LivingGLP1
Study S003271

A Phase 2, Double-blind Dose Escalation Regimen of Once-Weekly OPK-88003 in Subjects With Type 2 Diabetes

Registration

Registration
NCT03406377
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
TRIPLE
Status
COMPLETED
Enrollment
113
Start
2018-04-02
Primary completion
2019-03-08
Lead sponsor
OPKO Health, Inc.
Conditions
Type 2 Diabetes Mellitus
Interventions
DRUG:OPK-88003; DRUG:Placebo
Results posted
TRUE

Registered primary outcomes

  • Change in HbA1c in Subjects With Type 2 DM [From baseline to 30 weeks]

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