| 查看: 4155 | 回复: 17 | |||||
[交流]
达比加群酯的SWOT分析项
|
|||||
|
老大让我做一个SWOT分析,这对一个没有THOMSON、没有Pharmaproject的立项工作者来说,只能空手套白狼了,暂时只想出以下几个分析项,请各位虫友补充啦。 S分析 用药方法的便利性 出血安全性得到FDA、EMA等机构的屡次肯定 曾经获得FDA下属委员会全票支持 其对卒中的预防效果明显优于华法林 有间接比较研究显示,达比加群酯的成本-效益特征与有效性特征优于利伐沙班 先后在德国和加拿大被授予Prix Galien最佳药物奖 曾经获得NICE的有条件推荐 上市后市场表现强劲,已经实现了重磅炸弹级别的销售额 W分析 出血事件—达比加群酯挥之不去的阴影 肾功能损伤与P-gp是达比加群酯在其用药过程中需要调整剂量的主要因素 RE-ALLGN失败,使得人工心脏瓣膜成为达比加群酯的禁忌症之一 价格昂贵 O分析 适应证发病率高,用药市场规模庞大 需要开发新的药物,以弥补华法林的不足 利伐沙班于ROCKET-AF试验中仅证实与华法林相比的非劣性 T分析 将面临来自阿哌沙班、利伐沙班、依度沙班的激烈竞争 [ Last edited by williamxiang on 2013-4-3 at 16:31 ] |
» 收录本帖的淘帖专辑推荐
研发工艺 | 泮托拉唑 |
» 猜你喜欢
北京协和医学院杰青课题组招聘科研助理
已经有0人回复
北京协和医学院杰青课题组招聘科研助理
已经有0人回复
药理学论文润色/翻译怎么收费?
已经有229人回复
🔥速览|AACR 2026 mRNA肿瘤疫苗临床捷报
已经有0人回复
深圳理工大学和东南大学联合培养博士招生(2026年9月入学)
已经有11人回复
求助中国药典1995年版、二部
已经有0人回复
211高校2026年入学博士名额
已经有14人回复
211高校2026年入学博士名额
已经有15人回复
211高校2026年入学博士名额
已经有16人回复
海勃原辅料助力银屑病一线外用制剂开发
已经有0人回复
北京协和医学院杰青课题组招聘科研助理
已经有0人回复
» 本主题相关价值贴推荐,对您同样有帮助:
达比加群酯在中国获批
已经有17人回复
达比加群酯经过碱降解后产物会是什么结构?
已经有10人回复
达比加群酯甲磺酸盐 颜色
已经有10人回复
» 抢金币啦!回帖就可以得到:
西安电子科技大学保研: 挑战高速IP设计NVMe,RDMA及NVMe-oF
+1/288
福州大学化工学院电子化学品团队博士招生,还有一个名额!
+1/75
诚邀津门师者共研
+1/75
【通知】北京信息科技大学仪器科学与光电工程学院招收调剂生(2026),快来报名吧!
+1/38
安徽大学俞洋洋课题组招收化学方向博士生1人
+1/28
上海理工大学-赵斌教授课题组招收申请考核制博士【新能源材料】
+1/18
【26.9月入学】211大学补招学博1人
+1/14
【26.9月入学】211大学补招学博1人
+1/14
【急招】 北京工业大学 能动第二批博士申请-杰青课题组1-2名额,25日截止!!
+1/12
紧急招收2026年秋季入学博士生1名(湘潭大学 固体废弃物低碳利用湖南省工程研究中心)
+1/10
【截止2026年5月31日】石家庄铁道大学智能交通课题组诚招理工科背景博士
+1/10
南京农业大学2026年申请考核制博士招生:最后一批啦!
+1/8
紧急招收2026年秋季入学博士生1名(河北工大/北京科技大学联合 增材制造/生物材料)
+1/5
中科院博士后/特别研究助理招聘(光学工程、仪器科学、机械、电子、控制)
+1/5
三元结构理论 一个相对原创的社会学理论
+1/5
干货 | CD47/SIRPα通路
+1/2
四川大学招聘联合培养学生/科研助理/2027届博士
+1/2
海南大学药学院陈家良课题组2026年招聘博后、副高
+1/1
易度质量流量计在微孔加工流通性测试中的应用
+1/1
湖南师范大学国家杰青团队急招第二批博士研究生
+1/1
★ ★ ★ ★ ★ ★ ★ ★
小木虫: 金币+0.5, 给个红包,谢谢回帖
痴夷子皮: 金币+2, 谢谢交流,欢迎常来哦。 2013-04-07 08:32:30
williamxiang: 金币+5 2013-04-07 09:53:30
小木虫: 金币+0.5, 给个红包,谢谢回帖
痴夷子皮: 金币+2, 谢谢交流,欢迎常来哦。 2013-04-07 08:32:30
williamxiang: 金币+5 2013-04-07 09:53:30
|
楼上的就是来自TP中达比加群酯的SWOT分析。 给楼主个站内链接:http://muchong.com/bbs/viewthread.php?tid=5319066 建议:做产品SWOT分析的时候可结合国内情况,行业情况及本公司情况三级,给出相应的分析。 楼主对这个产品所述的SWOT分析,已相当专业了!除了专业方面的应该还有些上述建议的其他的。 个人意见,仅供参考! |
9楼2013-04-04 00:12:48
★ ★ ★
小木虫: 金币+0.5, 给个红包,谢谢回帖
痴夷子皮: 金币+2, 谢谢交流,欢迎常来哦。 2013-04-07 08:32:18
小木虫: 金币+0.5, 给个红包,谢谢回帖
痴夷子皮: 金币+2, 谢谢交流,欢迎常来哦。 2013-04-07 08:32:18
|
Strengths The first novel anticoagulant to secure approval for stroke prevention in atrial fibrillation (AF), entering the US market in November 2010 No requirement for anticoagulation monitoring and dose adjustment, and no food effect In the RE-LY trial in AF, Pradaxa showed comparable to superior efficacy in stroke prevention, compared with warfarin, with equal to lower bleeding risk A subgroup analysis from RE-LY showed that Pradaxa 150 mg bid reduced the rate of stroke by 35% compared with well-controlled warfarin, irrespective of a patient's stroke risk Comparable to Lovenox in the prevention of major venous thromboembolism (VTE) and VTE-related mortality after both knee and hip replacement, according to RE-NOVATE data Equal efficacy to well-controlled warfarin in the treatment of acute VTE, but with a 37% reduction in major or clinically relevant bleeding risk over 6 months, according to RECOVER data |
2楼2013-04-03 10:38:46
13楼2013-04-09 19:00:34
★ ★ ★ ★ ★ ★
小木虫: 金币+0.5, 给个红包,谢谢回帖
williamxiang: 金币+5 2013-04-03 10:47:53
小木虫: 金币+0.5, 给个红包,谢谢回帖
williamxiang: 金币+5 2013-04-03 10:47:53
|
