← Eichor
Study identifier: NCT07719023 Synced from ClinicalTrials.gov · July 28, 2026
● Not Yet Recruiting

A Phase 3 Study of Efficacy and Safety of AK3280 in Patients With Idiopathic Pulmonary Fibrosis

Condition: Idiopathic Pulmonary Fibrosis (IPF)  ·  Sponsor: Shanghai Ark Biopharmaceutical Co., Ltd.

PhasePhase 3
Planned participants263
Who can joinAll sexes, 40 Years to no upper limit
Healthy volunteersNo

About this study

This is a phase 3 clinical study conducted in China. The primary objective is to compare the efficacy and safety of AK3280 400 mg versus placebo and active control (pirfenidone) in IPF patients.

This description comes directly from the study's public registry record.

Talk to the study team

Jayson Zhou  ·  +8618796252099  ·  jayson.zhou@arkbiosciences.com

Always discuss trial participation with your own doctor first.

Locations (1)

China-Japan Friendship HospitalBeijing, Beijing Municipality, China

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07719023