Formulation for the treatment of obesity
    1.
    发明申请
    Formulation for the treatment of obesity 失效
    治疗肥胖症的配方

    公开(公告)号:US20040247694A1

    公开(公告)日:2004-12-09

    申请号:US10454538

    申请日:2003-06-05

    IPC分类号: A61K035/26 A61K035/78

    摘要: The present invention refers to a formulation for a slimming treatment comprising in certain quantities: hypothalamus powder, hypophysis powder, thyroid powder, suprarenal cortex powder and pancreas powder, and other polyglandular opotherapic extracts such as extract of ovary or testicle; said slimming treatment being evaluated and optimised thanks to an exponential mathematical model which models the accumulated weight loss of a patient by means of a differentiation and separation of the slimming effect due to the set of factors depending on the applied slimming treatment and, on the other hand, of the slimming effect due to the set of factors depending on the typology of the patient trying to slim.

    摘要翻译: 本发明涉及一种减肥治疗制剂,其包括一定量:下丘脑粉末,垂体粉末,甲状腺粉末,肾上皮质粉末和胰腺粉末,以及其它多腺体热疗提取物,例如卵巢或睾丸提取物; 所述减肥治疗被评估和优化,这是由于指数数学模型,其通过依赖于所应用的减肥治疗的一系列因素的减弱效应的分化和分离来模拟患者的累积体重减轻,并且在另一个 手的减肥效果由于一系列因素的影响,取决于患者尝试瘦身的类型。

    PEPTIDES FOR INHIBITING RETROVIRUSES
    2.
    发明申请
    PEPTIDES FOR INHIBITING RETROVIRUSES 无效
    抑制肝炎病毒的药物

    公开(公告)号:US20020037326A1

    公开(公告)日:2002-03-28

    申请号:US09054345

    申请日:1998-04-02

    发明人: MARK E. HOWARD

    IPC分类号: A61K035/26 A61K035/28

    摘要: Peptides derived from shark immunoglobulin preparations are used to prepare compositions, including pharmaceutical compositions, for inhibiting retrovirus replication in susceptible cells. The peptide preparations are useful for inhibiting diseases associated with retroviral infection, such as acquired immunodeficiency syndrome. The peptides also inhibit growth of tumor cells, especially sarcomas and leukemias.

    摘要翻译: 衍生自鲨鱼免疫球蛋白制剂的肽用于制备用于抑制易感细胞中的逆转录病毒复制的组合物,包括药物组合物。 肽制剂可用于抑制与逆转录病毒感染相关的疾病,例如获得性免疫缺陷综合征。 肽还抑制肿瘤细胞,特别是肉瘤和白血病的生长。

    METHODS FOR INDUCING ANTIGEN-SPECIFIC T CELL TOLERANCE
    4.
    发明申请
    METHODS FOR INDUCING ANTIGEN-SPECIFIC T CELL TOLERANCE 有权
    诱导抗原特异性T细胞耐受性的方法

    公开(公告)号:US20020187135A1

    公开(公告)日:2002-12-12

    申请号:US09164568

    申请日:1998-10-01

    摘要: Methods for inducing antigen-specific T cell tolerance are disclosed. The methods involve contacting a T cell with: 1) a cell which presents antigen to the T cell, wherein a ligand on the cell interacts with a receptor on the surface of the T cell which mediates contact-dependent helper effector function; and 2) an antagonist of the receptor on the surface of the T cell which inhibits interaction of the ligand on the antigen presenting cell with the receptor on the T cell. In a preferred embodiment, the cell which presents antigen to the T cell is a B cell and the receptor on the surface of the T cell which mediates contact-dependent helper effector function is gp39. Preferably, the antagonist is an anti-gp39 antibody or a soluble gp39 ligand (e.g., soluble CD40). The methods of the invention can be used to induce T cell tolerance to a soluble antigen or to an allogeneic cell. The methods of the invention can also be used to induce tolerance in cases of bone marrow transplantation and other organ transplants and to inhibit graft-versus-host disease.

