The primary objective of the study is to evaluate the efficacy of T-817MA in AD patients to treat dementia. Efficacy will be cognitive function, as measured by the ADAS-cog cognitive assessment. The secondary objectives of the study are to evaluate the safety of T-817MA and the activities of daily living (assessed with the ADCS-ADL) of AD patients taking T-817MA, and to evaluate the efficacy of T-817MA in AD patients with an overall global assessment using the ADCS-CGIC.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
373
Evaluation of the efficacy of T-817MA in AD patients to treat dementia. Efficacy will be cognitive function, as measured by the ADAS-cog cognitive assessment.
Time frame: 52 weeks
Secondary objectives are to evaluate the safety of T-817MA and the activities of daily living (ADCS-ADL) of AD patients taking T-817MA, and to evaluate the efficacy of T-817MA in AD patients with an overall global assessment using the ADCS-CGIC.
Time frame: 52 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Banner Alzheimer's Institute
Phoenix, Arizona, United States
Northwest NeuroSpecialists
Tucson, Arizona, United States
Collaborative Neuroscience Network, Inc.
Garden Grove, California, United States
Southwest Institute for Clinical Research, Inc.
Rancho Mirage, California, United States
Pacific Research Network, Inc.
San Diego, California, United States
San Francisco Clinical Research Center
San Francisco, California, United States
Radiant Research
Denver, Colorado, United States
Geriatric and Adult Psychiatry, LCC
Hamden, Connecticut, United States
Research Center for Clinical Studies, Inc.
Norwalk, Connecticut, United States
NeuroPsychiatric Center of the Palm Beaches
Boynton Beach, Florida, United States
...and 25 more locations