drugset / Trial / NCT07036029

NAL ER IPF Respiratory Function and Safety Study

NCT07036029

Phase 1 Recruiting 10 enrolled Trevi Therapeutics
NaSingle-groupOpen-labelTreatment

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.

Timeline

Start
2025-08-21
Primary completion
2026-06-30
Completion
2026-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Nalbuphine Small molecule Oral