PEARL-HD: [PETDE10] Imaging of PDE10A Enzyme Levels in Huntington's Disease Gene Expansion Carriers and Healthy Controls With PET.

• Sponsor: CHDI Foundation, Inc. (Other)
• Overall Status: Completed
• CT.gov ID: NCT02061722
• Collaborator: (none)
• Enrollment: 90
• Locations: 8
• Arm: 1
• Duration (Months): 40
• Patients Per Site: 11.3
• Patients Per Site Per Month: 0.3

Study Details

Study Description

Brief Summary

The aim of this study is to measure the availability of the PDE10A enzyme in Huntington disease gene expansion carriers (HDGECs) using the recently developed radioligand [18F]MNI-659. The study will be cross-sectional, examining HDGECs at different stages of the disease (pre-manifest, stage 1 and stage 2), in comparison with Healthy Controls (HCs). The HDGECs included in this study will be recruited from the large database of the REGISTRY (NCT01590589) or ENROLL-HD (NCT01574053) studies.

Condition or Disease	Intervention/Treatment	Phase
Huntington's Disease	Radiation: PET Imaging with [18F]MNI-659	Early Phase 1

Detailed Description

The study will be organized in an "adaptive-like" mode. Initially a cohort of 5 HDGECs and 5 HCs will be studied. The data obtained in the first cohort will be analysed and depending on the variability of the data, there will be approximately 10 HDGECs and an equal number of HCs in the second cohort and the size of the third cohort may be altered to in total include approximately 45 HDGECs and an equal number of HCs.

Study Design

• Study Type: Interventional
• Actual Enrollment: 90 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment
• Masking: None (Open Label)
• Primary Purpose: Diagnostic
• Official Title: [PETDE10] Imaging of Phosphodiesterase 10 A (PDE10A) Enzyme Levels in the Living Human Brain of Huntington´s Disease Gene Expansion Carriers and Healthy Controls With Positron Emission Tomography
• Study Start Date: Jan 1, 2013
• Actual Primary Completion Date: May 1, 2016
• Actual Study Completion Date: May 1, 2016

Arms and Interventions

Arm

Intervention/Treatment

Experimental: PET Imaging with [18F]MNI-659 All subjects (both HDGECs and HCs) will receive single intravenous doses of the radioligands [11C]raclopride (non-investigational medicinal product [NIMP]) and [18F]MNI-659 (investigational medicinal product [IMP]). The radioligands [11C]raclopride and [18F]MNI-659 will be administered at doses less than 10 micrograms, i.e. within the micro dosing concept, and no pharmacological effects are expected. The injected radioactivity of [11C]raclopride will be 300 MBq/70 kg of body weight ± 10%. The injected radioactivity of [18F]MNI-659 will be 185 MBq/70 kg of body weight ± 10%.

Radiation: PET Imaging with [18F]MNI-659; The radioligands [11C]raclopride and [18F]MNI-659 will be administered at doses less than 10 micrograms, i.e. within the micro dosing concept, and no pharmacological effects are expected. The injected radioactivity of [11C]raclopride will be 300 MBq/70 kg of body weight ± 10%. The injected radioactivity of [18F]MNI-659 will be 185 MBq/70 kg of body weight ± 10%.

Outcome Measures

Primary Outcome Measures

1. The primary outcome measure will be the distribution volume (VT) in the striatum (caudate and putamen), globus pallidus, and ventral striatum estimated using kinetic and graphical analysis. Thalamus, cortex and cerebellum will also be examined. [Visit 3: For HD subjects, this will occur within 90 days from the Screening Visit. For Healthy Controls, this will occur within 28 days of Screening visit.]

