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求助来那替尼上市信息?

在网上看到有公司挂来那替尼项目合作信息,在CDE上有来那替尼片的进口申请,但是我却查不到该药的具体上市信息,特此求助,望大侠相帮,谢谢!
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我查到信息该药也是在刚做完3期,预计明年才开始申报。但是CDE上怎么有来那替尼片的进口申请呢(截图未成功,但确实有该申请)?搞不清楚了…...
国内申报进口跟申请FDA和EMA上市并没有联系。nintedanib同样也是申请进口临床,而nintedanib也没有在FDA上市,只是被FDA授予突破性疗法。
来那替尼(neratinib)刚获做完Ⅲ期临床试验(ExteNET),现在还没上市。...
我查到信息该药也是在刚做完3期,预计明年才开始申报。但是CDE上怎么有来那替尼片的进口申请呢(截图未成功,但确实有该申请)?搞不清楚了…
还没有在国内外上市,不排除最后被毙掉的可能。你看看汤姆数据报告
现在应该是正在申请进口临床吧,等进口还得需要2-3年吧。
Puma Biotechnology, under license from Pfizer (previously Wyeth), is developing neratinib (PB-272; HKI-272), an irreversible pan-HER (Erbb1, ErbB2 and ErbB4) tyrosine kinase inhibitor, for the potential oral treatment of HER2-positive cancers, primarily breast cancer
    In July 2009, worldwide phase III breast cancer trials were initiated by Wyeth in patients who had received prior trastuzumab-based therapy ; in October 2011, following its acquisition of rights, Puma intended to terminate the ongoing Pfizer-sponsored trials , and the company began its own phase III trial in third-line metastatic breast cancer in June 2013 . In July 2014, Puma planned to file the drug for approval in the extended adjuvant setting for breast cancer in 1H15 .

Development in other HER2-positive cancer settings is ongoing. In April 2013, a phase II trial in patients with NSCLC was ongoing . In October 2013, a phase II study in patients with other solid tumors with a HER2 mutation was initiated ; in March 2014, initial data from the trial were expected in 2014
Puma Biotechnology, under license from Pfizer (previously Wyeth), is developing neratinib (PB-272; HKI-272), an irreversible pan-HER (Erbb1, ErbB2 and ErbB4) tyrosine kinase inhibitor, for the potential oral treatment of HER2-positive cancers, primarily breast cancer
    In July 2009, worldwide phase III breast cancer trials were initiated by Wyeth in patients who had received prior trastuzumab-based therapy ; in October 2011, following its acquisition of rights, Puma intended to terminate the ongoing Pfizer-sponsored trials , and the company began its own phase III trial in third-line metastatic breast cancer in June 2013 . In July 2014, Puma planned to file the drug for approval in the extended adjuvant setting for breast cancer in 1H15 .

Development in other HER2-positive cancer settings is ongoing. In April 2013, a phase II trial in patients with NSCLC was ongoing . In October 2013, a phase II study in patients with other solid tumors with a HER2 mutation was initiated ; in March 2014, initial data from the trial were expected in 2014
FDA刚刚批准上市,2017年9月正式上市。

Puma Biotechnology, under license from Pfizer (previously Wyeth), is developing neratinib (PB-272; HKI-272), an irreversible pan-HER (Erbb1, ErbB2 and ErbB4) tyrosine kinase inhibitor, for the potent ...
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