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biopure

97 Posts
Pagina: «« 1 2 3 4 5 | Laatste | Omlaag ↓
  1. linco 3 december 2006 22:11
    De meeste aandelen zijn rond 2000 allemaal hoog geweest.Ze betaalde hoge prijzen en er was nog totaal niets zie ook gnbt,gtcb zelfs met goedkeuring nu is vele dollars lager.Ik persoonlijk denk dat deze tijd niet meer terugkomt men overweegt en bestudeert het aandeel beter nu.
    Men steekt zijn geld niet meer blindelings in iets,alleen bepalen nu de grootte banken wanneer het stijgt of daalt helaas. Als men op het goede moment inspringt kan men mooie ritjes maken, want ze zetten het vast of omlaag als zij het willen.Ge moet maar de pech hebben en op het hoogste punt gekocht hebben,dan is het lang wachten eer we terug daar zijn.
  2. Nel 14 december 2006 16:21
    zit er nog niet in,maar kans op een mooie uitbraak naar de 1,30 is zeker aanwezig,wachten is op de uitslag vandaag,keerzijde is dat het ook kan terug zakken rond de 40 cent.70/30% .

    succes
  3. [verwijderd] 14 december 2006 19:21
    Ik heb er ook maar een paar gekocht op 0.63. Heeft natuurlijk niets met bewust en weloverwogen investeren te maken, maar alleen met goklust!
  4. [verwijderd] 14 december 2006 19:23
    quote:

    versatronics schreef:

    Ik heb er ook maar een paar gekocht op 0.63. Heeft natuurlijk niets met bewust en weloverwogen investeren te maken, maar alleen met goklust!
    hahahaha! zo denk ik er ook over! heb 10k in de portefeuille!
  5. [verwijderd] 14 december 2006 19:29
    quote:

    Eisbear schreef:

    [quote=versatronics]
    Ik heb er ook maar een paar gekocht op 0.63. Heeft natuurlijk niets met bewust en weloverwogen investeren te maken, maar alleen met goklust!
    [/quote]

    hahahaha! zo denk ik er ook over! heb 10k in de portefeuille!
    Als de uitkomst gunstig is kan je er een mooie lange-termijn investering van maken!
    Het is me alleen niet helemaal duidelijk wanneer die uitslag zal komen. Hopelijk vandaag of morgen..
  6. Nel 14 december 2006 19:38
    The panel is expected to decide later on Thursday whether the benefits of the trial would outweigh its risks

    afwachte maar
  7. Nel 14 december 2006 19:48
    dan wordt het een flinke gok als dit pas na de handel van vandaag wordt gebracht,maandag kop/munt of een start van 20%plus of 20% min

    succes
  8. [verwijderd] 15 december 2006 05:51
    Dit is de reden!

    FDA Panel Votes Against Blood-Substitute Study
    Despite Push From Navy,
    Test of Biopure's Treatment
    Fails to Win Endorsement
    By ZACHARY M. SEWARD and THOMAS M. BURTON
    December 15, 2006

    Bucking heavy pressure from the U.S. Navy, a federal advisory panel recommended against carrying out a controversial study of Biopure Corp.'s blood substitute. The treatment carries significant safety risks and often would have been administered to human trauma victims without their consent.

    The Food and Drug Administration usually follows advisory panels' advice, but it doesn't have to. The decision on testing Hemopure is vital for its developer, Biopure Corp., of Cambridge, Mass. Hemopure currently is only approved for limited human use in South Africa.

    The panel vote was 11 against, eight in favor and one abstention. Biopure's chairman and chief executive, Zafiris G. Zafirelis, declined to comment on the outcome immediately following the meeting. "I need to digest the comments," he said.

    Hemopure is controversial because it has been consistently linked to serious complications in earlier studies, documents show.

