Autopsy report · NCT00860093
Efficacy and Safety of Using MPC-5971 in Subjects Undergoing Shock Wave Lithotripsy
Cause of deathFunding or business
“Sponsor Corporate Business Decision”
Life of this trial
- Registered 1 year 1 month before it started.
- Ran for about 8 months before it stopped.
- 135 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2
- Sponsor
- Mission Pharmacal
- Sponsor type
- Industry
- Conditions
- Nephrolithiasis
- Interventions
- placebo; MPC-5971
- Participants
- 135
- Sites
- 3
- Countries
- United States
Trials that died the same way
- A Study of Telitacicept for the Treatment of Moderately to Severely Active Systemic Lupus Erythematosus (REMESLE-2)
“Sponsor business decision” - Study With Bispecific Antibody Engaging T-cells, in Patients With Progressive Cancer Diseases With Positive PSCA Marker
“business decision by sponsor” - Study of Vitespen (HSPPC-96, Oncophage ®) for Immune Response Assessment in Participants With Resectable Renal Cell Carcinoma at Intermediate Risk of Recurrence
“Sponsor's business decision” - A Phase 1a/1b Study of ACTM-838 in Patients With Advanced Solid Tumors
“Sponsor's strategic business decision” - Phase 1 Study of GEN2 in Patients With Advanced Solid Tumors
“Sponsor strategic business 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.