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公开(公告)号:US08765148B2
公开(公告)日:2014-07-01
申请号:US13578686
申请日:2011-02-21
申请人: Benjamin Wizel , Karin Riedl , Karen Lingnau , Ursula Schlosser , Jürgen Wruss , Robert Schlegl , Michael Weber , Christoph Reinisch , Ljubomir Paucz , Christoph Klade , Jee Loon Look , Christian Ruiz , Robert Seid
发明人: Benjamin Wizel , Karin Riedl , Karen Lingnau , Ursula Schlosser , Jürgen Wruss , Robert Schlegl , Michael Weber , Christoph Reinisch , Ljubomir Paucz , Christoph Klade , Jee Loon Look , Christian Ruiz , Robert Seid
CPC分类号: A61K39/39 , A61K9/0019 , A61K9/08 , A61K9/10 , A61K9/14 , A61K9/51 , A61K38/00 , A61K39/00 , A61K39/0011 , A61K39/092 , A61K39/118 , A61K39/12 , A61K39/145 , A61K39/40 , A61K39/42 , A61K48/00 , A61K2039/55516 , A61K2039/55555 , A61K2039/55561 , A61K2039/70 , C12N7/00 , C12N2760/16134 , C12N2760/16171 , C12N2760/16234 , Y02A50/386 , Y02A50/388 , Y02A50/39 , Y02A50/394 , Y02A50/396 , Y02A50/401 , Y02A50/412 , Y02A50/47
摘要: The invention discloses pharmaceutical compositions in liquid form comprising a peptide with the amino acid sequence KLKL5KLK and an oligodeoxynucleotide with the nucleic acid sequence (dIdC)13 and wherein the peptide and the oligodeoxynucleotide are present as sterile-filterable nanoparticles in the composition, thereby forming a suspension, characterized in that the mean particle size of the solid particles is less than 1 μm.
摘要翻译: 本发明公开了液体形式的药物组合物,其包含具有氨基酸序列KLKL5KLK的肽和具有核酸序列(dIdC)13的寡脱氧核苷酸的肽,并且其中肽和寡脱氧核苷酸作为无菌可过滤纳米粒子存在于组合物中,由此形成 悬浮液,其特征在于固体颗粒的平均粒径小于1μm。
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公开(公告)号:US20120308618A1
公开(公告)日:2012-12-06
申请号:US13578686
申请日:2011-02-21
申请人: Benjamin Wizel , Karin Riedl , Karen Lingnau , Ursula Schlosser , Jürgen Wruss , Robert Schlegl , Michael Weber , Christoph Reinisch , Ljubomir Paucz , Christoph Klade , Jee Loon Look , Christian Ruiz , Robert Seid
发明人: Benjamin Wizel , Karin Riedl , Karen Lingnau , Ursula Schlosser , Jürgen Wruss , Robert Schlegl , Michael Weber , Christoph Reinisch , Ljubomir Paucz , Christoph Klade , Jee Loon Look , Christian Ruiz , Robert Seid
IPC分类号: A61K39/39 , A61P31/14 , A61P31/18 , A61P31/20 , A61P35/00 , A61P33/00 , A61P33/02 , A61P31/04 , A61P31/10 , A61K9/14 , A61P31/22
CPC分类号: A61K39/39 , A61K9/0019 , A61K9/08 , A61K9/10 , A61K9/14 , A61K9/51 , A61K38/00 , A61K39/00 , A61K39/0011 , A61K39/092 , A61K39/118 , A61K39/12 , A61K39/145 , A61K39/40 , A61K39/42 , A61K48/00 , A61K2039/55516 , A61K2039/55555 , A61K2039/55561 , A61K2039/70 , C12N7/00 , C12N2760/16134 , C12N2760/16171 , C12N2760/16234 , Y02A50/386 , Y02A50/388 , Y02A50/39 , Y02A50/394 , Y02A50/396 , Y02A50/401 , Y02A50/412 , Y02A50/47
摘要: The invention discloses pharmaceutical compositions in liquid form comprising a peptide with the amino acid sequence KLKL5KLK and an oligodeoxynucleotide with the nucleic acid sequence (dIdC)13 and wherein the peptide and the oligodeoxynucleotide are present as sterile-filterable nanoparticles in the composition, thereby forming a suspension, characterized in that the mean particle size of the solid particles is less than 1 μm.
