic lupus erythematosus (SLE) has been lifted.

Thursday Nov 16, 2006
Anti-TNF-α Golimumab (CNTO 148), Under Development by Centocor and Schering-Plough, Provides Sustained Improvement in Moderately-to-Severely Active Rheumatoid Arthritis in Phase II Study
Centocor, Inc (HORSHAM, Pennsylvania), a wholly owned subsidiary of Johnson & Johnson, announced that 1-year data, presented at the 70th Annual Meeting of the American College of Rheumatology in Washington, DC, showed that nearly 75% of patients with moderately-to-severely active rheumatoid arthritis (RA) receiving golimumab (CNTO 148) and methotrexate experienced at least 20% improvement in arthritis symptoms (ACR 20) at week 52.

Wednesday Nov 15, 2006
Three-Year BeSt Results Suggest MTX Plus Infliximab Can Move Some RA Patients Into Drug-Free Remission
Three-year results from the BeSt study suggest that early induction therapy with infliximab plus MTX can bring about remission in RA patients…Van Der Kooij SM, et al. Presented at: ACR 2006 Meeting. 

Tuesday Nov 14, 2006
PROMPT Study Shows "Window of Opportunity" in Early Undifferentiated Arthritis
Early MTX treatment can delay and possibly prevent progression to RA among anti-CCP positive patients who have early, undifferentiated arthritis... van Dongen H, et al. Presented at: ACR 2006 Meeting.

Tuesday Nov 14, 2006
Successful Anti-TNF Treatment Restores Regulatory T-Cell Function in RA
TNF inhibitor treatment can restore some of the lost T regulatory (suppressor) cell functioning in patients with RA, which might contribute to suppression of disease flares... Valencia X, et al. Presented at: ACR 2006 Meeting.

Wednesday Nov 08, 2006
CombinatoRx Syncretic Drug Candidate CRx-102 Achieves Phase II Trial Endpoints in Rheumatoid Arthritis
CombinatoRx, Incorporated announced positive preliminary results of its phase II clinical trial of CRx-102, an oral synergistic combination drug candidate containing the generic cardiovascular agent dipyridamole and an unconventionally low dose (3mg, below the effective human dose) of the generic steroid prednisolone, in rheumatoid arthritis (RA).

Friday Nov 03, 2006
MTX Bests Sulfasalazine as DMARD of First Choice for Inflammatory Polyarthritis
Five-year data show that methotrexate and sulfasalazine have similar clinical effects as first DMARD in patients with inflammatory polyarthritis, but methotrexate is more effective at preventing radiological erosions...

Wednesday Oct 25, 2006
NSAIDs/DMARDs Can Thwart Antibiotic-Refractory Lyme Arthritis
Report highlights effective postantibiotic strategies for treating antibiotic-refractory Lyme arthritis and identifies risk factors for the rare but vexing condition... Steere AC, Angelis SM. Arthritis Rheum. 2006;54:3079-3086

Monday Oct 23, 2006
Etanercept/MTX Uncouple Inflammation and Joint Destruction in RA
RA patients treated with etanercept plus methotrexate have less radiographic progression of joint damage than patients who take either drug alone, even if they continue to have inflammation or other makers of active disease....

Tuesday Oct 10, 2006
Trubion Initiates Phase IIb Clinical Trial of CD20-Targeted TRU-015 for the Treatment of Rheumatoid Arthritis
Trubion Pharmaceuticals, Inc, a biopharmaceutical company focused on developing treatments for autoimmune diseases and cancer, announced it has initiated a phase IIb clinical trial of TRU-015, the company's lead Small Modular ImmunoPharmaceutical (SMIPâ„¢) CD20-targeted drug candidate for the treatment of rheumatoid arthritis (RA) via B-cell depletion...

Thursday Oct 05, 2006
Little Gained From Combining Etanercept and Sulfasalazine in RA
Patients whose RA is active despite treatment with sulfasalazine benefit from switching to etanercept, but combining the two drugs provides little additional benefit... Combe B, et al. Ann Rheum Dis. 2006;65:1357-1362.

Monday Oct 02, 2006
Pulmonary Alveolar Proteinosis Seen in Leflunomide-Treated RA Patient
A case of pulmonary alveolar proteinosis associated with leflunomide treatment for rheumatoid arthritis has been reported... Wardwell NR, et al. Respirology. 2006;11:663-665.

Thursday Sep 28, 2006
RA Skin Problems Related or Due to Disease or Treatment?
Skin problems are more common in RA patients than in those with non-inflammatory diseases, but only steroid-related bruising and athlete's foot appear to be related to either RA itself or its treatment.

Tuesday Sep 26, 2006
Genmab Completes Accrual in Anti-CD20 Antibody Phase II RA Study
Genmab A/S, a biotechnology company that creates and develops human antibodies for the treatment of rheumatoid arthritis (RA) and other inflammatory conditions, cancer, and infectious disease, announced it has completed enrollment in the HuMax-CD20â„¢ (ofatumumab) phase II study to treat patients with active RA who have failed treatment with one or more disease-modifying anti-rheumatic drugs (DMARDs), including biologics.

Monday Sep 25, 2006
Rituximab Quickly Reduces Disease Activity in Treatment-Resistant RA
Rituximab added to methotrexate significantly reduces disease activity in patients whose RA is resistant to TNF inhibitors... Cohen SB, et al. Arthritis Rheum. 2006;54:2793-2806.

Thursday Sep 21, 2006
Abatacept Should Not be Used with Etanercept to Treat RA
The combination of etanercept and abatacept increased serious adverse effects and provided little clinical benefit for patients with RA... Weinblatt M, et al. Ann Rheum Dis. 2006;25 August 2006 [Epub ahead of print]

Tuesday Sep 19, 2006
TNF Inhibitors Do Not Increase Cancer Risk More Than MTX in RA Patients
A study of 1152 RA patients who used biologics and 7306 treated with methotrexate concludes that the risk of cancer is about the same in both groups, once RA disease severity is considered. Setoguchi S, et al. Arthritis Rheum. 2006;54:2757-2764.

