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Found 17 result(s) FROM 1963 pages containing the term 'golimumab'.
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...
Wednesday Aug 05, 2009
Black Box Added to TNF Inhibitors for Kids, Teens
The FDA has expanded TNF blocker “black box” warnings to include lymphoma and other cancers in children and teens, leukemia in all patients, and new-onset psoriasis...
Tuesday Jun 16, 2009
Golimumab for Psoriatic Arthritis Still Effective at 2 Years
2-Year GO-REVEAL data show durable PsA response to golimumab...
Friday May 22, 2009
Johnson & Johnson Wants Remicade Back
J&J is going to court to end its Remicade partnership with Schering-Plough due to a merger with Merck...
Thursday May 07, 2009
Abbott Sues Centocor Over Simponi Rights
Court fights over TNF inhibitors expand with Simponi approval...
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)...
Tuesday Nov 18, 2008
Centocor's Golimumab Gives Durable Skin, Joint Relief in Psoriatic Arthritis, ACR Studies Say
More than half of active psoriatic arthritis patients receiving subcutaneous injections of 50 mg or 100 mg of golimumab (CNTO 148) every 4 weeks showed improvements that lasted through 1 year in the joint and skin symptoms...
Thursday Jul 03, 2008
Centocor Requests Approval From FDA of Golimumab for the Treatment of RA, Psoriatic Arthritis, and Ankylosing Spondylitis
Centocor submitted a Biologics License Application to the US FDA requesting the approval of golimumab, a human anti-TNFα monoclonal antibody, as a monthly subcutaneous treatment for adults with active forms of RA, PsA, and AS...
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...
Wednesday Mar 19, 2008
Centocor, Schering-Plough Submit Marketing Authorization Application Requesting EU Approval of Golimumab to Treat RA, PsA, AS
Centocor, Inc and Schering-Plough Corp are seeking EU approval of golimumab, which targets and neutralizes both the soluble and membrane-bound forms of TNFα, to treat RA, PsA, and AS...
Thursday Nov 08, 2007
Centocor, Schering-Plough's Anti-TNF Golimumab Significantly Improved Articular, Skin, and Nail Manifestations in Patients With Psoriatic Arthritis in Phase III Study; Met Primary and Major Secondary Endpoints
Centocor, Inc, a wholly owned subsidiary of Johnson & Johnson, announced that patients with active psoriatic arthritis (PsA) receiving monthly subcutaneous injections of golimumab experienced significant and sustained improvements in the joint and skin manifestations of the disease, according to findings from the largest phase III biologic study (GO-REVEAL trial) in PsA subjects...
Thursday Nov 08, 2007
Centocor, Schering-Plough's Anti-TNF Golimumab Significantly Reduced Signs and Symptoms of AS in Phase III Study; Monthly Treatment Yielded Marked Improvements in Physical Function
Centocor, Inc, a wholly owned subsidiary of Johnson & Johnson, announced that more than half of patients receiving monthly subcutaneous injections of golimumab 50 mg and 100 mg experienced significant and sustained improvements in the signs and symptoms of active ankylosing spondylitis (AS), according to the phase III study (GO-RAISE trial) results...
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.
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.
Wednesday Feb 01, 2006
EMEA Recommends Approval of Remicade® for Ulcerative Colitis
Centocor, Inc, has announced that the Committee for Medicinal Products for Human Use of the European Union's European Medicines Agency (EMEA) has recommended the approval of RemicadeR for ulcerative colitis...
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.
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