deltatrials

Relapsing remitting multiple sclerosis Trials in Ufa, Russia

Conditions / Relapsing remitting multiple sclerosis / Ufa, Russia

Relapsing remitting multiple sclerosis has been the subject of sustained clinical investigation across multiple research sites.

10 total trials for this combination

Trials

NCT ID Title Status Phase
NCT02255656 Phase IIIB-IV Long-Term Follow-up Study for Patients Who Participated in CAMMS03409 COMPLETED PHASE4
NCT00870740 Safety and Efficacy Extension Study of Daclizumab High Yield Process (DAC HYP) in Participants With Multiple Sclerosis Who Have Completed Study 205MS201 (NCT00390221) to Treat Relapsing-Remitting Multiple Sclerosis COMPLETED PHASE2
NCT01578785 An Efficacy, Safety and Tolerability Study of Glatiramer Acetate (GA) 20 mg/0.5 ml New Formulation Administered Daily by Subcutaneous (SC) Injection in Subjects With Relapsing-Remitting Multiple Sclerosis (RRMS) TERMINATED PHASE3
NCT01067521 A Study in Subjects With Relapsing-Remitting Multiple Sclerosis (RRMS) to Assess the Efficacy, Safety and Tolerability of Glatiramer Acetate (GA) Injection 40 mg Administered Three Times a Week Compared to Placebo COMPLETED PHASE3
NCT01963611 Efficacy, Safety, and Tolerability of Plovamer Acetate (Pathway 1) TERMINATED PHASE2
NCT00390221 Safety and Efficacy Study of Daclizumab High Yield Process (DAC HYP) to Treat Relapsing-Remitting Multiple Sclerosis COMPLETED PHASE2
NCT01064401 Efficacy and Safety of BIIB019 (Daclizumab High Yield Process) Versus Interferon β 1a in Participants With Relapsing-Remitting Multiple Sclerosis COMPLETED PHASE3
NCT01051349 Safety and Efficacy Extension Study of Daclizumab High Yield Process (DAC HYP) (BIIB019) in Participants Who Have Completed Study 205MS202 (NCT00870740) to Treat Relapsing Remitting Multiple Sclerosis COMPLETED PHASE2
NCT01534182 Evaluation of Patient Reported Outcomes in RRMS Patients Candidates for MS Therapy Change and Transitioned to Fingolimod 0.5 mg (EPOC) COMPLETED PHASE4
NCT01797965 Long-Term Extension Study in Participants With Multiple Sclerosis Who Have Completed Study 205MS301 (NCT01064401) to Evaluate the Safety and Efficacy of BIIB019 TERMINATED PHASE3

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