Wednesday Sep 13, 2006
Can-Fite BioPharma to Develop Its A3 Adenosine Receptor Agonist (CF101) for Psoriasis
Can-Fite BioPharma, a clinical-stage drug development company focused on a portfolio of orally bioavailable, highly selective, small-molecule A3 adenosine receptor (A3AR) agonists with potent activities in inflammation and cancer, announced the intent to initiate a phase II clinical trial in psoriasis for its lead drug candidate, CF101.

Monday Sep 11, 2006
Small, Portable In-Office MRI Can Monitor Response to Therapy in RA
As RA treatments become more effective and expensive, monitoring response to therapy becomes more important. Two new studies suggest that small, portable MRI devices might help...

Thursday Sep 07, 2006
Rigel Starts Phase II Study of its Oral Kinase Inhibitor, R788, in Rheumatoid Arthritis
Rigel Pharmaceuticals, Inc, announced that it has initiated enrollment and dosing of patients with rheumatoid arthritis (RA) in a phase II study evaluating the efficacy and safety of its lead product candidate, R788, an oral syk kinase inhibitor that blocks the activation of the mast cells, macrophages, and B-cells that promote swelling and an inflammatory response. This multicenter, randomized, double-blind, placebo-controlled, ascending dose, dose ranging study will evaluate up to three doses of R788...

Tuesday Aug 15, 2006
Centocor's REMICADE Receives Expanded Psoriatic Arthritis Indication
Centocor, Inc. announced that the US FDA has expanded marketing approval for Remicade® (infliximab) to inhibiting the progression of structural damage and improving physical function in patients with active psoriatic arthritis (PsA), in addition to reducing the signs and symptoms of active arthritis. 

Friday Aug 11, 2006
Fish Oil Reduces CV Risk Factors, NSAID Requirements in RA Patients
Two tablespoons of fish oil per day significantly improved some cardiovascular risk factors and reduced NSAID requirements in patients with rheumatoid arthritis... Cleland LG, et al. J Rheumatol. 2006 Aug 01; [Epub ahead of print]

Thursday Aug 03, 2006
British Registry Data Show Safety of First-Trimester TNF Inhibitor Exposure, Safety of Later Use Still Unclear
Data from a British registry of TNF inhibitor users suggest that brief exposure to TNF inhibitors during the first trimester of pregnancy is not harmful either to women who inadvertently become pregnant while taking these drugs or to their babies, but raise questions about safety in later pregnancy... Hyrich KL, et al. Arthritis Rheum. 2006;54:2701-2702.

Tuesday Aug 01, 2006
Schering-Plough's REMICADE Receives EU Approval as Monotherapy for Treatment of Psoriatic Arthritis; Abbott's HUMIRA Receives FDA Approval for Treatment of Ankylosing Spondylitis
Schering-Plough Corporation announced that the European Commission approved the use of REMICADE® (infliximab) as monotherapy in the treatment of active and progressive psoriatic arthritis (PsA) in patients who show intolerance to methotrexate (MTX) or for whom MTX is contraindicated.

Wednesday Jul 26, 2006
Can-Fite BioPharma Initiates Multi-National Phase IIb Study of A(3) Adenosine Receptor Agonist (CF101) in Rheumatoid Arthritis
Can-Fite BioPharma announced that it has initiated a phase IIb clinical study of CF101 (1-deoxy-1-[6-[[(3-iodophenyl)methyl]amino]-9H-purine-9-yl]-N-methyl-D-ribofuranuronamide), an A3AR agonist exclusively licensed from the National Institutes of Health (NIH) and Can-Fite's lead drug candidate for rheumatoid arthritis (RA).

Tuesday Jun 27, 2006
Keep Prescribing MTX, Using X-rays for RA, EULAR Told
Pre-symptomatic diagnosis and better drugs should make RA remission for all a possibility within 10 years...Smolen, J. Presented&nbsp;at: EULAR 2006, 21-24 June 2006, Amsterdam, The Netherlands.

Monday Jun 26, 2006
Lupus Treatment Moving "From Serendipity to Sense"
Lupus research has had a very good year... Isenberg DA. EULAR 2006 Meeting; June 21-24, 2006; Amsterdam, The Netherlands. Abstract SP0139.

Saturday Jun 24, 2006
PROMPT Trial Suggests Prompt MTX Stops Undifferentiated Arthritis Progression to RA
Patients with undifferentiated arthritis who are anti-CCP- or RF-positive are likely to have significantly slower progression to rheumatoid arthritis if treated with early MTX... Van Dongen H, et al. 2006 EULAR Meeting; June 21–24; Amsterdam, the Netherlands. Abstract OP0001.

Friday Jun 23, 2006
Tocilizumab Hot New Treatment for Rheumatoid Disorders
The interleukin-6 receptor blocker tocilizumab (Actemra®; Chugai/Roche) emerged at the 2006 EULAR meeting as one of the hottest new prospects for the treatment of rheumatoid disorders... Nishimoto N, et al. 2006 EULAR Meeting; June 21–24, 2006; Amsterdam, the Netherlands.

Friday Jun 23, 2006
Rituximab Inhibits Progression of Joint Damage in Rheumatoid Arthritis
Rituximab plus MTX significantly slows joint damage in RA... Keystone E, et al. 2006 EULAR Meeting; June 21–24, 2006; Amsterdam, the Netherlands.

Thursday Jun 22, 2006
JRA Patients Do Better With Adalimumab, With or Without MTX
Phase III data show that adalimumab quickly and durably reduces disease flares and improves response rates in children with juvenile rheumatoid arthritis... Ruperto N; 2006 EULAR Meeting. Ann Rheum Dis. 2006;65(suppl):OP0007.

Thursday Jun 22, 2006
EULAR Lupus Guidelines Make the Best of Sparse Data
While EULAR experts agree on the best treatment of SLE and recommend an integrated approach to medical care, the lupus task force also warns of a worrying lack of evidence on the benefits of lifestyle modifications and the impact of primary preventive measures... Boumpas D. 2006 EULAR Meeting.

Wednesday Jun 21, 2006
Thalidomide, IL-6 Inhibitors Seen As Possible Treatments in JIA
Thalidomide, IL-6 receptor inhibitors, and genomics were highlights of the overview of JIA presented by Patricia Woo, MD, at the 2006 EULAR Meeting...

Tuesday Jun 20, 2006
Abatacept Effective in MTX-Resistant RA
Abatacept (Orencia®) significantly reduces disease activity and retards radiographic progression in patients with active rheumatoid arthritis despite treatment with methotrexate... Kremer JM, et al. Ann Intern Med. 2006;144:865-876.

