drugset / Trial / NCT07115082

Clinical Study on the Safety and Efficacy of Human Amniotic Mesenchymal Stem Cells in the Treatment of Premature Ovarian Insufficiency

NCT07115082

Phase 1/2 Recruiting 50 enrolled Yan Hongli
Non-randomizedParallel-groupSingle-blindTreatment

Summary

There is a high incidence of women suffering from Primary Ovarian Insufficiency (POI). So far, there was no treatment sufficient enough to cure POI. Cell therapy is a rapidly developing field and have shown immense promise in the treatment of ovarian dysfunction. In this study, the investigator will evaluate the safety of human Amniotic mesenchymal stem cells (hA-MSCs) therapy in women suffering from POI.

Timeline

Start
2024-10-15
Primary completion
2025-12
Completion
2026-03-30

Drugs

EvaluationDrugModalityDoseRoute
Subject hA-MSCs Unknown 1e+06 cells/kg Intravenous
Background cyproterone acetate Small molecule 1 mg Oral
Background estradiol valerate Unknown 2 mg Oral