黄建平 的讨论

发布于: 雪球回复:8喜欢:0
风险投资可以看看,靶点都比较新,百济的pd1今年9月刚获得临床批件,1期还没开始做呢,已经落后恒瑞不止一点了,君实和信达也在他前面。

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2017-02-15 10:15

这类数据如何获得?谢谢LZ

2016-12-11 09:59

我以前分析过恒瑞的PD1. 基本上来看至少没有比已经上市的3家更好,所以incy才会放弃。但这并不代表在国内无法上市。 阿帕替尼和艾克替尼都不是最好的同类药品但是在国内也算是先进生产力。。。卖的有声有色

2016-12-10 23:47

不是进二期了么

2016-12-10 21:51

恒瑞的PD1据说临床一般

2016-12-10 10:03

哦你是说国内啊。嗯,进度比恒瑞和君实慢了

2016-12-10 09:30

Updated data from a Phase 1 clinical trial assessing BeiGene's (BGNE+2.6%) PD-1 inhibitor BGB-A317 in patients with advanced solid tumors showed greater than a 38% disease control rate. The results were presented at the Society for Immunotherapy of Cancer 31st Annual Meeting in National Harbor, MD.

In 99 evaluable patients as of September 30, 15 (15%) were partial responders and 23 (23%) had stable disease implying a disease control rate of 38%. 87% (n=13/15) of the partial responders remain on treatment  with duration of response ranging from 28 - 47 weeks. Responders include renal cell carcinoma, urothelial carcinoma, gastric cancer, Merkel cell carcinoma, naospharyngeal cancer and penis squamous cell carcinoma an duodenal carcinoma.

The most common treatment-related adverse events (TRAEs) were fatigue (19%), diarrhea (13%), rash (11%), pruritis (11%), nausea (8%), hypothyroidism (7%) and infusion-related reactions (6%).

The study will advance to a 1b phase during which flat dosing of 200 mg and 300 mg every three weeks will be explored.

详细的细分数据在conference里面我看了。一时间找不到。。

2016-12-10 09:28

不对的。1期已经开始做了。我都看到中期跟踪数据了。
应答15%。招募了100多个病人测试10多种癌症。我去找找数据