Clinical Research

Efficacy , safety and tolerability of Atorvastatin 40 mg in patients with relapsing remitting multiple sclerosis in treatment with interferon-beta-(ARIANNA) – Multicenter, randomised, double blind, placebo controlled, parallel-group-study. Studio Schering – prot. DR04-07-02.


An active extension of LAQ/5062 study – multinational, multi-center, randomised, double-blind, parallel-group study, to evacuate the safety, tolerability and efficacy of two doses (0.3mg and 0.6mg) of laquinimod, orally administered in relapsing-remitting (R-R) multiple sclerosis (MS) subjects. Teva Pharmaceutical Industries. Prot. N. LAQ/5063

FORTE – GA/9016 A multinational, multicenter, randomized, parallel-group, double-blind study, to compare the efficacy, tollerabilità and safety of glatiramer acetate injection 40mg/ml to rhat of glatiramer acetate injection 20 mg/ml administered once daily by subcutaneous injection in subjects with relapsing remitting (R-R) multiple sclerosis (MS)

Multicenter. Open-label, 12 weeks Phase IV study to assess adherence to treatment in relapsing multiple sclerosis (RMS) subjects switching from othr injectable DMDs using ReBiSmart to self-inject Rebif New Formulation (RNF) In a multi-dose cartriDGE – BRIDGE – Merck Serono prot. 701048-525

A double-blind, randomized, multicenter, placebo-controlled, parallel-group study comparing the efficacy and safety of 1,25 mg FTY20 administered orally once daily versus placebo in patients with primary progressive multiple sclerosis. Novartis Pharma, prot. CFTY720D2306

Research area

Clinical Research