Wednesday Jun 14, 2006
4-Year Follow-up Finds Etanercept Safe, Effective in JRA
Long-term data show continued improvement, acceptable safety in children with JRA treated with etanercept for 4 or more years... Lovell DJ, et al. Arthritis Rheum. 2006;5:1987-1994.

Monday Jun 05, 2006
PsA Enthesopathy As Cause of Plantar Fasciitis Responds to TNF Inhibitors
The TNF inhibitors infliximab and etanercept are both effective for the treatment of enthesopathy associated with psoriatic arthritis... Ritchlin CT. J Rheumatol. 15 May 2006; [Epub ahead of print]

Wednesday May 31, 2006
British Clinicians Challenge Restrictive TNF Inhibitor Guidelines
British guidelines for the use of TNF inhibitors are unduly restrictive and should be revised, practitioners charge... Deighton CM, et al. Rheumatology. 2006;45:649-652.

Wednesday May 31, 2006
Synta Initiates Phase II Clinical Trials in RA, CVID for Oral Inhibitor of IL-12 and IL-23
Synta Pharmaceuticals Corp announced the dosing of the first patients in its phase IIa clinical studies of apilimod mesylate in RA and CVID...

Wednesday May 24, 2006
Centocor's Remicade^R Approved by US FDA for Pediatric Crohn's Disease
Centocor Inc announced US FDA approval of Remicade® (infliximab) for reducing signs and symptoms and inducing and maintaining clinical remission in pediatric patients with moderately to severely active Crohn's disease...

Monday May 22, 2006
MTX Plus Steroid Injection Into Joints Helps Control Early RA
Combining MTX with intraarticular steroids provides prompt control of early RA... Hetland ML, et al. Arthritis Rheum. 2006;54:1401-1409.

Tuesday May 16, 2006
Low-Dose Prednisone Durably Slows Joint Damage in Early RA
Two years of low-dose prednisone slows radiographic progression in early RA and appears to change the course of the disease...  Jacobs JW, et al. Arthritis Rheum. 2006; 54:1422-1428.

Thursday May 11, 2006
Adding Zoledronic Acid Improves MTX Efficacy in Early RA
Zoledronic acid added to standard methotrexate treatment reduced the progression of MRI hand and wrist erosions by 61% in patients with early RA, apparently by inhibiting osteoclast activity... Jarrett AJ, et al. Arthritis Rheum. 2006;54:1410-1414.

Thursday May 04, 2006
Adding Alefacept Increases MTX Response in Psoriatic Arthritis
Alefacept plus methotrexate significantly increased response rates in patients with psoriatic arthritis... Mease PJ, et al. Arthritis Rheum. 2006;54:1638-1645.

Monday May 01, 2006
Abbott's Humira^R (Adalimumab) Receives Positive Opinion From EMEA for Ankylosing Spondylitis
Abbott Laboratories, of Abbott Park, Illinois, announced that the Committee for Medicinal Products for Human Use (CHMP), of the European Medicines Agency (EMEA), issued a positive opinion recommending approval of Humira® (adalimumab)...

Monday May 01, 2006
Rituximab Shown to Be Effective Without Steroids in DANCER Study
Two doses of rituximab were shown to be equally effective when added to methotrexate in patients with DMARD-resistant RA, and glucocorticoids did not increase the benefit... Emery P, et al. Arthritis Rheum. 2006;54:1390-1400.

Wednesday Apr 26, 2006
Infliximab Suspected of Worsening Rare MTX Lung Problem
Interstitial pneumonitis occurs in less than 1% of patients treated with methotrexate (MTX), but a recent case report suggests that adding infliximab might increase lung toxicity risk in certain vulnerable patients...  Villeneuve E, et al. J Rheumatol. 2006 Apr 15; [Epub ahead of print]

Monday Apr 17, 2006
Subcutaneous Infliximab Shows Promise in Treating RA
An experimental subcutaneous and intramuscular formulation of the tumor necrosis factor-alpha inhibitor infliximab is well tolerated and associated with a favorable American College of Rheumatology (ACR) response…Westhovens R, et al. J Rheumatol. 2006;33:5. First release April 1, 2006.

Friday Apr 14, 2006
Low Risk of Serious Infections With Infliximab When Used at Approved Dose of 3 mg/kg
New research suggests that the risk of serious infections in RA patients given the approved infliximab dose of 3 mg/kg plus methotrexate (MTX) is similar to the risk among patients receiving MTX alone... Westhovens R, et al. Arthritis Rheum. 2006;54:1075-1086.

Tuesday Apr 04, 2006
Merrimack Pharmaceuticals, Inc, Raises $65 Million to Support Continued Clinical Development of Human Alpha-fetoprotein in RA and Psoriasis
Merrimack Pharmaceuticals, Inc, of Cambridge, Massachusetts, announced that it has raised $65 million in a Series E private equity financing to advance the company's lead product, MM-093, a recombinant version of human alpha-fetoprotein (hAFP)...

Monday Mar 27, 2006
Genmab Reports Positive Phase I/II Clinical Data for HuMax-CD20â„¢ in RA
Genmab A/S, of Copenhagen, Denmark, reported encouraging safety and efficacy data from its 24-week multicenter, double-blind, randomized, placebo-controlled, dose-escalation phase I/II study of HuMax-CD20â„¢...

Monday Mar 27, 2006
EntreMed's 2ME2 Continues to Yield Positive Data in Preclinical Models of RA, Further Supporting the Potential for 2ME2 as a DMARD
EntreMed, Inc, of Rockville, Maryland, announced at the Inflammation and Immune Diseases Drug Discovery and Development Summit held this month in New Brunswick, New Jersey, that daily oral administration (100 mg/kg) of its lead compound, 2-methoxyestradiol (2ME2)...

Monday Mar 27, 2006
Remicade^R Approved in Australia for the Treatment of Early RA and Psoriatic Arthritis
Schering-Plough Corporation, of Kenilworth, New Jersey, announced that the Therapeutic Goods Administration of the Department of Health and Ageing in Australia has revised the indication of Remicade® (infliximab)...

