drugset / Trial / NCT01725802

A Safety, Tolerability, and Plasma Concentration Study of Levodopa/Carbidopa Subcutaneous Solution (ND0612) in Parkinson's Disease (PD) Patients

NCT01725802 ↗

Phase 1 Completed 8 enrolled NeuroDerm Ltd.
RandomizedCrossoverQuadruple-blindTreatment

Summary

In this Phase I/IIa study, the effect of continuous subcutaneous administration of LD/CD solution (ND0612) on the safety and PK profile of LD will be examined.

Timeline

Start
2012-12-16
Primary completion
2013-02-26
Completion
2013-02-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Levodopa/carbidopa Unknown — —

Indications