A Trial of 18F-AV-133 Positron Emission Tomography (PET) Imaging to Differentiate Subjects With Parkinson's Disease (PD) From Other Movement Disorders

NCT ID: NCT01550484

Last Updated: 2017-02-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2/PHASE3
• Total Enrollment: 170 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-04-30
• Study Completion Date: 2016-03-31

Brief Summary

The purpose of this study is to determine whether 18F-AV-133 PET scans can be used to differentiate subjects with Parkinson's Disease from other movement disorders.

Detailed Description

The early detection and monitoring of neurodegenerative diseases including Parkinson's disease (PD), Alzheimer's disease (AD), Dementia with Lewy Bodies (DLB), and other dementias and movement disorders represent a very significant unmet medical need. Disease mechanisms are gradually becoming understood, and disease-modifying drugs are emerging that target the specific molecular pathology underlying each of these diseases. Tools for accurate and early differential diagnosis are thus necessary to determine the appropriate treatment for patients and to minimize inappropriate use of potentially harmful treatments. In addition, such diagnostic imaging tools are expected to permit monitoring of disease progression and will thus accelerate testing and development of disease-modifying drugs. Furthermore, the new imaging test may be useful as a prognostic tool by identifying humans suffering from neurodegenerative diseases before the clinical manifestations become evident.

Conditions

Parkinson's Disease; Primary Parkinsonism; Lewy Body Parkinson's Disease

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: SINGLE

Interventions

18F-AV-133

222 MBq (6 mCi)

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Males or females ≥ 40 years of age;
• Presenting (within the last 3 months) for an initial evaluation to a movement disorders specialist with signs or symptoms suggestive of a movement disorder;
• The subject's signs or symptoms were previously evaluated by a physician who was not a movement disorders specialist during the previous six months;
• Absence of an established clinical movement disorder diagnosis;
• Symptoms mild in intensity, this includes Hoehn & Yahr ≤ 2 (Exceptions are allowed for subjects who meet criteria for Hoehn & Yahr stage 3 due to early onset of postural instability and/or gait impairment out of proportion to his/her other Parkinson signs and symptoms);
• Montreal Cognitive Assessment (MoCA) score ≥ 22;
• Can tolerate imaging visit procedures; and
• Provide written informed consent prior to study entry.

Exclusion Criteria

• Have been referred to the movement disorders clinic primarily for the purpose of disease management (no diagnostic uncertainty exists on the part of the non-specialist or referring physician);
• Have a previous movement disorder diagnosis given by a movement disorders specialist prior to the time of enrollment;
• Have received a total of more than 90 days treatment with dopaminergic medications, including direct dopamine agonists or precursors (levodopa) or have received a total of more than 180 days treatment with MAO-B inhibitors, amantadine, anticholinergics or primidone or beta-blockers prescribed for treatment of tremor or signs of parkinsonism;
• Have had a sustained and clinically meaningful response to anti-parkinsonian medications;
• Are currently taking or have taken MAO-B inhibitors in the past 4 weeks;
• Have a known CNS structural lesion such as stroke or tumor that likely accounts for their symptoms;
• Have clinically meaningful cognitive impairment or dementia (mild cognitive problems as might be expected in the earliest stages of PD are not exclusionary);
• Have current clinically significant cardiovascular disease or clinically important abnormalities on screening ECG (including but not limited to QTc > 450 msec);
• Are currently taking medications that are known to cause QT-prolongation;
• Are currently taking medications with narrow therapeutic windows (e.g. warfarin or other anticoagulant therapies);
• Are currently taking tetrabenazine (TBZ), amphetamine type drugs;
• Have a current clinically significant endocrine or metabolic disease, pulmonary, renal or hepatic impairment, or cancer (excluding localized basal cell carcinoma and in situ prostate cancer) that would interfere with completion of the study;
• Have a recent history (within the past year) of alcohol or substance abuse or dependence;
• Are females of childbearing potential who are not surgically sterile, not refraining from sexual activity or not using reliable contraception. Females must not be pregnant (negative serum beta-hCG at the time of screening and negative urine beta-hCG on the day of imaging), must not be breastfeeding at screening, must avoid becoming pregnant and use adequate contraceptive methods for 14 days prior to and 24 hours after administration of 18F-AV-133 for injection;
• Have had prior intracranial surgery; and
• Are receiving any investigational medications, or have participated in a trial with investigational medications within the last 30 days.

• Minimum Eligible Age: 40 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Avid Radiopharmaceuticals

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Chief Medical Officer

Role: STUDY_DIRECTOR

Avid Radiopharmaceuticals

Locations

Research Site

Scottsdale, Arizona, United States

Research Site

Sun City, Arizona, United States

Research Site

New Haven, Connecticut, United States

Research Site

Kansas City, Kansas, United States

Research Site

Shreveport, Louisiana, United States

Research Site

Baltimore, Maryland, United States

Research Site

Boston, Massachusetts, United States

Research Site

St Louis, Missouri, United States

Research Site

Las Vegas, Nevada, United States

Research Site

Cleveland, Ohio, United States

Research Site

Philadelphia, Pennsylvania, United States

Research Site

Providence, Rhode Island, United States

Research Site

Dallas, Texas, United States

Research Site

Houston, Texas, United States

Research Site

Sydney, New South Wales, Australia

Countries

United States; Australia

Other Identifiers

18F-AV-133-B04

Identifier Type: -

Identifier Source: org_study_id