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A Study in Healthy Male Volunteers to Investigate a New Drug for the Treatment of Parkinson's Disease

Phase 1
Completed
Conditions
Parkinson's Disease
Interventions
Registration Number
NCT02764892
Lead Sponsor
Vernalis (R&D) Ltd
Brief Summary

The main purpose of the study is to identify the best dose of V81444 to use in future trials in patients with Parkinson's disease. The study will also explore the effects of V81444 on brain activity and blood flow with tests of mental ability ("cognitive function tests"). It will also check how safe V81444 is and how well it is tolerated after dosing.

Detailed Description

In this Phase I, single-centre, open-label, adaptive, single-dose study at multiple dose levels, the relationship between dose and plasma concentration of orally administered V81444 to brain A2A RO was investigated in 6 healthy male volunteers. In addition, the effects of V81444 on regional brain activity and perfusion during tests of cognitive function, and the safety and tolerability of V81444 were assessed. For each subject, the study consisted of a screening visit, a baseline visit, a treatment period, and a safety follow-up visit. The dose of V81444 and timing of scans performed were defined in the protocol for the first 2 subjects only. The dose, nature and timings of assessments for subsequent subjects were determined based on review of emerging receptor binding, pharmacokinetic (PK), pharmacodynamic (PD) and safety information.

In each treatment period, subjects were admitted to the unit on the day before dosing (Day -1), received a single oral dose of V81444 on Day 1 and, subject to satisfactory medical review, were discharged a minimum of 12 h after dosing. Overall, 3 doses of V81444 were assessed (250 mg, 50 mg, and 100 mg), with 2 subjects included at each dose level. PD assessments were performed at baseline and after each dose of V81444 using PET (with the A2A radioligand, to measure brain A2A RO, as well as MRI techniques to investigate the effects of V81444 on regional brain activity and perfusion during cognitive function tests. PK parameters were assessed by assay of V81444 concentration in plasma. Safety and tolerability were assessed by monitoring physical examination findings, adverse events (AEs), vital signs, 12 lead electrocardiogram (ECG) and clinical laboratory safety tests.

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
6
Inclusion Criteria
  • Healthy male volunteers: aged 25 to 55 years, in good general health as determined by medical history, physical examination and screening investigations, and taking no regular medication.
  • Confirmation to be sought for all volunteers that their general practitioner has provided an acceptable medical history.
Exclusion Criteria
  • Any significant medical condition or a history of such a condition that the Investigator considers should exclude the subject from the study.

Specific exclusion criteria relate to

  • usual caffeine intake and willingness to abstain from caffeine
  • history or evidence of clinically significant gastro-intestinal disease
  • presence of structural brain abnormality
  • contraindications or cautions for MRI scanning
  • clotting test results
  • exposure to significant levels of ionising radiation in the past

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
V81444V81444Single oral dose of V81444
Primary Outcome Measures
NameTimeMethod
Plasma concentration V81444 corresponding with 50% brain A2A receptor occupancy.Up to 27 hours after a single dose

Plasma concentrations of V81444 and binding of \[11C\]SCH442416 radioligand to brain A2A receptors using PET before and after V81444 dosing to determine occupancy of A2A receptors by V81444.

Secondary Outcome Measures
NameTimeMethod
Change versus placebo in proportion of subjects with adverse eventsUp to 7 Days after last dose
Change versus placebo in proportion of subjects with abnormal laboratory findingsUp to 7 Days after last dose
Change versus placebo in proportion of subjects with clinically significant abnormalities on vital signsUp to 7 Days after last dose
Change versus placebo in proportion of subjects with clinically significant abnormalities in 12-lead ECGUp to 7 Days after last dose
Cognitive function using functional MRI5 hours after dosing
Change versus placebo in proportion of subjects with clinically significant abnormalities on physical examinationUp to 7 Days after last dose
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