包含imtokenpte.ltd.的词条

　　本文转载自肖恩大侠

　　反向并购再上市imtokenpte.ltd.，Valeritas纳斯达克挂牌

　　大麻也疯狂！Therapix Biosciences纳斯达克成功IPO

　　FGFR3靶点膀胱癌单抗再获3000万美元B轮融资

　　点石成金imtokenpte.ltd.，原GSK高管受资本青睐imtokenpte.ltd.，新公司再获3040万美金B轮投资

　　大手笔！Hologic 16.5亿美元收购Cynosure进军医美

　　Xenon制药股价狂跌44%，痤疮药临床试验终止

　　IPO挂牌

　　1.一次性胰岛素泵生产商Valeritas纳斯达克上市

　　概要：Valeritas于3月23日在纳斯达克IPO发行股票，通过以每股10美元的价格出售525万股股份，希望筹集5250万美元。Valeritas是一家专注糖尿病治疗的医疗技术公司，致力于创新型药物供应解决方案的开发和商业化，为患者带去临床和人道解决方案。值得一提的是，Valeritas曾于去年3月撤回上市计划，之后缩减规模重新申请上市。

　　相关报道：

　　Valeritas prices IPO at $10, within the range

　　Mar 23, 2017

　　Valeritas Holdings, which markets a disposable device that delivers insulin therapy for Type 2 diabetes, raised $53 million by offering 5.3 million shares at $10, within the range of $9 to $11. Valeritas Holdings plans to list on the Nasdaq under the symbol VLRX. Cowen & Company and Wedbush PacGrow acted as lead managers on the deal.

　　The article Valeritas prices IPO at $10, within the range originally appeared on IPO investment manager Renaissance Capital's web.

　　PS: Renaissance Capital, the Renaissance IPO ETF (symbol: IPO) or the Global IPO Fund (symbol: IPOSX) , may have investments in securities of companies mentioned.

　　Source: NASDAQ

　　https://www.nasdaq.com/article/valeritas-prices-ipo-at-10-within-the-range-cm764581

　　2. 以色列大麻制药公司Therapix Biosciences纳斯达克成功IPO

　　概要：Therapix Biosciences在纳斯达克IPO发行200万股ADS，发行价为6美元每ADS，其原先预定价位为5-7美元每ADS。Therapix Biosciences是一家以色列大麻制药公司，现阶段公司正在开展两个大麻药物临床试验，分别是处于临床2b期适应症为图雷特氏综合症的THX-TS01和临床1期针对轻度认知障碍的THX-ULD01。

　　相关报道：

　　Therapix Biosciences Ltd. Announces Pricing of U.S. InitialPublic Offering and NASDAQ Listing

　　Mar 22, 2017

　　Therapix Biosciences Ltd. (NASDAQ:TRPX) (TASE:THXBY), a specialty clinical-stage pharmaceutical company specializing in the development of cannabinoid-based drugs, today announced the pricing of its initial publicoffering in the United States of 2,000,000 American Depository Shares("ADSs"). Each ADS, representing 40 ordinary shares of the Company,is offered at a price to the public of $6.00.

　　The gross proceeds to Therapix from this offering are expected tobe $12,000,000, prior to deducting underwriting discounts, commissions and other offering expenses. Therapix has granted the underwriters a 45-day optionto purchase up to an additional 300,000 ADSs to cover over-allotments, if any.

　　Therapix plans to use the net proceeds from the offering to advance the formulation and clinical development efforts for its two lead product candidates, including Phase II clinical trials, and for working capital and other general corporate purposes.

　　Therapix's ADSs are scheduled to begin trading on the NASDAQ Capital Market on March 22, 2017, under the symbol "TRPX". The offering is expected to close on or about March 27, 2017, subject to customary closing conditions.

