Improving Beta-2 Adrenergic Signaling in Alzheimer's Disease

Palo Alto Veterans Institute for Research

Status and phase

Withdrawn

Phase 2

Conditions

Alzheimer's Disease

Cognitive Dysfunction

Treatments

Other: Formoterol B (placebo)

Drug: Formoterol A

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT02500784

ASJ0015

Details and patient eligibility

About

The purpose of this study is to test the effects of long-term therapeutic doses of formoterol, on a) cerebrospinal fluid (CSF) tau levels, and Amyloid Beta protein 40/42 levels in the CSF, and b) cognitive function in people with mild to moderate Alzheimer' Disease (AD).

Full description

The purpose of this study is to test the effects of long-term therapeutic doses of formoterol, on a) cerebrospinal fluid CSF tau levels, and A-beta amyloid protein 40/42 levels, and b) cognitive function: NE-ergic neurons undergo significant degeneration in AD. This system plays a significant role in cognition. Recent studies have indicated that increasing NE levels in the brain would significantly improve microglia migration and clearance of A-beta amyloid protein 40/42 levels in mouse models of AD. The investigators plan to test whether long- term daily treatment with inhaled formoterol solution would improve the structure and function of hippocampal neurons in AD. Study Design: Randomization and initiation of experimental treatment: All participants will be given formoterol daily for 52 weeks. The active regimen will be initiated as (20 micro gram, BID). The dose will be decreased if there is evidence of side effects, including cardiac or respiratory alteration changes, gastro-intestinal disturbances or neurological issues.

Sex

All

Ages

50 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Males and females between the ages of 50-85,
Mild-to-moderate AD (NINCDS/ADRDA criteria for probable AD will be used to establish AD diagnosis).
MMSE 16-26.

Exclusion criteria

Non-AD dementia or significant neurological disease such as Parkinson's disease, stroke, brain tumor,multiple sclerosis, seizure disorder, focal brain lesion, or head injury with loss of consciousness.
Hypothyroidism, congestive heart failure (New York Heart Association Class III or IV), significant extrapyramidal symptoms on neurological examination, serum creatinine>1.3 mg/dl, significant arrhythmias or conduction defect abnormalities on ECG,
Use of another beta2 adrenergic drug within the last 2 months.
Residence in a long-term care facility.
Evidence of any significant clinical disorder or laboratory finding that renders the person unsuitable for receiving an investigational new drug.
Known hypersensitivity or prior exposure to formoterol.
Active asthma or family history of asthma.