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ENCY

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  1. [verwijderd] 23 november 2007 20:16
    Vandaag maar helve dag handel en waarschijnlijk grijpt men dat om de koers in een dunne handel weer boven de 1 use te zetten. Onthouden voor het volgende jaar rond thanksgivingday.
  2. gustaaf1e 23 november 2007 20:23
    quote:

    BlueGiant schreef:

    Vandaag maar helve dag handel en waarschijnlijk grijpt men dat om de koers in een dunne handel weer boven de 1 use te zetten. Onthouden voor het volgende jaar rond thanksgivingday.
    Ja, dat is wel een goeie. Blijkbaar vandaag hetzelfde idee bij GTCB.
    G
    die schrijf ik even in mijn agenda voor volgend jaar.
  3. [verwijderd] 26 november 2007 08:23
    Encysive Pharmaceuticals Launches Thelin (sitaxentan sodium) in Italy

    First Selective, Once-Daily Oral Endothelin A Receptor Antagonist Now Available to Patients in All Big Five EU Countries
    November 26, 2007: 02:00 AM EST

    HOUSTON, Nov. 26, 2007 (PRIME NEWSWIRE) -- Encysive Pharmaceuticals Inc. (Nasdaq:ENCY) today announced the commercial availability of THELIN(r)(1) (sitaxentan sodium(2)) 100 mg tablets in Italy for the treatment of pulmonary arterial hypertension (PAH). Encysive received European Union (EU) marketing authorization for THELIN from the European Commission in August 2006. THELIN is the first selective endothelin A receptor antagonist, and the first once-daily oral treatment available for patients with PAH.

    THELIN is indicated for improving exercise capacity in PAH patients classified as World Health Organization (WHO) functional class III. Efficacy has been shown in primary pulmonary hypertension(3) and pulmonary hypertension associated with connective tissue disease (CTD).

    "Italy joins the countries in which two different endothelin receptors antagonists are marketed for the PAH indication," said Nazzareno Galie, M.D., Director of the Pulmonary Hypertension Centre of the University of Bologna. "The possibility of alternative drugs of the same class can be utilized by clinicians to identify the optimal benefit-to-risk ratio in the individual patient."

    The European Commission's centralized licensing procedure permits Encysive to market THELIN in all 27 member states of the EU. THELIN has already been launched in the United Kingdom, Germany, Ireland, Spain, France and the Netherlands and will be launched in additional EU member states as local government approval for reimbursement is obtained.

    "The launch of Thelin in Italy marks an important achievement for Encysive Pharmaceuticals," commented George Cole, President and CEO of Encysive. "Thelin is now being commercialized in the five largest markets in the EU, positioning us for substantial sales growth in 2008."

    THELIN(r) (sitaxentan sodium) Overview

    THELIN is an endothelin A receptor antagonist, a small molecule that blocks the action of endothelin, a potent mediator of blood vessel constriction and growth of smooth muscle in vascular walls. Endothelin receptor antagonists may prove to be effective in the treatment of a variety of diseases where the regulation of vascular constriction is important. THELIN is 6,500-fold selective in the targeting of the endothelin A receptor versus the endothelin B receptor. Highly selective endothelin A receptor antagonism has been shown to increase blood flow and reverse vasoconstriction in human clinical pharmacology studies. For more information, please visit www.encysive.com.

    Important Safety Information

    In placebo-controlled clinical trials, the most frequent adverse events that occurred in patients receiving THELIN, which were considered to possibly be related to THELIN treatment, were headache, peripheral edema and nasal congestion. Other adverse events that occurred in at least 2% of THELIN patients, at a rate greater than placebo and considered to possibly be related to THELIN treatment, included dizziness, constipation, epistaxis, flushing, international normalized ratio (INR) increase, insomnia, nausea, upper abdominal pain, vomiting, dyspepsia, diarrhea, fatigue, muscle cramp, and prothrombin time (PT) prolongation. THELIN is also associated with liver function abnormalities. Because THELIN inhibits the metabolism of warfarin and other vitamin K antagonists, a dose adjustment for these drugs is needed when co-administered with THELIN. THELIN and other endothelin receptor antagonists have potential for liver toxicity and are teratogenic. Testing of liver enzymes is required prior to the initiation of THELIN and monthly thereafter. THELIN should not be used during pregnancy unless clearly necessary. THELIN is contraindicated in patients receiving cyclosporine A, patients with mild to severe hepatic impairment (Child-Pugh Class A-C), patients with elevated liver aminotransferases prior to starting treatment (elevation in liver enzymes to levels greater than 3 times the upper limit of normal), lactating patients, or patients with hypersensitivity to the active substance or any excipients.

