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公开(公告)号:US20110135645A1
公开(公告)日:2011-06-09
申请号:US12311587
申请日:2007-10-04
申请人: R. Anthony Williamson , Zhifeng Chen , Pietro Paolo Sanna , Dennis R. Burton , James Crowe , John V. Williams
发明人: R. Anthony Williamson , Zhifeng Chen , Pietro Paolo Sanna , Dennis R. Burton , James Crowe , John V. Williams
CPC分类号: C07K16/1027 , A61K2039/505 , C07K2317/21 , C07K2317/55 , C07K2317/56 , C07K2317/565 , C07K2317/76 , C07K2317/92
摘要: The present invention discloses methods for generating antibodies to human metapneumovirus (HMPV) polypeptides, including antibodies that immunospecifically bind to a HMPV F-protein. The invention also discloses methods for preventing, treating, or ameliorating symptoms associated with HMPV infection.
摘要翻译: 本发明公开了产生针对人类偏肺病毒(HMPV)多肽的抗体的方法,包括免疫特异性结合HMPV F蛋白的抗体。 本发明还公开了用于预防,治疗或改善与HMPV感染相关的症状的方法。
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公开(公告)号:US08119854B2
公开(公告)日:2012-02-21
申请号:US12085381
申请日:2006-11-21
申请人: Pietro Paolo Sanna
发明人: Pietro Paolo Sanna
IPC分类号: A01K67/00
CPC分类号: C07K14/705 , A61K31/00
摘要: The invention provides methods of preventing or treating drug addiction, or ameliorating the craving for an addictive drug, as well as compounds, peptides, and pharmaceutical compositions that may be used to prevent or treat drug addiction or ameliorate the craving for an addictive drug. The invention also provides methods for identifying agents that may be used to prevent or treat drug addiction, or ameliorate the craving for an addictive drug.
摘要翻译: 本发明提供了预防或治疗药物成瘾或改善上瘾药物渴求的方法,以及可用于预防或治疗药物成瘾或改善成瘾药物渴求的化合物,肽和药物组合物的方法。 本发明还提供了用于鉴定可用于预防或治疗药物成瘾或改善对上瘾药物的欲望的药剂的方法。
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公开(公告)号:US6156313A
公开(公告)日:2000-12-05
申请号:US852147
申请日:1997-05-06
CPC分类号: C07K16/4216 , C07K16/087 , A61K38/00 , A61K39/00 , C07K2317/55 , C07K2317/622 , C07K2319/00
摘要: The present invention describes human monoclonal antibodies which immunoreact with Herpes simplex virus Type-1 and Type-2. Also disclosed are immunotherapeutic and diagnostic methods of using the monoclonal antibodies, as well as nucleic acids and cell lines for producing the monoclonal antibodies.
摘要翻译: 本发明描述了与单纯疱疹病毒1型和2型免疫反应的人单克隆抗体。 还公开了使用单克隆抗体以及用于产生单克隆抗体的核酸和细胞系的免疫治疗和诊断方法。
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公开(公告)号:US10039772B2
公开(公告)日:2018-08-07
申请号:US15350052
申请日:2016-11-12
申请人: Pietro Paolo Sanna
发明人: Pietro Paolo Sanna
IPC分类号: A61K31/585 , A61K31/56 , A61K31/4965 , A61K31/58
摘要: Disclosed are methods and compositions for treating alcohol dependence by administration to a patient of an inhibitor of 11β-hydroxysteroid dehydrogenases (11β-HSD) to modulate glucocorticoid effects. One such compound is the 11β-HSD inhibitor carbenoxolone (18β-glycyrrhetinic acid 3β-O-hemisuccinate), which has been extensively employed in the clinic for the treatment of gastritis and peptic ulcer. Carbenoxolone is active on both 11β-HSD1 and 2 isoforms. Here, carbenoxolone is surprisingly shown to reduce both baseline and excessive drinking in rats and mice. The carbenoxolone diastereomer 18α-glycyrrhetinic acid 3β-O-hemisuccinate (αCBX), which the applicants discovered to be selective for 11β-HSD2, was also effective in reducing alcohol drinking in mice. Thus, 11β-HSD inhibitors are a new class of candidate alcohol abuse medications and existing 11β-HSD inhibitor drugs may be re-purposed for alcohol abuse treatment.
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公开(公告)号:US20170232007A1
公开(公告)日:2017-08-17
申请号:US15350052
申请日:2016-11-12
申请人: Pietro Paolo SANNA
发明人: Pietro Paolo SANNA
IPC分类号: A61K31/585 , A61K31/4965 , A61K31/58 , A61K31/56
CPC分类号: A61K31/585 , A61K31/22 , A61K31/4965 , A61K31/56 , A61K31/573 , A61K31/58 , A61K38/39 , A61K45/06 , C07J63/008 , A61K2300/00
摘要: Disclosed are methods and compositions for treating alcohol dependence by administration to a patient of an inhibitor of 11β-hydroxysteroid dehydrogenases (11β-HSD) to modulate glucocorticoid effects. One such compound is the 11β-HSD inhibitor carbenoxolone (18β-glycyrrhetinic acid 3β-O-hemisuccinate), which has been extensively employed in the clinic for the treatment of gastritis and peptic ulcer. Carbenoxolone is active on both 11β-HSD1 and 2 isoforms. Here, carbenoxolone is surprisingly shown to reduce both baseline and excessive drinking in rats and mice. The carbenoxolone diastereomer 18α-glycyrrhetinic acid 3β-O-hemisuccinate (αCBX), which the applicants discovered to be selective for 11β-HSD2, was also effective in reducing alcohol drinking in mice. Thus, 11β-HSD inhibitors are a new class of candidate alcohol abuse medications and existing 11β-HSD inhibitor drugs may be re-purposed for alcohol abuse treatment.
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