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Study identifier: NCT06267183 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Clinical Study to Evaluate Safety, Tolerability and Pharmacokinetics of SV001 in Chinese Healthy Adult Volunteers.

Condition: Idiopathic Pulmonary Fibrosis  ·  Sponsor: Shanghai Synvida Biotechnology Co.,Ltd.

PhaseEARLY_Phase 1
Planned participants53
Who can joinAll sexes, 18 Years to 45 Years
Healthy volunteersNo

About this study

The purpose of this study is to evaluate safety, tolerability, PK and immunogenicity of SV001 compare to placebo in Chinese healthy adult volunteers.

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

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Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (1)

Shanghai Xuhui District Central HospitalShanghai, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06267183