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UnknownNCT06204419

A Phase I Study of XH-S002 in Healthy Volunteers

A Phase I Study to Assess the Safety, Tolerability, and Pharmacokinetics of XH-S002 After Single Ascending Doses, Multiple Ascending Doses and Evaluation of Food Effects in Healthy Volunteers

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
86 (estimated)
Sponsor
S-INFINITY Pharmaceuticals Co., Ltd · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The purpose of the study is to assess the safety, tolerability and pharmacokinetics of XH-S002 in healthy volunteers under SAD (Single ascending dose) and MAD (Multiple ascending dose) studies. In addition, this study evaluates the food effects of XH-S002.

Conditions

Interventions

TypeNameDescription
DRUGXH-S002 (A)XH-S002 powder will be administered orally as per assigned treatment regimen.
OTHERPlacebo(B)XH-S002 Placebo (matched) will be administered orally as per assigned treatment regimen.

Timeline

Start date
2023-12-26
Primary completion
2024-07-01
Completion
2024-10-01
First posted
2024-01-12
Last updated
2024-01-12

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06204419. Inclusion in this directory is not an endorsement.

A Phase I Study of XH-S002 in Healthy Volunteers (NCT06204419) · Clinical Trials Directory