FAU's clinical trial to evaluate efficacy of RVT-101 tablet for Lewy body dementia

NewsGuard 100/100 Score

Florida Atlantic University's Charles E. Schmidt College of Medicine is spearheading the South Florida site for the first U.S. clinical trial for Lewy body dementia (LBD), the second-most common dementia after Alzheimer's disease. The HEADWAY-DLB is a phase 2b multi-center, double-blind, placebo-controlled study to evaluate an investigational medicine, RVT-101, for dementia with Lewy bodies.

Currently, there are no medications available to specifically treat LBD, and patients are typically treated with medications for Alzheimer's.

The six-month study will enroll approximately 240 patients nationally to evaluate the safety and efficacy of RVT-101, a tablet that works by raising levels of acetylcholine, a vital chemical in the brain that helps with cognition and performing daily activities. Deficits in acetylcholine are a prominent feature of dementia with Lewy bodies.

Because symptoms of LBD mimic other diseases like Parkinson's and Alzheimer's, it is very difficult to diagnose often taking up to 18 months, with patients seeing a number of physicians over multiple visits. Patients, who are often misdiagnosed, are given medications for psychiatric disorders, Alzheimer's and Parkinson's. The only way to confirm whether someone has LBD is with a post-mortem brain autopsy.

The late Robin Williams had this form of dementia as did legendary NHL coach Alger Joseph "Radar" Arbour, legendary radio personality Casey Kasem, and most recently, Hall of Famer Gerald Eugene "Jerry" Sloane, former NBA player and head coach of the Utah Jazz.

Dementia with Lewy bodies is a progressive type of dementia that affects more than 1 million people in the U.S. LBD is characterized by fluctuations in cognition, particularly in alertness and attention, and can make depression worse. Many LBD patients also have visual hallucinations and REM sleep behavior disorder. LBD is characterized by the buildup of abnormal protein clusters (known as "Lewy bodies") within the brain.

The South Florida clinical trial is directed by one of the world's leading neuroscientists and an expert on LBD, James E. Galvin, M.D., M.P.H., a professor of clinical biomedical science in FAU's College of Medicine, a professor in FAU's Christine E. Lynn College of Nursing, and medical director of FAU's Louis and Anne Green Memory and Wellness Center.

Galvin developed the "Lewy Body Composite Risk Score" (LBCRS) to quickly and effectively diagnose LBD and Parkinson's disease dementia (PDD) in about three minutes. The LBCRS is a brief rating scale that can be completed by a clinician to assess clinical signs and symptoms highly associated with the pathology of this disease.

"Diagnosing dementia with Lewy bodies early is critical, and with this important tool, a clinician can assess whether the patient has bradykinesia, rigidity, postural instability, or rest tremor without having to grade each extremity," said Galvin. "We are hopeful that we also will be able to assist patients who have dementia with Lewy bodies with a medication that is designed to address their specific needs and condition."

Comments

The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
Post a new comment
Post

While we only use edited and approved content for Azthena answers, it may on occasions provide incorrect responses. Please confirm any data provided with the related suppliers or authors. We do not provide medical advice, if you search for medical information you must always consult a medical professional before acting on any information provided.

Your questions, but not your email details will be shared with OpenAI and retained for 30 days in accordance with their privacy principles.

Please do not ask questions that use sensitive or confidential information.

Read the full Terms & Conditions.

You might also like...
Antipsychotics for dementia associated with elevated risks of serious adverse outcomes