CompletedPhase 1NCT03619616

Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Single Ascending Dose of ZSP1603 in Healthy Adults

Studying Idiopathic pulmonary fibrosis

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Key facts

Sponsor
Guangdong Zhongsheng Pharmaceutical Co., Ltd.
Principal Investigator
Guoping Yang, MD
The Third Xiangya Hospital of Central South University
Intervention
ZSP1603 7.5 mg(drug)
Enrollment
40 enrolled
Eligibility
18-50 years · All sexes
Timeline
20182019

Study locations (1)

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.

Open NCT03619616 on ClinicalTrials.gov

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