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 70 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

• Capacity to give full informed consent in writing, and have read and signed the informed consent

• Age 18 to 70 years, inclusive

• HCs: Healthy according to medical history, physical examination, ECG, vital signs, laboratory assessment and MRI, with a body mass index between 19 and 27 (both inclusive)

• HDGECs: Otherwise healthy according to medical history, no co-morbidity of psychotic disorders, physical examination, vital signs and laboratory assessments

• HDGECs:

(A) HD Stage 1 or HD Stage 2: Patients with a clinical diagnosis of HD, defined by the presence of noticeable motor disorder and 40 CAG repeats (HD stage 1: Total Functional Capacity (TFC) 11-13, HD stage 2: TFC 7-10); (B) Pre-manifest: Subjects that are carriers of the mutant Huntingtin gene with ≥40 CAG repeats, a disease burden score ≥ 275 (calculated by the equation ((CAGn-35.5) X age)), and a Total Motor Score (TMS) ≤ 5.

• Able and willing to travel to Stockholm

• Willing to comply with use of adequate contraceptive measures:

Exclusion Criteria:

• Any disease, condition or concomitant medications that significantly compromises the function of the body systems and that, in the opinion of the Investigator might interfere with the conduct of the study or the interpretation

• Regular use of any medication prohibited by this protocol with the exception for Viagra, Levitra and Cialis, which may be temporarily discontinued prior to the PET measurements

• HDGECs: History of other neurological condition (including brain surgery, intracranial haematoma, stroke/cerebrovascular disorders, epilepsy), co-morbidity of psychotic disorders

• HCs: Anamnesis/medical history of neurological conditions (Alzheimer´s disease, dementia, Parkinson´s disease, brain surgery, intracranial haematoma, stroke/cerebrovascular disorders, epilepsy) or psychiatric conditions schizophrenia, depression, bipolar disorder, attention-deficit hyperactivity disorder)

• HCs: Family history of HD

• History of or current alcohol or drug abuse or dependence

• History of anaphylactoid or anaphylactic reactions to any allergen including drugs and contrast media

• Haematological or biochemical parameters that are outside the normal range and are considered clinically significant by the Investigator

• Clinical relevant findings in the 12-lead ECG as determined by the evaluating physician

• Donation of blood (450 mL) within three months prior to Visit 3

• Contraindication to MRI, such as known claustrophobia, presence of metal devises or implants (e.g. pacemaker, vascular- or heart- valves, stents, clips), metal deposited in the body (e.g. bullets or shells), or metal grains in the eyes

• Participating in a clinical trial within the past 3 months

• HCs: previous participation in another PET study

• Positive viral test result for Hepatitis B or C or HIV 1 or 2

• Female subjects: breast-feeding or positive pregnancy test at screening or at Visit 3

• Contraindication for arterial cannulation (by assessment of Allen's test)

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	The Memory Clinic, Rigshopitalet	Copenhagen		Denmark
2	Leiden University Medical Center, Department of Neurology	Leiden		Netherlands	K5Q112
3	University of Oslo, Nevrologisk poliklinikk	Oslo		Norway	0372 Oslo
4	Skane Universitetssjukhus Lund, Neurologiska kliniken	Lund		Sweden	SE-221 85
5	Karolinska Universitetssjukhus, Huddinge	Stockholm		Sweden	SE-141 86
6	Karolinska University Hospital	Stockholm		Sweden	SE-171 76
7	KTA Karolinska Trial Alliance	Stockholm		Sweden	SE-171 76
8	Neurologkliniken Akademiska sjukhuset, ing 85	Uppsala		Sweden	SE-751 85

Sponsors and Collaborators

• CHDI Foundation, Inc.

Investigators

• Principal Investigator: Bernhard Landwehrmeyer, MD, PhD, Ulm University Hospital
• Study Director: Cristina Sampaio, MD, PhD, CHDI Foundation, Inc.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: CHDI Foundation, Inc.
• ClinicalTrials.gov Identifier: NCT02061722
• Other Study ID Numbers: CHDIKI1201/PET-HD-PDE10A
• First Posted: Feb 13, 2014
• Last Update Posted: Jun 1, 2016
• Last Verified: Mar 1, 2016

• Additional relevant MeSH terms: Huntington Disease

Study Results

No Results Posted as of Jun 1, 2016