Monday Mar 20, 2006
Vertex's Investigational p38 MAP Kinase Inhibitor Meets Primary Objectives in Phase II Trials for RA
Vertex Pharmaceuticals Inc, of Cambridge, Massachusetts, announced that its oral drug candidate, the p38 mitogen-activated protein (MAP) kinase inhibitor VX-702...

Wednesday Mar 15, 2006
New Single-Blind Trial Suggests Potential Role for Combined Antibiotics in RA
Combined antibiotic therapy using intravenous clindamycin and oral tetracycline may be useful in the management of active rheumatoid arthritis... Gompels LL, et al. J Rheumatol. 2006;33:224-227.

Tuesday Mar 07, 2006
High, Prolonged Inflammatory Activity in Rheumatoid Arthritis Increases Lymphoma Risk
The severity of disease, not its treatments, is a risk factor for the development of malignant lymphomas in rheumatoid arthritis patients... Baecklund E, et al. Arthritis Rheum. 2006;54:692-701.

Monday Mar 06, 2006
Phase III Data for Centocor's Remicade® Show Rapid and Marked Improvement in Moderate to Severe Plaque Psoriasis
Centocor, Inc, of Horsham, Pennsylvania, announced the results from its phase III EXPRESS II study of Remicade® (infliximab)...

Friday Mar 03, 2006
Rituximab Approved for Rheumatoid Arthritis Patients Refractory to TNF-Antagonists
The US Food and Drug Administration has approved the anti-CD20+ B-cell-targeted monoclonal antibody rituximab (Rituxan®) in combination with methotrexate for adult patients with moderate to severe rheumatoid arthritis who experienced an adequate response to one or more tumor necrosis factor antagonists...

Wednesday Mar 01, 2006
Rigel Completes R788 Plus Methotrexate Drug Interaction Study in Patients With RA; Will Initiate Further Clinical Studies This Year
Rigel Pharmaceuticals, Inc, of San Francisco, California, announced preliminary data from a phase I double-blind, placebo-controlled trial to investigate the safety and pharmacokinetics of R788...

Tuesday Feb 21, 2006
TNF Inhibitors May Benefit Refractory Dermatomyositis and Polymyositis
Tumor necrosis factor-alpha inhibitors may be useful for the treatment of some cases of refractory dermatomyositis and polymyositis... Efthimiou P, et al. Ann Rheum Dis. [serial online]. February 13, 2006; doi.10.1136/ard.2005.048744.

Friday Feb 17, 2006
Chelsea Therapeutics Raises $21.5 Million in a Private Placement to Advance Its Antifolate Compound into Phase II trials for RA and Psoriasis
Chelsea Therapeutics International, Ltd, of Charlotte, NC, announced that it has completed a private placement of its common stock...

Thursday Feb 16, 2006
Infliximab Effective Treatment for Refractory Childhood Uveitis
Tumor necrosis factor-alpha inhibition is effective for treatment of childhood uveitis refractory to standard immunosuppressive therapy... Saurenmann RK, et al. Rheumatology Advance Access. February 3, 2006.doi:10.1093/rheumatology/ke1030.

Friday Feb 10, 2006
Adding Doxycycline to Methotrexate Improves Efficacy in Early RA Patients
Initial therapy with methotrexate (MTX) plus doxycycline is more effective than MTX alone among patients with early seropositive rheumatoid arthritis... O'Dell JR, et al. Arthritis Rheum. 2006;54:621-627.

Thursday Feb 09, 2006
Low-Dose Prednisone Increases Risk of Pneumonia in RA Patients
New research showing a dose-related relationship between prednisone use and pneumonia risk in rheumatoid arthritis calls into question the commonly held belief that low-dose prednisone is safe... Wolfe F, et al. Arthritis Rheum. 2006;54:628-634.

Wednesday Feb 08, 2006
Etanercept in Combination with Sulfasalazine, Hydroxychloroquine, or Gold Is Safe and Effective Treatment for RA
Etanercept in combination with sulphasalazine, hydroxychloroquine, or intramuscular gold is an effective and well-tolerated treatment for rheumatoid arthritis. O'Dell JR, et al. J Rheumatol. 2006;33:213-218.

Monday Jan 30, 2006
Can-Fite BioPharma Submits Clinical Protocol to FDA for Multinational Phase IIb Study of A₃ Adenosine Receptor Agonist for RA
Can-Fite BioPharma, of Petach Tikva, Israel, announced that it has submitted a draft protocol to the US Food and Drug Administration...

Wednesday Jan 25, 2006
Insurance Coverage May Influence How TNF-Alpha Inhibitors Are Prescribed
A new observational study of the TNF-α inhibitors infliximab and etanercept has found that Medicare patients with RA are 30% more likely to receive infliximab than those covered by private insurance, findings that suggest that reimbursement policies may drive physicians' prescribing decisions independent of efficacy. However, the emergence of Medicare Part D prescription coverage may change prescribing behavior to favor self-injectable drugs... DeWitt EM, et al. Arch Intern Med. 2006;166:57-63.

Tuesday Jan 10, 2006
ARMADA Trial Supports Long-Term Safety and Efficacy of Adalimumab and Background Methotrexate for RA

Adalimumab plus background methotrexate is a safe and well-tolerated combination that has demonstrated a sustained clinical response and remission in patients with active rheumatoid arthritis (RA) for up to 4 years... Weinblatt ME, et al. Ann Rheum Dis. Published online Dec. 16, 2005; doi:10.1136/ard.2005.044404.

Wednesday Jan 04, 2006
Bristol-Myers Squibb Receives US Approval for Orencia® (Abatacept) for RA
Bristol-Myers Squibb Company announced that the US Food and Drug Administration (FDA) has approved Orencia® (abatacept) for the treatment of rheumatoid arthritis (RA)

Wednesday Jan 04, 2006
Rigel Initiates Phase I Methotrexate Interaction Trial for R788 in Rheumatoid Arthritis
Rigel Pharmaceuticals, Inc, of South San Francisco, California, announced the start of a phase I double-blind, placebo-controlled trial to evaluate R788, an oral syk kinase inhibitor...

