Kidney drug tested to restart egg growth in early menopause
NCT ID NCT07815509
First seen Sep 11, 2026 · Last updated Sep 11, 2026
Summary
Researchers are testing whether finerenone, a medicine used for kidney and heart protection, can help women with premature ovarian insufficiency grow ovarian follicles and produce eggs for IVF. About 46 women under 40 with POI will take finerenone or a placebo twice weekly for 24 weeks. The main goal is to see whether more women in the finerenone group have eggs successfully retrieved during an IVF cycle.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- finerenone, a drug used to protect the kidneys and heart
- What this could lead to
- If it works, finerenone could offer a way to help some women with premature ovarian insufficiency produce eggs for IVF.
- What could go wrong
- This is a small, early-phase trial of 46 women, so results may not hold up in larger studies. Finerenone can cause high potassium and low blood pressure, and it may not restart egg growth in ovaries that have stopped working.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 46 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 39 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age of women \<40 years. * Diagnosis of POI according to ESHRE 2024 guidelines, defined as: * Oligomenorrhea or amenorrhea for at least 4 months; and * Elevated FSH levels (≥25 mIU/mL) on a single measurement. Exclusion Criteria: * Known hypersensitivity to Finerenone or any of its excipients. * Severe uncontrolled systemic diseases (cardiovascular, hepatic, renal, or endocrine disorders) that may interfere with study participation. * Active malignancy or history of hormone-dependent cancer. * Currently participating in another interventional trial. * Known chromosomal abnormalities or clinically significant genetic syndromes associated with POI.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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The University of Hong Kong Shenzhen Hospital
Shenzhen, Guangdong, 518000, China
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Other studies related to the condition(s) this trial covers.
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