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  1. orchid 3 maart 2007 09:32
    DE nieuwe ontwikkelingen zijn op het gebied van gemodificeerde planten en zelfs van schimmels, techniek eigenlijk hetzelfde als met GTCB maar dan met planten en schimmels.( technisch natuurlijk een dag en nacht verschil)

    Voor grote bedrijven is dit minder bedreigend dan met dieren, alleen...die technieken staan nog zeker 6 tot 8 jaar tot achter tot er werkelijk een productie gemaakt kan worden.

    Er zal in de markt plaats zijn voor GTCB achtige oplossingen en in een later stadium natuurlijk ook voor productie via planten en schimmels.

    Denk dat de US politiek en het extreem behoudende geld wereldje een grotere rol speelt.
    Zodra de eerste grote contracten binnen zijn en er is acceptatie dan gaat het aandeel vliegen.

    Alles een kwestie van tijd. en das niet makkelijk..
  2. [verwijderd] 3 maart 2007 10:08
    vergeet vooral niet huidige goedgekeurde indicatie=relatief kleine markt

    en met beursklimaat willen beleggers vooral in blockbusters investeren

    maar gtcb nu n100mln market cap
    als je naar een 500-1bln market cap gaan
    dan ben ik al tevreden

    downwaards risico klein, cash tot eind 2008
    EN als pharma deal inderdaad wat geld opbrengt als is maar 10-20mln, daar kan gtcb gezien hun cashburn een aardige tijd op teren

    dus iedere cashflow goed nu.. enige nadeel gtcb is evt te weinig revenue waardoor ze eind 2007/begin 2008 weer geld willen hebben (ze houden totnutoe 1 jaar cash in reserve)
    dus alle revenue nu is extreem positief voor de toekomstige waarde

    en ze hebben nog geen blockbuster... maaarrrr daarom de LFB deal zo belangrijk..dat is nml wel een potentiele 2 miljard markt
  3. $rob$ 3 maart 2007 10:28
    Als ik me niet vergis zit er ook nog geld van LEO aan te komen bij verkoop van ATryn? Was er niet toen een deal van 73 miljoen dollar uitgesmeerd over een aantal jaren....?
  4. [verwijderd] 3 maart 2007 11:36

    GTC BIOTHERAPEUTICS ENTERS INTO PROCESS DEVELOPMENT AND CLINICAL SUPPLY MANUFACTURING SERVICES AGREEMENT WITH PHARMATHENE FOR PROTEXIA®


    FRAMINGHAM, MA and ANNAPOLIS, MD – March 2, 2007 -- GTC Biotherapeutics, Inc. ("GTC", Nasdaq: GTCB) and PharmAthene, Inc. have entered into an agreement under which GTC will provide process development and clinical supply manufacturing services for PharmAthene’s Protexia®program. Protexia® is a recombinant form of human butyrylcholinesterase (rBChE) produced in the milk of transgenic goats, which is being developed by PharmAthene as a pre- and post-exposure therapy for military or civilian victims of a chemical nerve agent attack.



    “We are pleased to expand our relationship with PharmAthene to provide the processing and analytical expertise for the development of Protexia®,” stated Geoffrey F. Cox, Ph.D., GTC’s Chairman and Chief Executive Officer. “rBChE is a prime example of a protein that is difficult to express in other production systems and is well suited to the transgenic technology platform.”



    “GTC is an industry leader in transgenic protein technology and we look forward to working with them to ensure that the manufacturing of Protexia® is developed in accordance with all the appropriate regulatory requirements,” stated David P. Wright, President and Chief Executive Officer of PharmAthene.



    While the utility of human plasma derived butyrylcholinesterase (hBChE) to protect against nerve agent toxicity is well documented, a major limitation hindering its commercial development has been the inability to produce commercial quantities of hBChE due to a limited availability of appropriate blood supplies, low levels of the protein in plasma, and low production yields using traditional biotechnology methods. PharmAthene’s recombinant hBChE overcomes these limitations by enabling substantially larger production yields than are possible using other expression systems or through purification of the native protein from human plasma. Transgenic production and manufacturing is estimated to be capable of supplying sufficient rBChE to make Protexia® available for use by the military and civilian populations.



    About Nerve Agents

    Organophosphate nerve agents, or anti-cholinesterase agents, cause toxicity by binding to and inhibiting acetylcholinesterase, an enzyme in the body that is essential for nervous system function. This leads to increases in acetylcholine and “cholinergic crisis” that can cause loss of muscle control, respiratory failure, paralysis, convulsions, permanent brain damage and eventually death.



    These so-called nerve gases, which are actually all liquids at room temperature, are lethal in low quantities when inhaled or absorbed through the skin. Nerve agents can be classified as either G-agents (sarin, soman, tabun) or V agents (VX), both of which are exceedingly volatile and toxic.



    About Protexia: Recombinant Human Butyrylcholinesterase

    Protexia® is a form of recombinant human butyrylcholinesterase (rBChE), a potent

    organophosphate (OP) scavenger protein produced in the milk of transgenic goats, which is being developed for use as a prophylactic and therapeutic against acute organophosphate (OP) nerve agent toxicity. In September 2006 PharmAthene was awarded amulti-year contract valued at up to $213 million from the Department of Defense (DoD) U.S. Army Space and Missile Command, for advanced development of Protexia®.



    About PharmAthene, Inc.

    PharmAthene, a privately-held biotechnology company, was formed to meet the critical needs of the United States by developing biodefense products. PharmAthene is dedicated to the rapid development of important and novel biotherapeutics to address biological pathogens and chemicals that may be used as weapons of bioterror. PharmAthene’s lead programs include

    Valortim™, a treatment for anthrax, and Protexia®, a treatment for nerve agent exposure.

