发布于: 修改于:雪球转发:1回复:2喜欢:0
怎么看$Day One(DAWN)$的这款药?@薛定谔之猫 FIREFLY-1的数据不错,在69名携带BRAF突变的低级别胶质瘤儿童患者中,Tovorafenib使得67%的患者肿瘤大幅度缩小,其中17%的患者肿瘤完全消失。26%的患者疾病稳定,没有进一步加重。$诺华制药(NVS)$ $百济神州(BGNE)$
引用:
2023-04-20 21:46
DAWN Tovorafenib data in BRAF-fusion Melanoma 1PR,1CR, 1uPR from 1st 3 patients
$Day One(DAWN)$ BRAF新药

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04-18 22:37

期待一下

05-24 06:58

现在才看到这个。我发现我雪球名字有好几个近似的,很容易弄混。
这只在观察池里,靠谱的小公司。2024-04-23 FDA accelerated 批准,还获得一张儿科罕见病优先评审券(价值$1亿?)。接下来得看至少两个季度的销售如何、从而决定被收购的价格吧(如果有收购的话)?
兄台另外还关注哪些?
==2024-04-23
Day One Biopharmaceuticals, Inc. (Nasdaq: DAWN) (“Day One” or the “Company”), a commercial-stage biopharmaceutical company dedicated to developing and commercializing targeted therapies for people of all ages with life-threatening diseases, today announced that the U.S. Food and Drug Administration (FDA) has approved OJEMDA (tovorafenib), a type II RAF inhibitor, for the treatment of patients 6 months of age and older with relapsed or refractory pLGG harboring a BRAF fusion or rearrangement, or BRAF V600 mutation. This indication is approved under accelerated approval based on response rate and duration of response. With the approval, Day One received a rare pediatric disease priority review voucher from the FDA.