A Safety and Efficacy Study of Setipiprant Tablets in Androgenetic Alopecia in Males

Completed · Phase 2 · Has a placebo group

Conditions studied: Alopecia

In brief

This study will evaluate the safety, tolerability and efficacy of the oral administration of setipiprant tablets 1000 mg twice daily (BID) relative to placebo in 18 to 49 years old males with androgenetic alopecia (AGA).

Key facts

Study ID
NCT02781311
Run by
Allergan
People needed
169
Starts
2016-07-14
Expected to finish
2018-05-22
Last updated by the study team
2019-04-05

Who can join

Age: 18 and older, up to 49. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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