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NCT06225336: AUR-201

Subcutaneous Implant Combination Product (AUR-201) in Patients With Unilateral Microtia (Australia)

Terminated Phase 1 Last updated 19 November 2025
What this trial tests

Phase 1 trial testing AUR-201 in Microtia in 2 participants. Terminated before completion.

Timeline
4 November 2022
Primary endpoint
10 September 2025
10 September 2025

Quick facts

Lead sponsorAuregen Biotherapeutics, SA
PhasePhase 1
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment2
Start date4 November 2022
Primary completion10 September 2025
Estimated completion10 September 2025
Sites1 location across Australia

Drugs / interventions tested

Conditions studied

Sponsor

Auregen Biotherapeutics, SA

Who can join

Adults 8 to 29, any sex, with Microtia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

AUR-201 is indicated for the treatment of Grade II, III, or IV unilateral microtia in patients 8 to 29 years of age.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of AUR-201

Trials testing the same drug.

Other recruiting trials for Microtia

Currently open trials in the same condition.

Other Auregen Biotherapeutics, SA trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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/NCT06225336.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing