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Found 37 result(s) FROM 1963 pages containing the term 'TNF-alpha'.
Thursday Nov 05, 2009
TNFα Weakens Bones in Diabetes
High levels of TNF-α in diabetics accelerates cartilage loss, weakens bones, and slows fracture healing...
Wednesday Oct 07, 2009
TNF Blockade in SLE? The Plot Thickens
Brief therapy with 4 infusions of infliximab plus azathioprine produces relatively safe, durable improvements in refractory lupus nephritis...
Tuesday Jul 07, 2009
Quercetin Boosts Exercise Capacity
New research shows that quercetin supplementation boosts endurance and maximal oxygen capacity in healthy, active but untrained men and women...
Tuesday Jun 16, 2009
Golimumab for Psoriatic Arthritis Still Effective at 2 Years
2-Year GO-REVEAL data show durable PsA response to golimumab...
Thursday May 07, 2009
Abbott Sues Centocor Over Simponi Rights
Court fights over TNF inhibitors expand with Simponi approval...
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...
Thursday Jul 19, 2007
ACR REF Campaign Taps Brightest Minds to Cure RA
The American College of Rheumatology Research and Education Foundation has awarded $6 million in grant money to 15 arthritis researchers as part of a new "Within Our Reach: Finding a Cure for Rheumatoid Arthritis" campaign.
Friday Jul 06, 2007
Chi-Med Announces Positive Phase II Data for Botanical Compound, HMPL-004, in Ulcerative Colitis
Chi-Med, the Hutchison Whampoa-backed pharmaceutical and healthcare group, announced positive results for its phase II proof-of-concept study for HMPL-004 in mild-to-moderate ulcerative colitis (UC).
Wednesday May 23, 2007
Celgene to Advance Clinical and Regulatory Development of Oral Anti-Inflammatory Agents Based on Successful Phase II Trial in Psoriasis; Expands Clinical Program to Include RA and PsA
Celgene Corp (SUMMIT, New Jersey), an integrated global biopharmaceutical company engaged in the discovery, development, and commercialization of novel therapies for the treatment of inflammatory diseases and cancer, announced plans to advance its leading oral anti-inflammatory candidates to address a broad range of inflammatory diseases...
Monday Dec 04, 2006
Hollis-Eden's Steroid Hormone Preclinical Drug Candidate HE3286 Gains Positive Data in Model of RA
Hollis-Eden Pharmaceuticals, Inc, developing a proprietary new class of small molecule compounds that are metabolites or synthetic analogs of adrenal steroid hormones, announced data on an experimental drug candidate, HE3286, an orally active, second-generation, synthetic steroid hormone currently in preclinical study for the treatment of autoimmune diseases and inflammatory disorders.
Monday Nov 27, 2006
Synovial Cells Predict Response to TNF Inhibitors
The secret to why some RA patients respond to anti-TNF-α drugs and others do not may lie in the synovium…Tak P, et al. Presented at ACR 2006 Meeting.
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.
Monday Jul 31, 2006
Expert Scientific Group Proposes Recommendations to Improve Safety of First-In-Man Clinical Trials Following TeGenero's TGN 1412 Drug Trial
The Expert Scientific Group on phase I clinical trials, an independent committee established by the UK Secretary of State for Health to examine the safety and design of first-in-man clinical studies involving biologic molecules with novel mechanisms of action, new investigational agents with a highly species-specific action, and new drugs directed toward immune system targets, has published its interim report for public comment.
Wednesday May 24, 2006
Centocor's RemicadeR 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 08, 2006
Additional Neuropathies Linked to TNF Inhibitors
Guillain-Barré syndrome, demyelinating and axonal neuropathies, and a central nervous system syndrome have been reported recently in patients treated with TNF inhibitors... Shin I-SJ, et al. Arthritis Rheum. 2006;54:1429-1434; Jarand J, et al. J Rheumatol. 2006;33:1018-1020.
Monday May 01, 2006
Abbott's HumiraR (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)...
Wednesday Apr 26, 2006
Direvo Biotech Appears Poised to Advance Its Lead Preclinical Candidate, a Protease Specific for TNF-Alpha
Direvo Biotech Appears Poised to Advance Its Lead Preclinical Candidate, a Protease Specific for TNF-Alpha
Wednesday Apr 26, 2006
TNF-alpha Inhibitors Increase Postop Infection Risk in RA Patients
The first systematic investigation linking TNF inhibitor therapy in RA to postoperative infections suggests that clinicians should consider interrupting anti-TNF treatment prior to orthopaedic surgery procedures... Giles JT, et al. Arthritis Rheum. 2006;55:333-337
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
RemicadeR 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...
