check_circleStudy Completed

Contraception

Bioequivalence chlormadinone acetate/ethinylestradiol

Trial purpose

Please see attached Study Results Summary below

Key Participants Requirements

Sex

N/A

Age

55 - 75 Years
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Trial summary

Enrollment Goal
40
Trial Dates
March 2008 - May 2008
Phase
Phase 1
Could I Receive a placebo
N/A
Products
EV/Chlormadinone Acetate (BAY86-6356)
Accepts Healthy Volunteer
N/A

Where to participate

StatusInstitutionLocation
Completed
SocraTec R&D Clinical WardErfurt, 99084, Germany

Trial design

Characterization of relative bioavailability and assessment of bioequivalence of a newly developed formulation containing chlormadinone acetate and ethinylestradiol in comparison to Belara in a single dose, two way crossover, open, randomized study under fasting conditions in postmenopausal women
Trial Type
Interventional
Intervention Type
N/A
Trial Purpose
N/A
Allocation
N/A
Blinding
N/A
Assignment
N/A
Trial Arms
N/A