← Eichor
Study identifier: NCT05937191 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Leflunomide for Idiopathic Pulmonary Hemosiderosis in Children

Condition: Idiopathic Pulmonary Hemosiderosis · Leflunomide  ·  Sponsor: Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

PhasePhase 1/Phase 2
Planned participants34
Who can joinAll sexes, 5 Months to 18 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to compare Leflunomide in Idiopathic pulmonary hemosiderosis. The main questions it aims to answer are: * The efficacy and safety of Leflunomide in Idiopathic pulmonary hemosiderosis * The mechanism of leflunomide in treating Idiopathic pulmonary hemosiderosis Participants will be treated with leflunomide plus stroid. A comparison group: Researchers will compare the control group treated with stroid to see if the efficacy of Leflunomide would be better than control group.

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

Talk to the study team

Haiyan Wang, MD  ·  8613560489257  ·  wanghy78@mail.sysu.edu.cn

Weiping Tan, PhD  ·  8613556196566  ·  tanweip@mail.sysu.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Sun Yat-sen Memorial Hospital of Sun Yat-sen UniversityGuangzhou, Guangdong, ChinaRecruiting

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/NCT05937191