Last reviewed · How we verify
NCT01739530
Phase I Study to Evaluate Safety of Repaircell in Healthy Volunteers
Phase 1 trial testing Repaircell in Healthy in 5 participants. Completed in 1 December 2009.
1 November 2009
Quick facts
| Lead sponsor | Anterogen Co., Ltd. |
|---|---|
| Phase | Phase 1 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 5 |
| Start date | 1 March 2009 |
| Primary completion | 1 November 2009 |
| Estimated completion | 1 December 2009 |
| Sites | 1 location across South Korea |
Drugs / interventions tested
- Repaircell — full drug profile →
Conditions studied
- Healthy — all drugs for Healthy →
Sponsor
Anterogen Co., Ltd. — full company profile →
Who can join
19 and older, male only, with Healthy. Healthy volunteers can join.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
Number of Adverse events
Time frame: week 8
Evaluate the safety at week 8 whether any kind of Adverse event occurs
Sponsor's own description
Allogenic differentiated adipocytes (ANT-adip-AL) is produced by well-established techniques including cell harvesting from lipoaspirates obtained from healthy donors, expansion of adipose tissue derived stem cells, and differentiation into pure and immature adipocytes. This was an open-label study. Subjects were received subcutaneous injection of ANT-adip-AL and followed for 8 weeks according to the clinical trial protocol.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
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Adipose-Derived Stem Cells for Tissue Engineering and Regenerative Medicine Applications.
Dai R, Wang Z, Samanipour R, Koo KI, et al · · 2016 · cited 191× · PMID 27057174 · DOI 10.1155/2016/6737345 -
Clinical implication of allogenic implantation of adipogenic differentiated adipose-derived stem cells.
Kim I, Bang SI, Lee SK, Park SY, et al · · 2014 · cited 31× · PMID 25273542 · DOI 10.5966/sctm.2014-0109
Verify or expand the search:
- PubMed search for NCT01739530
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Anterogen Co., Ltd. trials
Trials by the same sponsor.
- NCT06539429 — Clinical Study to Evaluate Efficacy and Safety of ANT-301 in Patients With Knee Osteoarthritis in Grade III/IV by K/L · Phase 1 · active not recruiting
- NCT05157958 — Study to Evaluate Safety and Efficacy of ALLO-ASC-SHEET in Subjects With Dystrophic Epidermolysis Bullosa · Phase 2 · recruiting
- NCT06141811 — A Follow-up Study to Evaluate the Safety of ALLO-ASC-DFU in ALLO-ASC-DFU-302 Clinical Trial · recruiting
- NCT04569409 — Clinical Study to Evaluate Efficacy and Safety of ALLO-ASC-DFU in Patients With Diabetic Wagner Grade 2 Foot Ulcers. · Phase 3 · completed
- NCT04590703 — A Follow-up Study to Evaluate the Safety of ALLO-ASC-DFU in ALLO-ASC-DFU-301 Clinical Trial · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT01739530 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Anterogen Co., Ltd.
- Last refreshed: 3 December 2012
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01739530.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing