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A D2 Receptor Occupancy and fMRI Study in Schizophrenic Subjects Treated With Lurasidone

Primary Purpose

Schizophrenia

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Lurasidone 80 mg
Lurasidone 120 mg
Lurasidone 160 mg
Sponsored by
University of California, Irvine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Subjects are eligible to participate in this study if they:

  • are 18 to 60 years of age at the day of first dosing.
  • are diagnosed with schizophrenia or schizoaffective disorder.
  • are female, subject must be using an acceptable method of birth control or be surgically sterile or postmenopausal. Postmenopausal is defined as no period for at least 12 months. Acceptable methods of birth control include oral, injectable or implanted contraceptives, and barrier methods such as condoms, diaphrams, and spermicides.
  • are able to provide written informed consent.
  • can safety have an MRI (no metal in the body, not claustrophobic).

Exclusion Criteria:

Subjects are not eligible to participate in this study if they:

  • are treatment resisitant or intolerant to lurasidone.
  • have had extensive radiation exposure (the study doctor will discuss this with the subject).
  • if they have tremors or shaking of the limbs.
  • are pregnant or trying to become pregnant or breastfeeding.
  • are colorblind.
  • have a current or past history of a major medical illness or have abnormal lab values which the study doctor feels is significant (any abnormal lab values will be discussed with the subject).
  • are taking certain medications. The study doctor will discuss these medicines with the subject.
  • have a history of alcohol, cannabis or cocaine abuse within two weeks prior to the study.

Sites / Locations

  • UCI Medical Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Lurasidone 80 mg per day

Lurasidone 120 mg per day

Lurasidone 160 mg per day

Arm Description

Lurasidone 80 mg per day

Lurasidone 120 mg per day

Lurasidone 160 mg per day

Outcomes

Primary Outcome Measures

D2 receptor occupancy
To determine whether additional D2 receptor occupancy can be accomplished with doses of 160 mg of lurasidone per day.

Secondary Outcome Measures

Full Information

First Posted
November 1, 2013
Last Updated
November 1, 2013
Sponsor
University of California, Irvine
Collaborators
Dainippon Sumitomo Pharma America
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1. Study Identification

Unique Protocol Identification Number
NCT01979679
Brief Title
A D2 Receptor Occupancy and fMRI Study in Schizophrenic Subjects Treated With Lurasidone
Official Title
A D2 Receptor Occupancy and fMRI Study in Schizophrenic Subjects Treated With Lurasidone
Study Type
Interventional

2. Study Status

Record Verification Date
November 2013
Overall Recruitment Status
Completed
Study Start Date
December 2008 (undefined)
Primary Completion Date
October 2013 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, Irvine
Collaborators
Dainippon Sumitomo Pharma America

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this research study is to measure how many of the dopamine receptors lurasidone occupies throughout the brain of patients with schizophrenia or schizoaffective disorder and over what time period the occupancy occurs. This is research because lurasidone is an investigational medication that has not yet been approved by the Food and Drug Administration (FDA). Dopamine receptors have key roles in many processes, including the control of motivation, learning, and fine motor movement. The degree of occupancy and the transience of occupancy D2 receptor occupancy for optimal clinical response and to prevent relapses is a controversial area that this study will address. In this study Positron Emission Tomography (PET) scanning will be performed with D2/D3 ligand 18F-fallypride (a radioactive, injectable substance) to help the researchers measure the use of these receptors. Researchers hope that quantifying the amount of receptors being occupied by the medication will help them to determine the best dose of study medication in terms of improvement and least side effects related to body size and gender as well as in preventing relapse that may be related to hypersensitivity. Magnetic Resonance Imaging (fMRI) will also be performed. MRI is a scanning method which makes pictures of parts of the brain using a large magnetic field. This study will use a particular kind of MRI called fMRI, or functional MRI. fMRI takes pictures of the brain while the person is thinking or doing a simple task. fMRI will allow the researchers to investigate patients regional brain activation during cognitive (mental) and emotional tasks.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
28 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Lurasidone 80 mg per day
Arm Type
Active Comparator
Arm Description
Lurasidone 80 mg per day
Arm Title
Lurasidone 120 mg per day
Arm Type
Active Comparator
Arm Description
Lurasidone 120 mg per day
Arm Title
Lurasidone 160 mg per day
Arm Type
Active Comparator
Arm Description
Lurasidone 160 mg per day
Intervention Type
Drug
Intervention Name(s)
Lurasidone 80 mg
Intervention Type
Drug
Intervention Name(s)
Lurasidone 120 mg
Intervention Type
Drug
Intervention Name(s)
Lurasidone 160 mg
Primary Outcome Measure Information:
Title
D2 receptor occupancy
Description
To determine whether additional D2 receptor occupancy can be accomplished with doses of 160 mg of lurasidone per day.
Time Frame
Up to 6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects are eligible to participate in this study if they: are 18 to 60 years of age at the day of first dosing. are diagnosed with schizophrenia or schizoaffective disorder. are female, subject must be using an acceptable method of birth control or be surgically sterile or postmenopausal. Postmenopausal is defined as no period for at least 12 months. Acceptable methods of birth control include oral, injectable or implanted contraceptives, and barrier methods such as condoms, diaphrams, and spermicides. are able to provide written informed consent. can safety have an MRI (no metal in the body, not claustrophobic). Exclusion Criteria: Subjects are not eligible to participate in this study if they: are treatment resisitant or intolerant to lurasidone. have had extensive radiation exposure (the study doctor will discuss this with the subject). if they have tremors or shaking of the limbs. are pregnant or trying to become pregnant or breastfeeding. are colorblind. have a current or past history of a major medical illness or have abnormal lab values which the study doctor feels is significant (any abnormal lab values will be discussed with the subject). are taking certain medications. The study doctor will discuss these medicines with the subject. have a history of alcohol, cannabis or cocaine abuse within two weeks prior to the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven G Potkin, MD
Organizational Affiliation
University of California, Irvine
Official's Role
Principal Investigator
Facility Information:
Facility Name
UCI Medical Center
City
Orange
State/Province
California
ZIP/Postal Code
92868
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
24073841
Citation
Potkin SG, Keator DB, Kesler-West ML, Nguyen DD, van Erp TG, Mukherjee J, Shah N, Preda A. D2 receptor occupancy following lurasidone treatment in patients with schizophrenia or schizoaffective disorder. CNS Spectr. 2014 Apr;19(2):176-81. doi: 10.1017/S109285291300059X. Epub 2013 Sep 30.
Results Reference
result

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A D2 Receptor Occupancy and fMRI Study in Schizophrenic Subjects Treated With Lurasidone

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