TrialAutopsyBuilt by Jawad Momani (Pwnedl0l)

Autopsy report · NCT02397395

An Efficacy, Safety, Tolerability and Pharmacokinetics Study of 12 Weeks Treatment With Simeprevir and Daclatasvir in Participants With Chronic Hepatitis C Virus Genotype 1b or 4 Infection and Either Severe Renal Impairment or End-stage Renal Disease on Hemodialysis.

Cause of deathSlow enrollment Automatic label, confidence 0.5, unverified. How labels are made.
“Trial has been cancelled due to availability of new therapeutic options for patient population”

The sponsor’s own words in the registry.

Life of this trial

201520162017Registered2015-03-19Planned start2015-05 (planned)Withdrawn (as of)2015-07-17

Vital statistics

Status
Withdrawn
Phase
Phase 2
Sponsor
Janssen R&D Ireland
Sponsor type
Industry
Conditions
Renal Impairment; End-stage Renal Disease
Interventions
Simeprevir (SMV) 150 mg; Daclatasvir (DCV) 60 mg
Participants
0
Sites
6
Countries
France, Spain

Trials that died the same way

Look deeper

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.