　　Source: PR News Wire

　　https://www.prnewswire.com/news-releases/therapix-biosciences-ltd-announces-pricing-of-us-initial-public-offering-and-nasdaq-listing-616794734.html

　　私募融资

　　1.药物公司BioClin宣布完成3000万美元的B轮融资

　　概要：BioClin Therapeutics宣布完成imtokenpte.ltd.了3000万美元的B轮融资。此轮投资是由Sofinnova Ventures和Ysios Capital领投的，原投资方HealthCap、Life Sciences Partners(LSP)以及TeklaCapital Management继续跟投。BioClin Therapeutics是一家临床阶段药物公司，该公司候选药物B-701是一种靶向FGFR3（成纤维细胞生长因子受体3）的人源单克隆抗体，有成为领域内首个药物（first-in-class）的潜力。该轮融资能够使BioClin扩大使用B-701与多西紫杉醇联合的1b/2期试验，并启动了一项评估B-701联用atezolizumab单抗的1b/2期试验。

　　相关报道：

　　BioClin Gets $30M to Back More Bladder Cancer Drug Trials

　　Mar 22, 2017

　　BioClin Therapeutics has raised $30 million in funding to move forward with more tests of its experimental treatment for bladder cancer.

　　New investors Sofinnova Ventures and Ysios Capital led the Series B round of financing for San Ramon, CA-based BioClin. Earlier investors HealthCap, Life Sciences Partners, and Tekla Capital Management also participated in the investment. BioClin says it has now raised a total of $59million from investors.

　　BioClin’s lead drug candidate, B-701, is a monoclonal antibody developed to target fibroblast growth factor receptor 3 (FGFR3), a protein thatis often mutated in patients with bladder cancer. So far, BioClin has testedits treatment in two Phase 1 clinical trials, one of which studied patients with advanced solid tumors, including bladder cancer.

　　With the new capital, BioClin says it will test its drug inpatients who have metastatic bladder cancer or metastatic urothelial carcinoma and have either relapsed or failed to respond to first-line cancer treatments.The company says it will also expand a Phase 1b/2 clinical trial evaluating its drug in combination with the chemotherapy docetaxel.

　　BioClin also plans to start a a Phase 1b/2 trial evaluating itsdrug in combination with atezolizumab (Tecentriq), a Genentech immunotherapy drug that the FDA approved last year to treat the most common form of bladder cancer.

　　Source: Xconomy

　　https://www.xconomy.com/san-francisco/2017/03/22/bioclin-lands-30m-to-back-more-bladder-cancer-drug-trials/

　　2. 英国新药研发公司Pulmocide 完成3040万美元B轮融资

　　概要：Pulmocide是一家成立于2013年的英国公司,近日宣布完成了总额为3040万美元的B轮融资，业内知名风险投资机构SROne领投。目前公司有两款拥有自主知识产权的产品，一款叫做PC786的产品能以雾状制剂的形式，被患者吸入呼吸道，治疗呼吸道合胞病毒感染；另一款产品PC945能针对肺部的真菌感染。B轮融资将用于这两款创新化合物到早期临床阶段。Pulmocide公司首席执行官Rapeport博士曾出任葛兰素史克的高级副总裁长达6年，并曾担任“卓越中心”（Centre of Excellence）的呼吸疾病主任。先前，Rapeport博士曾出任一家初创公司Respivert的首席执行官，并帮助它在2010年被强生以近1亿美元的价格收购。

　　相关报道：

　　Ex-GSK team raises $30M for respiratory infection trials

　　Mar 20, 2017

　　Researchers who worked at GlaxoSmithKline before leading RespiVertto a takeover by Johnson & Johnson have raised $30.4 million (?24.5million) for their latest venture, Pulmocide. The Series B will allow Pulmocideto take inhaled treatments for respiratory syncytial virus (RSV) and pulmonary aspergillosis through early clinical trials.

　　New investor SR One, the VC arm of GSK, led the round with the support of backers who helped Pulmocide to its ?17 million Series A in 2013,including SV Life Sciences, F-Prime Capital, Johnson & Johnson Innovationand Touchstone Innovations. London, United Kingdom-based Pulmocide has attracted the big name financiers on the strength of its management team andthe potential of the two candidates they have started to develop.

　　“Pulmocide's core asset is the management team's proprietary expertise in the design of highly potent compounds with extended lung retentiontime and limited systemic exposure. This has enabled the development of two anti-infective drugs for serious diseases of the lung, where an inhaled therapy should deliver the optimal clinical outcome,” SR One Partner Matthew Foy saidin a statement.

　　Many on the management team, including CEO Garth Rapeport, M.D.and CSO Pete Strong, Ph.D., list stints at GSK on their résumés. Rapeport,Strong and other members of the Pulmocide team subsequently showed they couldturn the expertise in inhaled medicines they accrued at GSK and elsewhere intobiotech success when they set up RespiVert. J&J bought the biotech and itspipeline of programs in COPD, cystic fibrosis and severe asthma in 2010 for an undisclosed sum reported by The Telegraph to be around $100 million.

