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
“Trial has been cancelled due to availability of new therapeutic options for patient population”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
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- Withdrawn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
- Exploratory Study of Farletuzumab to Treat Resectable, Non-functioning Pituitary Adenomas
“Trial terminated due to focus of primary therapeutic areas.” - Phase 3 Trial to Evaluate the Efficacy and Safety of DKP21102_B Added on to DKP21102_A Compared With DKP21102_A
“The clinical trial was withdrawn due to a commercial decision.” - Effect of Citalopram on Chest Pain in Patients With Functional Chest Pain
“The clinical trial has ended prematurely due to low patient recruitment” - A Study to Evaluate the Efficacy and Safety of Liso-cel Compared to Standard of Care in Adults With Relapsed or Refractory Follicular Lymphoma
“Replaced with another clinical trial.” - Neoadjuvant Lu-PSMA Radioligand Therapy and Ipilimumab in Men With Very High-risk Prostate Cancer
“The clinical trial has been terminated due to the revocation of funding. Although one subject was enrolled, the participant withdrew prior to receiving any treatment. No trial-related procedures generating evaluable clinical data were performed.”
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.