Autopsy report · NCT07489560
Evaluation of Safety and Efficacy of Dehydrated Human Amnion-Intermediate-Chorion Membrane (dHAICM) Allograft in Treatment of Partial Thickness Thermal Burns
Cause of deathFunding or business
“Change in company strategy.”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Phase 4
- Sponsor
- Cellution Biologics
- Sponsor type
- Industry
- Conditions
- Partial Thickness Burn
- Interventions
- Amnion-Intermediate-Chorion; Standard of Care (SOC)
- Participants
- 0
Trials that died the same way
- Automated Breast Ultrasound Case Collection Registry
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“Business strategy change” - Dose-escalation Study of APG-1387 and Toripalimab in Solid Tumors
“Company Strategy” - Study of SIM0501 Alone and in Combination in Patients With Advanced Solid Tumors
“Company development strategy change” - Pharmacokinetics of Repeat Oral Doses of Dabrafenib and the Combination of Dabrafenib and Trametinib in Chinese Subjects With Melanoma
“Change in strategy”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.