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Completed NCT07185321

A Phase 1 Study of Mosliciguat in Healthy, Adult Males

Conditions: Healthy Volunteer

Sex: Male
Ages: 18 Years – 50 Years
Healthy volunteers: Yes
Phase: PHASE1
Enrollment: 8
Sponsor: Pulmovant, Inc.

Location: Pharmaron Baltimore Maryland

Summary

This is a single-center, Phase 1, open-label, 3-period, fixed-sequence study to investigate the bioavailability, absorption, metabolism, excretion and the safety of mosliciguat administered to healthy male adults.

Eligibility Criteria

Inclusion Criteria: * Participants willing and able to provide informed consent. * Considered to be in good health by the Investigator, as determined by medical history, physical examination, vital sign measurements, 12 lead electrocardiogram (ECG), and laboratory test results. Exclusion Criteria: * History or presence of any condition (e.g., chronic diarrhea, urinary incontinence), or prior surgery (e.g., gastric bypass) that, in the opinion of the Investigator, poses a significant risk to participant safety and/or achievement of study objectives * History or presence of COPD, moderate or persistent asthma, other chronic lung disease, or chronic respiratory condition within the last 5 years * Acute or recent respiratory infection symptoms not resolved at least 3 days prior to Period 1 check-in.

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07185321). StuddyBuddy aggregates publicly available trial information.