Autopsy report · NCT07585734
Clinical Trial of CD38 Monoclonal Antibody Combined With Chemotherapy for T-Cell Acute Lymphoblastic Leukemia
Cause of deathSafety
“drug-associated adverse reactions”
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- Withdrawn before it enrolled anyone.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- Withdrawn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 1, Phase 2
- Sponsor
- Institute of Hematology & Blood Diseases Hospital, China
- Sponsor type
- University, hospital or other
- Conditions
- T-ALL
- Interventions
- Pediatric-Inspired Chemotherapy Regimen
- Participants
- 0
Trials that died the same way
- Study to Evaluate the Efficacy, Safety and Immunogenicity of Subcutaneous HX575 in the Treatment of Anemia Associated With Chronic Kidney Disease (SWEEP)
“investigation of adverse events in a related clinical study” - Safety and Bioactivity of AXT107 in Subjects With Diabetic Macular Edema
“Adverse Events” - Safety and Preliminary Efficacy Study of V404 PDS in Uveitis
“Study terminated due to unacceptable frequency of drug related adverse events” - Development of Cocktail for Measuring the Activity of Important Cytochrome P450 Enzymes
“Unexpected non-serious adverse events” - Phase I Trial of AZD1775 and Belinostat in Treating Patients With Relapsed or Refractory Myeloid Malignancies or Untreated Acute Myeloid Leukemia
“Other - Adverse Events”
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.