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Study on the Bioavailability of Three Different Prescription Processes of SHR4640 Tablets in Healthy Volunteers

Hyperuricemia Clinical Trial

Official title:
Study on the Bioavailability of Three Different Prescription Processes of SHR4640 Tablets in Healthy Volunteers (Single Center, Randomized, Open, 3 Cycles, 6 Sequences)

Clinical Trial Summary

The primary objective of the study is to evaluate the relative bioavailability of three different prescription processes of SHR4640 tablets in healthy volunteers. The secondary objective of the study is to observe the safety of SHR4640 tablets in healthy subjects.

Clinical Trial Description

Study Type: Interventional Enrollment: Number of Subjects: 24 Type: Anticipated

Allocation : Yes Intervention Model : Single center, randomized, open Intervention Model Description: 3 cycles, 6 sequences Masking: No Masking

Subjects were randomly divided into the group A, B, C, D, E and F. On D1, D8 and D15, six groups of subjects were respectively given A version or C version or D version of SHR4640 tablet. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04586803
Study type Interventional
Source Jiangsu HengRui Medicine Co., Ltd.
Contact Sheng Zhong, Master
Phone 13564101315
Email zhongsheng@hrglobe.cn
Status Not yet recruiting
Phase Phase 1
Start date October 2020
Completion date December 2020
View Details
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