Rebif (human IFN-β-1a) / EMD Serono |
NCT00367484 / 2004-000337-12: Study To Evaluate The Immunogenicity And Safety Of r-hIFN Beta-1a (Rebif®) Using Clone 484-39 In Multiple Sclerosis |
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| Completed | 4 | 460 | Europe | Rebif® (clone 484-39), Recombinant-human interferon beta-1a, r-hIFN Beta-1a | Merck KGaA, Darmstadt, Germany | Relapsing Remitting Multiple Sclerosis | 01/06 | 01/06 | | |
NCT00078338: Rebif® Versus Copaxone® in the Treatment of Relapsing Remitting Multiple Sclerosis |
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| Completed | 4 | 764 | US, Europe, RoW | Rebif®, Recombinant interferon beta-1a, Copaxone®, Glatiramer acetate | EMD Serono, Pfizer | Relapsing-remitting Multiple Sclerosis | 11/06 | 11/06 | | |
NCT00202995: Randomized Study Designed to Look at Disease Progression Using 2 Currently FDA Approved Drugs for the Treatment of RRMS |
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| Terminated | 4 | 91 | US | Glatiramer Acetate, Betaseron, Rebif | Teva Branded Pharmaceutical Products R&D, Inc. | Relapsing Remitting Multiple Sclerosis | 10/07 | 10/07 | | |
NCT00317941: Safety Study in Relapsing-remitting Multiple Sclerosis (RRMS) Patients Receiving Betaferon or Rebif |
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| Completed | 4 | 220 | Europe | Betaferon/Betaseron, Rebif | Bayer | Relapsing-remitting Multiple Sclerosis | 04/08 | 04/08 | | |
REMAIN, NCT01142466: A Phase IV Study of Rebif ® 44mcg Administered Three Times Per Week by Subcutaneous Injection Compared With no Treatment in the Therapy of Relapsing Multiple Sclerosis After Mitoxantrone |
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| Completed | 4 | 30 | Europe | Interferon beta-1a (Rebif), Rebif | Merck KGaA, Darmstadt, Germany, Gesellschaft für Therapieforschung mbH | Multiple Sclerosis, Relapsing-Remitting | 12/09 | 01/10 | | |
SEPTIME, NCT01201343: Evaluation of Emotional Disorders During Treatment by Interferon Beta in Relapsing-remitting Multiple Sclerosis Patients |
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| Completed | 4 | 79 | Europe | Interferon beta-1a, Rebif | Merck KGaA, Darmstadt, Germany, Merck Serono S.A.S, France | Multiple Sclerosis, Relapsing, Remitting | 07/10 | 07/10 | | |
| Completed | 4 | 324 | US | Blood sampling | EMD Serono | Relapsing Multiple Sclerosis | 11/10 | 11/10 | | |
NCT01085318: Rebif Advanced Magnetic Resonance Imaging (MRI) and Immunology Pilot Trial |
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| Completed | 4 | 38 | US | Rebif | EMD Serono | Multiple Sclerosis | 02/12 | 03/12 | | |
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EPOC, NCT01216072: A 6-month, Randomized, Open-label, Patient OutComes, Safety and Tolerability Study of Fingolimod (FTY720) 0.5 mg/Day vs. Comparator in Patients With Relapsing Forms of Multiple Sclerosis |
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| Completed | 4 | 1053 | US, Canada | Fingolimod, GILENYA™, Standard MS DMTs, Avonex®,, Copaxone®,, Rebif®,, Betaseron®,, Extavia® | Novartis Pharmaceuticals | Relapsing Forms of Multiple Sclerosis | 08/12 | 08/12 | | |
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EPOC, NCT01534182: Evaluation of Patient Reported Outcomes in RRMS Patients Candidates for MS Therapy Change and Transitioned to Fingolimod 0.5 mg |
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| Completed | 4 | 298 | RoW | Fingolimod, Gilenya, Interferon beta - 1a (IFN), Rebif, Glatiramer acetate (GA), Copaxone | Novartis Pharmaceuticals | Relapsing Remitting Multiple Sclerosis | 06/13 | 06/13 | | |
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NCT00101959: Implementation Study of Treatment Optimization Recommendations on Relapsing-Remitting Multiple Sclerosis (RR MS) Subjects |
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| Withdrawn | 4 | 0 | US | Rebif | EMD Serono | Relapsing-Remitting Multiple Sclerosis | | | | |
| Completed | 4 | 61 | Europe | Fingolimod, GILENYA™, Standard MS DMT, Avonex®,, Copaxone®,, Rebif®,, Betaferon®,, Extavia® | Novartis Pharmaceuticals | Relapsing Remitting Multiple Sclerosis | 06/14 | 06/14 | | |
OUCH, NCT01834586: Anesthetic Topical Adhesive (Syneraâ„¢) to Reduce Injection Pain With Subcutaneous Multiple Sclerosis Medications |
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| Completed | 4 | 30 | US | Anesthetic Topical Adhesive Synera, Synera | Brown, Theodore R., M.D., MPH | Multiple Sclerosis | 03/15 | 03/15 | | |
| Terminated | 4 | 1 | US | Rebif®, interferon-beta-1a | EMD Serono | Multiple Sclerosis | 04/15 | 04/15 | | |
NCT02019550: Rebif® Rebidose® Versus Rebiject II® Ease-of-Use |
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| Completed | 4 | 97 | US | Rebif Rebidose, Rebiject II | EMD Serono | Multiple Sclerosis, Relapsing-Remitting | 01/16 | 01/16 | | |
RebiQoL, NCT01791244: A Phase 4 Study to Assess the Impact of Patient Support Program on Health Related Quality of Life and Adherence in Subjects With Relapsing-Remitting Multiple Sclerosis Administered Rebif® With the RebiSmart™ Device |
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| Completed | 4 | 93 | Europe | Rebif® | Merck KGaA, Darmstadt, Germany | Multiple Sclerosis, Relapsing-Remitting | 02/16 | 02/16 | | |
| Completed | 4 | 200 | Europe | Rebif® | Merck KGaA, Darmstadt, Germany | Multiple Sclerosis, Relapsing-Remitting | 04/16 | 04/16 | | |
| Completed | 4 | 106 | Europe | Rebif, Interferon beta-1a | Merck KGaA, Darmstadt, Germany, Merck Romania SRL, an affiliate of Merck KGaA, Darmstadt, Germany | Relapsing Multiple Sclerosis, Clinically Isolated Syndrome | 08/16 | 08/16 | | |
| Withdrawn | 4 | 0 | US | Interferon Beta, Rebif or Betaseron/Betaferon, BIIB017 (Peginterferon beta-1a), PEGylated interferon beta-1a (IFN β-1a) | Biogen | Relapsing Multiple Sclerosis | 02/17 | 03/18 | | |