LivingGLP1
Study S002717

A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Fasiglifam (TAK-875) Compared to Placebo as Add-on to Preexisting Antihyperglycemic Therapy Over 16 Weeks With 36-week Extension in Type 2 Diabetic Subjects With Chronic Kidney Disease Stage 4 or Stage 5 on Dialysis

Registration

Registration
NCT02015780
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
QUADRUPLE
Status
WITHDRAWN
Enrollment
0
Start
2013-12
Primary completion
2016-01
Lead sponsor
Takeda
Conditions
Type 2 Diabetes Mellitus; Chronic Kidney Disease
Interventions
DRUG:Fasiglifam; DRUG:Placebo; DRUG:Antihyperglycemic therapy
Results posted
FALSE
Secondary identifiers
OTHER:U1111-1146-5546; EUDRACT_NUMBER:2013-003414-40

Registered primary outcomes

  • Change from Baseline in Glycosylated Hemoglobin (HbA1c) at Week 16 [Baseline and Week 16]

Linked records (0)

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