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.
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.
| Metric | Value |
|---|---|
| Registered studies (all statuses) | 18 |
| Interventional studies in the sample | 17 |
| Recruiting right now | 2 |
| Completed | 3 |
| Terminated, withdrawn or suspended | 2 |
| Phase 3 or Phase 4 records | 0 |
| Countries with at least one site | 8 |
| Median planned enrolment | 34 participants |
| Largest single planned enrolment | 320 participants |
| First / most recent start year | 2012 — 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 label | Records | Share |
|---|---|---|
| Phase 1 | 15 | 54% |
| Phase 2 | 11 | 39% |
| Not applicable | 2 | 7% |
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.
| Country | Studies with a site there |
|---|---|
| China | 9 |
| Ukraine | 1 |
| South Korea | 1 |
| United States | 1 |
| Egypt | 1 |
| Jordan | 1 |
| Mongolia | 1 |
| Iran | 1 |
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.
| Study | Phase | Status | Planned n | Lead sponsor | Start |
|---|---|---|---|---|---|
| NCT07775391 — Phase Ⅰ/Ⅱa Trial Evaluating Intravenous hUC-MSCs Injection for Safety, Tolerability and Efficacy in Patients With POI | Phase 1, Phase 2 | Recruiting | 59 | Shenzhen 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 Insufficiency | Phase 1, Phase 2 | Recruiting | 50 | Yan Hongli | 2024-10-15 |
| NCT07510139 — A Clinical Study of Umbilical Cord Mesenchymal Stem Cell-Derived Exosomes for the Treatment of Premature Ovarian Insufficiency | Phase 1, Phase 2 | Active Not Recruiting | 60 | International Peace Maternity and Child Health Hospital | 2026-03-20 |
| NCT07551895 — Umbilical Cord Mesenchymal Stem Cells (UC-MSC) in the Treatment of Primary Ovarian Insufficiency | Phase 1, Phase 2 | Not Yet Recruiting | 21 | Shenzhen Huishan Biotechnology Co., Ltd. | 2026-04-15 |
| NCT03816852 — The Safety and Efficiency Study of Mesenchymal Stem Cell (19#iSCLife®-POI) in Premature Ovarian Insufficiency | Phase 2 | Suspended | 12 | Sclnow 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 2 | Unknown | 320 | Chinese Academy of Sciences | 2016-02 |
| NCT02644447 — Transplantation of HUC-MSCs With Injectable Collagen Scaffold for POF | Phase 1, Phase 2 | Completed | 23 | Chinese Academy of Sciences | 2015-10 |
| NCT03069209 — Autologous Bone Marrow-Derived Stem Cell Transplantation in Patients With Premature Ovarian Failure (POF) | Phase 1, Phase 2 | Unknown | 50 | Stem Cells Arabia | 2015-01 |
| NCT02603744 — Autologous Adipose Derived Mesenchymal Stromal Cells Transplantation in Women With Premature Ovarian Failure (POF) | Phase 1, Phase 2 | Unknown | 9 | Royan Institute | 2015-06 |
| NCT01742533 — Stem Cell Therapy Combined Hormone Replacement Therapy in Patients With Premature Ovarian Failure | Phase 1, Phase 2 | Unknown | 40 | Shenzhen 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.
More on this condition
- Premature Ovarian Insufficiency: cell-therapy evidence and registered trials
- How much does stem cell therapy for Premature Ovarian Insufficiency cost? (2026)
- Premature Ovarian Insufficiency stem cell therapy — your questions answered (2026)
- Premature Ovarian Insufficiency: cell-therapy evidence by therapy class
- MSC vs PRP for Premature Ovarian Insufficiency: what the registries show
Download the query data
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.