NAL ER IPF Respiratory Function and Safety Study

Recruiting Phase 1 Interventional Study
Idiopathic Pulmonary Fibrosis
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
10 (estimated)
Sponsor
Trevi Therapeutics · Industry
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About This Trial

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.

Trial Locations
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Eligibility Criteria
Inclusion criteria: * Diagnosis of IPF as determined by a pulmonologist based on American Thoracic Society (ATS)/ European Respiratory Society (ERS) / Japanese Respiratory Society (JRS) / Asociación Latinoamericana de Tórax (ALAT) guidelines. * SpO2 ≥ 92%, taken after at least 5 minutes in a sittin…
Contacts

Connie Crum

203-654-3287

Connie.crum@trevitherapeutics.com

CONTACT

Paula Buckley

203-680-3864

Paula.buckley@trevitherapeutics.com

CONTACT