Remicade
Company: Centocor
Approval Status: Approved February 2002
Treatment for: Rheumatoid arthritis
Areas: Musculoskeletal; Rheumatology
| General Information | Clinical Results | Side Effects | Mechanism of Action | Additional Information |
General Information
RA is a debilitating, chronic disease that affects more than two million Americans. This autoimmune disease causes the body's immune system to attack multiple joints, leading to pain, swelling and eventually to irreversile joint damage.
Clinical Results
The approval of Remicade for improvement in physical function compromised by RA is supported by a two year double-blind, placebo-controlled study that evaluated changes in physical function due to treatment with Remicade and methotrexate, compared to methotrexate alone. The primary endpoint of the trials, which included 428 subjects, was the changes in physical function and disability from baseline to study end.
Those who received Remicade and methotrexate experienced statistically significant improvement compared to those adminstered only methotrexate. Improvements were evident after 54 weeks of treatment and were sustained through out the entire 102 weeks.
Side Effects
Adverse events associated with the use of Remicade may include (but are not limited to) the following:- Upper respiratory infection
- Cough
- Sinusitis
- Headache
- Rash
- Abdominal pain
Mechanism of Action
Remicade (infliximab) is a chimeric monoclonal antibody that targets and binds to tumor necrosis factor alpha (TNF-a). TNF-a is a key factor in regulating the inflammation in RA. By inactivating TNF-a, the inflammatory process is significantly diminished from the start.Additional Information
For additional information on Remicade, please visit Remicade.The FDA drug information shown here is licensed from Thomson CenterWatch. The information provided here is for general educational purposes only and does not constitute medical or pharmaceutical advice which should be sought from qualified medical and pharmaceutical advisers.