    About PAH

    It is estimated that PAH afflicts approximately 100,000 to 200,000 people in North America and Europe. The disease is characterized by high blood pressure and structural changes in the walls of the pulmonary arteries, the blood vessels that connect the right side of the heart to the lungs. As these arteries become increasingly constricted, blood flow and oxygenation may be inadequate to meet the body's demands. Since the heart must then pump harder to overcome the resistance, patients are susceptible to heart failure.

    Vriendelijke groet.
  4. [verwijderd] 28 december 2007 22:32
    ENCY: Patent Infringement Lawsuit Filed Against Barr Laboratories
    Friday, December 28, 2007; Posted: 04:06 PM


    Ridgeland, MS, DEC 28, 2007 (EventX/Knobias.com via COMTEX) -- MUCCY | charts | news | PowerRating -- By Fain Hughes, fhughes@knobias.com

    Encysive Pharmaceuticals Inc. (ENCY) announced that Mitsubishi Chemical Corporation, the patent holder for Argatroban injections, Mitsubishi Tanabe Pharma Corporation, Encysive and GlaxoSmithKline have filed a patent infringement lawsuit in the U.S. District Court for the Southern District of New York against Barr Laboratories, Inc. related to Argatroban injections. Argatroban is approved by the FDA for the treatment of heparin-induced thrombocytopenia. Encysive is the holder of the New Drug Application for Argatroban, and has licensed the North American marketing rights for the drug to GlaxoSmithKline.

    KNOBIAS DISCLAIMER: All statements made in this article were made by the Company and do not in any way reflect the opinions of Knobias. Knobias is not a registered broker-dealer, nor investment advisor, and does not endorse or recommend any securities mentioned. This story is provided for informational purposes only and is not intended for trading purposes. Knobias shall not be liable for any actions taken in reliance of any information provided herein. Republication or redistribution of Knobias content is expressly prohibited without prior written consent of Knobias.com, LLC.

    ABOUT KNOBIAS: Knobias is a premier financial information provider of trading and investing data covering all U.S. equities for investors and security professionals. Knobias is best described by its three major components: Real-time desktop applications providing quotes, charts, level 2, analysis etc.; Knobias RAiDAR providing thousands of real-time news stories, alerts and documents daily; Knobias fundamentals providing a comprehensive database of fundamental research information.

    If your company wishes to participate in the EventX newswire, please contact Knobias: www.knobias.com

    Knobias.com, LLC 601-978-3399 601-978-3675 info@knobias.com www.knobias.com/cmtx

    Vriendelijke groet.
  5. [verwijderd] 2 januari 2008 18:33



    Associated Press
    Barr Pharma Confirms Encysive Lawsuit
    Associated Press 01.02.08, 10:57 AM ET









    MONTVALE, N.J. - Generic drug maker Barr Pharmaceuticals Inc. on Wednesday confirmed it is challenging a patent held by biopharmaceutical company Encysive Pharmaceuticals Inc. for blood-clotting injection Argatroban.

    Argatroban is approved by the Food and Drug Administration for the treatment of heparin-induced thrombocytopenia, a serious side effect of the blood thinner heparin.

    Barr said it believes it was the first to file an abbreviated new drug application for Argatroban, containing a so-called paragraph IV certification, which indicates that its generic version of Argatroban would infringe an existing patent, but contends that Encysive's patent is invalid.

    Barr said it has notified the new drug application holder and patent owner, Encysive.

    On Friday, Encysive said it formally launched a patent challenge under the Hatch-Waxman Act, which Congress passed in 1984 to establish procedures to encourage generic companies to challenge patents for brand-name drugs before their expiration.