    摘要翻译: 公开了诱导抗原特异性T细胞耐受性的方法。 所述方法包括使T细胞接触:1)向T细胞呈递抗原的细胞,其中细胞上的配体与介导接触依赖性辅助效应子功能的T细胞表面上的受体相互作用; 和2)T细胞表面上的受体拮抗剂,其抑制抗原呈递细胞上的配体与T细胞上的受体的相互作用。 在优选的实施方案中,向T细胞呈递抗原的细胞是B细胞,介导接触依赖性辅助效应子功能的T细胞表面上的受体是gp39。 优选地,拮抗剂是抗gp39抗体或可溶性gp39配体(例如可溶性CD40)。 本发明的方法可用于诱导对可溶性抗原或同种异体细胞的T细胞耐受性。 本发明的方法还可用于在骨髓移植和其他器官移植的情况下诱导耐受性并抑制移植物抗宿主病。

    Pharmaceutical composition for the medical treatment of the benign prostatic hyperplasia, its preparation method and its therapeutic application
    5.
    发明申请
    Pharmaceutical composition for the medical treatment of the benign prostatic hyperplasia, its preparation method and its therapeutic application 审中-公开
    用于治疗良性前列腺增生的药物组合物及其制备方法及其治疗应用

    公开(公告)号:US20040131694A1

    公开(公告)日:2004-07-08

    申请号:US10697264

    申请日:2003-10-31

    申请人: H.P.B. S.A.

    IPC分类号: A61K035/26 A61K031/739

    摘要: A pharmaceutical composition for the treatment of benign prostate hyperplasia comprising between about 0.002 g and about 0.05 g of polysaccharide from a gram negative bacteria, between about 0.1 mg and about 2 mg water soluble thymus extract, between about 0.01 mg and about 1 mg water soluble prostate extract, and between about 0.02 mg and about 2 mg of total carbohydrates, per mL of solution in a physiologically acceptable solvent A method of preparing a pharmaceutical composition comprising isolating a polysaccharide from a culture of gram negative bacteria in a liquid medium, the culture raised under rigorous conditions of bacteriological asepsis and the bacteria culture typified by biochemical tests, combining between about 0.002 g to about 0.05 g of the polysaccharide with between 0.1 mg and about 2 mg water soluble thymus extract, between about 0.01 mg and about 1 mg of water soluble prostate extract, and between about 0.02 mg and 2 mg of total carbohydrates, in a physiologically acceptable solvent to obtain about 1 mL of solution.

    摘要翻译: 一种用于治疗良性前列腺增生的药物组合物,其包含约0.002g至约0.05g来自革兰氏阴性细菌的多糖,约0.1mg至约2mg水溶性胸腺提取物之间,约0.01mg至约1mg水溶性 前列腺提取物,以及约0.02mg至约2mg总碳水化合物/ mL生理学上可接受的溶剂中的溶液。一种制备药物组合物的方法,包括在液体培养基中从革兰氏阴性细菌培养物中分离多糖,培养物 在严格的细菌无菌条件下培养,细菌培养以生化试验为代表,将约0.002g至约0.05g多糖与0.1mg至约2mg水溶性胸腺提取物之间,约0.01mg至约1mg的 水溶性前列腺提取物,以及约0.02mg至2mg的总碳水化合物 得到约1mL的溶液。

    TREATMENT OF HEMATOLOGIC DISORDERS
    7.
    发明申请
    TREATMENT OF HEMATOLOGIC DISORDERS 有权
    治疗病理性疾病

    公开(公告)号:US20010048921A1

    公开(公告)日:2001-12-06

    申请号:US09191970

    申请日:1998-11-13

    摘要: The inventors have discovered that hematologic disorders, e.g., both neoplastic (hematologic cancers) and non-neoplastic conditions, can be treated by the induction of mixed chimerism using myeloreductive, but not myeloablative, conditioning. Methods of the invention reduce GVHD, especially GVHD associated with mismatched allogeneic or xenogeneic donor tissue, yet provide, for example, significant graft-versus-leukemia (GVL) effect and the like.

    摘要翻译: 本发明人已经发现,血液学障碍,例如肿瘤(血液癌)和非肿瘤性病症都可以通过使用骨髓来引导混合嵌合体来治疗,而不是骨髓切除术,调理。 本发明的方法降低GVHD,特别是与错配的同种异体或异种供体组织相关的GVHD,但提供例如显着的移植物抗白血病(GVL)效应等。