Autopsy report · NCT05041972
ARX788 in Selected HER2-mutated or HER2-amplified/Overexpressed Solid Tumors (ACE-Pan Tumor-02)
Cause of deathFunding or business
“Business strategy change”
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- Withdrawn before it enrolled anyone.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- Withdrawn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 2
- Sponsor
- Ambrx, Inc.
- Sponsor type
- Industry
- Conditions
- HER2 Mutation-Related Tumors; HER2 Amplified Solid Tumors
- Interventions
- ARX788
- Participants
- 0
- Sites
- 2
- Countries
- United States
Trials that died the same way
- Automated Breast Ultrasound Case Collection Registry
“Change in business strategy” - A Phase I, the Study to Evaluate the Safety, Immunogenicity and Efficacy of YS-HBV-002
“Business strategy” - Observational Trial of Real-World Treatment Utilization and Effectiveness of PI3K-inhibitors in CLL/SLL and FL
“Strategy Change” - Evaluation of Safety and Efficacy of Dehydrated Human Amnion-Intermediate-Chorion Membrane (dHAICM) Allograft in Treatment of Partial Thickness Thermal Burns
“Change in company strategy.” - 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.