Autopsy report · NCT05073458
Study of the Efficacy and Safety of Parsaclisib in Participants With Primary Warm Autoimmune Hemolytic Anemia
Cause of deathFunding or business
“A business decision was made to discontinue further enrollment. There were no safety concerns that contributed to this decision.”
Life of this trial
- Registered 6 months before it started.
- Ran for about 2 years 1 month before it stopped.
- 13 participants enrolled.
- Results were posted on the registry 9 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 3
- Sponsor
- Incyte Corporation
- Sponsor type
- Industry
- Conditions
- Warm Autoimmune Hemolytic Anemia (wAIHA)
- Interventions
- parsaclisinib; placebo
- Participants
- 13
- Sites
- 56
- Countries
- Austria, Belgium, Canada, France, Germany, Israel, Italy, Japan, Netherlands, Poland, Spain, United Kingdom and more
Trials that died the same way
- EnligHTN IV Trial - Multicenter Sham-controlled RCT of Renal Denervation for Hypertension
“There were no safety or effectiveness concerns. There were concerns about completing enrollment due to a competitive device's potential approval.” - A Study of TAK-659 in Combination With Bendamustine (+/-Rituximab), Gemcitabine, Lenalidomide, or Ibrutinib for the Treatment of Participants With Advanced Non-Hodgkin Lymphoma
“Business decision, insufficient enrollment, no safety or efficacy concerns.” - A Study to Evaluate INCB177054 in Participants With Select Advanced or Metastatic Solid Tumors
“This was a strategic business decision. There were no safety concerns contributing to this decision.” - A Safety Study of IV Stem Cell-derived Extracellular Vesicles (UNEX-42) in Preterm Neonates at High Risk for BPD
“The study was discontinued due to a business decision; no safety concerns were noted.” - Dual-Orexin Antagonism As a Mechanism for Improving Sleep and Drug Abstinence in Opioid Use Disorder
“Did not meet enrollment goals.”
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.