Neurodegenerative

Parkinson's Disease: 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 70 registered studies for the stored condition/intervention query, including 15 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 accelerated: 40 newly registered studies in 2021–2025 against 14 in 2016–2020. The first study in this registry query was posted in 2009; the registry now holds 70 in total, of which 15 are recruiting. Counting is by first-posted date, so the series reflects when research was registered — not enrolment, completion or results.

Newly registered Parkinson's Disease studies by year
20162
20174
20183
20192
20203
20217
20222
202310
20247
202514
20265

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 parkinson disease 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
Status not updated by sponsor1623%
Recruiting now1521%
Not yet recruiting1115%
Completed1014%
Active, closed to entry57%
Withdrawn before enrolling46%
Enrolling by invitation only46%
No longer available34%
Terminated early34%
All registered studies71100%

Reading it: 7 stopped before finishing — terminated, withdrawn or suspended, 10% of the total; 21 carry no assigned trial phase, meaning they sit outside the phased development path that leads to an approved medicine; 9 reached Phase 2 or later, against 41 still at Phase 1 or earlier; 16 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.

Mesenchymal stromal cells19Exosomes13Haematopoietic transplant3
Cell familyStudies
Mesenchymal stromal cells19
Exosomes13
Haematopoietic transplant3

Mesenchymal cells dominate the registered work here: 19 studies against 3 using haematopoietic transplant.

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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