摘要翻译: 本发明公开了液体形式的药物组合物,其包含具有氨基酸序列KLKL5KLK的肽和具有核酸序列(dIdC)13的寡脱氧核苷酸的肽,并且其中肽和寡脱氧核苷酸作为无菌可过滤纳米粒子存在于组合物中,由此形成 悬浮液,其特征在于固体颗粒的平均粒径小于1μm。
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公开(公告)号:US08101352B2
公开(公告)日:2012-01-24
申请号:US12305258
申请日:2007-06-26
申请人: Guido Sauter , Ronald Simon , Phillip Stahl , Frederik Holst , Khawla Al-Kuraya , Christian Ruiz
发明人: Guido Sauter , Ronald Simon , Phillip Stahl , Frederik Holst , Khawla Al-Kuraya , Christian Ruiz
IPC分类号: C12Q1/68
CPC分类号: C12Q1/6886 , C12Q2600/106
摘要: The present invention relates to an in-vitro method of identifying a tumor resulting from a proliferative breast disease as responsive to anti-estrogen treatment. Further, the invention relates to an in-vitro method of identifying a candidate patient with a proliferative breast disease as suitable for anti-estrogen treatment. In a further aspect, the invention provides an in-vitro method of identifying an individual with a non-cancerous proliferative breast disease who is at risk of developing breast cancer. The invention also provides kits for performing the above methods.
摘要翻译: 本发明涉及鉴定由抗雌激素治疗反应的增殖性乳腺疾病引起的肿瘤的体外方法。 此外,本发明涉及鉴定具有适合于抗雌激素治疗的增殖性乳腺疾病的候选患者的体外方法。 在另一方面,本发明提供了一种鉴定患有具有发展为乳腺癌风险的非癌性增殖性乳腺疾病的个体的体外方法。 本发明还提供了用于执行上述方法的试剂盒。
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公开(公告)号:US20100086915A1
公开(公告)日:2010-04-08
申请号:US12305258
申请日:2007-06-26
申请人: Guido Sauter , Ronald Simon , Philip Stahl , Frederik Holst , Khawla A-Kuraya , Christian Ruiz
发明人: Guido Sauter , Ronald Simon , Philip Stahl , Frederik Holst , Khawla A-Kuraya , Christian Ruiz
IPC分类号: C12Q1/68 , C07H21/00 , C07C217/00 , C07D409/02 , C07J71/00 , C07D249/08 , C07J1/00
CPC分类号: C12Q1/6886 , C12Q2600/106
摘要: The present invention relates to an in-vitro method of identifying a tumor resulting from a proliferative breast disease as responsive to anti-estrogen treatment. Further, the invention relates to an in-vitro method of identifying a candidate patient with a proliferative breast disease as suitable for anti-estrogen treatment. In a further aspect, the invention provides an in-vitro method of identifying an individual with a non-cancerous proliferative breast disease who is at risk of developing breast cancer. The invention also provides kits for performing the above methods.
摘要翻译: 本发明涉及鉴定由抗雌激素治疗反应的增殖性乳腺疾病引起的肿瘤的体外方法。 此外,本发明涉及鉴定具有适合于抗雌激素治疗的增殖性乳腺疾病的候选患者的体外方法。 在另一方面,本发明提供了一种鉴定患有具有发展为乳腺癌风险的非癌性增殖性乳腺疾病的个体的体外方法。 本发明还提供了用于执行上述方法的试剂盒。
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