Study: Enbrel Safe After Six-Month Treatment For Rheumatoid Arthritis
Unregistered User
If this is not your name, click here.
Contact Us | Order Now | Journals | Bookstore | Register a colleague
 
  SEARCH  
News
Bookstore
Medline
The Web
Meetings & Congresses
Complete Doctor's Guide
 


 EXPLORE :
 news  All News
 webcasts All Webcasts
 All cases All Cases
 Meetings All Meetings & Congresses
 Medical All Medical Resources

top





New drugs / indications

English Dictionary

Medical Dictionary

Thesaurus



Warning | Privacy | Awards



 Favourite Journals 

Click here to choose your favourite journals


 Favourite Sites 

Click here to choose your favourite sites


 Languages 



  




Study: Enbrel Safe After Six-Month Treatment For Rheumatoid Arthritis

SEATTLE, April 11, 1997-- Preliminary results from an ongoing safety trial for Enbrel(TM) suggest that the drug can be safely administered to patients with rheumatoid arthritis for six months. Enbrel is a soluble (free-floating) tumor necrosis factor receptor (TNFR) and part of a new class of biologic drugs aimed at inhibiting the biological effects of TNF.

Study results were reported today at the regional American College of Rheumatology Meeting in Chicago by Investigator Larry W. Moreland, MD, of the University of Alabama at Birmingham.

"This trial has so far shown that TNF receptor can be given safely to patients for six months with infrequent and tolerable side effects," said Dr. Moreland. "This is important for patients with a chronic disease like rheumatoid arthritis."

The ongoing, open-label, multi-center study is designed to measure the long-term safety of Enbrel and clinical effects as determined by improvements in tender and swollen joints. Improvements in clinical endpoints were consistent with previously reported results. Forty-one patients received the drug for at least six months in this trial. All patients had previously received the drug for a maximum of three months in earlier clinical trials. Injection site reactions, which are seen with some biologic drugs, were relatively mild and infrequent (146 injection site reactions out of a total 3,708 injections given).

Sixteen of 41 patients reported infections (including colds) during 260 patient months of treatment. All infections resolved and no patient withdrew from the study due to injection site reactions or infections. No antibodies against the drug were detected.

This long-term safety study continues. Patients on the study are scheduled to receive the drug for a minimum of one year. This study is part of the company's clinical development program in rheumatoid arthritis.

Immunex Corporation, who developed the drug, is a biopharmaceutical company engaged in developing immune system science to protect human health.

E-mail this page
to a friend or colleague!
To print,
use this version




Any question regarding a medical diagnosis, treatment, referral, drug availability or pricing should be directed to either a licensed physician or to the product's manufacturer.

If you have any technical questions or other concerns about this site, feel free to contact us at webmaster@docguide.com.

All contents Copyright (c) 1995- Doctor's Guide Publishing Limited. All rights reserved.


Employment opportunities | Partnering opportunities