Tocotrienols in Parkinson's Disease (PD): A Pilot, Randomised, Placebo-controlled Trial

Who is this study for? Patients with Parkinson's disease
What treatments are being studied? Tocovid Suprabio
Status: Recruiting
Location: See all (2) locations...
Intervention Type: Other, Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

A study using Parkinson's disease animal model, transgenic fruit flies, demonstrated the potential of using tocotrienols (HOV-12020) as a therapeutic agent for delaying Parkinsonian motor dysfunctions. The proposed study aims to enrol 100 PD patients in a randomized placebo-controlled trial to investigate the effects of tocotrienols (HOV-12020) in motor and non-motor outcomes. Patients will be given oral tocotrienols (400mg/day) or placebo for 104 weeks. They will be assessed using the standard assessments scales in PD at baseline, Week 52 and Week 104. Neuropsychological evaluation will also be completed at these intervals to monitor progression of cognitive impairment (if any). Additional PD staging using MDSUPDRS (Part III), Hoehn \& Yahr (H\&Y) will be conducted at Week 26 and week 78. Blood samples will be collected to evaluate PD biomarkers and for safety monitoring (liver function, renal function and hematology).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Maximum Age: 90
Healthy Volunteers: f
View:

• Men or women aged between 40 - 90 years (inclusive).

• Able to provide written informed consent and able to comply with study protocol.

• Idiopathic PD of more than 1 years duration from diagnosis. The diagnosis must be confirmed by presence of bradykinesia and at least 1 other cardinal sign (resting tremor, rigidity), without any other known or suspected cause of parkinsonism.

• Hoehn \& Yahr =\> 2 with treatment.

• Patients on PD medication(s) e.g. levodopa, dopamine agonists, amantadine and/or Monoamine oxidase (MAO)-B inhibitors, must be on stable dose, for at least 30 days prior to screening. Medication and dose adjustments are allowed but must be documented.

• Patients on anti-depressant or anxiolytic medication must be on stable dose for at least 90 days prior to screening.

• The patient is willing to abstain from Vitamin E supplements (tocopherols and tocotrienols) and other dietary supplements which contain Vitamin E (tocopherols and tocotrienols) up to 14 days before baseline visit, and throughout the clinical study, unless prescribed by their physician for medical reasons.

Locations
Other Locations
Singapore
National Neuroscience Institute
RECRUITING
Singapore
Singapore General Hospital
RECRUITING
Singapore
Contact Information
Primary
Elaine Ang
elaine_sl_ang@nni.com.sg
(65) 65762660
Time Frame
Start Date: 2021-04-01
Estimated Completion Date: 2025-07-31
Participants
Target number of participants: 100
Treatments
Experimental: Tocovid Suprabio (HOV-12020)
200mg, twice 1 day, 12 months
Placebo_comparator: Placebo
200mg, twice 1 day, 12 months
Related Therapeutic Areas
Sponsors
Leads: National Neuroscience Institute

This content was sourced from clinicaltrials.gov