Nabilone for Non-motor Symptoms in Parkinson's Disease

Last updated: February 10, 2021
Sponsor: Medical University Innsbruck
Overall Status: Completed

Phase

3

Condition

N/A

Treatment

N/A

Clinical Study ID

NCT03773796
1.3
  • Ages 30-100
  • All Genders

Study Summary

This is an open-label extension study for participants of the randomized placebo-controlled, double-blind, parallel-group, enriched enrolment randomized withdrawal NMS-Nab Study, assessing the long-term safety and efficacy of nabilone for non-motor symptoms in patients with Parkinson´s Disease (PD). 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.

Eligible patients will be re-tapered in an open-label nabilone dose optimization phase followed by an open-label period of 6 months on a stable nabilone dose.

Eligibility Criteria

Inclusion

Inclusion Criteria: In order to be eligible for participation in the study, subjects must meet all inclusioncriteria:

  1. In order to be eligible for the study, patients must have completed the double-blindphase of the NMS-Nab trial as responders within the last 2 months.
  2. For patients that completed NMS-Nab Study over 2 months prior to the Screening /Baseline Visit, and meet all other inclusion criteria, eligibility should be discussedon a case-by-case basis.
  3. Only patients without a drug-related serious adverse event (SAE) or (drug-related)moderate or severe AE during the NMS-Nab Study can be included in the study
  4. Patients must be able and willing to provide written informed consent prior to anystudy related procedure being performed. Patients with a legal guardian should beconsented according to local requirements.
  5. Patients must be willing and able to take oral medication and able to comply with thestudy specific procedures.
  6. The patient is in good health as determined by medical examination and based on theinvestigator's judgement

Exclusion

Exclusion Criteria: Patients with any of the following characteristics will be excluded from entering thestudy:

  1. Patients with PArkinson´s Disease (PD) who have not participated in the randomizeddouble-blind phase of the previous NMS-Nab Study.
  2. Patients that experienced a drug-related SAE or had a (drug-related) moderate orsevere AE during the NMS-Nab Study will be excluded in the study.
  3. Patients who are unable or unwilling to comply with the study procedures in theinvestigator´s opinion.
  4. Patients with any clinically significant or unstable medical or surgical condition atthe Screening / Baseline Visit that may preclude safety and the completion of thestudy participation (based on the investigator's judgement).

Study Design

Total Participants: 22
Study Start date:
August 06, 2018
Estimated Completion Date:
January 31, 2020

Study Description

This is an open-label extension study for participants of the randomized placebo-controlled, double-blind, parallel-group, enriched enrolment randomized withdrawal NMS-Nab Study, assessing the long-term safety and efficacy of nabilone for non-motor symptoms in patients with Parkinson´s Disease. Nabilone is an analogue of tetrahydrocannabinol (THC), the psychoactive component of cannabis.

Eligible subjects will be re-tapered with open-label nabilone, optimally up to the dose the patient had in the NMS-Nab Trial. It is the investigator´s decision to modify this dose, if necessary. The re-tapering will be performed up to a maximum dose of 1 mg twice daily. Treatment responders will enter the open-label treatment period for 6 months with visits being performed every 3 months in the context of the patient´s regularly scheduled visits in the specialized outpatient department. The last visit will be the Termination Visit. Following this, nabilone will be tapered. During this period the patients will receive phone calls every other day. A Safety Follow-Up Visit will be performed.

Connect with a study center

  • Department of Neurology - Medical University Innsbruck

    Innsbruck, Tyrol 6020
    Austria

    Site Not Available

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