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DDSS

159 Posts
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  1. [verwijderd] 25 juni 2009 12:38
    quote:

    crackedtooth schreef:

    heb je grote positie eisbear?

    Volum exit hier lastig bij lage volumes
    Mijn positie is zeker omvangrijk. Exit/lage volume valt nog wel mee bij dit aandeel, heb voor hetere vuren gestaan. Moet zeggen dat de volumes de laatste weken flink zijn en verwacht ook dat dit zeker gaat toenemen tot 18 juli. Ik bekijk het per dag. Mocht die flink oplopen richting 18 juli dan verkoop ik in ieder geval de helft en bij goedkeuring gooi ik de andere helft gelijk bij opening beurs eruit. Ik wacht daarna tot de koers weer gaat dalen en stap in met een kleine positie (max 5k) voor de LT.

    Succes
  2. [verwijderd] 2 juli 2009 21:46
    Begint weer op gang te komen, volume inmiddels bijna 800000 stukken en stijging van bijna 12%. De uptrend is gestart, 18 juli begint te naderen.
  3. [verwijderd] 2 juli 2009 22:31
    quote:

    crackedtooth schreef:

    kleine positie

    welke upside denk je dat max haalbaar is op nieuws?
    Persoonlijk denk ik dat hij gaat vertrekken naar de 3 - 3,50 voor 18 juli. Bij goedkeuring opening boven de 5. Bij afkeuring terugval tot net onder de 1 en dan wachten op goede omzetten Tramadol, zodat de koers weer rond de 2 gaat komen.
  4. [verwijderd] 2 juli 2009 23:07
    Ik denk dat deze ook wel behoorlijk hoger gaat. Er zijn namelijk redelijk wat beleggers die de FDA kalender volgen, en DDSS is de volgende op de lijst. Ik denk dat er vandaag ook aardig geswitcht is van SPPI (helaas nog geen nieuws) naar DDSS. Ms vandaar wel de stijging wat later op de dag. Als je naar de FDA-lijst kijkt is DDSS van vanaf 1 januari behooorlijk achter gebleven t.o.v. het geweld van o.a. VNDA, ARCA, HEB, BDSI en SPPI. Ik geloof uit mn hoofd sinds 1 jan 2009 slechts +40%, dus nog genoeg ruimte naar boven vergleken met de voorgenoemde aandelen.
  5. [verwijderd] 7 juli 2009 17:37
    quote:
    Dank voor rapport! INSM ingeruild voor dit fonds (oa nav dit rapport)...iig tot aan de 18de in een aantrekkelijke stijgende lijn. Na de 18de bij goed bericht, is de sky de limit!
    online.wsj.com/article/BT-CO-20090706...

    Geluk, F.
  6. [verwijderd] 7 juli 2009 21:29
    Hallo,

    waar kopen jullie je aandelen over het algemeen ?
    Zoals deze DDSS ?

    Ik koop via de tradebox (ABN) en surprise surprise, nog niet verhandelbaar via de tradebox.

    Ik heb 'm 6x staan hier: de Nas, de TSE, Berlijn, Munchen, Frankfurt en Xetra.

    Welke is het beste?

    Groet,
    Martin
  7. [verwijderd] 7 juli 2009 22:16
    quote:

    marnop schreef:

    Hallo,

    waar kopen jullie je aandelen over het algemeen ?
    Zoals deze DDSS ?

    Ik koop via de tradebox (ABN) en surprise surprise, nog niet verhandelbaar via de tradebox.

    Ik heb 'm 6x staan hier: de Nas, de TSE, Berlijn, Munchen, Frankfurt en Xetra.

    Welke is het beste?

    Groet,
    Martin
    Binck is mijn beleggingsbank en ik koop via Binck DDSS aandelen op de US Nasdaq
  8. [verwijderd] 7 juli 2009 22:24
    TORONTO (DOW JONES)--Labopharm Inc. (DDSS) has made a great deal of progress in partnership talks for its Trazodone drug, but it sees no reason at this point to sign a deal until a U.S. regulatory decision is made, its top executive said.

    In an interview with Dow Jones, James Howard-Tripp said that, with only two weeks to go until the U.S. Food and Drug Administration makes a decision, there would be "no logic" in finalizing a marketing pact now.

    The FDA is expected to make a decision by July 18.

    "With most groups, once you get to within a couple of weeks of the (FDA's deadline) date, (they're) probably a little reluctant to sign," he said, adding that Labopharm would also prefer to wait.

