A Molecular and Functional Brain Imaging Study in Individuals With Down Syndrome and Healthy Controls Following Single Dose RG1662

NCT ID: NCT01667367

Last Updated: 2015-09-02

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 13 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-08-31
• Study Completion Date: 2013-10-31

Brief Summary

This single-center, single-blind, placebo-controlled, parallel-group study with crossover component will evaluate the GABAAalpha5 receptor expression, occupancy and functional connectivity in the brains of individuals with Down syndrome and healthy controls following single dose RG1662. Participants will receive a single dose of placebo before the imaging session (PET and MRI), and a single dose of RG1662 before the second imaging session.

Conditions

Healthy Volunteer, Down Syndrome

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Blinding Strategy: SINGLE

Study Groups

Placebo

Group Type: PLACEBO_COMPARATOR

placebo

Intervention Type: DRUG

Single oral dose

RG1662

Group Type: EXPERIMENTAL

RG1662

Intervention Type: DRUG

Single oral dose

Interventions

RG1662

Single oral dose

Intervention Type: DRUG

placebo

Single oral dose

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

Healthy controls and individuals with Down syndrome:

• Male and female adults, 18 to 40 years of age
• Body mass index (BMI) 18 - 40 kg/m2 inclusive
• Females of child-bearing potential and males with female partners of child-bearing potential must agree to use two medically approved methods of contraception, one of which must be a barrier method, for the duration of the study and for 4 months after the last study drug administration
• Clinical laboratory values within normal limits or abnormalities considered not significant by the investigator and sponsor; individuals with thyroid disease may be included in the study provided they are euthyroid and stable on treatment for at least one month prior to screening

Individuals with Down syndrome must also meet the following:

• Diagnosis of Down syndrome confirmed by karyotype; subjects may have free trisomy 21 or Robertsonian translocations; mosaic Down syndrome will be excluded
• Individuals must have a parent or other reliable caregiver who agrees to accompany the inidvidual to all clinic visits, provide information about the individual as required by protocol, and be willing to give informed consent

Exclusion Criteria

• Regular smoker (>5 cigarettes or equivalent: 3 cigars, 6 cigarillos, 3 pipes per day)
• Concomitant disease or condition or any clinically significant finding at screening that could interfere with, or for which the treatment might interfere with the conduct of the study, or that would, in the opinion of the investigator, pose an unacceptable risk to the subject in this study
• Severe head trauma or CNS infections (e.g. meningitis)
• History of epilepsy or seizures other than benign febrile convulsions of childhood
• Any confirmed significant allergic reactions against any drug, anaphylaxis or severe environmental allergies as judged by the investigator
• Positive for hepatitis B, hepatitis C or HIV infection
• Positive urine test at screening or at follow-up for drugs of abuse, or positive alcohol breath test at screening and prior to dosing
• Previous inclusion in research and/or medical protocol involving nuclear medicine, PET or radiological investigations with significant radiation burden (as defined by protocol)
• Pregnant or lactating women
• Individuals with evidence or meeting clinical diagnosis of dementia

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 40 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Hoffmann-La Roche

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Clinical Trials

Role: STUDY_DIRECTOR

Hoffmann-La Roche

Locations

London, , United Kingdom

Countries

United Kingdom

Other Identifiers

2012-001301-24

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

BP25611

Identifier Type: -

Identifier Source: org_study_id