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

Status unconfirmed · Phase 2 · Has a placebo group

Conditions studied: Alopecia Areata

In brief

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.

Key facts

Study ID

NCT05865041

Run by

ASLAN Pharmaceuticals

People needed

60

Starts

2023-04-14

Expected to finish

2024-10-31

Last updated by the study team

2023-12-18

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adult (≥18 years of age and a weight of ≥40 kg at the time of signing the informed consent)
• Moderate, severe, or very severe Alopecia Areata (AA), as determined by meeting the following criteria:
• Clinical diagnosis of AA with no other etiology of hair loss (e.g., telogen effluvium, androgenetic alopecia, etc.)
• At least 30% scalp hair loss, as defined by a SALT score ≥30
• Current episode of hair loss lasting at least 6 months and not exceeding 7 years at the time of Screening. Participants who have AA for longer than 7 years may be enrolled if episodes of regrowth, spontaneous or under treatment, have been observed on the affected areas over the past 7 years
• No appreciable change (i.e., change exceeding 20 points on SALT score) in terminal hair regrowth within 6 months

You may not qualify if…

• Known history of androgenic alopecia or female pattern hair loss prior to AA
• Other types of alopecia (including, but not limited to traction and scarring alopecia, telogen effluvium, diffuse type of AA)
• History or presence of hair transplants
• Other scalp disease that may impact AA assessment or require topical treatment (including, but not limited to scalp psoriasis, seborrheic dermatitis, actinic keratosis)

Where it is running

• 1 Site — Birmingham, Alabama, United States (enrolling)
• 1 Site — Fountain Valley, California, United States (enrolling)
• 1 Site — Santa Ana, California, United States (enrolling)
• 1 Site — New Haven, Connecticut, United States (enrolling)
• 1 Site — Washington D.C., District of Columbia, United States (enrolling)
• 1 Site — Coral Gables, Florida, United States (enrolling)
• 1 Site — Indianapolis, Indiana, United States (enrolling)
• 1 Site — Louisville, Kentucky, United States (enrolling)
• 1 Site — Brighton, Massachusetts, United States (enrolling)
• 1 Site — Minneapolis, Minnesota, United States (enrolling)
• 1 Site — New Brighton, Minnesota, United States (enrolling)
• 1 Site — Saint Joseph, Missouri, United States (enrolling)
• 1 Site — Omaha, Nebraska, United States (enrolling)
• 1 Site — Cleveland, Ohio, United States (enrolling)
• 1 Site — Columbus, Ohio, United States (enrolling)
• 1 Site — Nashville, Tennessee, United States (enrolling)
• 1 Site — Pflugerville, Texas, United States (enrolling)
• 2 Sites — San Antonio, Texas, United States (enrolling)
• 1 Site — Webster, Texas, United States (enrolling)

Full record on ClinicalTrials.gov

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