LivingGLP1
Study S000168

The Safety, Preliminary Pharmacodynamics and Pharmacokinetics Study of rExenatide-4 in Chinese T2DM

Registration

Registration
NCT01342042
Acronym
SPPS
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
NONE
Status
UNKNOWN
Enrollment
36
Start
2011-03
Primary completion
2011-12
Lead sponsor
CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
Conditions
Type 2 Diabetes
Interventions
BIOLOGICAL:rExenatide-4
Results posted
FALSE

Registered primary outcomes

  • To compare treatment arms in terms of change from baseline to endpoint in HbA1c [12 Weeks]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0011151Pharmacokinetics and Preliminary Pharmacodynamics of Single- and Multiple-dose Lyophilized Recombinant Glucagon-like Peptide-1 Receptor Agonist (rE-4) in Chinese Patients with Type 2 Diabetes Mellitus.
Wang Y, Clinical drug investigation
2017Randomized trialPMID 28932995DOIcites ClinicalTrials.gov:NCT01342042; registry reference DERIVED:28932995