Viewing Study NCT02392494


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Study NCT ID: NCT02392494
Status: COMPLETED
Last Update Posted: 2019-01-22
First Post: 2015-03-16
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: Evaluation of MK-1075 in Participants With Hepatitis C Virus (HCV) Infection (MK-1075-002)
Sponsor: Merck Sharp & Dohme LLC
Organization:

Study Overview

Official Title: A Single Rising Dose Study to Evaluate Safety, Pharmacokinetics and Pharmacodynamics of MK-1075 in HCV-Infected Patients
Status: COMPLETED
Status Verified Date: 2019-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to evaluate the safety and pharmacokinetics of MK-1075, and to determine the ability of MK-1075 to reduce HCV viral load, following administration of a single dose in HCV-infected participants.
Detailed Description: Per protocol, panels may be omitted if the objectives of the study are met in preceding panels.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
2015-000127-93 EUDRACT_NUMBER None View
MK-1075-002 OTHER Merck Protocol Number View