Clinical Trial

A Clinical Study to Evaluate the Safety, Tolerability and Pharmacokinetic Characteristics of RC010 Inhalation Powder in Healthy Participants

Not Yet Recruiting Phase 1
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Summary
This is a Phase 1A, first in human, randomized, double-blinded, placebo-controlled, dose escalation study of RC010 in healthy adult volunteers. RC010 is a small-molecule drug , being developed as a novel therapeutic treatment for patients with Idiopathic Pulmonary fibrosis (IPF). This study aims to evaluate the safety, tolerability and pharmacokinetics of RC010 after Single ascending doses .
Trial Details
NCT Number NCT07528703
Lead Sponsor Nanjing Reju Therapeutics Co., Ltd
Conditions IPF
Enrollment 42 participants
Start Date 2026-04
Primary Completion 2027-04 (estimated)
Study Completion 2027-12 (estimated)
Updated on ClinicalTrials.gov 2026-04-14