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UnknownNCT03159052

Efficacy and Safety of SHR3824 as Monotherapy in Subjects With Type 2 Diabetes

A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel Group, Clinical Trial to Evaluate the Efficacy and Safety of SHR3824 as Monotherapy in in Chinese Type 2 Diabetic Patients With Inadequate Glycemic Control by Diet and Exercise

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
450 (estimated)
Sponsor
Jiangsu HengRui Medicine Co., Ltd. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to obtain information on efficacy and safety of SHR3824 over 24 weeks and 52 weeks in Chinese patients with Type 2 Diabetes. This will be done by comparing the effect of SHR3824 to placebo when given in oral doses.

Conditions

Interventions

TypeNameDescription
DRUGSHR3824Once daily, 52 weeks
DRUGPlaceboOnce daily, 24 weeks

Timeline

Start date
2017-06-01
Primary completion
2018-10-01
Completion
2019-06-01
First posted
2017-05-18
Last updated
2017-05-18

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03159052. Inclusion in this directory is not an endorsement.