Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Pulmonary Hypertension
Type
Interventional
Phase
Phase 1
Design
Allocation: RandomizedIntervention Model: Sequential AssignmentMasking: Double (Participant, Investigator)Primary Purpose: Treatment

Participation Requirements

Age
Between 40 years and 80 years
Gender
Both males and females

Description

Part 1 of this study will assess safety, tolerability, and PK of MK-5475 compared to placebo. Part 2 of this study will assess safety, tolerability, PK, and changes in PVR and PBV of MK-5475 compared to placebo.

Part 1 of this study will assess safety, tolerability, and PK of MK-5475 compared to placebo. Part 2 of this study will assess safety, tolerability, PK, and changes in PVR and PBV of MK-5475 compared to placebo.

Tracking Information

NCT #
NCT04370873
Collaborators
Not Provided
Investigators
Study Director: Medical Director Merck Sharp & Dohme Corp.