Monday Mar 20, 2006
Centocor's Remicade® First Biologic to Receive EU Marketing Authorization for Ulcerative Colitis
Centocor, Inc, of Horsham, Pennsylvania, and Schering-Plough Corporation, of Kenilworth, New Jersey, have announced that the European Commission has granted marketing authorization for Remicade®...
Monday Feb 13, 2006
Inflabloc Pharmaceuticals Closes $6 Million in Series C Financing and Announces Merger With MantiCore Pharmaceuticals
Inflabloc Pharmaceuticals, Inc, of Salt Lake City, Utah, has announced the closing of $6 million in Series C financing, co-led by Friedli Corporate Finance...
Wednesday Jan 25, 2006
Targeted Genetics Restructures to Advance Anti-TNF-Alpha Agent tgAAC94 for Inflammatory Arthritis
Targeted Genetics Corporation, of Seattle, Washington, announced the restructuring of its operations...
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 Dec 20, 2005
Borean Achieves Preclinical Validation of TNF-Alpha Antagonist Derived from C-Type Lectin Domain Library
Borean Pharma A/S of Aarhus, Denmark, announced that its proprietary C-Type Lectin Domain (CTLD)–derived trimeric tumor necrosis factor-alpha (TNF-a) antagonist demonstrated a dose-dependent slowing of polyarthritis disease progression in transgenic mice expressing human TNF-a...
Tuesday Dec 13, 2005
Domantis Raises $29 Million in Series B Financing to Advance Its Human Domain Antibody (dAb) Therapeutics
Domantis Ltd has announced the acquisition of $29 million in series B financing from existing investors as well as new investors Novo Nordisk and MC Life Science Ventures...
Tuesday Nov 15, 2005
Despite Demonstrated Efficacy of Anti-TNF Therapies, Many Patients Stop Treatment
While biologic therapies targeted against tumor necrosis factor-alpha (TNF-α) have built a "satisfactory" track record in rheumatologic conditions, this emerging standard of care is still marked by a loss of efficacy over time and the withdrawal of patients from their initial therapy, indicating a need for improvement... Presented at: 69th 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.
Thursday Jun 30, 2005
Debiopharm and Neovacs to Develop Anti-TNF-Alpha Therapeutic Vaccine
Debiopharm SA, a Swiss drug development company, and Neovacs SA, a French biotechnology company specializing in anticytokine immunogens, announced the execution of a license and equity agreement for the development of Neovacs' tumor necrosis factor-alpha (TNF-α) kinoidR, a nontoxic immunogenic cytokine derivative that, in the presence of a T-helper carrier protein, triggers an active human polyclonal antibody immune response against TNF-α, while avoiding the generation of anti-idiotypic antibodies (antibody resistance).
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.
Thursday Jun 09, 2005
AVANIR/Novartis Agreement: Develop MIF Therapies for Inflammatory Diseases
AVANIR Pharmaceuticals, a drug discovery and development company, announced the signing of an agreement with Novartis Pharmaceutical Corp to develop orally active small molecule therapeutics targeting macrophage migration inhibitory factor (MIF), a proinflammatory cytokine that is thought to play a critical role in the pathology of inflammatory diseases such as rheumatoid arthritis, psoriasis, and inflammatory bowel disease.
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.
Monday Oct 18, 2004
MRI Has Modest Predictive Value in Detecting Response to TNF Therapy in Ankylosing Spondylitis
Treatment responders had a higher activity index on MRI than did nonresponders, but the difference was less marked than investigators expected... Rudwaleit M, Listing J, Brandt J, Braun J October 18, 2004, Sieper J. Prediction of a major clinical response (BASDAI 50) to TNF-alpha blockers in ankylosing spondylitis. Ann Rheum Dis. 2004; 63:665-670.
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 Jul 28, 2004
Survey Raises Awareness About the Impact of Psoriasis on Relationships and Daily Life
The results of a national survey emphasize the impact of psoriasis on intimate relationships, social activities, and other aspects of daily life.
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