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
brief summary
Bioequivalence study of two injectable formulation of progesterone in healthy post-menopausal women
detailed description
An open-label, randomized, single-dose, two-treatment, four-period, fully replicate crossover bioequivalence study in healthy female adult post-menopausal participants under fasting conditions comparing the test product, Prontogest 100mg/2mL Solution for IM injection with the reference product, Progesterone Injection, USP 500mg per 10mL.
official title
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 100mg/2mL Solution for IM Injection With the Reference Product, Progesterone Injection, USP 500mg Per 10mL.