Haematologic

Anemia: cell-therapy evidence and registered trials

A source-first research page for the exact condition. It does not recommend a cell product, clinic or private treatment.

Medical review statusPending clinical sign-offLast evidence update: 2026-08-05Methodology 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.

Registry snapshot

ClinicalTrials.gov returned 538 registered studies for the stored condition/intervention query, including 86 recruiting records, retrieved 2026-08-05T06:02:03+00:00. A registry count does not establish efficacy, approval, relevance or eligibility; inspect each study's design, product, status and inclusion criteria.

Research activity over time

Registration of new studies stayed broadly flat: 107 newly registered studies in 2021–2025 against 112 in 2016–2020. The first study in this registry query was posted in 1999; the registry now holds 538 in total, of which 86 are recruiting. Counting is by first-posted date, so the series reflects when research was registered — not enrolment, completion or results.

Newly registered Anemia studies by year
201616
201734
201826
201922
202014
202112
202223
202320
202434
202518
202627

Source: ClinicalTrials.gov API v2, retrieved 2026-08-05. A registration count is not evidence of efficacy, approval or eligibility. Open the exact query ↗

What the trial registry actually shows

Our own count of every study registered on ClinicalTrials.gov for anemia with a stem-cell intervention, retrieved 2026-09-05. A registration is a declaration of intent, not a result — which is why the status column matters more than the total.

Status in the registryStudiesShare
Completed24445%
Recruiting now8416%
Terminated early6111%
Status not updated by sponsor5711%
Active, closed to entry407%
Not yet recruiting214%
Withdrawn before enrolling194%
Enrolling by invitation only51%
Expanded access31%
No longer available20%
Suspended20%
Approved for marketing10%
All registered studies539100%

Reading it: 82 stopped before finishing — terminated, withdrawn or suspended, 15% of the total; 144 carry no assigned trial phase, meaning they sit outside the phased development path that leads to an approved medicine; 215 reached Phase 2 or later, against 180 still at Phase 1 or earlier; 57 have had no status update from the sponsor and may be dormant.

Which cell family is actually studied here

The same condition, split by the three families that registries can distinguish. Sub-types such as Muse, placental or fetal preparations are not separated in the registry and sit inside the mesenchymal count.

Haematopoietic transplant425Mesenchymal stromal cells19Exosomes2
Cell familyStudies
Haematopoietic transplant425
Mesenchymal stromal cells19
Exosomes2

Here the transplant route is the larger body of work: 425 registered studies against 19 using mesenchymal cells. Those are different treatments with different risks, and evidence for one is not evidence for the other.

Counts are our own extraction from the ClinicalTrials.gov API, retrieved 2026-09-05. The query behind them is published with the dataset so anyone can repeat the count. Nothing here is evidence of benefit or a treatment recommendation.

What to verify before interpreting a study or offer

  1. The exact product, cell source, processing, dose and delivery route.
  2. The indication, study phase, comparator, endpoints, status and eligibility criteria.
  3. Whether the proposed use is authorised, part of a registered trial or otherwise investigational.
  4. Provider and manufacturing authorisations, release testing, traceability and adverse-event reporting.
  5. How the proposal compares with current standard care, reviewed by an independent physician.

Sources & further reading

Registry data is a discovery aid, not evidence that a treatment works or is suitable for an individual patient.

Compare cell-therapy evidence, registered studies and published price observations.

StemCellAtlas is a source-first research and cost-planning guide. It separates registry and regulator evidence from heterogeneous commercial observations.

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