Abstract in simplified Chinese:本发明描述与布鲁顿氏酪胺酸激酶(Btk)形成共价键的化合物。亦描述Btk之不可逆抑制剂。另外,亦描述Btk之可逆抑制剂。亦揭示包括此等化合物的医药组合物。揭示单独或与其他治疗剂组合地使用Btk抑制剂治疗自体免疫疾病或病状、异质免疫疾病或病状、癌症(包括淋巴瘤)及发炎疾病或病状的方法。
Abstract in simplified Chinese:此处描述布鲁顿氏酪胺酸激酶(Btk)抑制剂1-((R)-3-(4-胺基-3-(4-苯氧基苯基)-1H-吡唑并[3,4-d]嘧啶-1-基)哌啶-1-基)丙-2-烯-1-酮,包括其结晶型、溶剂合物及药学上可接受之盐类。也揭示含括该Btk抑制剂之药学组成物,以及使用该Btk抑制剂单独使用或组合其它治疗剂用以治疗自体免疫病或病况、异种免疫病或病况、癌症包括淋巴瘤、及发炎病或病况之方法。
Abstract:
Described herein are methods for preventing or delaying the onset of Type 1 Diabetes, or inhibiting the maturation of anti-insulin B cells, in an individual in need thereof. The methods include administering to an individual in need thereof ibrutinib, alone or in combination with other Type 1 Diabetes treatments.
Abstract:
Described herein are combinations of ACK inhibitors and HDAC inhibitors in the treatment of diseases and disorders characterized by the presence or development of solid tumors.
Abstract:
Described herein are compounds and pharmaceutical compositions containing such compounds, which inhibit the acitivy of histone deacetylase 8 (HDAC8). Also described herein are methods of using such HDAC8 inhibitors, alone and in combination with other compounds, for treating diseases or conditions that would benefit from inhibition of HDAC8 activity.
Abstract:
A packaging system is described for a drug that provides protection from contamination, crystallization and/or degradation of the drug during storage of the system prior to its use. The packaging of the drug does not significantly absorb, react with, or otherwise adversely affect the therapeutic effectiveness of the drug or other excipients or components during storage of the system prior to its use. The packaging system is also used for preserving a drug, particularly a drug containing high-purity texaphyrin metal complexes, by providing a product packaging system that prevents, limits or otherwise controls degradation reactions that can result from exposure to oxygen and/or light.
Abstract:
Novel coordination polymers, their pharmaceutical formulations, useful for treating atheroma, tumors and other neoplastic tissue, as well as other conditions that are responsive to the induction of targeted oxidative stress, are disclosed.