Autopsy report · NCT04482699
RAPA-501-Allo Therapy of COVID-19-ARDS
Cause of deathSlow enrollment
“Change in eligible patient population”
Life of this trial
- Registered 5 months before it started.
- Ran for about 8 months before it stopped.
- 1 participant enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1, Phase 2
- Sponsor
- Rapa Therapeutics LLC
- Sponsor type
- Industry
- Conditions
- Severe COVID-19 Disease
- Interventions
- RAPA-501-Allo off-the-shelf Therapy of COVID-19; Placebo
- Participants
- 1
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Hepatic Arterial Infusion With FOLFOX Alone or in Combination With IV Chemotherapy in Colon Cancer With Liver Metastasis
“patient population” - Endothelial Protection in Convalescent COVID-19 Patients
“Lack of the eligible patients” - The Use of Tolvaptan to Prevent Renal Dysfunction in High Risk Patients With Heart Failure-Pilot Study
“Lack of eligible patients” - Non-alcoholic Fatty Liver Disease (NAFLD) in HIV: The Role of Nutritional Interventions
“Not enough eligible patients available” - Efficacy and Safety Study of Cetuximab or Cetuximab Plus Docetaxel to Treat Prostate Cancer Before Prostatectomy
“lack of patient population - slow accrual”
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.