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Clinical Trial Summary

This is a Phase I Clinical Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of SSD8432 in Healthy Adult Subjects


Clinical Trial Description

108 healthy adult subjects (including 72 subjects in Part A to C, 16-24 subjects in Part D, and 8-12 subjects in optional Part E), including both males and females, will be enrolled in the phase I study. This study will include Five parts: SSD8432 single dose and SSD8432 co-administrated with ritonavir (Part A), SSD8432 multiple dose (Part B), SSD8432 co-administrated with ritonavir multiple dose (Part C), SSD8432 co-administered ritonavir single dose in fasting and postprandial states (Part D: assessment of food effects) and optional part (Part E: Assessment of the safety and pharmacokinetics of SSD8432 in white healthy adult subjects) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05339646
Study type Interventional
Source Jiangsu Simcere Pharmaceutical Co., Ltd.
Contact Lily Chen
Phone +86 025-85566666
Email chenlihua2@simcere.com
Status Recruiting
Phase Phase 1
Start date April 7, 2022
Completion date December 2022

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