BMS TARGET-TAU This study is being done to learn more about the safety and efficacy of an investigational medication called BMS-986446 in adults aged 50-80 years with mild cognitive impairment due to Alzheimer’s disease, or mild Alzheimer’s dementia. Inclusion Criteria: Are 50-80 years old Have a diagnosis of mild cognitive impairment due to Alzheimer’s disease, […]
TG ENABLE The purpose of this study is to evaluate safety, effectiveness, and to gain insight into the treatment experience of participants prescribed BRIUMVI® (ublituximab-xiiy) in the real-world setting. Inclusion Criteria: Participants with a confirmed Multiple Sclerosis (MS) diagnosis who have been prescribed BRIUMVI® (ublituximab-xiiy) but have not yet received their first infusion. For more
EVIDERA EVA-38569-03 This is a cognitive interview study to evaluate Phase 2 Trial Anchors in Patients with Parkinson’s Disease. What to Expect This study involves in-depth interviews with adults who have been diagnosed with PD who meet specific criteria. For more information, contact Heather Macnamara at hmacnamara@dentinstitute.com or 716-819-4117
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TEVA IMPACT TD Registry (Tardive Dyskinesia) The purpose of this study is to uncover how tardive dyskinesia (TD) develops over time and its impact on individuals. Inclusion Criteria: Patients who are newly initiating deutetrabenazine as part of routine clinical practice. What to Expect As part of your usual care, you will complete questionnaires and visit
Alzheimer’s National Registry for Treatment and Diagnostics(ALZ-NET) (Mild Cognitive Impairment and Alzheimer’s Disease) ALZ-NET collects clinical and safety data about patients being evaluated for memory concerns or receiving new FDA-approved treatments for Alzheimer’s disease, including drugs/medications and devices, and tracks the long-term health outcomes associated with their use in real-world settings. ALZ-NET is a voluntary
Migraine prevention injection in patients with unsuccessful prior preventive treatments The objective of the trial is to assess the efficacy of the study drug for prevention of migraine at different doses compared to placebo in patients who have failed multiple preventive treatments. Inclusion Criteria: In order to be eligible, you have to have at least
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Chronic Migraine Implant for Migraine Prevention (RELIEV-CM2) The purpose of the RELIEV-CM2 study is to evaluate ShiraTronics Migraine Therapy System’s ability to reduce the frequency of headaches for those living with chronic migraine. Inclusion Criteria: You may be eligible for this study if your doctor has diagnosed you with chronic migraine and you meet the
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Menstrual Migraine Prevention using Ubrelvy This study will evaluate the Efficacy, Safety, and Tolerability of Ubrogepant for the Preventive Treatment of Menstrual Migraine with an Open-Label Extension Inclusion Criteria: In order to be eligible for this study, you must be at least 18 years old and have a diagnosis of Menstrual Migraine What to Expect
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JAZZ PATAGONIA (Parkinson’s Disease) This is a 17-week double-blind, placebo-controlled, randomized, flexible-dosing, parallel-group, multicenter study designed to evaluate the efficacy and safety of suvecaltamide for the treatment of moderate to severe residual tremor in adult participants with Parkinson’s disease (PD). The target population represents participants who have tremor that is not adequately controlled by PD
BIOGEN CELIA In this study, researchers will learn more about a study drug called BIIB080. The study will focus on participants with mild cognitive impairment or mild dementia due to AD. The main question researchers are trying to answer is if BIIB080 can slow the worsening of AD more than placebo. It will focus on
