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RECRUITING
NCT07036029
PHASE1

NAL ER IPF Respiratory Function and Safety Study

Sponsor: Trevi Therapeutics

View on ClinicalTrials.gov

Summary

The primary purpose of this study is to assess the safety and tolerability of escalating doses of NAL ER and to evaluate its effect on respiratory function in participants with IPF.

Official title: An Open Label, In-Clinic Study to Assess Respiratory Function and Safety of Escalating Doses of Nalbuphine Extended-Release Tablets (NAL ER) in Subjects With Idiopathic Pulmonary Fibrosis (IPF)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

10

Start Date

2025-08-21

Completion Date

2026-06-30

Last Updated

2026-04-09

Healthy Volunteers

No

Interventions

DRUG

NAL ER

Oral tablets

DRUG

Placebo

Oral tablets

Locations (2)

Mayo Clinic

Rochester, Minnesota, United States

Medicines Evaluation Unit Ltd.

Manchester, United Kingdom