Weaknesses A superiority claim over warfarin in stroke prevention was rejected for inclusion in the label by the FDA A 110 mg doseage was not approved for use in patients at higher bleeding risk A higher risk of myocardial infarction was seen in RE-LY Twice daily dosing, compared with once daily for Xarelto Not approved in the US for VTE prevention post-surgery, unlike Xarelto which was approved in July 2011 Has faced some safety concerns, and the label was updated to mandate renal testing in high-risk patients Associated with a 6% rate of major gastrointestinal hemorrhage during each patient year on treatment Other gastrointestinal side effects, including dyspepsia, nausea and gastritis, are increased compared with warfarin (35% vs 24%) Current lack of antidote Very short half-life once removed from specially designed desiccant-containing packaging |
3楼2013-04-03 10:41:12
★
小木虫: 金币+0.5, 给个红包,谢谢回帖
小木虫: 金币+0.5, 给个红包,谢谢回帖
|
Opportunities Approval in AF opens up a blockbuster market, and Pradaxa could garner a greater share of the market in the near term due to its first mover advantage Pradaxa could be viewed as superior to Xarelto given Xarelto's lack of superiority to warfarin on an intent-to-treat basis seen in the ROCKET AF trial Despite the proven efficacy of warfarin in stroke prevention, it has a number of limitations, such as an increased risk of bleeding and the need for patient monitoring and dose adjustment, which has created an unmet need for safe and effective alternatives Approval in acute coronary syndrome (ACS); phase III trials in this setting began in December 2007 Development of competitor Eliquis in ACS was discontinued following high rates of bleeding in trials High cost and considerable copay required for Pradaxa may fade as insurers realize potential savings from increased avoidance of ischemic events and hospitalization AF is the most common sustained cardiac rhythm disturbance, and prevalence increases with age Up to 60% of cases of AF are caused by hypertension or coronary artery disease, which are increasing in prevalence in most Western societies ACS is the leading cause of death in the US and one of the most prevalent non-communicable diseases in the world |
4楼2013-04-03 10:53:35
★ ★ ★ ★
williamxiang: 金币+4 2013-04-03 13:01:31
williamxiang: 金币+4 2013-04-03 13:01:31
|
Threats Commercial threat from Eliquis; current phase III data appear to support a superiority claim over warfarin which would differentiate the product Increased competition in the oral anticoagulant category; the marketing battle between Pradaxa, Xarelto and Eliquis will be key In Japan, Lixiana is in development for stroke prevention in AF, and could present competition in this market following Pradaxa's launch in March 2011 The drug may not gain approval in ACS given concerns about bleeding If approved, use in ACS may be limited given the availability of new, more potent antiplatelet regimes, such as AstraZeneca's Brilinta, that improve outcomes with less increased bleeding Physicians may be reluctant to switch patients who are well controlled on warfarin to other treatment options Price: the significant price difference between Pradaxa and warfarin could present reimbursement issue Self administration of low-molecular-weight heparins out of hospital by patients with AF undergoing elective cardioversion is a promising approach that may result in cost savings Low-molecular-weight heparins, in particular enoxaparin which presents a generic and efficacious option for DVT treatment and prophylaxis following orthopedic surgery |
5楼2013-04-03 10:54:50
6楼2013-04-03 10:56:14
7楼2013-04-03 11:15:17
8楼2013-04-03 13:02:42
10楼2013-04-04 00:54:08
11楼2013-04-06 12:19:13
12楼2013-04-06 21:54:49
14楼2013-04-10 00:30:10
15楼2013-04-11 20:08:46
16楼2013-04-26 06:35:02
17楼2013-09-03 16:57:58
18楼2013-09-10 18:04:01












回复此楼