drugset / Trial / NCT02617615
A Trial to Evaluate Safety, Tolerability, PK and Antiviral Activity of MB-110 in Hepatitis C Virus Infected Patients
RandomizedParallel-groupDouble-blindTreatment
Summary
A Phase 1, First-in-Human, Randomized, Placebo-Controlled, Double-Blind Study to Evaluate the Safety, Tolerability, and Pharmacokinetic Profiles of Single Ascending and Multiple Oral Doses of MB-110 in Healthy Volunteers and to Evaluate the Antiviral Activity of MB-110 in Hepatitis C Virus Infected Subjects
Timeline
- Start
- 2017-12-01
- Primary completion
- 2018-06
- Completion
- 2018-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | MB-110 | Unknown | 50 mg | Oral |
| Subject | MB-110 | Unknown | 100 mg | Oral |
| Subject | MB-110 | Unknown | 200 mg | Oral |