Carolinas HealthCare System

Research and Clinical Trials

Title  
OBS14527 LEM-COG
Brief Description  
This study is to describe neurocognitive function in patients with relapsing multiple sclerosis (RMS) treated with LEMTRADA® in routine clinical practice as measured by the Multiple Sclerosis Cognitive (MS-COG) composite score. Additional neurocognitive tests will also be administered and reviewed as well as MRI data when available. The study includes a screening period of up to 30 days followed by a baseline visit, month 12 and month 24/EQS visit for a total of four visits.
Who may be Eligible  
Patients with relapsing forms of MS aged 25-55 years old who are selected for treatment for treatment with Lemtrada(® and enrolled in the LEMTRADA Risk Evaluation and Mitigation Strategy (REMS) Program in the US are eligible for this study. The decision to treat with LEMTRADA(® will be done prior to and independent of the proposal to enroll in this study. To participate, patients must be able to give signed written informed consent.
Start Date  
07/20/2016
IRB Number  
07-16-12E
Principal Investigator  
Graves, Donna
Contact Name  
Nicol

For More Information, Contact   Nicol  M.  Brandon
Phone:  (704) 446-1910  Fax:  (704) 446-6208 
Email:  Nicol.Brandon@carolinashealthcare.org

Address:  1010 Edgehill Road, North
Charlotte, NC 28207
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