Autopsy report · NCT05831995
Safety and Effectiveness of ABM-168 in Adults with Advanced Solid Tumors.
Cause of deathFunding or business
“Due to development strategy change.”
Life of this trial
- Ran for about 1 year 3 months before it stopped.
- 12 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1
- Sponsor
- ABM Therapeutics Corporation
- Sponsor type
- Industry
- Conditions
- Advanced Solid Tumor; RAS Mutation; RAF Mutation; NF1 Mutation
- Interventions
- ABM-168
- Participants
- 12
- Sites
- 6
- Countries
- United States
Trials that died the same way
- Study of NIB101 in Participants With Advanced Solid Tumors
“due to the reconsideration of development strategy” - IBI397 or Combination Therapies in Patients With Advanced Malignancies
“Due to the company's development strategy adjustment” - Mesenchymal Stem Cells in the Treatment of Refractory Primary Immune Thrombocytopenia
“Due to corporate strategic adjustment.” - Improving End-of-life Care by Continuing Medical Education and Electronic Decision Making Support for General Practitioners
“due to organisational changes” - Safety and Efficacy of Periodontal Surgery in Supra-alveolar-type Defects With or Without Straumann® Emdogain
“Due to change in strategy and decision not to expand indication.”
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.