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NCT06787690: Cohealyx I
A Prospective Multicenter Single-arm Clinical Study to Investigate Clinical Outcomes When Cohealyx™ is Used for the Management of Full Thickness Wounds Post-surgical Excision
NA trial testing Cohealyx in Burn in 41 participants. Participants enrolled and being followed up; not accepting new ones.
10 February 2026
Quick facts
| Lead sponsor | Avita Medical |
|---|---|
| Phase | NA |
| Status | Active, enrolled |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 41 |
| Start date | 15 May 2025 |
| Primary completion | 10 February 2026 |
| Estimated completion | 1 August 2026 |
| Sites | 18 locations across United States |
Drugs / interventions tested
- Cohealyx
Conditions studied
- Burn — all drugs for Burn →
- Trauma Wound — all drugs for Trauma Wound →
- Full Thickness Wounds — all drugs for Full Thickness Wounds →
- Surgical Wound — all drugs for Surgical Wound →
Sponsor
Avita Medical — full company profile →
Who can join
Eligibility, any sex, with Burn or Trauma Wound. Patients with the condition only — healthy volunteers not accepted.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
Time for Cohealyx to generate tissue capable of supporting definitive closure
Time frame: Up to 30 days
Defined as the number of days from placement of Cohealyx until placement of an autologous split-thickness skin graft
Sponsor's own description
The goal of this study is to look at clinical outcomes when Cohealyx Collagen Matrix is used to treat full thickness wounds after surgical excision in patients that require a skin graft to heal their wounds. The main question it aims to answer is how long does it take for Cohealyx to support definitive closure.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06787690
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Currently open trials in the same condition.
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Other Avita Medical trials
Trials by the same sponsor.
- NCT05971381 — Repigmentation of Stable Vitiligo Lesions Using Spray-On Skin™ Cells · NA · completed
- NCT04271501 — Feasibility Study to Evaluate RECELL and Melanocyte Keratinocyte Transplantation Procedure for Repigmentation of Stable · NA · terminated
- NCT04547998 — Clinical Study to Investigate the Safety and Effectiveness of RECELL for Repigmentation of Stable Vitiligo Lesions · NA · completed
- NCT03626701 — RES® Prepared With RECELL® Compared to Standard of Care Dressings of Partial-thickness Burns in Ages 1-16 Years · NA · terminated
- NCT04091672 — RECELL® System Combined With Meshed Autograft for Reduction of Donor Skin Harvesting in Soft Tissue Reconstruction · NA · 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 NCT06787690 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Avita Medical
- Last refreshed: 10 March 2026
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/NCT06787690.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing