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. 2020 Jul 23;2020(7):CD012990. doi: 10.1002/14651858.CD012990.pub2

ClinicalTrials.gov Identifier: NCT03439943.

Study name Study to evaluate the effect of lixisenatide in patients with Parkinson's disease (LixiPark)
Methods Multi‐centre, randomised, placebo‐controlled, double‐blind, parallel‐arm proof‐of‐concept trial
Participants With early PD
Interventions Intervention: lixisenatide (10 μg/d for 14 days, then 20 μg/d), once daily subcutaneously
Comparator: placebo, once‐daily subcutaneous injection
Outcomes Change from baseline to end point (M12) in MDS‐UPDRS III motor examination score, evaluated in the best ON condition in patients with early Parkinson's disease
Starting date June 2018
Contact information olivier.rascol@univ-tlse3.fr
Notes