    The lawsuit against Barr stops the FDA from approving the generic version for 30 months, Encysive said last week. That could be reversed, however, if a final district court decision finds the patent invalid, unenforceable or not infringed.

    Encysive said the company along with Mitsubishi Chemical Corp. (other-otc: MUCCF.PK - news - people ) - the patent holder for Argatroban injections - Mitsubishi (other-otc: MSBHY.PK - news - people ) Tanabe Pharma Corp. and GlaxoSmithKline (nyse: GSK - news - people ) PLC had filed suit in the U.S. District Court for the Southern District of New York to prevent Barr from bringing the product to market.

    Barr Pharma's subsidiary Barr Laboratories Inc. (nyse: BRL - news - people ) initiated the patent challenge.

    Shares of Pomona, N.Y.-based Barr Pharmaceuticals fell 30 cents to $52.80 in morning trade, while Houston-based Encysive rose a penny to 86 cents.

    Copyright 2007 Associated Press. All rights reserved. This material may not be published broadcast, rewritten, or redistributed

    Vriendelijke groet.

  6. [verwijderd] 14 januari 2008 11:34
    Encysive Pharma Introduces THELIN 100 Mg Tablets In Belgium And Luxembourg [ENCY]

    1/14/2008 4:04:06 AM Encysive Pharmaceuticals Inc. (ENCY), a global biopharmaceutical company, announced on Monday that THELIN(r)(1) (sitaxentan sodium(2)) 100 mg tablets for the treatment of pulmonary arterial hypertension (PAH) are commercially available in Belgium and Luxembourg. The company said that in August 2006, it obtained European Union, or EU, marketing authorization for THELIN from the European Commission, thereby allowing it to market THELIN in all 27-member states of the EU.

    Encysive already introduced THELIN in the United Kingdom, Germany, Ireland, Spain, France, Italy and the Netherlands and will launch in additional EU member states after getting local government approval for reimbursement.

    THELIN is the first selective endothelin A receptor antagonist, and the first once-daily oral treatment commercially available for PAH patients in the EU. It is indicated for improving exercise capacity in PAH patients classified as World Health Organization functional class III. Efficacy has been shown in primary pulmonary hypertension (3) and pulmonary hypertension associated with connective tissue disease.

    Thierry Plouvier, M.D., Vice President, Europe Operations, for Encysive (UK) Ltd., commented, “With the availability of THELIN to physicians and patients in Belgium and Luxembourg, our European commercialization strategy continues to move forward. THELIN adds an additional therapeutic option for treating patients with pulmonary arterial hypertension in the EU.”

    ENCY closed trade on Friday at $0.67.

    Vriendelijke groet.
  7. [verwijderd] 28 januari 2008 21:16
    Can Encysive Catch the Competition?
    By Brian Lawler January 28, 2008

    After two years of spectacular mismanagement, will 2008 be the year that Encysive Pharmaceuticals (Nasdaq: ENCY) is finally able to capitalize on its very marketable lead drug, Thelin?

    Thelin is Encysive's only in-house marketed drug. It treats a condition called pulmonary arterial hypertension (PAH) and is approved for marketing in the European Union and a few other places around the world, but not in the United States. Sales guidance provided by Encysive calls for 2007 sales to be a bit above the company's previous $10.5 million to $11.5 million forecast, with 2008 estimates for worldwide sales in the $40 million to $50 million range.

    Last week, both of Encysive's most direct competitors, Actelion and Gilead Sciences (Nasdaq: GILD) reported fourth-quarter sales numbers for their similar compounds. In the fourth quarter, sales of Actelion's Tracleer were up an incredibly strong 34% year over year, topping $300 million and showing no signs of a sales slowdown despite having been on the market for more than six years in some places.

    Sales of other PAH treatments have been strong as well in the fourth quarter. Gilead's Letairis, which is only approved in the U.S., brought in a respectable $15 million in the fourth quarter, in only its second full quarter on the market. Sometimes competitor and sometimes complementary treatment Revatio (known more commonly as Viagra) from Pfizer (NYSE: PFE) also experienced another solid quarter of 10% sales growth, although Pfizer doesn't break out the portion of Viagra sales meant for treating pulmonary arterial hypertension.

