Neurology Department Research Activities

Contact Information

Phone: 202/741-2719
Primary Investigator: Ted Rothstein, MD

Protocol Description

A historical-controlled, multicenter, double-blind, randomized trial to assess the efficacy and safety of conversion to Lacosamide 400mg/day Monotherapy in subjects with partial-onset seizures. Protocol No: SP902

 

TYSABRI Global Observational Program in Safety (TYGRIS).

Protocol No:101-MS-402

 

Double-blind, placebo-controlled, randomized, parallel-group phase II study in subjects with relapsing forms of multiple sclerosis (MS) to evaluate the safety, tolerability, and effects of two doses of CDP323 over 24 weeks with a rater-blind MRI follow-up over 12 weeks.

Protocol No: C32322

 

Insulin resistance intervention after stroke trial (IRIS): a randomized, placebo-controlled trial of pioglitazone, compared with placebo, for prevention of stroke and myocardial infarction after ischemic stroke and transient ischemic attack).

 

Clinical Trial of Ceftriaxone in subjects with ALS.

Protocol No: CEF-ALS -2006

An International, multi-center, randomized, double-blind, placebo-controlled, parallel group study to evaluate the efficacy and safety of two year treatment with teriflunomide 7 mg once daily and 14 mg once daily versus placebo in patients with a first clinical episode suggestive of multiple sclerosis.                                                                                                                   

Protocol No: EFC6260 

 

A Phase 3 Randomized Rater-and-dose-blinded Study Comparing Two Annual Cycles of low- and high-dose atemtuzumab to three-times weekly interferon Beta-la (Rebif) in patients with RRMS who have relapsed on therapy. 

Protocol No: CAMMS32400507-CARE MS II

Eligibility Criteria

 TBD

Last Update

October 10, 2008
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