    Nevertheless, the Navy, whose medics treat wounded Marines in battle zones, contends that Hemopure may lower the death rate among severely injured trauma patients by possibly 15% from what it believes will be about a 58% death rate among patients getting standard therapy. Saline solution, the standard therapy administered in the ambulance, merely raises blood pressure, while Hemopure is an oxygen-carrying resuscitative fluid that can be carried onto the battlefield and doesn't require matching blood types, as would real human blood.

    John Mateczun, the Navy's deputy surgeon general, told the committee that 90% of military trauma fatalities occur before the soldier reaches "hospital-level care," where they could receive real human blood. "In terms of benefit, we believe that many lives might be saved in Operation Iraqi Freedom with this capability," Dr. Mateczun said, referring to Hemopure. "It would be worth our efforts if it saved only one life."

    Among those addressing the panel in Silver Spring, Md., was Sgt. Eddie Wright, who was struck by a rocket-propelled grenade outside of Fallujah, Iraq, in 2004. He said he was willing to accept "a slight risk to my health" for the benefits of Hemopure in combat. "Any risks that I've been hearing today are not applicable to my situation," Sgt. Wright said.

    Some committee members expressed skepticism that results from any trial among citizens in the U.S. could be applied to the use of Hemopure during war. They also questioned whether the potential benefits to the military in combat should be weighed in considering a stateside study.

    The FDA had sought to hold the Biopure/Navy hearing behind closed doors in July. After The Wall Street Journal wrote about the issue of the planned closed hearings, the consumer group Public Citizen brought a lawsuit and the FDA rescheduled yesterday's hearing as a public one.

    Hemopure has shown an elevated level of medical "serious adverse events" in a large study of the blood substitute in orthopedic-surgery patients, 353 of whom got Hemopure and 340 of whom received donor blood. Government documents show the Hemopure patients had 25 deaths, versus 14 in the blood group; 54 cases of heart failure and fluid overload, compared with 22 who got blood; and 14 heart attacks, against four in the donated-blood population. The same sorts of imbalances arose when Hemopure was compared with other resuscitative fluids, including saline solution, in other surgical studies.

    The FDA's reviewer on the proposed Navy/Biopure study, Laurence Landow, has consistently opposed the Navy's plans. Dr. Landow has declined to comment on the issue.

    The FDA has acted with apparent inconsistency on the blood-substitute issue, blocking the Navy study while allowing a competing trauma study by Biopure competitor Northfield Laboratories Inc. to proceed. The Northfield trial finished enrolling patients this summer. Northfield is expected to release some results this month.

    The importance of Hemopure to Biopure was underscored as the company released financial results for the year ended Oct. 31. It said that it expects its independent accountants to include a "going concern" warning in its annual report because Biopure said it has only enough money to survive through August and needs to raise additional funds even though it just completed an offering of stock and warrants that raised $16.6 million.

    For the fourth quarter, Biopure reported a net loss of $6.3 million, or 13 cents a share, narrowed from a year-earlier net loss of $8.2 million, or 34 cents a share. Revenue rose to $431,000 from $328,000. Biopure shares fell four cents to 59 cents in 4 p.m. Nasdaq Stock Market composite trading.

    Write to Thomas M. Burton at tom.burton@wsj.com

  9. Nel 15 december 2006 14:56
    eerst maar eens laten uitrazen de eerste 10/15 min dan maar eens kijken of er een leuk rittje in zit.

    succes
  10. linco 15 december 2006 16:13
    Te ver gedaald voor weg te doen, een tijdje laten laten berusten.Stond aan de verkeerde kant van de lijn helaas.
  11. Nel 15 december 2006 16:28
    wat dacht je van deze investeerder

    25 mln shares at 64 cents 14 dec 2006
  12. [verwijderd] 15 december 2006 16:47
    quote:

    papaa schreef:

    wat dacht je van deze investeerder

    25 mln shares at 64 cents 14 dec 2006
    Nou dan hoop ik dat ie dit opvangt want hij hangt nu rond de 0.43 met een low van 0.32, was idd een leuk ritje geweest..............
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