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NOT YET RECRUITING
NCT07815509
PHASE2

Finerenone for Premature Ovarian Insufficiency (POI)

Sponsor: The University of Hong Kong-Shenzhen Hospital

View on ClinicalTrials.gov

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

Interventions

DRUG

Finerenone

Finerenone 20 mg oral tablet, administered twice weekly for 24 weeks.

DRUG

Placebo

Matching placebo tablet, oral, administered twice weekly for 24 weeks.

Locations (1)

The University of Hong Kong Shenzhen Hospital

Shenzhen, Guangdong, China