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Clinical Trial: A Rheumatoid Arthritis (RA) Study Treating Signs and Symptoms of RA in People With RA & Receiving Methotrexate
This study has been terminated.
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Purpose
This clinical study is investigating AMG 719, an investigational drug, for the treatment of patients who have Rheumatoid Arthritis and who are taking Methotrexate. AMG 719 is a drug which is self-injected beneath the skin (similarly to the way insulin is self-injected by diabetics). Patients on this study are on study for 28-weeks. They visit the study facility at least 11 times while participating in the study.
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| Arthritis, Rheumatoid | Drug: AMG 719 | Phase II |
MedlinePlus related topics: Rheumatoid Arthritis
Study Type: Interventional
Study Design: Treatment
Eligibility
Ages Eligible for Study: 18 Years and above, Genders Eligible for Study: Both
Criteria
- Men or women, at least 18 years of age at screening
- Diagnosed with Rheumatoid Arthritis, with a disease duration of at least 24 weeks, receiving methotrexate, and having no recent history of substance or alcohol abuse
Location Information
Arizona
Research Center, Paradise Valley, Arizona, United States
Research Center, Phoenix, Arizona, United States
California
Research Center, San Diego, California, United States
Research Center, Santa Maria, California, United States
Indiana
Research Center, Indianapolis, Indiana, United States
Maine
Research Center, Bangor, Maine, United States
Maryland
Research Center, Hagerstown, Maryland, United States
Research Center, Frederick, Maryland, United States
New Jersey
Research Center, Voorhees, New Jersey, United States
Pennsylvania
Research Center, Wyomissing, Pennsylvania, United States
Research Center, Duncansville, Pennsylvania, United States
Texas
Research Center, Dallas, Texas, United States
More Information
AmgenTrials -- Amgen's clinical trial resource site
CenterWatch - Clinical Trial Resource Site
Record last reviewed: October 2002
Last Updated: October 13, 2004
Record first received: May 29, 2002
ClinicalTrials.gov Identifier: NCT00038298
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005

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