Monday Dec 05, 2005
Trials Demonstrate That Earlier Use of DMARDs and MTX Improve Juvenile Arthritis Outcomes 
Earlier use of second-line medications such as methotrexate or disease-modifying antirheumatic drugs (DMARDs) in juvenile arthritis may account for the improved outcomes that rheumatologists have observed in recent years…  Presented at: Annual Meeting of the American College of Rheumatology; November 12–17, 2005; San Diego, Calif. Abstract 126.

Tuesday Nov 22, 2005
Belimumab Data Show Only Modest Clinical Effect in RA
While belimumab is biologically active, safe, and somewhat effective for RA, the magnitude of its effect may not portend a bright future for the novel anti-BlyS agent... Presented at: 69th Annual Meeting of the American College of Rheumatology; November 12–17, 2005; San Diego, Calif. Abstract 1920.

Tuesday Nov 22, 2005
RA Patients Less Likely to Take Prophylactic Aspirin Despite Increased MI Risk
Despite a growing body of evidence suggesting that the inflammation that is a hallmark of rheumatoid arthritis (RA) increases a patient's risk of myocardial infarction or stroke, RA patients are less likely to take prophylactic aspirin than RA-free controls. These findings call attention to the need for rheumatologists to address this discrepancy in care... Presented at: the 69th Annual Meeting of the American College of Rheumatology; November 12–17, 2005; San Diego, Calif. Abstract 1904.

Monday Nov 21, 2005
Genentech, Biogen IDEC's Rituxan® Benefits RA Patients Unresponsive to Methotrexate and Anti-TNF Therapies
Genentech, Inc, and Biogen IDEC, who filed in October for US Food and Drug Administration approval to market rituximab (Rituxan®)...

Thursday Nov 17, 2005
Three Novel and Distinct Agents Show Promise in RA
Three promising new rheumatoid arthritis (RA) drugs—including an oral small-molecule inhibitor that targets a novel adenosine receptor (AR) and a new anti-tumor necrosis factor-alpha (TNF-α) agent—may soon augment the rheumatologist's ever-expanding armamentarium... Presented at: Annual Meeting of the American College of Rheumatology; November 12–17, 2005; San Diego, Calif.

Wednesday Nov 16, 2005
Long-Term Follow-Up Results Show Durable RA Responses with Abatacept
Abatacept, the selective co-stimulation modulator of T-cell activation, has demonstrated sustained clinical benefit during 18 months of treatment in rheumatoid arthritis (RA) patients who had inadequate responses to anti-tumor necrosis factor-alpha (anti-TNF-α) therapy... Presented at: Annual Meeting of the American College of Rheumatology; November 12–17, 2005; San Diego, Calif.

Wednesday Nov 16, 2005
REFLEX Trial Demonstrates Efficacy of Rituximab in RA Resistant to Anti-TNF Therapy
Rituximab, an anti-CD20+ B-cell-targeted monoclonal antibody with an established therapeutic record in the treatment of non-Hodgkin's lymphoma, has shown statistically significant and clinically meaningful improvement in rheumatoid arthritis (RA) patients who are refractory to anti-tumor necrosis factor-alpha (TNF-α) therapy... Presented at: Annual Meeting of the American College of Rheumatology; November 12–17, 2005; San Diego, Calif.

Sunday Nov 13, 2005
Targeted Anti-Cytokine Therapies Emerging as the Future of RA Treatment
Although tumor necrosis factor-alpha (TNF-α) blockade is the new standard of care for patients with moderate-to-severe rheumatoid arthritis (RA), other targeted therapies—including abatacept, B-cell-depleting agents, and anti-interleukin-6 monoclonal receptor antibodies—are emerging to fill the unmet needs of RA patients ... Maini R. Presented at: 69th Annual Meeting of the American College of Rheumatology; November 12–17, 2005; San Diego, Calif.

Friday Nov 04, 2005
BeSt Study Reinforces Importance of Aggressive Combination Therapy for Early RA
The latest results from the BeSt study show that initial combination therapy with either prednisone or infliximab resulted in earlier functional improvement and less radiographic damage after 1 year among early rheumatoid arthritis patients when compared with either sequential monotherapy or step-up combination therapy... Goekoop-Ruiterman YPM, et al. Arthritis Rheum. 2005;52:3381–3390.

Tuesday Nov 01, 2005
US FDA Accepts sBLA and Grants Priority Review Status for Rituxan® for RA
Biogen Idec, Inc, of Cambridge, Massachusetts, and Genentech, Inc, of South San Francisco, California, announced that the US Food and Drug Administration (FDA) has granted priority status to the supplemental Biologics License Application (sBLA) for  Rituxan®...

Monday Oct 31, 2005
Meta-Analysis Points to the Need to Customize Treatment for Subtypes of Juvenile Idiopathic Arthritis
With the increased recognition that radiologic joint and cartilage damage occurs earlier in the course of juvenile idiopathic arthritis than originally thought, a recently released literature review underlines the importance of taking a customized approach to treatment of the disease. However, despite treatment advances, researchers argue that there is no evidence-based consensus on the optimal treatment regimen for several subtypes of JIA. Hashkes PJ, Laxer RM. JAMA. 2005;294:1671-1684.

Monday Oct 24, 2005
Chugai and Roche to Present Phase III Efficacy Data for Tocilizumab in RA at ACR Annual Meeting
Chugai Pharmaceutical Co, Ltd, of Tokyo, Japan, and its strategic partner, F. Hoffmann-La Roche of Switzerland, will jointly present phase III clinical trial results on MRA (tocilizumab)...

Monday Oct 17, 2005
Autoimmune Disease May Contribute to Increase in Non-Hodgkin's Lymphoma, Particularly Among Women
Providing further insight into the dramatic rise in the incidence of non-Hodgkin's lymphoma (NHL) over the last 20 years, a new study suggests that autoimmune diseases, as well as the potent immunosuppressive drugs commonly used for their treatment, may partly account for the increase in NHL, especially among women... Cuttner J, et al. J Rheumatol. 2005;32:1884-1887.

Wednesday Oct 12, 2005
Centocor Obtains Approval in Europe for Remicade® for Psoriasis
Centocor, Inc, and its marketing partner, Schering-Plough Corporation, have announced that the European Commission has granted approval of Remicade^R (infliximab)...

Thursday Oct 06, 2005
Abbott's HumiraR (Adalimumab) Approved in Europe for Psoriatic Arthritis and Severe Rheumatoid Arthritis
Abbott Laboratories announced that it has received US Food and Drug Administration (FDA) approval to market HumiraR (adalimumab)...

