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The use of a neutralizing anti TNFa Antibody, High affinity, in the manufacture of a Drug and a set of elements

机译:高亲和力的中和抗TNFa抗体在制造药物和一组药物中的用途

摘要

1. The use of a neutralizing antibody against TNFa, which is closely related to the development of a drug for the treatment of TNFa disorders, and includes a series of pharmaceutical components containing this anti TNFa antibody. 1. Characteristic 1: a method for treating TNFa related disorders in experimental subjects. In the experimental subjects, TNFa related disorders are selected from a group of people including sporozoites, pulmonary disorders, coronary artery disorders, metabolic disorders, anemia, pain, liver disorders, and skin disorders, A disorder or vasculitis of the nailscharacterized in that it comprises administering to the subject an effective amount for therapeutic use of a neutralizing anti-TNFa antibody, of great affinity, whereby said TNFa-related disorder is managed. Claim 4: The method of any of clauses 1, 2 or 3, characterized in that the antibody is an isolated human antibody, or a portion thereof that binds to the antigen, which dissociates from human TNFa with a Kᵈ of 1 x 10 ⁻⁸ M ᵒ ᵐᵉⁿᵒˢ ʸ ᵘⁿᵃ ᶜᵒⁿˢᵗᵃⁿᵗᵉ ᵈᵉ ᵛᵉˡᵒᶜⁱᵈᵃᵈ Kₒᶠᶠ of 1 x 10⁻³ s⁻¹ or less, both determined by surface plasmon resonance,and that neutralizes the cytotoxicity of human TNFa in a standard in vitro L929 assay with an IC₅₀ of 1 X 10⁻⁷ M ᵒ ᵐᵉⁿᵒˢ. Claim 15: A set of elements, characterized in that it comprises: a) a pharmaceutical composition comprising an anti-TNFa antibody, or a portion that binds to the antigen thereof, and a vehicle acceptable for pharmaceutical use; and b) instructions for administration to the subject of the pharmaceutical composition with the anti-TNFa antibody to treat a subject suffering from a TNFa-related disorder.
机译:1.针对TNFα的中和抗体的用途,其与用于治疗TNFα疾病的药物的开发密切相关,并且包括一系列含有该抗TNFα抗体的药物成分。 1.特征1:一种治疗实验对象中与TNFα相关的疾病的方法。在实验对象中,TNFa相关疾病选自子孢子,肺疾病,冠状动脉疾病,新陈代谢疾病,贫血,疼痛,肝病和皮肤疾病,其特征在于指甲疾病或指甲炎包括:向受试者施用有效量的,具有高亲和力的中和性抗TNFa抗体用于治疗,从而控制了所述TNFa相关疾病。权利要求4:条款1、2或3中任一项的方法,其特征在于所述抗体是分离的人抗体或其与抗原结合的部分,该人抗体以1×10 6的K 3从人TNFα解离。 M x K等于或小于1 x 10 3 s -1,两者均由表面等离振子共振确定,并且在标准体外L929分析中以1 X 10的IC 50中和人TNFa的细胞毒性。 ⁻⁷Mᵒ。 15.权利要求15的元素集,其特征在于它包括:a)药物组合物,所述药物组合物包含抗TNFα抗体或其结合抗原的部分,以及药学上可接受的载体。 b)给予抗TNFα抗体药物组合物给受试者以治疗患有TNFα相关疾病的受试者的说明书。

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