A randomized, double-blind, placebo-controlled, phase I study of MEDI-545, an anti-interferon-alfa monoclonal antibody, in subjects with chronic psoriasis
被引:61
作者:
Bissonnette, Robert
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Innovaderm Res Inc, Montreal, PQ, CanadaMedimmune LLC, Gaithersburg, MD 20878 USA
Bissonnette, Robert
[2
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Papp, Kim
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Prob Med Res, Waterloo, ON, CanadaMedimmune LLC, Gaithersburg, MD 20878 USA
Papp, Kim
[3
]
Maari, Catherine
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Innovaderm Res Inc, Laval, PQ, CanadaMedimmune LLC, Gaithersburg, MD 20878 USA
Background: Interferon alfa (IFN-alpha) has been implicated in the pathogenesis of psoriasis. Objective: To evaluate the safety profile of MEDI-545, a fully human anti-IFN-alpha monoclonal antibody and to explore its effect on the involvement of type 1 IFN-alpha activity in the maintenance of established plaque psoriasis. Methods: We conducted an 18-week, randomized, double-blind, placebo-controlled, close-escalating study in 36 subjects with chronic plaque psoriasis. Subjects received one intravenous close of MEDI-545 (0.3-30.0 mg/kg) or placebo. Study outcomes were safety profile, pharmacokinetics, immunogenicity, and clinical effects. Results: There eras no difference in adverse events between MEDI-545 and placebo. Two serious adverse events were reported; one drug-related hypotensive infusion reaction occurred in one subject in the 30.0 mg/kg MEDI-545 dose group, causing discontinuation of study drug in that subject and study dismissal of the other subjects in the same cohort; and a myocardial infarction occurred in one subject in the 10 mg/kg MEDI-545 dose group; which eras considered to be unrelated to treatment. MEDI-545 was nonimmunogenic, had a half-life of 21 clays; showed no significant inhibition of the type I IFN gene signature, and had no clinical activity. Limitations: The study addressed only IFN-alpha and chronic psoriatic lesions. Conclusion: The safety profile of MEDI-545 supports further clinical development. IFN-alpha does not appear to be significantly involved in the maintenance of established plaque psoriasis. (J Am Acad Dermatol 2010;62:427-36.)