AUR-201 clinical trials
Also written AUR-201.
- studies test it
- 3
- open now
- 0
- in phase 3
- 0
- first study started
- 2022
How each study uses AUR-201 is sorted by a rule, right about nine times in ten. Readers can ask us to read every study one by one.Ask us to read each study
Approvals
The first approval found in each region, with its record
- United States
- Not in FDA's approval records
- European Union
- Not in EMA's list of EU-wide authorisations
From FDA's Drugs@FDA and Purple Book (through openFDA) and the European Medicines Agency, files of Sept 2026 and 27 Oct 2026. National approvals in Europe and other countries are not included. How this is worked out
How studies write it
Studies that test it under each name
Development codes
- AUR-201
- 3
Studies by the year they started
3 studies that test it; most in 2024 (2)
| Year | Studies |
|---|---|
| 2022 | 1 |
| 2024 | 2 |
Who runs them
Industry 3 · Other 0
Auregen Biotherapeutics, SA (3)
Studies
Open first, then newest update. How each study uses AUR-201 is read from its arms, and is right about nine times in ten. Ask us to read each study. These are the studies that list it as an intervention; a search of ClinicalTrials.gov also finds studies that mention it only in a description, such as earlier treatment.
Testing it · 3
- Long-Term Follow-Up Study of Unilateral Microtia Patients Implanted With AUR-201TerminatedPhase 1/2Auregen Biotherapeutics, SANCT06078566Written as AUR-201
- Subcutaneous Implant Combination Product (AUR-201) in Patients With Unilateral MicrotiaTerminatedPhase 1/2Auregen Biotherapeutics, SANCT06072040Written as AUR-201
- Subcutaneous Implant Combination Product (AUR-201) in Patients With Unilateral Microtia (Australia)TerminatedPhase 1Auregen Biotherapeutics, SANCT06225336Written as AUR-201