    Assuming a positive decision, Labopharm would want to complete the partnership "fairly rapidly" after approval, with the aim of launching the drug "very early" in 2010, he said.

    Trazodone has many generics available, but Labopharm's version is taken only once daily and can help patients sleep better.

    Labopharm's stock has been on a tear, up 28% in July alone, mainly on anticipation of a regulatory decision on Trazodone and/or a partnership.

    Canaccord Adams analyst Neil Maruoka said in a note Monday that he believes Trazodone has a "better-than-average" approval chance.

    "A positive decision would likely result in a pop in the stock and point to a potential partnership for the drug in the near-term," he wrote. He rates the stock a buy.

    On Nasdaq Monday, Labopharm is up 7 cents to $2.53 on 980,000 shares.

    Company Web Site: www.labopharm.com
    Lucky=never making the same mistake twice
  9. ludwig mack 8 juli 2009 22:09
    frederik, je had wel ff een post bij insm kunnen doen, dat je daar weg bent;
    maar ieder voor zich natuurlijk, maar geeft wel los/vast idee hier om erg vrijblijvend te posten, terwijl we juist ook willen leren;
    vraag: dit bedrijf met produkten is interessant, maar dan voor mij eerder l.t. dan winst meteen na goedkeuring, die wellicht tegenvalt en misschien maar heel kort is;
    akzo had zijn kaskraker, en dit zou er ook een kunnen zijn nl.
    dus wellicht moet ik wachten en goedkeuring afwachten, want heb al genoeg mijn neus gestoten bij afwijzingen ........

    graag jullie reaktie.

    gr
  10. [verwijderd] 16 juli 2009 06:00
    quote:

    ludwig mack schreef:

    frederik, je had wel ff een post bij insm kunnen doen, dat je daar weg bent;
    maar ieder voor zich natuurlijk, maar geeft wel los/vast idee hier om erg vrijblijvend te posten, terwijl we juist ook willen leren;
    vraag: dit bedrijf met produkten is interessant, maar dan voor mij eerder l.t. dan winst meteen na goedkeuring, die wellicht tegenvalt en misschien maar heel kort is;
    akzo had zijn kaskraker, en dit zou er ook een kunnen zijn nl.
    dus wellicht moet ik wachten en goedkeuring afwachten, want heb al genoeg mijn neus gestoten bij afwijzingen ........

    graag jullie reaktie.

    gr
    Onderstaand een duidelijk beeld hoe Labopharm momenteel in elkaar steekt. Wachten is op het grote nieuws.

    Labopharm Inc. - In High Spirits
    Mon. July 06, 2009; Posted: 03:54 AM
    Are you looking to increase your ETF knowledge?
    (RTTNews) - A little less than two weeks now remain for the FDA to announce its decision on Labopharm Inc.'s (DDSS | Quote | Chart | News | PowerRating) (DDS.TO) investigational depression drug DDS-04A, a novel once-daily formulation of trazodone. The FDA is scheduled to decide on the drug on July 18. In the face of a looming regulatory decision, shares of Labopharm hit a new 52-week high of $2.48 on July 2 on the Nasdaq.

    The Canadian biotech company filed its New Drug Application, or NDA, for DDS-04A last September under Section 505(B | Quote | Chart | News | PowerRating)(2 | Quote | Chart | News | PowerRating) of the Federal Food, Drug and Cosmetic Act. This section typically applies to reformulations of drugs that are already approved and being marketed, allowing the company to refer to existing efficacy and safety data on trazodone.

    Labopharm's NDA was based on data from five pivotal pharmacokinetic studies and the positive results from its North American phase III placebo controlled clinical trial, which enrolled over 400 patients.

    DDS-04A is the rapid-onset formulation of Trazodone that was approved by the FDA in 1982 for the treatment of depression in adults. Trazodone was sold under the brand name Desyrel by Bristol-Myers Squibb Co. (BMY | Quote | Chart | News | PowerRating). Following the expiry of the drug's patent, generic version of Trazodone became available and the brand-name version is no longer being manufactured.

    According to Labopharm, in the phase III study dubbed 04ACL3-001, the primary endpoint achieved statistical significance providing an improvement from baseline to the end of the study as measured by the Hamilton Rating Scale for Depression (HAMD-17).

