A Study to Evaluate Safety and Efficacy of OLX72021 in Healthy Males With Androgenetic Alopecia

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexMale
Age18-59
SponsorOlix Pharmaceuticals, Inc.

About this trial

This study is designed to evaluate the safety, tolerability, and pharmacokinetics (PK) of OLX72021 in medically healthy men with mild to moderate androgenetic alopecia.

Eligibility criteria

Qualifiers

Adult male.

18 to 59 years.

Androgenetic Alopecia (Hamilton-Norwood III-V).

Body mass index (BMI) ≥ 18.0 kg/m2, with a body weight ≥ 50 kg at screening.

Disqualifiers

History or presence of significant pulmonary, hepatic, renal, hematological, gastrointestinal, endocrine, immunologic, or neurological disease, including any acute illness or major surgery within the past 3 months determined by the PI to be clinically significant.

Uncontrolled diabetes mellitus.

Immunodeficiency disorders.

History of clinically significant heart disease.

Trial design

Treatments tested in this trial

  • OLX72021
  • OLX72021
  • OLX72021
  • Placebo

Treatment groups

158 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Olix Pharmaceuticals, Inc.

Lead sponsor

Avance Clinical Pty Ltd.

Collaborator