Status:

COMPLETED

A Safety and Pharmacokinetics Study in Participants With Rheumatoid Arthritis

Lead Sponsor:

Eli Lilly and Company

Conditions:

Arthritis, Rheumatoid

Eligibility:

All Genders

18-75 years

Phase:

PHASE1

PHASE2

Brief Summary

The purpose of this study is to examine the safety and efficacy of this antibody in participants with rheumatoid arthritis. Part A of the study is an initial dose escalation phase Part B of the stud...

Eligibility Criteria

Inclusion

  • diagnosis of rheumatoid arthritis
  • regular use of methotrexate
  • active rheumatoid arthritis

Exclusion

  • Juvenile Rheumatoid Arthritis
  • evidence of tuberculosis
  • women who are pregnant or become pregnant during study, or are breast-feeding

Key Trial Info

Start Date :

November 1 2005

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 1 2007

Estimated Enrollment :

121 Patients enrolled

Trial Details

Trial ID

NCT00380744

Start Date

November 1 2005

End Date

November 1 2007

Last Update

February 6 2019

Active Locations (14)

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Page 1 of 4 (14 locations)

1

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Tucson, Arizona, United States, 85712

2

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Upland, California, United States, 91786

3

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Miami, Florida, United States, 33169

4

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Port Orange, Florida, United States, 32127