Overview

A Study of Single Doses of MK -5475 on Pulmonary Vascular Resistance (MK-5475-002)

Status:
Completed
Trial end date:
2020-12-11
Target enrollment:
Participant gender:
Summary
This is a 2-part, 4-panel study of MK-5475 in participants with Group 1 pulmonary arterial hypertension (PAH). Part 1 is a double-blind, randomized, single-ascending dose assessment of the safety, tolerability and pharmacokinetics (PK) of inhaled MK-5475. Part 2 of this study is an open-label study and will assess the safety, tolerability, PK and pharmacodynamics of inhaled MK-5475 at dose determined by results of Part 1 and Period 1 of Part 2 of the study. There is no formal hypothesis to be tested.
Phase:
Phase 1
Details
Lead Sponsor:
Merck Sharp & Dohme Corp.