drugset / Trial / NCT03769896

Nabilone for Non-motor Symptoms in Parkinson's Disease

NCT03769896

Phase 2 Completed 48 enrolled Medical University Innsbruck
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a randomized placebo-controlled, double-blind, parallel-group, enriched enrollment randomized withdrawal study assessing the efficacy and safety of nabilone for non-motor symptoms in patients with Parkinson´s Disease. Nabilone is an analogue of tetrahydrocannabinol (THC), the psychoactive component of cannabis. Nabilone acts as a partial agonist on both Cannabinoid 1 (CB1) and Cannabinoid 2 (CB2) receptor in humans and therefore mimics the effect of THC but with more predictable side effects and less euphoria. Part 1 is an open-label dose adjustment phase of the study. In eligible patients, a screening period is followed by an open-label nabilone dose optimization phase and a stable phase for at least 1 week. Treatment responders will be included in Part 2 of the study (randomized placebo-controlled, double-blind, parallel-grouped). Part 2 is the placebo-controlled, double-blind, parallel-group randomized withdrawal phase of the study.

Timeline

Start
2017-10-03
Primary completion
2019-07-15
Completion
2019-07-15

Drugs

EvaluationDrugModalityDoseRoute
Comparator Nabilone Other / unclassified 0.25 mg Oral

Indications