    Almost every approved PAH treatment has shown strong sales growth in recent quarters, and there are a host of drugmakers, like United Therapeutics (Nasdaq: UTHR) and BioMarin (Nasdaq: BMRN), with innovative new treatments in development.

    Pulmonary arterial hypertension is a market that is undoubtedly (and unfortunately) experiencing a large market expansion as more and more patients are correctly diagnosed and put on PAH drugs. The market opportunity in the U.S. and Europe is huge.

    It will probably be another two years before Encysive's Thelin will be on the market in the United States, because the FDA wants more efficacy data before approving it. Encysive is planning to begin a phase 3 study in the second quarter. The main question now is what highly diluted shape Encysive will be in by the time Thelin gets to the U.S. market.

    Vriendelijke groet.

  8. [verwijderd] 20 februari 2008 15:19
    Pfizer to Acquire Encysive Pharmaceuticals
    Last update: 2/20/2008 9:14:01 AM
    Acquisition Will Extend Presence in Pulmonary Arterial Hypertension with Product Launched in Several EU Countries; Pfizer Plans Pivotal Trial to Support Registration in the U.S. NEW YORK & HOUSTON, Feb 20, 2008 (BUSINESS WIRE) -- Pfizer Inc today announced that it has entered into an agreement to acquire Encysive Pharmaceuticals Inc. (ENCY), a publicly held biopharmaceutical company whose product for the treatment of pulmonary arterial hypertension (PAH) is commercially available in much of the European Union and is approved in other markets. Under the terms of the agreement, Pfizer will make a cash tender offer for all issued and outstanding shares of Encysive for $2.35 per share, representing an equity value of approximately $195 million. Following completion of the tender offer, a subsidiary of Pfizer will merge with Encysive, with the outstanding Encysive shares not tendered pursuant to the tender offer converted into the right to receive the per share price paid under the offer. Upon Pfizer's acquisition of Encysive, Pfizer will assume Encysive's change of control repurchase obligations under its 2.5% convertible senior notes. The Board of Directors of Encysive has unanimously approved the merger agreement and unanimously recommends that Encysive stockholders accept the tender offer and tender their shares. Pfizer will acquire the rights to THELIN(R) (sitaxsentan sodium), an oral, once-daily endothelin A receptor antagonist (ETRA) for the treatment of PAH, as well as Encysive's other pipeline candidates. THELIN has been approved for marketing in the European Union (EU), and is currently available in many EU states, including the United Kingdom, Germany, Ireland, Spain, France, Italy, Belgium, Luxembourg and the Netherlands. THELIN has also been approved in Australia and Canada. In the United States, THELIN has been the subject of three approvable letters from the U.S. Food and Drug Administration (FDA). Pfizer plans to conduct a pivotal Phase III trial to support registration in the U.S. "The process initiated in July of 2007 to review Encysive's strategic alternatives led us to consider a range of opportunities for increasing shareholder value," commented George W. Cole, president and chief executive officer of Encysive. "After a thorough analysis, Encysive's Board of Directors concluded that this cash transaction with Pfizer represents the best option for our shareholders now. Pfizer has come with a superior offer and with an in-depth understanding of pulmonary arterial hypertension, our primary therapeutic focus. We look forward to working with representatives of Pfizer in finalizing this transaction, and in transitioning our U.S. and EU operations." "The acquisition of Encysive will add growing, near-term revenue from the European market and increase our already strong presence in the cardio-respiratory arena with a product that complements REVATIO(TM), a PAH treatment that was discovered and developed by Pfizer researchers," said Ian Read, president of Pfizer's Worldwide Pharmaceutical Operations. "We look forward to applying Pfizer's significant resources to the launch of THELIN in additional countries." "Our commitment to pursue compelling science taking place outside of our laboratories is ongoing, and the acquisition of Encysive is an example of that effort," added Martin Mackay, Ph.D., president of Pfizer Global Research and Development. "With this agreement, we will gain an important marketed product in PAH and will have the opportunity to complete the development of this new medicine to treat this devastating disease." PAH is a progressive, incurable disease that is estimated to affect 100,000 to 200,000 people in North America and Europe, including about 55,000 persons in the United States. It may be of unknown cause (idiopathic) or secondary to other disorders such as connective tissue disease. Though relatively rare, the disease affects men and women of all races and ages, but is more common among women aged 20 through 40. The disease may be misdiagnosed as asthma, anemia or chronic obstructive pulmonary disease. PAH is characterized by high blood pressure and structural changes in the walls of the pulmonary arteries, the blood vessels that connect the right side of the heart to the lungs. In PAH, the pulmonary arteries become thickened and constricted, forcing the heart to work harder to pump blood through the lungs. Over time, the heart is unable to keep up, and blood flow and oxygenation become inadequate to meet the body's demands. This can lead to breathlessness, fatigue, dizziness, fainting, edema, chest pain and the development of heart failure. THELIN works by blocking the action of endothelin-1, a potent mediator of blood vessel constriction. THELIN acts to dilate the constricted blood vessels, thereby reducing pulmonary arterial pressure and thus the demands on the right side of the heart improving exercise tolerance. The transaction is expected to close in the second quarter of 2008, subject to customary closing conditions, including approval under the Hart-Scott-Rodino Antitrust Improvements Act of 1976 and the acquisition by Pfizer of a majority of Encysive's shares in the tender offer. Lazard Freres and Co., LLC, and Weil, Gotshal & Manges LLP advised Pfizer on this transaction. Morgan Stanley and Covington & Burling LLP advised Encysive. More information on both companies, THELIN and PAH is available at and .
  9. [verwijderd] 20 februari 2008 15:21
    quote:

