Registry evidence

Premature Ovarian Insufficiency and Mesenchymal stem/stromal cells (MSC): what the trial registry contains

The ClinicalTrials.gov registry holds 18 records for MSC in Premature Ovarian Insufficiency: 2 recruiting now, 0 labelled Phase 3 or 4, across 8 countries. Snapshot 2026-08-29.

Medical review statusMedically reviewedReviewed by: Stem Plus medical teamReviewed on: 2026-08-29Last evidence update: 2026-08-29Methodology and editorial standards
Clinical review team: Dr Kamelia Milcheva, Hematologist · Dr Vadym Uvarov, Board-Certified Physician · Hepatobiliary Surgeon · Candidate of Medical SciencesEditorial responsibility: StemCellAtlas research teamEducational information only. This page does not provide medical advice, diagnosis or a treatment recommendation.

Why this is studied in Premature Ovarian Insufficiency

Primary ovarian insufficiency is loss of ovarian function before forty, from genetic, autoimmune or iatrogenic causes. Cell and platelet-based 'ovarian rejuvenation' aims to restore folliculogenesis. Occasional spontaneous ovulation occurs in this condition — including spontaneous pregnancies — which is the fact most often exploited by uncontrolled case reports.

What MSC means in this table

Mesenchymal stromal cells are the workhorse of commercial cell therapy: easy to source from fat, cord or marrow, easy to expand, and rarely characterised in the same way twice. Their proposed action is paracrine — signalling molecules that damp inflammation — rather than replacement of lost tissue. That matters when reading counts like these, because two studies filed under the same label can test materially different products at different doses by different routes.

The numbers

Every figure below comes from one reproducible query (primary ovarian insufficiency x mesenchymal stem cell) run against ClinicalTrials.gov API v2 on 2026-08-29.

MetricValue
Registered studies (all statuses)18
Interventional studies in the sample17
Recruiting right now2
Completed3
Terminated, withdrawn or suspended2
Phase 3 or Phase 4 records0
Countries with at least one site8
Median planned enrolment34 participants
Largest single planned enrolment320 participants
First / most recent start year2012 — 2026

How mature is this evidence?

Registration activity is thin and early: 18 records in total, none at confirmatory phase, 2 recruiting.

Registrations do not all survive contact with recruitment — 3 completed here, 2 stopped early, giving a 11% attrition rate.

Phase labelRecordsShare
Phase 11554%
Phase 21139%
Not applicable27%

Median planned enrolment is 34 participants (largest single study: 320). Trials of this size can describe safety and generate hypotheses; detecting a modest clinical benefit reliably usually needs substantially larger numbers with a control group.

Where the studies are

8 countries host at least one site. China is the largest single contributor at roughly 56% of country mentions in this sample.

CountryStudies with a site there
China9
Ukraine1
South Korea1
United States1
Egypt1
Jordan1
Mongolia1
Iran1

Legal pathway differs by country — see where cell therapy is legal, by country.

Who runs them

Among the top lead sponsors, 3 are universities or hospitals and 5 are companies, making this a commercial area.

  • Chinese Academy of Sciences — 3 records
  • Ukraine Association of Biobank — 1 record
  • Shenzhen Wingor Biotechnology Co., Ltd. — 1 record
  • CHABiotech CO., Ltd — 1 record
  • Bright Cell, Inc. — 1 record
  • Vitti Labs, LLC — 1 record

Representative registered studies

Recruiting studies first, then the most advanced phases. Each identifier links to the registry record, where eligibility criteria, outcome measures and contacts are published.

StudyPhaseStatusPlanned nLead sponsorStart
NCT07775391 — Phase Ⅰ/Ⅱa Trial Evaluating Intravenous hUC-MSCs Injection for Safety, Tolerability and Efficacy in Patients With POIPhase 1, Phase 2Recruiting59Shenzhen Wingor Biotechnology Co., Ltd.2026-08-03
NCT07115082 — Clinical Study on the Safety and Efficacy of Human Amniotic Mesenchymal Stem Cells in the Treatment of Premature Ovarian InsufficiencyPhase 1, Phase 2Recruiting50Yan Hongli2024-10-15
NCT07510139 — A Clinical Study of Umbilical Cord Mesenchymal Stem Cell-Derived Exosomes for the Treatment of Premature Ovarian InsufficiencyPhase 1, Phase 2Active Not Recruiting60International Peace Maternity and Child Health Hospital2026-03-20
NCT07551895 — Umbilical Cord Mesenchymal Stem Cells (UC-MSC) in the Treatment of Primary Ovarian InsufficiencyPhase 1, Phase 2Not Yet Recruiting21Shenzhen Huishan Biotechnology Co., Ltd.2026-04-15
NCT03816852 — The Safety and Efficiency Study of Mesenchymal Stem Cell (19#iSCLife®-POI) in Premature Ovarian InsufficiencyPhase 2Suspended12Sclnow Biotechnology Co., Ltd.2018-10-01
NCT03033277 — Human Umbilical Cord Mesenchymal Stem Cells (HUC-MSCs) Transplantation in Women With Primary Ovarian Insufficiency (POI)Phase 1, Phase 2Unknown320Chinese Academy of Sciences2016-02
NCT02644447 — Transplantation of HUC-MSCs With Injectable Collagen Scaffold for POFPhase 1, Phase 2Completed23Chinese Academy of Sciences2015-10
NCT03069209 — Autologous Bone Marrow-Derived Stem Cell Transplantation in Patients With Premature Ovarian Failure (POF)Phase 1, Phase 2Unknown50Stem Cells Arabia2015-01
NCT02603744 — Autologous Adipose Derived Mesenchymal Stromal Cells Transplantation in Women With Premature Ovarian Failure (POF)Phase 1, Phase 2Unknown9Royan Institute2015-06
NCT01742533 — Stem Cell Therapy Combined Hormone Replacement Therapy in Patients With Premature Ovarian FailurePhase 1, Phase 2Unknown40Shenzhen Beike Bio-Technology Co., Ltd.2012-03

What this page does and does not tell you

None of these numbers say the therapy works. They say how much organised research exists and how far along it is; effect sizes live in published results, not registry entries.

If a clinic offers you this today, the useful question is not "is there research?" but "which of these registered studies is mine part of, and if none, what evidence applies to the exact product I am being sold?" The Provider Question Builder turns that into a scored checklist.

Frequently asked

How many MSC studies for Premature Ovarian Insufficiency are recruiting right now?

2 of 18 registered records were listed as recruiting in the 2026-08-29 snapshot. Recruitment status changes frequently; the registry record is authoritative.

Is MSC an approved treatment for Premature Ovarian Insufficiency?

Registration on ClinicalTrials.gov is not approval. Approval is granted by a regulator for a specific product and indication after review of submitted evidence. 18 registered studies tell you research exists, not that a product cleared review.

How advanced is the research on MSC for Premature Ovarian Insufficiency?

0 of 18 records carry a Phase 3 or Phase 4 label and 3 are marked completed. Registrations run from 2012 to 2026.

Registry and literature counts retrieved 2026-08-29 (ClinicalTrials.gov API v2; PubMed E-utilities). Registration or publication volume measures research activity, not effectiveness or approval. Educational information — not medical advice; verify product, indication, legal pathway and evidence with an independent qualified physician. Page generated 2026-08-29. See our editorial standards.

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Query totals are full API matches; status, phase and country counts describe the first up to 400 returned records per query. Query classes overlap and must not be summed as unique trials. Counts are not treatment outcomes. Snapshot: 2026-08-29. Methods and field definitions.