Evaluation of the Efficacy and Safety of Azeliragon (TTP488) in Patients With Mild Alzheimer's Disease
Status: | Terminated |
---|---|
Conditions: | Alzheimer Disease |
Therapuetic Areas: | Neurology |
Healthy: | No |
Age Range: | 50 - Any |
Updated: | 6/10/2018 |
Start Date: | April 2015 |
End Date: | June 1, 2018 |
Randomized, Double-blind, Placebo Controlled, Multi-center Registration Trial to Evaluate the Efficacy and Safety of Azeliragon (TTP488) in Patients With Mild Alzheimer's Disease Receiving Acetylcholinesterase Inhibitors and/or Memantine
This is a study to evaluate the efficacy and safety of azeliragon in patients with mild
Alzheimer's disease. Patients will receive either azeliragon or placebo with a patient's
participation lasting approximately 18 months.
Alzheimer's disease. Patients will receive either azeliragon or placebo with a patient's
participation lasting approximately 18 months.
Inclusion Criteria:
- Diagnosis of probable Alzheimer Disease (AD) with documented evidence of progression
of disease
- Mini Mental State Examination (MMSE) score of 21-26, inclusive
- Clinical Dementia Rating global score of 0.5 or 1
- Rosen-Modified Hachinski Ischemia Score less than or equal to 4
- Brain magnetic resonance imaging (MRI) consistent with the diagnosis of probable AD
- Concurrent use of cholinesterase inhibitor or memantine with stable dose for at least
3 months prior to randomization
- Caregiver willing to participate and be able to attend clinic visits with patient
- Ability to ingest oral medications
Exclusion Criteria:
- Significant neurological or psychiatric disease other than Alzheimer's disease
- Participants with evidence or history of severe drug allergies (resulting in dyspnea
or severe rash).
- Any contraindications to MRI (e.g., clinically significant claustrophobia,
non-removable ferromagnetic implants). Patients with contraindications to MRI may
undergo computed tomography (CT) on approval by sponsor.
- Any contraindications to the FDG-PET study (e.g. allergy to any component of the FDG
dose) in the cohort undergoing a PET scan.
- Previous exposure to investigational or non-investigational therapies for Alzheimer's
disease within 6 months of screening
- History of cancer within the last 5 years except adequately treated cervical carcinoma
in-situ, cutaneous basal cell or squamous cell cancer, or non-progressive prostate
cancer not requiring treatment
- Women of childbearing potential
- Uncontrolled blood pressure and/or blood pressure above 160/100
- Prescription medical food intended for dietary management of the metabolic processes
associated with Alzheimer's disease.
- Diagnosis or history of cerebrovascular stroke, severe carotid stenosis, cerebral
hemorrhage, intracranial tumor, subarachnoid hemorrhage.
- Patients with unstable, uncontrolled diabetes (HbA1c > 7.7%) and those requiring
insulin.
We found this trial at
75
sites
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