Friday Sep 16, 2005
Abatacept Beneficial to Patients with RA Refractory to TNF-α Inhibitors
Abatacept has shown benefit to rheumatoid arthritis patients with inadequate response to tumor necrosis factor (TNF)-α inhibitors, according to the results of a randomized, double-blind study...Genovese MC, et al. N Engl J Med. 2005;353:1114-1123.

Monday Sep 12, 2005
Genmab's HuMax-CD20 in Phase II for RA
Genmab A/S (Copenhagen, Denmark), a biotechnology company that creates and develops human antibodies for the treatment of life-threatening and debilitating diseases, has announced...

Friday Sep 09, 2005
Roche Files RA Indication for MabThera (Rituximab) in Europe
Roche Holding AG (Basel, Switzerland) announced the regulatory filing of MabTheraâ„¢ (rituximab) in Europe...

Friday Sep 09, 2005
FDA Arthritis Advisory Committee Gives Preliminary Go-ahead to Abatacept
A Food and Drug Administration Arthritis Advisory Committee unanimously recommended approval of Orencia®  (abatacept) Tuesday, stating that the benefits of the costimulation blocker for rheumatoid arthritis (RA) outweighed the risks of serious infections like pneumonia and some cancers.

Thursday Sep 01, 2005
RA May Be Becoming Milder With Time
New research suggests that rheumatoid arthritis may have become a milder disease in recent years, perhaps due to more aggressive treatment... Welsing PMJ, et al. Arthritis Rheum. 2005;52:2616-2624.

Monday Aug 29, 2005
Is There a Role for TNF Inhibitors in Refractory Subacute Cutaneous Lupus Erythematosus?
New research demonstrating expression of tumor necrosis factor-α (TNF-α) in refractory subacute cutaneous lupus erythematosus (SCLE) skin lesions suggests a possible role for TNF blockade in the treatment of this disease. Zampieri S, et al. Ann Rheum Dis. August 11, 2005. [Epub ahead of print]

Monday Aug 29, 2005
Entremed's 2ME2 Generates More Positive Preclinical Data in Arthritis Models
EntreMed, Inc, of Rockville, Maryland, a clinical-stage company developing treatments for cancer and inflammatory diseases...

Monday Aug 15, 2005
Abbott's Humira Approved in Europe for Psoriatic Arthritis and Early RA
Abbott Laboratories has received approval from the European Commission to market Humira^R...

Wednesday Aug 10, 2005
Abatacept Reduces Disease Activity and Improves Function in RA Patients Who Failed MTX
Results of a 12-month study show that the first in a class of agents designed to block a costimulatory pathway required for optimum activation of T cells may play an important role in the treatment of rheumatoid arthritis (RA), particularly among patients unresponsive to methotrexate (MTX)... Kremer JM, et al. Arthritis Rheum. 2005;52:2263-2271.

Friday Aug 05, 2005
RA Patients With High BMI Have Lower Mortality
In a finding that runs contrary to the recognized relationship between increased weight and mortality, a new study has found that rheumatoid arthritis (RA) patients with a high body mass index had a lower risk of death than their leaner counterparts... Escalante A, Haas RW, del Rincón I. Arch Intern Med. 2005;165:1624-1629.

Sunday Jul 31, 2005
UCB's Cimzia Demonstrates Positive Results in Phase III Trials for Crohn's Disease
USB Pharma, Inc, of Atlanta, Georgia, the biopharmaceutical subsidiary of international pharmaceutical...

Thursday Jul 21, 2005
Swedish Study Clarifies Connection Between TB, RA, and Use of TNF-α Inhibitors
Irrespective of whether TNF-α inhibitors were administered, Swedish patients with RA were at an increased risk of TB, and TB risk is further heightened by use of biologic agents... Askling J, et al. Arthritis Rheum. 2005;52:1986-1992

Wednesday Jun 29, 2005
EMEA Recommends HumiraR as First Line for Moderate-to-Severe RA
Abbott Laboratories announced that the European Medicines Agency (EMEA) has recommended approval of HumiraR (adalimumab) for first-line treatment of moderate-to-severe early rheumatoid arthritis (RA).

Friday Jun 17, 2005
Vertex Inhibitor of p38 MAP Kinase Starts Phase II in RA
Vertex Pharmaceuticals Inc has initiated a 3-month Phase II clinical trial of VX-702, an orally administered small molecule inhibitor of p38 mitogen-activated protein (MAP) kinase, for the treatment of rheumatoid arthritis (RA).

Thursday Jun 16, 2005
Chelsea Launches Phase I Trial of Its Lead Antifolate Compound
Chelsea Therapeutics, Inc. announced the initiation of a Phase I clinical trial in the UK of its lead orally available, metabolically inert antifolate (CH-1504), which, in a nonpivotal, independent, 6-month pilot clinical study involving 20 rheumatoid arthritis (RA) patients in Peru suggested a lower toxicity and improved tolerability, and increased effectiveness versus methotrexate (MTX), even among patients who had previously failed to demonstrate improvement with MTX.

Thursday Jun 16, 2005
TEMPO Demonstrates Effects of TNF-α Blockade Over 3 Years
The benefits of continuous treatment with etanercept and methotrexate persist for at least 3 years, and, as more patients achieve remission, researchers' focus may turn to determining whether patients can safely discontinue TNF inhibitors...Presented at: Annual European Congress of Rheumatology of EULAR; June 8-11, 2005; Vienna, Austria.

Wednesday Jun 15, 2005
Apratastat, an Experimental Dual Acting Biologic Agent Shows Early Promise for RA
A novel, oral, small-molecule dual inhibitor of TNF-α-converting enzyme and matrix metalloproteinases has been shown in early trials to target two of the factors known to cause inflammation in RA... Fleischmann R, et al. Presented at: Annual European Congress of Rheumatology of EULAR; June 8-11, 2005; Vienna, Austria.

Wednesday Jun 15, 2005
Alefacept in Combination With Methotrexate Evaluated for the Treatment of Psoriatic Arthritis
A 6-month study of the memory T cell suppressor alefacept suggests that the agent will be an effective tool in the armamentarium against PsA... Presented at: Annual European Congress of Rheumatology of EULAR; June 8-11, 2005; Vienna, Austria.

