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Trials / Completed

CompletedNCT06168929

Bioequivalence Study of 2 Sizes of SHR4640 Tablets Orally in Healthy Subjects

Bioequivalence Study of 2 Sizes of SHR4640 Tablets in Healthy Subjects (Randomized, Open, Single Dose, Two Sequences, Two Cycles, Self-Crossover Control)

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
34 (actual)
Sponsor
Jiangsu HengRui Medicine Co., Ltd. · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The study is being conducted to evaluate the pharmacokinetic, and safety of two sizes of SHR4640 tablets in healthy adults, to explore the bioequivalence between two sizes of SHR4640 tablets.

Conditions

Interventions

TypeNameDescription
DRUGSHR4640SHR4640, 2.5mg\*4 - 10mg\*1
DRUGSHR4640SHR4640, 10mg\*1 - 2.5mg\*4

Timeline

Start date
2023-12-13
Primary completion
2024-01-13
Completion
2024-01-13
First posted
2023-12-13
Last updated
2024-01-23

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06168929. Inclusion in this directory is not an endorsement.

Bioequivalence Study of 2 Sizes of SHR4640 Tablets Orally in Healthy Subjects (NCT06168929) · Clinical Trials Directory