RecruitingPhase 2NCT07192939
Multicenter, Randomized, Double-blind, Placebo-controlled Phase II Trial to Evaluate the Efficacy and Safety of HRS-9813 in Subjects With Pulmonary Fibrosis
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
- Guangdong Hengrui Pharmaceutical Co., Ltd
- Intervention
- HRS-9813 capsules(drug)
- Enrollment
- 270 target
- Eligibility
- 21 years · All sexes
- Timeline
- 2025 – 2028
Study locations (1)
- Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, Beijing Municipality, China
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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