LivingGLP1
Study S002075

Phase IIa Study to Evaluate the Efficacy and Safety of Subcutaneous SR-Exenatide (PT320) in Patients With Early Parkinson's Disease

Registration

Registration
NCT04269642
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
UNKNOWN
Enrollment
99
Start
2020-03-19
Primary completion
2021-09-29
Lead sponsor
Peptron, Inc.
Conditions
Early Parkinson's Disease
Interventions
DRUG:PT320 2.0mg Placebo; DRUG:PT320 2.0 mg; DRUG:PT320 2.5 mg
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Change of MDS-UPDRS part 3 score [48 week]

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