    Patients treated with DDS-04A experienced rapid onset of action as demonstrated by a clinically significant improvement in HAMD scores within the first two weeks of treatment. In addition, the study demonstrated an improvement in the overall quality of sleep and a favorable adverse event profile, including transient mild to moderate somnolence, no difference from placebo in anxiety, agitation, sexual dysfunction and weight change.

    Major depression is one of the most prevalent central nervous disorders, affecting more than 120 million people worldwide. The antidepressants that are currently used are plagued by certain limitations like delayed onset of therapeutic response, insomnia or sleep disturbance, sexual dysfunction and anxiety to name a few. According to the World Health Organization, 40% of patients treated with current antidepressants discontinue treatment within the first 12 weeks due to limitations with existing products and their unwanted side effects.

    Labopharm believes that the profile of DDS-04A, which is at the altar awaiting the FDA decision, addresses the limitations of the existing antidepressants. What's more, the company also hopes to capture a significant share of the global anti-depressant market.

    According to market research firm, IMS Health, global sales of antidepressants total about $21 billion a year. In the U.S. antidepressants racked up sales of $12 billion in 2007, the last year for which data are available, according to IMS Health.

    Labopharm began the year 2009 on a high note. On December 31, 2008 Ryzolt, a once-daily formulation of the analgesic tramadol, was approved by the FDA for the management of moderate to moderately severe chronic pain in adults.

    The approval of Ryzolt is the first U.S. FDA approval that Labopharm has obtained for a drug using its patented Contramid controlled-release technology for oral administration of solid dosage medications. The drug was launched in the U.S. as recently as May by Labopharm's U.S. marketing partner, Purdue Pharma.

    Labopharm's once-daily tramadol product is already marketed in Europe, Canada, South Korea, Australia, and a number of countries. The company markets its product primarily through licensing and distribution arrangements with local pharmaceutical companies.

    The company has completed phase III trials evaluating an investigational drug, which is a twice-daily formulation that combines the analgesics tramadol and acetaminophen. According to the company, the results of the trial are insufficient to support the acceptance of a New Drug Application by the FDA in the United States. However, the company believes that the trial results may be accepted for the evaluation of analgesics in Europe, Canada and other jurisdictions.

    Labopharm is also developing a series of abuse deterrent products based on its proprietary Contramid-based technology platform. Having completed proof-of-principle studies for an abuse-deterrent formulation of a widely prescribed combination pain product, the company is preparing to advance the product to clinical studies.

    The company made its trading debut on the Nasdaq on April 28 2006, with its IPO priced at $8 per share. However, the company's shares have been trading on the Toronto Stock Exchange since 1996.

    The company was founded in 1990 and was formerly known as Centre de recherche appliquee pharmaceutique CRAP inc. The name was changed to Labopharm Inc. in September 1994.

    Labopharm has incurred substantial operating losses since its inception and as of March 31, 2009, had an accumulated deficit of C$255 million. For the first-quarter ended March 31, 2009, net loss narrowed to C$8.0 million or C$0.14 per share from C$9.7 million or C$0.17 per share in the year-ago quarter, thanks to higher revenues and lower research and development expenses.

    The company generates revenue from product sales, research and development collaborations, and licensing arrangements.

    Quarterly revenue increased to C$5.0 million from C$3.2 million in the comparable year-ago quarter as sales of the company's once-daily tramadol product rose an impressive 76%. The once-daily tramadol product logged in sales of C$3.8 million in the first-quarter of 2009, up from C$2.2 million in the first-quarter of 2008. Licensing revenue for the recent first-quarter totaled C$1.2 million compared to C$1.1 million in the same period a year before.

    Now that, the company's once-daily tramadol has been launched in the U.S. too, its sales can be expected to grow appreciably, which may ultimately improve its bottom-line results. In addition, the looming FDA decision on depression drug DDS-04A, if positive, is a near term catalyst that could drive Labopharm's share price higher and traders and investors are placing their bets. Will DDS-04A reach the finish line? ...Stay tuned.

    For comments and feedback: con
  11. [verwijderd] 17 juli 2009 20:13
    quote:

    Eisbear schreef:

    Wordt flink aan de boom geschud!
    Ben er ingestapt aan 2.15 USD

    Wel verwarrend dat koers in USD wordt weergegeven, maar order in CAD

    Verschoot wel toen ik zag dat order uitgevoerd was aan 2.4 CAD, had hem op dagprijs gezet omdat order niet wou doorgaan. Nogal logisch natuurlijk
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