Autopsy report · NCT02392572
ONC201 in Treating Patients With Relapsed or Refractory Acute Leukemia or High-Risk Myelodysplastic Syndrome
Cause of deathSlow enrollment
“\<75% participants”
Life of this trial
- Registered 8 months before it started.
- Ran for about 10 years 9 months before it stopped.
- 58 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1, Phase 2
- Sponsor
- M.D. Anderson Cancer Center
- Sponsor type
- University, hospital or other
- Conditions
- Recurrent Acute Lymphoblastic Leukemia; Recurrent Acute Myeloid Leukemia; Recurrent Myelodysplastic Syndrome; Refractory Acute Lymphoblastic Leukemia; Refractory Acute Myeloid Leukemia; Refractory Myelodysplastic Syndrome
- Interventions
- Akt/ERK Inhibitor ONC201; Venetoclax
- Participants
- 58
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Erdafitinib for the Treatment of Patients With Castration-Resistant Prostate Cancer
“\<75% participation” - Vapocoolant Analgesia for Breast Lymphoscintigraphy
“\<75% accrued participants” - Amikacin Pharmacokinetic Profile in Plasma and Tissue After an Administration Using Impregnated Dressings in Burned Patient Population
“not enough participants to include” - Impact of Daylight on Patients With Acute Myocardial Infarction
“not enough participants” - Supplementation With Polyphenol-Rich Foods and Atrial Fibrillation After a Cardiac Surgery
“low participation rate”
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.