Autopsy report · NCT05731947
Evaluation of Revumenib in Participants With Colorectal Cancer and Other Solid Tumors
Cause of deathFunding or business
“Study was terminated by sponsor after Phase 1b as pre-defined signals of efficacy were not met in the Phase 1b dose expansion cohort.”
Life of this trial
- Registered 2 months before it started.
- Ran for about 2 years 3 months before it stopped.
- 41 participants enrolled.
- Results were posted on the registry 1 year after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1, Phase 2
- Sponsor
- Syndax Pharmaceuticals
- Sponsor type
- Industry
- Conditions
- Colorectal Cancer; Solid Tumors
- Interventions
- Revumenib; Chemotherapy
- Participants
- 41
- Sites
- 6
- Countries
- United States
Trials that died the same way
- A Safety, Tolerability and Efficacy Study of NC410 Plus Pembrolizumab in Participants With Advanced Unresectable or Metastatic Solid Tumors
“Following completion of Phase 1b, the Sponsor decided not to initiate Part 2 of the trial.” - A Study of THE-630 in Patients With Advanced Gastrointestinal Stromal Tumors (GIST)
“The Sponsor terminated the study due to early dose-limiting toxicities.” - PROPEL - A Prospective Observational Patient Registry to Evaluate ENPP1 and ABCC6 Deficiency
“The study was terminated by the sponsor prior to planned completion based on a review of the data across indications and overall program considerations. Study termination was not related to participant safety.” - Nab-Sirolimus and Pazopanib Hydrochloride in Treating Patients With Advanced Nonadipocytic Soft Tissue Sarcomas
“Study was terminated at completion of the Phase 1 dose escalation due to loss of financial support.” - A Study of De-immunized DI-Leu16-IL2 Administered Subcutaneously in Participants With B-cell NHL
“Clinical benefit was noted in the earlier portion of the trial; hence, participants were not enrolled in 2 expansion cohorts and the study was terminated early.”
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.