    Dirk R. Wijnen schreef:

    Pfizer to Acquire Encysive Pharmaceuticals
    Last update: 2/20/2008 9:14:01 AM
    Acquisition Will Extend Presence in Pulmonary Arterial Hypertension with Product Launched in Several EU Countries; Pfizer Plans Pivotal Trial to Support Registration in the U.S. NEW YORK & HOUSTON, Feb 20, 2008 (BUSINESS WIRE) -- Pfizer Inc today announced that it has entered into an agreement to acquire Encysive Pharmaceuticals Inc. (ENCY), a publicly held biopharmaceutical company whose product for the treatment of pulmonary arterial hypertension (PAH) is commercially available in much of the European Union and is approved in other markets. Under the terms of the agreement, Pfizer will make a cash tender offer for all issued and outstanding shares of Encysive for $2.35 per share, representing an equity value of approximately $195 million. Following completion of the tender offer, a subsidiary of Pfizer will merge with Encysive, with the outstanding Encysive shares not tendered pursuant to the tender offer converted into the right to receive the per share price paid under the offer. Upon Pfizer's acquisition of Encysive, Pfizer will assume Encysive's change of control repurchase obligations under its 2.5% convertible senior notes. The Board of Directors of Encysive has unanimously approved the merger agreement and unanimously recommends that Encysive stockholders accept the tender offer and tender their shares. Pfizer will acquire the rights to THELIN(R) (sitaxsentan sodium), an oral, once-daily endothelin A receptor antagonist (ETRA) for the treatment of PAH, as well as Encysive's other pipeline candidates. THELIN has been approved for marketing in the European Union (EU), and is currently available in many EU states, including the United Kingdom, Germany, Ireland, Spain, France, Italy, Belgium, Luxembourg and the Netherlands. THELIN has also been approved in Australia and Canada. In the United States, THELIN has been the subject of three approvable letters from the U.S. Food and Drug Administration (FDA). Pfizer plans to conduct a pivotal Phase III trial to support registration in the U.S. "The process initiated in July of 2007 to review Encysive's strategic alternatives led us to consider a range of opportunities for increasing shareholder value," commented George W. Cole, president and chief executive officer of Encysive. "After a thorough analysis, Encysive's Board of Directors concluded that this cash transaction with Pfizer represents the best option for our shareholders now. Pfizer has come with a superior offer and with an in-depth understanding of pulmonary arterial hypertension, our primary therapeutic focus. We look forward to working with representatives of Pfizer in finalizing this transaction, and in transitioning our U.S. and EU operations." "The acquisition of Encysive will add growing, near-term revenue from the European market and increase our already strong presence in the cardio-respiratory arena with a product that complements REVATIO(TM), a PAH treatment that was discovered and developed by Pfizer researchers," said Ian Read, president of Pfizer's Worldwide Pharmaceutical Operations. "We look forward to applying Pfizer's significant resources to the launch of THELIN in additional countries." "Our commitment to pursue compelling science taking place outside of our laboratories is ongoing, and the acquisition of Encysive is an example of that effort," added Martin Mackay, Ph.D., president of Pfizer Global Research and Development. "With this agreement, we will gain an important marketed product in PAH and will have the opportunity to complete the development of this new medicine to treat this devastating disease." PAH is a progressive, incurable disease that is estimated to affect 100,000 to 200,000 people in North America and Europe, including about 55,000 persons in the United States. It may be of unknown cause (idiopathic) or secondary to other disorders such as connective tissue disease. Though relatively rare, the disease affects men and women of all races and ages, but is more common among women aged 20 through 40. The disease may be misdiagnosed as asthma, anemia or chronic obstructive pulmonary disease. PAH is characterized by high blood pressure and structural changes in the walls of the pulmonary arteries, the blood vessels that connect the right side of the heart to the lungs. In PAH, the pulmonary arteries become thickened and constricted, forcing the heart to work harder to pump blood through the lungs. Over time, the heart is unable to keep up, and blood flow and oxygenation become inadequate to meet the body's demands. This can lead to breathlessness, fatigue, dizziness, fainting, edema, chest pain and the development of heart failure. THELIN works by blocking the action of endothelin-1, a potent mediator of blood vessel constriction. THELIN acts to dilate the constricted blood vessels, thereby reducing pulmonary arterial pressure and thus the demands on the right side of the heart improving exercise tolerance. The transaction is expected to close in the second quarter of 2008, subject to customary closing conditions, including approval under the Hart-Scott-Rodino Antitrust Improvements Act of 1976 and the acquisition by Pfizer of a majority of Encysive's shares in the tender offer. Lazard Freres and Co., LLC, and Weil, Gotshal & Manges LLP advised Pfizer on this transaction. Morgan Stanley and Covington & Burling LLP advised Encysive. More information on both companies, THELIN and PAH is available at and .
    Wou gisteren nog kopen tijdens de stijging.
    Niet gedaan natuurlijk..
  10. [verwijderd] 20 februari 2008 17:57
    www.streetinsider.com/Insiders+Blog/A...

