Safety, Tolerability and Pharmacokinetics of KX826 in Healthy Male Subjects With Androgenetic Alopecia Following Topical Single Ascending Dose Administration
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Dose Escalation Study in Healthy Male Subjects With Androgenetic Alopecia to Evaluate the Safety, Tolerability and Pharmacokinetics of KX-826 Following Topical Single Ascending Dose Administration
In the register
The register attaches this trial to Pyrilutamide (Kintor Pharmaceutical), currently at “Phase 3” in the register. The programme's phase is checked by hand; the trial's is declared by its sponsor.
What the registry records
- Status
- Completed
- Declared phase
- Phase 1
- Sponsor
- Suzhou Kintor Pharmaceutical Inc,
- Participants (registry)
- 40
- Start
- January 2019
- Primary completion
- April 2019
- Study completion
- October 2019
- Last registry update
- July 2021
- Countries
- United States
Conditions studied: Androgenetic Alopecia
Interventions: KX0826, Pyrilutamide, KX-826, Placebo
Other trials of Pyrilutamide
To Evaluate Efficacy and Safety of TopicalKX-826 Solution in Chinese Male Patients With Androgenetic Alopecia
To Evaluate Efficacy, Safety, and Tolerability of KX-826 in Male Subjects With Androgenetic Alopecia
Phase III Study of KX-826 With Adult Male Patients With AGA
To Evaluate Safety and Efficacy of KX-826 in Chinese Female Subjects With Androgenetic Alopecia
Phase II Study Evaluating the Efficacy and Safety of KX-826
the Safety, Tolerability and PK of KX-826 in Healthy Males With Alopecia Following Topical Multiple Dose Ascending
Listing a trial is not a recommendation to join one. Eligibility, risks and costs vary enormously — discuss any trial with your own doctor first. A registration proves a sponsor declared a study, not that it is progressing or will succeed. We're not doctors.