Autopsy report · NCT02956629
Efficacy and Safety of Uprifosbuvir (MK-3682) + Ruzasvir (MK-8408) in Treating Hepatitis C Virus Infection Genotypes 1-6 (MK-3682-041)
Cause of deathFunding or business
“The study was terminated based on review of Phase 2 efficacy data”
Life of this trial
- Ran for about 1 year 4 months before it stopped.
- 282 participants enrolled.
- Results were posted on the registry 10 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2
- Sponsor
- Merck Sharp & Dohme LLC
- Sponsor type
- Industry
- Conditions
- Hepatitis C
- Interventions
- Uprifosbuvir; Ruzasvir; Ribavirin
- Participants
- 282
Trials that died the same way
- A Dose Exploration Study With Birabresib (MK-8628) in Participants With Selected Hematologic Malignancies (MK-8628-005)
“This study was terminated due to limited efficacy and not due to safety reasons” - Avelumab in Previously Untreated Patients With Epithelial Ovarian Cancer (JAVELIN OVARIAN 100)
“The study was terminated based on the results of a planned interim analysis that showed futility of efficacy.” - Relative Bioavailability Study of Ropinirole Implants in Parkinson's Patients on L-Dopa Switched From Oral Ropinirole
“This study was terminated for reasons not related to efficacy or safety” - A Study of Tadalafil for Duchenne Muscular Dystrophy
“The study is being terminated for lack of efficacy” - Dasatinib in Polycythemia Vera
“This study was terminated due to lack of efficacy.”
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.