An Open-label, Randomized, Single-dose, Two-treatment, Four-period, Fully Replicate Crossover Bioequivalence Study in Healthy Female Adult Participants Under Fasting Conditions Comparing the Test Product, Prontogest Solution for IM Injection With the Reference Product, Progesterone Injection
CompletedNCT07495007
Zi Diligence BiocenterBioequivalance, Post-menopause
Start: 2025-11-10End: 2025-12-28Updated: 2026-03-27