A Study of RO4602522 in Patients With Alzheimer Disease and in Healthy Volunteers

Roche

Status and phase

Completed

Phase 1

Conditions

Healthy Volunteer, Alzheimer's Disease

Treatments

Drug: 11C-L-deprenyl-D2

Drug: RO4602522

Study type

Interventional

Funder types

Industry

Identifiers

NCT01701089

BP28253

Details and patient eligibility

About

This open-label, multiple dose, parallel group study will assess the monoamine oxidase in the brain by in vivo positron emission tomography (PET) and safety of RO4602522 in patients with Alzheimer disease and in healthy volunteers. Patients and volunteers will receive multiple doses of RO4602522 and up to three injections of C11-L-deprenyl-D2 used in the PET.

Enrollment

17 patients

Sex

All

Ages

50 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

General:

Adults between 50-80 years of age. Females must be of non-child-bearing potential or if of child-bearing potential must use an acceptable form of contraception
Body mass index (BMI) 18.0-32.0 kg/m2 inclusive

Healthy volunteers:

Healthy, with no clinically relevant finding on physical examination at screening and Day -1
No suspicion of cognitive impairment/early dementia from neuropsychological battery as judged by the investigator
Able to participate and willing to give informed consent, and comply with the study restrictions.

Alzheimer Disease (AD) patients:

Probable Alzheimer's disease, based on the National Institute of Neurological and Communicative
Disorders and Stroke (NINCDS/ADRDA) and DSM-IV criteria
Have a MMSE score at screening between 17 and 26 inclusive
Modified Hachinski Ischemia Scale score of </=4
A neuroimaging evaluation of the brain by MRI which supports a diagnosis of AD, with no evidence of focal disease to account for dementia or MRI exclusion criteria
Medications taken for symptomatic treatment of AD must be maintained on a stable dosage regimen for at least 1 month before Day 1.
Able to participate in all scheduled evaluations
The patient has an appropriate caregiver or community dwelling with caregiver capable of accompanying subject on all visits to the center as judged by the investigator.
In the opinion of the investigator the patient and caregiver will be compliant and have a high probability of completing the study.
Signed and dated written informed consent obtained from the patient, co-signed by the patient's closest relatives and legally authorized representative, as required by national law for patients that are incapable of giving informed consent.

Exclusion criteria

General:

Any active disease of the gastrointestinal (GI) system, liver, or kidneys that could result in altered absorption, excess accumulation, or impaired metabolism or excretion of drugs, including a history of major upper or middle GI tract surgery or current significant chronic disease of the GI tract
Clinically relevant abnormal history, physical findings, ECG, or laboratory values at the screening assessment
History of cancer in the past five years, except for fully treated local basal carcinoma, or fully treated carcinoma in situ of cervix
Any major illness occurring within 1 month prior to the screening examination or febrile illness within 5 days prior to first dose
History of psychotropic medicine abuse
At risk of suicide in the opinion of the investigator or having a Yes to question number 4 or 5 of the Suicidal Ideation section of the C-SSRS
Administration of ionizing radiation or radioisotope for research, diagnostics test or therapy within 12 months prior to the present study which would exceed the local yearly radiation dose exposures for participation in research studies (except for dental x-rays, minimal plain films such as chest and ankle X-rays) or subjects who regularly work with ionizing radiation or radioactive material.
Participation in a clinical study with an investigational drug within 3 months before screening
Positive test for hepatitis B, hepatitis C, or HIV at screening
Loss or donation of more than 450 mL blood in the 4 months before screening or donation of plasma within 14 days of screening.
History of drug abuse or evidence of drug abuse in urine test performed at screening
Current alcohol abuse, or regular intake of more than 2 units of alcohol daily
Coffee (or tea) consumption > 5 cups per day or xanthine containing drinks >/1.5 liter/day

Healthy volunteers:

Family history of Alzheimer's disease in 1st and 2nd degree relative under 75 years.
Evidence or history of clinically significant neurological or psychiatric disorders.

AD Patients: