Efficacy and Safety of Tamibarotene (OAM80) for Alzheimer's Disease

Osaka City University

Status and phase

Unknown

Phase 2

Conditions

Alzheimer's Disease

Treatments

Drug: Placebo

Drug: Tamibarotene

Study type

Interventional

Funder types

Other

Identifiers

NCT01120002

OAM80-01

Details and patient eligibility

About

A double blind, placebo-controlled randomized study to evaluate the efficacy and safety of orally administered Tamibarotene to patients of Alzheimer's Disease

Full description

Tamibarotene is a synthetic retinoid presently approved in Japan for the treatment of APL, which has a higher receptor selectivity and activity for the Retinoic Acid Receptor subtypes compared to the natural retinoid.

Tamibarotene decreased insoluble amyloid-beta (Ab) 42 deposition in APP mice, and also increased TTR, VAChT and ACh in the brain of SAMP8 mice, which suggest the enhancement of neurotransmission. In the behavioral model such as reduced anxiety of SAMP8 mice and rat passive avoidance test, tamibarotene showed improvement.

Tamibarotene as in other retinoids are known to moderate the immune system and reduce inflammatory cytokines and chemokines, which may control the excessive stimulation of astrocyte and microglia around the Ab plaque. Tamibarotene reduced cytokines and showed clinical efficacy in the rat experimental autoimmune encephalitis model.

Furthermore, retinoids are known to have critical roles during the regeneration stage in the differentiation from neural stem cells (NSC).

In spinal cord injured rats treated with tamibarotene showed better recovery compared to the control.

By these preclinical results, we plan by this study to evaluate the efficacy together with the safety of tamibarotene to the patients of Alzheimer's Disease.

Tamibarotene is used clinically in Japan since 2005. It's side effects are known to be similar to that of other clinically used retinoids.

Enrollment

50 estimated patients

Sex

All

Ages

55 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Japanese patients who are diagnosed as probable Alzheimer' Disease according to NINCDS-ADRDA criteria
Diagnosed by brain diagnostic imaging (CT, MRI) within six months before the consent and no occurrence of the event after that to suggest cerebral vascular disease
Mild to Moderate Alzheimer's Disease of MMSE from 10 to 26
Age from 55 to 80
Treated for a minimum of 12 weeks with a stable dose of donepezil and willing to continue the same during the trial period
For women Menopause ≥ 2 years
For men contraceptive measures are required during the study and after 6 months
In principle patients should be living at their home in the presence of a caregiver who is defined as a healthy person in contact with the patient for more than 10 hours a week, could provide required information of the behavior and activities of daily living, accompany all the clinical examination, and supervise the handling and administration of the drug throughout the study period.
Patients who could take pills as a whole
Patient, caregiver and patient surrogate are able and willing to comply with study visits and procedures per protocol, understand, sign, and date the written voluntary informed consent form

Exclusion criteria

Any cause of dementia not due to Alzheimer's disease
Past history of other central nervous condition or psychiatric disease
Symptom of depression and drug addiction
Impairment in the physical function by other factor than the Alzheimer's Disease
Patients who are expected to move in to care facilities during the study period
triglyceride > 400 mg/dL