    Analyst Call of the Year: Collins Stewart on Encysive (ENCY)
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    February 20, 2008 10:49 AM EST
    Normally, Wall Street analysts get beat up in the media for their bad calls. So today we wanted to highlight an outstanding call by an analyst.

    The stock: Encysive Pharmaceuticals Inc. (Nasdaq: ENCY).
    The analyst: Andrew Fein at Collins Stewart

    Yesterday, Fein upgraded Encysive to Buy. Today, the company announced a deal to be acquired by Pfizer (NYSE: PFE) for $2.35 per share, a huge premium to yesterday's $1.08 close. If you followed Fein's advice and bought the stock yesterday before the close you would be up over 100% today. Friday's close was $0.85, so if you bought yesterday morning, after the call, you would be up even more.

    Fein was positive on Encysive's pulmonary hypertension drug THELIN in the EU and potential US approval. Pfizer saw the same thing and jumped at the chance to buy the entire company.

    Great Call!

    Some other pharmaceutical stocks Fein has Buy ratings on: Inspire Pharmaceuticals, Inc. (Nasdaq: ISPH), United Therapeutics Corp. (Nasdaq: UTHR), Array BioPharma, Inc. (Nasdaq: ARRY), GTC Biotherapeutics, Inc. (Nasdaq: GTCB), OSI Pharmaceuticals Inc. (Nasdaq: OSIP), Tercica Inc. (Nasdaq: TRCA), Metabasis Therapeutics Inc. (Nasdaq: MBRX), Cyclacel Pharmaceuticals, Inc. (Nasdaq: CYCC), Rosetta Genomics, Ltd. (Nasdaq: ROSG), Insmed Incorporated (Nasdaq: INSM), Hana Biosciences Inc. (Nasdaq: HNAB), Allos Therapeutics, Inc. (Nasdaq: ALTH), Sunesis Pharmaceuticals Inc. (Nasdaq: SNSS).

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