Monday Jun 13, 2005
IL-6 Blocker Shows Promise in Systemic Onset Juvenile Idiopathic Arthritis
More evidence emerging on the therapeutic potential of the experimental IL-6 blocker tocilizumab in the management of severe SJIA... Presented at: Annual European Congress of Rheumatology of EULAR; June 8-11, 2005; Vienna, Austria.

Saturday Jun 11, 2005
Methotrexate Together With Folic Acid Slashes Cardiovascular Risk in RA Patients
Study highlights cardioprotective role for MTX plus folic acid in RA and identifies disease activity as an important risk factor for heart disease...Presented at: Annual European Congress of Rheumatology of EULAR; June 8-11, 2005; Vienna, Austria.

Friday Jun 10, 2005
Treatment of RA Reduces Cardiovascular Mortality
Analysis of a large RA database reveals that treatment with MTX or anti-TNF-α drugs causes a significant decrease in mortality, specifically in death due to cardiovascular and pulmonary disease... Presented at: Annual European Congress of Rheumatology of EULAR; June 8-11, 2005; Vienna, Austria.

Thursday Jun 09, 2005
Trials Examine Efficacy and Safety of B-cell Depletion in RA
Favorable results from the DANCER trial and other studies of rituximab suggest that this anti-CD20 monoclonal antibody may be a promising therapy, particularly for refractory patients... Emery P, et al. Presented at: Annual European Congress of Rheumatology of EULAR;  June 8-11, 2005; Vienna, Austria.

Thursday Jun 09, 2005
Abatacept Inhibits Structural Damage in RA Patients with Inadequate Response to Methotrexate
New studies help define and clarify potential niche for costimulation blockade in autoimmunity...Presented at: Annual European Congress of Rheumatology of EULAR; June 8-11, 2005; Vienna, Austria.

Monday Jun 06, 2005
Trials Outline Effective Strategies for the Use of Existing Therapies in Ankylosing Spondylitis
Four new studies highlight ways to use non-steroidals, biologics, and methotrexate in ankylosing spondylitis. Marzo-Ortega H, et al. Ann Rheum Dis. 2005 May 26; [Epub ahead of print].

Friday Jun 03, 2005
Recombinant Version of Alpha-Fetoprotein May Hold Promise in RA and Other Autoimmune Diseases
As a Phase II trial begins, experts are cautiously optimistic that the experimental immunomodulating agent may be safer than existing RA treatments, and that the work may help explain why RA tends to remit during pregnancy...National Jewish Medical and Research Center [press release]; June 2, 2005.

Tuesday May 17, 2005
Study Suggests That Standardized Criteria Are Needed to Gauge Remission in RA
Rates of remission vary by criteria, but experts agree that new standards should include both clinical and radiographic measures. Mäkinen H, et al. J Rheumatol. 2005;32:796-800.

Tuesday May 17, 2005
Infliximab Approved for Treatment of Psoriatic Arthritis
Infliximab joins etanercept as an anti-TNF-α treatment option for patients with active psoriatic arthritis...FDA approves Remicade® for ninth indication: psoriatic arthritis [press release]. Malvern, Pa: Centocor, Inc; May 17, 2005.

Thursday May 12, 2005
Arakis RA Drug Completes Phase IIa Trial
Arakis Ltd announced that in a multicenter Phase IIa, placebo-controlled study, its candidate rheumatoid arthritis compound AD 452, a novel small-molecule cytokine modulator, demonstrated acceptable pharmacokinetics, safety, and tolerability in RA patients already receiving methotrexate.

Friday May 06, 2005
Use of DMARDs and Referral to Rheumatologists Too Low in Rheumatoid Arthritis Patients
A pre-biologic therapy era population study in British Columbia suggests that too few physicians are adhering to treatment guidelines for rheumatoid arthritis for early and aggressive intervention, delaying the "window of opportunity" when effective therapy can induce radiographic regression... Lacaille D, et al. Arthritis Rheum. 2005;53:241-248.

Friday Apr 22, 2005
High-Dose Methotrexate Particularly Effective for Polyarticular Juvenile Rheumatoid Arthritis
A head-to-head trial comparing leflunomide and methotrexate monotherapy showed that both drugs demonstrated significant improvement in ACR Pediatric 30 responses through a 48-week course of therapy...Silverman E, et al. New Engl J Med. 2005;352:1655-1666.

Thursday Apr 14, 2005
Phase III RituxanR Study Demonstrates Clinical Improvement in Treatment-resistant RA
Following positive preliminary findings from a Phase IIb study that evaluated the efficacy and safety of the approved cancer drug Rituxan in rheumatoid arthritis (RA) patients, Genentech Inc, Biogen Idec and Roche Pharmaceuticals announced that a recent Phase III study has met its primary endpoint based on clinical improvement (ACR 20 responses) at week 24.

Tuesday Apr 12, 2005
Limited Dose Increase Effective in Patients Initially Unresponsive to Infliximab
RA patients who show an insufficient clinical response to 3 mg/kg infliximab every 8 weeks can benefit from a limited dose increase of 100 mg from week 30 onward... Durez P, et al. Rheumatology. 2005;44:465-468.

Wednesday Mar 23, 2005
IL-1 Blocker Anakinra Safe and Effective in Small Study of Severe Lupus Arthritis Patients
Accumulating evidence suggests that anakinra may find a niche in IL-1-driven diseases such as juvenile arthritis, adult onset Still's disease, and severe lupus arthritis...Ostendorf B, et al. Ann Rheum Dis. 2005;64:630-633.

Sunday Mar 13, 2005
Markers of Systemic Inflammation May Be Independent Risk Factors for Cardiovascular Death in Patients With Rheumatoid Arthritis
A new study indicates that ESR may be predictive of CV mortality and suggests that tighter control of inflammation may help improve long-term outcomes for RA patients...Maradit-Kremers H, et al. Arthritis Rheum. 2005;52:722-732.

Wednesday Dec 22, 2004
UVA-1 Light Useful as Adjuvant Therapy for Systemic Lupus Erythematosus
A new study by Dutch researchers has found that UVA-1 cold light therapy significantly decreases validated disease activity indices in patients with moderately active systemic lupus erythematosus (SLE) without causing significant adverse effects... Polderman MCA, et al. Rheumatology. 2004;43:1402-1404.

