Clinical Trials Directory

Trials / Unknown

UnknownNCT05865041

Investigate the Efficacy and Safety of Farudodstat Compared With Its Placebo in Adult Alopecia Areata Participants

A Parallel Group Treatment, Phase 2a, Double-blind, Two-arm Study to Investigate the Efficacy and Safety of Farudodstat Tablets Compared With Its Placebo in Male or Female Alopecia Areata Participants Aged 18 Years and Older With 30% or Greater Scalp Hair Loss

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
ASLAN Pharmaceuticals · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The main purpose of this study is to measure the efficacy of farudodstat compared to placebo at Week 12 from the treatment start, in adult participants with Alopecia Areata (AA) with 30% or greater scalp hair loss.

Conditions

Interventions

TypeNameDescription
DRUGFarudodstatFarudodstat tablets administered orally
DRUGPlaceboPlacebo tablets administered orally

Timeline

Start date
2023-04-14
Primary completion
2024-09-12
Completion
2024-10-31
First posted
2023-05-18
Last updated
2023-12-18

Locations

19 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05865041. Inclusion in this directory is not an endorsement.

Investigate the Efficacy and Safety of Farudodstat Compared With Its Placebo in Adult Alopecia Areata Participants (NCT05865041) · Clinical Trials Directory