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Finerenone for Premature Ovarian Insufficiency (POI)
Sponsor: The University of Hong Kong-Shenzhen Hospital
Summary
This study is testing whether finerenone, a medicine currently used to protect the kidneys and heart, can help women with premature ovarian insufficiency (POI) grow ovarian follicles and produce eggs that can be collected for in vitro fertilization (IVF). Women with POI often have very few or no active egg-containing follicles, making it hard for them to conceive. About 46 women with POI will be randomly assigned, without either the participants or their doctors knowing the assignment, to take either finerenone or a matching placebo twice weekly for 24 weeks. Participants will be monitored regularly with ultrasound and blood tests. If follicle growth is observed, participants may undergo ovarian stimulation so that eggs or embryos can be collected and frozen. The main goal is to see whether more women in the finerenone group have eggs successfully retrieved during an IVF cycle, compared with the placebo group. The study will also look at other measures of ovarian reserve, egg and embryo quality, and pregnancy outcomes among participants who go on to embryo transfer.
Official title: A Randomized, Double-Blind, Placebo-Controlled Trial of Finerenone in Women With Premature Ovarian Insufficiency
Key Details
Gender
FEMALE
Age Range
18 Years - 39 Years
Study Type
INTERVENTIONAL
Enrollment
46
Start Date
2026-09-15
Completion Date
2028-09
Last Updated
2026-09-11
Healthy Volunteers
No
Conditions
Interventions
Finerenone
Finerenone 20 mg oral tablet, administered twice weekly for 24 weeks.
Placebo
Matching placebo tablet, oral, administered twice weekly for 24 weeks.
Locations (1)
The University of Hong Kong Shenzhen Hospital
Shenzhen, Guangdong, China