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Clinical Trial Summary

This is a phase Ib study to investigate the safety, pharmacokinetics and preliminary efficacy of ginsenoside compound K (GCK) tablets in patients with rheumatoid arthritis. This study is to be run in China involving 10-12 sites. It will enroll approximately 240 patients to ensure 128 randomized with active rheumatoid arthritis. The treatment period is 12 weeks and total study duration per patient is approximately 14 weeks.


Clinical Trial Description

In this double-blind, placebo-controlled, phase Ib study, 128 patients with active RA are planned to be enrolled and randomly assigned 1:1:1:1 to receive placebo, or different doses of GCK tablet (100/200/300 mg). This study will evaluate the safety, pharmacokinetics and preliminary efficacy of GCK tablets in patients with rheumatoid arthritis ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03755258
Study type Interventional
Source Zhejiang Hisun Pharmaceutical Co. Ltd.
Contact Jianwei Liao, Master
Phone +8657688827869
Email jwliao@hisunpharm.com
Status Recruiting
Phase Phase 1
Start date March 16, 2017
Completion date December 11, 2019

See also
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