drugset / Trial / NCT05387785

Study to Assess the Safety and Tolerability of ANG-3070 in Subjects With Idiopathic Pulmonary Fibrosis

NCT05387785 ↗

Phase 1 Unknown 20 enrolled Angion Biomedica Corp
RandomizedCrossoverTriple-blindTreatment

Summary

The purpose of this study is to assess safety and tolerability of once daily (QD) and twice daily (BID) dosing of ANG-3070 in subjects with idiopathic pulmonary fibrosis (IPF) who are treatment-naïve, refused therapy, or discontinued for any reason current standard of care with nintedanib or pirfenidone.

Timeline

Start
2022-06
Primary completion
2022-11
Completion
2022-11

Drugs

EvaluationDrugModalityDoseRoute
Subject ANG-3070 Unknown 300 mg Oral
Subject ANG-3070 Unknown 500 mg Oral