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标题标题2专利权人发明人附图摘要摘要2优先权号IPC专利类型
首页123456下页尾页127 条记录, 当前第1/13页。
公开号 公开日 申请号 申请日
1. CN103509048A 2014/1/15
专利标题:A kind of preparation method of green amifostine 法律状态
专利权人


2. CN103509049A 2014/1/15
专利标题:A kind of method of preparing medicinal amifostine 法律状态
专利权人


3. CN103396439A 2013/11/20 CN20131331345 2013/8/1
专利标题:Synthetic method for thiophosphate cell protective agent-amifostine 法律状态


4. CN102399238B 2013/6/12
专利标题:The preparation method of amifostine 法律状态


5. US2013090312A1 2013/4/11 US201213689652 2012/11/29
专利标题:METHODS OF USE RELATED TO XEROSTOMIA 法律状态
The present invention relates to new uses of thermally stable, crystalline S-2-(3-aminopropylamino)ethyl dihydrogen phosphorothioate, (amifostine) and other aminothiol compounds to treat and reverse toxicities caused by radiation treatment. In particular, the invention provides a method for treating or preventing xerostomia associated with the administration of radiation treatment of head and neck cancer.


6. CN102659836A 2012/9/12 CN20121110491 2012/4/16
专利标题:Method for preparing amifostine 法律状态


7. US2012082736A1 2012/4/5 US201113244594 2011/9/25
专利标题:Small-molecule TNF modulator to reduce the side effects of chemotherapy and radiotherapy 法律状态
Cancer patients treated by chemotherapy and/or radiotherapy often suffer serious side effects. Currently, there is only one FDA approved and used as both a chemoprotector and a radioprotector, amifostine, which is associated with significant problems. Disclosed in the present invention are novel methods of using UTL-5g as both a chemoprotector and radioprotector for treating cancer patients in addition to other related methods.


8. CN102399238A 2012/4/4 CN20111431844 2011/12/21
专利标题:Preparation method for amifostine 法律状态


9. CN102210694A 2011/10/12 CN2011191377 2011/4/12
专利标题:Oral amifostine preparation and preparation method thereof 法律状态


10. EP1764103A3 2011/8/24
专利标题:Crystalline amifostine compositions and methods for the preparation and use of same 法律状态
专利权人Medimmune Oncology, Inc.;
The present invention relates to a sterile stable vacuum dried crystalline amifostine composition and optionally pharmaceutically acceptable excipient(s). Typically the crystalline compositions of the present invention exhibit enhanced stability at temperatures ranging from about 4°C to about ambient temperature for a period of at least 2 years relative to existing solid vacuum dried amorphous amifostine preparations. The reconstituted compositions of the present invention are suitable for admin...



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