WHO ICTRP trial

Multi center clinical study to evaluate the safety and efficacy of CB-03-01 for…

EUCTR2019-000950-78-DE · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2019-000950-78-DE
Public title Multi center clinical study to evaluate the safety and efficacy of CB-03-01 for the treatment of female pattern hair loss, versus Minoxidil and placebo at different dosage of CB-03-01
Scientific title A Phase 2, multicenter, prospective, randomized, double-blind, Minoxidil and vehicle controlled, dose-ranging study to evaluate the efficacy and safety of CB-03-01 (Cortexolone 17a-propionate) solution for the treatment of androgenetic alopecia in females - NA
Primary sponsor Cassiopea S.p.A.
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): yes Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): no
Countries Germany
Conditions Female Androgenic Alopecia (AGA) is scalp hair loss that occurs due to an underlying susceptibility of hair follicles to androgenic miniaturization. In the hair follicle, testosterone is converted by 5a-reductase into 5a-dihydrotestosterone…
Interventions Product Name: Cortexolone 17a-propionate solution 5% Product Code: CB-03-01 solution 5% Pharmaceutical Form: Cutaneous solution INN or Proposed INN: Cortexolone 17a-propionate CAS Number: 19608-29-8 Current Sponsor code: CB-03-01 Other…
Registration date Apr 30, 2019
Target size 280
Secondary IDs CB-03-01/35
Registry page clinicaltrialsregister.eu

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