RecruitingPhase 3NCT07464912
A Adaptive Design Clinical Trial to Evaluate the Efficacy and Safety of TDI01 Suspension in the Treatment of Idiopathic Pulmonary Fibrosis (IPF)
Studying Idiopathic pulmonary fibrosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Beijing Tide Pharmaceutical Co., Ltd
- Intervention
- TDI01(drug)
- Enrollment
- 508 enrolled
- Eligibility
- 40-80 years · All sexes
- Timeline
- 2025 – 2029
Study locations (1)
- China-Japan Friendship Hospital, Beijing, Beijing Municipality, China
Collaborators
China-Japan Friendship Hospital
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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