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

• ClinicalTrials.gov Identifier: NCT02764892
• Recruitment Status: Completed
• First Posted: May 6, 2016
• Last Update Posted: May 6, 2016
• Sponsor: Vernalis (R&D) Ltd
• Information provided by (Responsible Party): Vernalis (R&D) Ltd

Study Description

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.

Condition or disease	Intervention/treatment	Phase
Parkinson's Disease	Drug: V81444	Phase 1

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.

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 6 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment
• Masking: None (Open Label)
• Primary Purpose: Basic Science
• Official Title: An Open Label Study of V81444 Using Positron Emission Tomography to Assess Occupancy of Brain Adenosine A2A Receptors & Functional & Perfusion MRI to Explore Effects on Regional Brain Activity & Perfusion in Healthy Male Volunteers
• Study Start Date: August 2012
• Actual Primary Completion Date: November 2012
• Actual Study Completion Date: March 2013

Arms and Interventions

Arm	Intervention/treatment
Experimental: V81444; Single oral dose of V81444	Drug: V81444; Single oral dose of V81444

Outcome Measures

Primary Outcome Measures :

1. Plasma concentration V81444 corresponding with 50% brain A2A receptor occupancy. [ Time Frame: 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 :

1. Cognitive function using functional MRI [ Time Frame: 5 hours after dosing ]
2. Change versus placebo in proportion of subjects with adverse events [ Time Frame: Up to 7 Days after last dose ]
3. Change versus placebo in proportion of subjects with abnormal laboratory findings [ Time Frame: Up to 7 Days after last dose ]
4. Change versus placebo in proportion of subjects with clinically significant abnormalities on vital signs [ Time Frame: Up to 7 Days after last dose ]
5. Change versus placebo in proportion of subjects with clinically significant abnormalities in 12-lead ECG [ Time Frame: Up to 7 Days after last dose ]
6. Change versus placebo in proportion of subjects with clinically significant abnormalities on physical examination [ Time Frame: Up to 7 Days after last dose ]

Eligibility Criteria

• Ages Eligible for Study: 25 Years to 55 Years (Adult)
• Sexes Eligible for Study: Male
• Accepts Healthy Volunteers: Yes

Criteria

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

Contacts and Locations

No Contacts or Locations Provided

More Information

• Responsible Party: Vernalis (R&D) Ltd
• ClinicalTrials.gov Identifier: NCT02764892
• Other Study ID Numbers: V81444-1PD-02
• First Posted: May 6, 2016
• Last Update Posted: May 6, 2016
• Last Verified: May 2016

Additional relevant MeSH terms:

Parkinson Disease; Parkinsonian Disorders; Basal Ganglia Diseases; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Movement Disorders; Neurodegenerative Diseases