drugset / Trial / NCT02309918
HepNet Acute HCV IV - LDV/SOF FDC in Acute Genotype 1 Hepatitis C Virus Infection
Phase 2
Completed
20 enrolled
HepNet Study House, German Liverfoundation
Gilead Sciences · collabHannover Medical School · collab
NaSingle-groupOpen-labelTreatment
Summary
This is an open-label, single arm, multicenter, pilot-study to compare the efficacy and safety of LDV/SOF fixed dose combination (FDC) in subjects with acute genotype 1 HCV infection. A total of 20 subjects will be assigned to receive LDV/SOF FDC tablet (LDV 90 mg/SOF 400 mg/) once daily for 6 weeks.Patients will be followed up for 24 weeks.
Timeline
- Start
- 2014-11
- Primary completion
- 2016-08
- Completion
- 2016-08
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ledipasvir | Small molecule | 90 mg | Oral |
| Subject | Sofosbuvir | Small molecule | 400 mg | Oral |