Autopsy report · NCT01337518
A Phase 1a/1b Study to Evaluate the Safety of EZN-4176, in Adult Patients With Castration-Resistant Prostate Cancer
Cause of deathFunding or business
“Reassessment of strategic direction”
Life of this trial
- Suspended: paused, and may or may not restart.
- 150 participants planned (an estimate, not an actual count).
Vital statistics
- Status
- Suspended
- Phase
- Phase 1
- Sponsor
- Enzon Pharmaceuticals, Inc.
- Sponsor type
- Industry
- Conditions
- Prostatic Neoplasm
- Interventions
- EZN-4176
- Participants
- 150 (planned, not actual)
- Sites
- 2
- Countries
- United Kingdom, United States
Trials that died the same way
- PEPI-TiDP23-C104 is a First in Human Study With a Single Dose Escalation Part and a Multiple Dosing Part for Compounds TMC589337 and TMC589354.
“strategic decision” - Study to Evaluate Adverse Events and Movement of Intravenously (IV) Infused ABBV-787 in Adult Participants With Relapsed/Refractory (R/R) Acute Myeloid Leukemia (AML)
“Strategic considerations” - Rapid Amniotic Fluid (AF) Test and a Non-Invasive Vaginal Fluid (VF) Test
“Business Strategic Decision” - Clinical and Microbial Efficacy of Besifloxacin Ophthalmic Suspension, 0.6% in the Treatment of Bacterial Conjunctivitis
“Strategic business decision” - Dendritic Cell Immunotherapy Plus Standard Treatment of Advanced Renal Cell Carcinoma
“Strategic corporate decision”
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.