Tuesday Dec 21, 2004
SLE Patients Treated with TNF-ÃŽalpha Blockade Show Improvement
Study indicates that TNF-alpha blocker may reduce SLE disease activity in patients' joints and kidneys, without serious adverse events; need for larger clinical trials cited... Aringer M, et al. Arthritis Rheum. 2004;50: 3161-3169.

Monday Dec 13, 2004
Synovial Tissue Interleukin-18 Expression Correlates With Inflammatory Arthritis Disease Activity
New study underscores the important proinflammatory role of IL-18 in the pathophysiology of inflammatory arthritis, and suggests that treatment that inhibits or neutralizes endogenous IL-18 may become an effective tool in controlling synovial tissue inflammation&Rooney T, et al. Ann Rheum Dis. 2004;63:1393-1398.

Friday Dec 03, 2004
Leflunomide Associated With Lower Rate of Adverse Events Than Other DMARDs, Large Cohort Study Finds
Study of more than 40,000 patients showed that the AE profile of leflunomide, alone or in combination with methotrexate, was comparable to that of other DMARDs used in the treatment of rheumatoid arthritis...Cannon GW. J Rheumatol. 2004;31:1906-1911.

Monday Oct 25, 2004
Leflunomide-Methotrexate Combination Equivalent in Safety to Leflunomide Alone for RA
A five-year study involving over 5000 RA patients showed no increase in mortality or long-term serious adverse events... Ta KT, et al. Presented at: Annual Meeting of the American College of Rheumatology; October 20, 2004; San Antonio, Tex.

Monday Oct 25, 2004
Leflunomide-Methotrexate Combination Equivalent in Safety to Leflunomide Alone for RA

A five-year study involving over 5000 RA patients showed no increase in mortality or long-term serious adverse events... Ta KT, et al. Presented at: Annual Meeting of the American College of Rheumatology; October 20, 2004; San Antonio, Tex.

Thursday Oct 21, 2004
Leflunomide-Methotrexate Combination Equivalent in Safety to Leflunomide Alone for RA
A five-year study involving over 5000 RA patients showed no increase in mortality or long-term serious adverse events... Ta KT, et al. Presented at: Annual Meeting of the American College of Rheumatology; October 20, 2004; San Antonio, Tex.

Thursday Oct 21, 2004
State-of-the-Art Lectures Reflect Pioneering Research in Rheumatology in the Past Year

The speakers highlighted new research in basic science, including genetic mechanisms at work in RA, and in clinical studies that further understanding of the efficacy of various therapeutic strategies…Barton A, et al. Arthritis Rheum. 2004.;50:1117-1121; Edwards JC, et al. N Engl J Med. 2004;350:2572-2581.

Thursday Oct 21, 2004
Treating Early and in Combination May Lessen Damage in Rheumatoid Arthritis
An emerging body of clinical evidence supports the concept that combination therapy with an antitumor necrosis factor-α agent and methotrexate brings symptomatic relief and reduces radiographic progression... Breedveld FC, et al. Presented at: Annual Meeting of the American College of Rheumatology; October 20, 2004; San Antonio, Tex.

Wednesday Oct 20, 2004
New Phase III Trial With Abatacept Gives Hope to Methotrexate Nonresponders

A phase III clinical trial reported that nearly half of rheumatoid arthritis patients receiving monthly injections of the T-cell inactivator abatacept achieved at least a 50% reduction in symptoms... Kremer J, et al. Presented at: Annual Meeting of the American College of Rheumatology; October 19, 2004; San Antonio, Texas.

Tuesday Oct 19, 2004
Studies of TNF-Alpha Blockers in Rheumatoid Arthritis Focus on Understanding Safety Issues

A new postmarketing surveillance analysis shows that infliximab is safe at approved doses, and patients have no greater risk of infection than those taking methotrexate ... Yocum DE et al. Presented at: Annual Meeting of the American College of Rheumatology; October 19, 2004; San Antonio, Tex.

Tuesday Oct 19, 2004
Emerging Data Underscore Long-Term Efficacy of Adalimumab in Combination With Methotrexate for RA

Several clinical trials presented at the ACR annual meeting demonstrated that the combination of adalimumab and MTX achieved clinical remission and inhibition of structural damage for up to 4 years... Schiff MH et al. Presented at: Annual Meeting of the American College of Rheumatology; October 19, 2004; San Antonio, Tex.

Tuesday Oct 12, 2004
Combination Step-Down Regimen Enhances Disease Control Over Sulfasalazine Monotherapy for RA, Without Adding Cost

A combination regimen consisting of prednisolone, methotrexate, and sulfasalazine may produce more robust clinical responses at equal or lower cost than sulfasalazine alone for the treatment of early rheumatoid arthritis... Korthals-de Bos I et al. J Rheumatol. 2004;31:1709–1716.

Monday Oct 04, 2004
FDA Approves Etanercept as Pre-Filled Syringe, Infliximab as First-Line Therapy for Moderate to Severe RA

The FDA has approved etanercept (Enbrel) as a pre-filled syringe formulation for once weekly use, and granted approval for a supplemental labeling change stating that the medication can induce a major clinical response in patients with rheumatoid arthritis (RA). In another regulatory decision, the FDA has approved the use of infliximab (Remicade) in combination with methotrexate as a first-line treatment for patients with RA.

Wednesday Sep 15, 2004
Advances in anti-TNF Therapy for RA

Two studies give insight regarding the time after RA onset to introduce anti-TNF therapy, and which doses to use to get an optimal response. (Baumgartner SW, et al. J Rheumatol. 2004;31:1532-1537; Stern R, Wolfe F. J Rheumatol. 2004;31:1538-1545.)

Thursday Sep 02, 2004
B Lymphocyte Depletion Seen with Rituximab in Seropositive RA Patients
A treatment often used in B-cell non-Hodkin's lymphoma may have promise for methotrexate-refractory RA patients.

Monday Jun 28, 2004
The Best Trial: Clinical and Radiological Outcomes in Patients with Early RA

Results from the BeSt trial show favorable results for aggressive strategies using combination DMARDs and regimens with TNF antagonists. (De Vries-Bouwstra JW, et al. BeSt Trial Group.)