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Clinical Trial Results Highlight Diverse Ways to Treat Alzheimer’s Disease
Researchers are exploring new pharmacologic and nutritional methods of preserving patients’ independence and cognitive function.
2012;20(10):22

VANCOUVER—New pharmaceuticals and a recently developed nutritional product are among the strategies being explored for the treatment of Alzheimer’s disease, according to research presented at the 2012 Alzheimer’s Association International Conference. Investigators described clinical trials of three drugs and a medical food product designed to reduce various symptoms of the neurodegenerative disease.


EVP-6124 May Have Cognitive and Clinical Benefits
EVP-6124, a selective alpha-7 partial agonist, had cognitive and clinical benefits for patients with mild to moderate Alzheimer’s disease, according to Dana C. Hilt, MD, Senior Vice President of Clinical Development and Chief Medical Officer of EnVivo Pharmaceuticals in Watertown, Massachusetts. The drug had statistically significant effects on patients’ Alzheimer’s Disease Assessment Scale (ADAS)-Cog 13 scores, ADAS-Cog 11 scores, and Clinical Dementia Rating Scale sum of boxes (CDR-SB).


Dr. Hilt and colleagues enrolled 409 patients in a double-blind, placebo-controlled phase IIb trial. Eligible patients had a Mini-Mental State Examination (MMSE) score between 14 and 24 and a CDR-SB score greater than 2. The study population included patients who were taking acetylcholinesterase inhibitors and patients who were not. Participants were assigned to placebo, 0.3 mg of drug per day, 1 mg of drug per day, or 2 mg of drug per day for 24 weeks.


EVP-6124 had a highly statistically significant effect on the primary end points, ADAS-Cog 13 and CDR-SB. The drug was associated with fewer adverse events than acetylcholinesterase inhibitors, according to Dr. Hilt. Typical adverse events were mild constipation and mild nausea. “The drug is well tolerated and safe, and it has a relatively mild adverse event profile,” concluded Dr. Hilt.


Citicoline May Preserve Cognition
MMSE score increased by 0.5 points for patients who took citicoline for nine months, according to Pietro Gareri, MD, PhD, Head of Research at the Ambulatory Center for Dementia in Catanzaro, Italy. MMSE score declined by approximately two points for untreated patients.
Citicoline had no effect on activities of daily living (ADL) or instrumental activities of daily living (IADL),
however.


Dr. Gareri and colleagues enrolled 387 patients with vascular mild cognitive impairment in the IDEALE study—an open, multicentric project to assess the effectiveness and safety of oral citicoline. Eligible patients were 65 or older, had an MMSE score of 21 or higher, and underwent a CT or MRI scan of the brain to confirm vascular lesions. Patients with probable Alzheimer’s disease were excluded. Investigators evaluated patients with the ADL and IADL scales and gauged their mood with the Geriatric Depression Scale (GDS).



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