　　Source: Fierce Biotech

　　https://www.fiercebiotech.com/biotech/ex-gsk-team-raises-30m-for-respiratory-infection-trials

　　并购

　　1. Hologic 16.5亿美元收购Cynosure进军医美界

　　概要：Hologic（NASDAQ：HOLX）最终确定收购Cynosure（NASDAQ：CYNO）,收购价为16.5亿美元,每股66美元，Hologic是一家诊断产品、医疗成像系统和手术产品制造商，Cynosure是一家专注于产品用于非侵入性身体造型，脱毛，皮肤再生的女性健康的公司，并购后Hologic战略定位为打造女性健康第一医疗品牌。

　　相关报道：

　　Hologic (HOLX) Completes Acquisition of Cynosure (CYNO)

　　Mar 22, 2017

　　Hologic,Inc. (Nasdaq: HOLX) announced today that it has completed the acquisition of Cynosure, Inc., a leader in medical aesthetics systems and technologies, for$66 per share in cash.

　　"Weare pleased to complete our acquisition of Cynosure, and look forward toworking with Michael Davin and the entire Cynosure team to achieve even greater success in the large, rapidly growing medical aesthetics market," saidSteve MacMillan, Hologic's Chairman, President and Chief Executive Officer."Acquiring Cynosure, combined with divesting our blood screening business,fundamentally reshapes our business portfolio and makes us a stronger, faster-growing company."

　　Thetender offer by a subsidiary of Hologic for all the outstanding shares ofCynosure Class A Common Stock expired as scheduled at midnight ET on March 21,2017. A total of 17,047,830 shares of Cynosure Class A Common Stock,representing approximately 70.6% of Cynosure's outstanding shares, were validly tendered into and not validly withdrawn from the tender offer. As a result,Hologic and its subsidiary have accepted for payment and will promptly pay forall shares that were validly tendered and not validly withdrawn.

　　Source: Street Insider

　　https://www.streetinsider.com/Corporate+News/Hologic+(HOLX)+Completes+Acquisition+of+Cynosure+(CYNO)/12695012.html

　　行业盘点

　　1.Xenon制药候选药物2期临床未取得积极结果

　　概要：Xenon制药(NASDAQ：XENE)宣布，该公司治疗中重度痤疮的重要候选药物XEN801在2期临床试验中未能达到关键药效学终点。具体来说，与安慰剂相比，临床数据无法证明从基线到第12周的病变计数在统计学上有明显差异，该公司将终止发展此候选药物，Xenon制药股价应声下跌44%。

　　相关报道：

　　Xenon acne drug misses efficacy endpoints in phase 2

　　Mar 24, 2017

　　A phase 2trial of Xenon Pharmaceuticals’ acne candidate XEN801 has missed its primary and key secondary efficacy endpoints. The comprehensive failure prompted Xenonto admit the data don’t support continued development of XEN801 and wiped 44%off its stock price in premarket trading.

　　Xenonenrolled 165 patients with moderate-to-severe facial acne and randomized them toreceive either a gel formulation of XEN801 or placebo. After 12 weeks in which participants applied a gel to their faces each evening, investigators looked for changes against baseline. The study’s primary endpoint was the percent change in lesion count after 12 weeks. Secondary endpoints looked at lesioncounts after four and eight weeks, and the change on an investigator assessmentscale.

　　Managementat Xenon thought small molecule SCD1 inhibitor XEN801 could improve outcomes byreducing the size and number of sebaceous glands, but the data fell well shortof expectations. XEN801 failed to outperform placebo against the primaryefficacy endpoint. And it came up short against “key secondary efficacyendpoints.”

　　Faced with a clean sweep of negative efficacy endpoints, Xenon CEO Simon Pimstone,M.D., Ph.D. held his hands up and admitted it looks like the end of the linefor XEN801.

　　PS:这种因临床试验或其imtokenpte.ltd.他重大影响而暴涨暴跌的情形非常多，如能提前研判或及时知晓/预测，这能力该多强啊。

　　Source: Fierce Biotech

　　https://www.fiercebiotech.com/biotech/xenon-acne-drug-misses-efficacy-endpoints-phase-2

　　以上，难免有疏漏或不正确之处，请多多指出，并在文下留言处留言，谢谢！