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Ofatumumab versus
Teriflunomide in Multiple
Sclerosis
S.L. Hauser, A. Bar-Or, J.A. Cohen, G. Comi, J. Correale, P.K. Coyle, A.H. Cross, J. de Seze, D. Leppert, X. Montalban, K.
Selmaj, H. Wiendl, C. Kerloeguen, R. Willi, B. Li, A. Kakarieka, D. Tomic, A. Goodyear, R. Pingili, D.A. H辰ring, K.
Ramanathan, M. Merschhemke, and L. Kappos, for the ASCLEPIOS I and ASCLEPIOS II Trial Groups*
e UCSF Weill Institute for Neurosciences, Department of Neurology, University of California, San Francisco, San
Francisco (S.L.H.); the Center for Neuroinflammation and Experimental Therapeutics and Department of Neurology,
Perelman School of Medicine, University of Pennsylvania, Philadelphia (A.B.-O.); the Department of Neurology, Mellen
Center for Multiple Sclerosis, Neurological Institute, Cleveland Clinic, Cleveland (J.A.C.); the Institute of Experimental
Neurology and Multiple Sclerosis Center IRCCS, San Raffaele Hospital, Milan (G.C.); the Department of Neurology,
Fleni, Buenos Aires (J.C.); the Department of Neurology, Stony Brook University, Stony Brook, NY (P.K.C.); Washington
University School of Medicine, St. Louis (A.H.C.); the University Hospital of Strasburg and Clinical Investigation Center
INSERM 1434, Strasburg, France (J.S.); University Hospital Basel (D.L.), Novartis Pharma (C.K., R.W., A.K., D.T., D.A.H.,
K.R., M.M.), and the Neurologic Clinic and Policlinic, Departments of Medicine, Clinical Research, Biomedicine, and
Biomedical Engineering, University Hospital and University of Basel (L.K.)  all in Basel, Switzerland; the Department
of NeurologyNeuroimmunology, Centre dEsclerosi M炭ltiple de Catalunya (Cemcat), Hospital Universitari Vall
dHebron, Barcelona (X.M.); the University of Warmia and Mazury, Olsztyn, and the Center of Neurology, Lodz  both
in Poland (K.S.); the Department of Neurology with Institute of Translational Neurology, University of M端nster,
M端nster, Germany (H.W.); and Novartis Pharmaceuticals, East Hanover, NJ (B.L., A.G., R.P.).
NEW ENGLAND JOURNAL OF MEDICINE AUGUST 2020
 Ofatumumab, a subcutaneous anti-CD20 monoclonal antibody,
selectively depletes B cells. Teriflunomide, an oral inhibitor of
pyrimidine synthesis, reduces T-cell and B-cell activation. The relative
effects of these two drugs in patients with multiple sclerosis are not
known
 METHODS In two double-blind, double-dummy, phase 3 trials, we
randomly assigned patients with relapsing multiple sclerosis to
receive subcutaneous ofatumumab or oral teriflunomide
 Overall, 946 patients were assigned to receive ofatumumab and 936
to receive teriflunomide; the median follow-up was 1.6 year
Ofatumumab versus teriflunomide  in multiple sclerosis
Ofatumumab versus teriflunomide  in multiple sclerosis
DISCUSSION
 Annualised Relapse rate defined as the total number of relapses divided
by the total person-day at risk of relapse multiplied by 365
 In these two simultaneously conducted active controlled trials involving patients
with relapsing multiple sclerosis, both ofatumumab and teriflunomide were
associated with low relapse rates. The relapse rate was significantly lower with
ofatumumab than with teriflunomide in each of the two trials
 Ofatumumab was also superior to teriflunomide in suppressing lesion activity on
MRI
 Injection-related reactions were more frequent with ofatumumab

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Ofatumumab versus teriflunomide in multiple sclerosis

  • 1. Ofatumumab versus Teriflunomide in Multiple Sclerosis S.L. Hauser, A. Bar-Or, J.A. Cohen, G. Comi, J. Correale, P.K. Coyle, A.H. Cross, J. de Seze, D. Leppert, X. Montalban, K. Selmaj, H. Wiendl, C. Kerloeguen, R. Willi, B. Li, A. Kakarieka, D. Tomic, A. Goodyear, R. Pingili, D.A. H辰ring, K. Ramanathan, M. Merschhemke, and L. Kappos, for the ASCLEPIOS I and ASCLEPIOS II Trial Groups* e UCSF Weill Institute for Neurosciences, Department of Neurology, University of California, San Francisco, San Francisco (S.L.H.); the Center for Neuroinflammation and Experimental Therapeutics and Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia (A.B.-O.); the Department of Neurology, Mellen Center for Multiple Sclerosis, Neurological Institute, Cleveland Clinic, Cleveland (J.A.C.); the Institute of Experimental Neurology and Multiple Sclerosis Center IRCCS, San Raffaele Hospital, Milan (G.C.); the Department of Neurology, Fleni, Buenos Aires (J.C.); the Department of Neurology, Stony Brook University, Stony Brook, NY (P.K.C.); Washington University School of Medicine, St. Louis (A.H.C.); the University Hospital of Strasburg and Clinical Investigation Center INSERM 1434, Strasburg, France (J.S.); University Hospital Basel (D.L.), Novartis Pharma (C.K., R.W., A.K., D.T., D.A.H., K.R., M.M.), and the Neurologic Clinic and Policlinic, Departments of Medicine, Clinical Research, Biomedicine, and Biomedical Engineering, University Hospital and University of Basel (L.K.) all in Basel, Switzerland; the Department of NeurologyNeuroimmunology, Centre dEsclerosi M炭ltiple de Catalunya (Cemcat), Hospital Universitari Vall dHebron, Barcelona (X.M.); the University of Warmia and Mazury, Olsztyn, and the Center of Neurology, Lodz both in Poland (K.S.); the Department of Neurology with Institute of Translational Neurology, University of M端nster, M端nster, Germany (H.W.); and Novartis Pharmaceuticals, East Hanover, NJ (B.L., A.G., R.P.). NEW ENGLAND JOURNAL OF MEDICINE AUGUST 2020
  • 2. Ofatumumab, a subcutaneous anti-CD20 monoclonal antibody, selectively depletes B cells. Teriflunomide, an oral inhibitor of pyrimidine synthesis, reduces T-cell and B-cell activation. The relative effects of these two drugs in patients with multiple sclerosis are not known METHODS In two double-blind, double-dummy, phase 3 trials, we randomly assigned patients with relapsing multiple sclerosis to receive subcutaneous ofatumumab or oral teriflunomide Overall, 946 patients were assigned to receive ofatumumab and 936 to receive teriflunomide; the median follow-up was 1.6 year
  • 5. DISCUSSION Annualised Relapse rate defined as the total number of relapses divided by the total person-day at risk of relapse multiplied by 365 In these two simultaneously conducted active controlled trials involving patients with relapsing multiple sclerosis, both ofatumumab and teriflunomide were associated with low relapse rates. The relapse rate was significantly lower with ofatumumab than with teriflunomide in each of the two trials Ofatumumab was also superior to teriflunomide in suppressing lesion activity on MRI Injection-related reactions were more frequent with ofatumumab