On Open-Label Study in Participants With Systemic Lupus Erythematosus
Stopped early · Phase 3 · Has a placebo group
Conditions studied: Systemic Lupus Erythematosus, Connective Tissue Disease, Autoimmune Disease
In brief
The purpose of this SLE study is to evaluate the long-term safety and efficacy of LY2127399 in eligible SLE participants who have completed the core studies (NCT01196091) (NCT01205438).
Key facts
- Study ID
- NCT01488708
- Run by
- Eli Lilly and Company
- People needed
- 1518
- Starts
- 2012-01-01
- Expected to finish
- 2015-10-01
- Last updated by the study team
- 2018-05-17
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Have completed 52 weeks of treatment in core studies (NCT01196091) (NCT01205438)
- Given written informed consent
- Test negative for pregnancy at the time of enrollment
- Agree to use a reliable method of birth control
You may not qualify if…
- Unwilling to comply with study procedures
- Any condition that renders the participants unable to understand the nature and scope and possible consequences of the study
- Any condition that in the opinion of the investigator poses an unacceptable risk to the participants if study drug would be administered
Where it is running
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9AM to 5 PM Eastern Time (UTC/GMT-5 hours, EST) or speak with your personal physician — Irving, Texas, United States
Full record on ClinicalTrials.gov
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