Trial intelligence / Profile preview

Safety, Tolerability, and PK of HRS-9813 in Healthy Volunteers

NCT06514963Phase 1Completed

Sponsor
Hengrui Therapeutics
Start
Jul 2024
Primary completion
Jan 2025
Modality
Small Molecules
Countries
1
01

Overview

Phase 1, randomised, double-blind trial of HRS-9813 in idiopathic pulmonary fibrosis (IPF) (2 arms), sponsored by Hengrui Therapeutics. Primary endpoint: Incidence of Adverse Event (AE) and Serious Adverse Event (SAE) at 14 days. Started Jul 2024; status: completed.

02

Drugs

HRS-9813
03

Conditions

idiopathic pulmonary fibrosis (IPF)

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