    For more information on PharmAthene, please visit www.PharmAthene.com.



    About GTC Biotherapeutics, Inc.

    GTC Biotherapeutics develops, produces, and commercializes therapeutic proteins through transgenic animal technology. In August 2006, ATryn®, GTC’s recombinant form of human antithrombin, was approved by the European Commission for use in patients with hereditary antithrombin deficiency undergoing surgical procedures. This was the first approval anywhere in the world of a therapeutic protein produced from a transgenic animal.



    GTC has also recently been granted a patent in the United States through 2021 for the production of any therapeutic protein in the milk of any transgenic mammal. GTC’s transgenic production

    platform is particularly well suited to enabling cost effective development of proteins that are difficult to express in traditional recombinant production systems as well as those that are required in large volumes. Additional information is available on the GTC web site, www.gtc-bio.com.



    This press release contains forward-looking statements as defined in the Private Securities Litigation Reform Act of 1995, including without limitation statements regarding the development of downstream processing and transgenic production capacity for Protexia®, PharmAthene’s plans for developing Protexia® for military and civilian markets, and plans for meeting the anticipated preclinical and clinical requirements for approval. Such forward-looking statements are subject to a number of risks, uncertainties and other factors that could cause actual results to differ materially from future results expressed or implied by such statements. Factors that may cause such differences include, but are not limited to, the risks and uncertainties discussed in GTC's most recent Annual Report on Form 10-K and its other periodic reports filed with the Securities and Exchange Commission, including the risks and uncertainties associated with the development of therapeutic proteins and dependence upon the actions of partners and regulatory and other governmental agencies. GTC cautions investors not to place undue reliance on the forward-looking statements contained in this release. These statements speak only as of the date of this document, and GTC undertakes no obligation to update or revise the statements, except as may be required by law.



    CONTACT:
    GTC Biotherapeutics, Inc.
    Thomas E. Newberry
    Vice President, Corporate Communications
  5. [verwijderd] 3 maart 2007 11:58
    Als de heren beleggers doordenken dan weten ze dat GTCB zo sterk in zijn patenten zit dat elke biotransgene bedrijf er niet omheen kan en dat zijn de klanten die het geld binnen brengen.
    Dus vele kleintjes maken een grote hoop
    En van die grote hoop daar zijn wij aandeelhouders van.
    als je alleen kijk naar de mogelijkheden van M.093
    Die ontwikkeld word voor een zeer grote markt potentie dan kan je wel degelijk praten van een blockbuster.


    quote:

    crackedtooth schreef:

    vergeet vooral niet huidige goedgekeurde indicatie=relatief kleine markt

    en met beursklimaat willen beleggers vooral in blockbusters investeren

    maar gtcb nu n100mln market cap
    als je naar een 500-1bln market cap gaan
    dan ben ik al tevreden

    downwaards risico klein, cash tot eind 2008
    EN als pharma deal inderdaad wat geld opbrengt als is maar 10-20mln, daar kan gtcb gezien hun cashburn een aardige tijd op teren

    dus iedere cashflow goed nu.. enige nadeel gtcb is evt te weinig revenue waardoor ze eind 2007/begin 2008 weer geld willen hebben (ze houden totnutoe 1 jaar cash in reserve)
    dus alle revenue nu is extreem positief voor de toekomstige waarde

    en ze hebben nog geen blockbuster... maaarrrr daarom de LFB deal zo belangrijk..dat is nml wel een potentiele 2 miljard markt

  6. [verwijderd] 3 maart 2007 13:24
    PharmAthene, Inc. was formed in March 2001 with a mission to become the premier company worldwide specializing in the development of medical countermeasures to prevent and treat morbidity and mortality associated with the use of biological and chemical weapons.
    www.pharmathene.com/contact_us.html

    Alleen nu nog de vraag, WELKE is hier de impact naar GTCb toe ???

  7. [verwijderd] 3 maart 2007 13:24
    quote:

    rschilders schreef:

    Als ik me niet vergis zit er ook nog geld van LEO aan te komen bij verkoop van ATryn? Was er niet toen een deal van 73 miljoen dollar uitgesmeerd over een aantal jaren....?
    [/quote]
    GTCB – Economics of the Leo partnership (updated):

    1. The milestone payments from Leo are as follows:

    $5M already received for EMEA approval in HD indication
    $38M for clinical/regulatory milestones in the DIC/sepsis indication
    $30M for sales-based milestones
    -------
    $73M Total

    2. The combined royalty and manufacturing transfer payment payable by Leo to GTC on commercial sales of ATryn is in the mid-to-high teens as a percentage of end-user sales, and this figure is net of GTC’s production costs. If we assume to be conservative that a 2.5% royalty is payable by GTC to third parties for IP licenses (the size of these payments has not been disclosed), then the net (pre-tax) income to GTC comes out to about 15% of Leo’s end-user sales.

    3. For ATryn used by Leo in clinical trials, Leo will reimburse GTC for its cost of production up to an undisclosed cap. (Unlike commercial sales, there is no built-in profit margin for GTC on Leo’s use of ATryn for clinical trials.)

    4. Leo will fund 100% of the phase-2 development in the DIC indication. When this program enters phase-3, GTC will have the option—but not the obligation—to fund half of the clinical-trial expenses. If GTC exercises this option, it will have access to all of Leo’s phase-3 data for use in the U.S. and Japan—territories not covered by the Leo partnership; if GTC declines to exercise the option, it will have access to only the phase-2 data. (GTC’s decision to exercise or not exercise this option will presumably depend on how important the European data will be to the FDA and the Japanese regulators.)

    [quote=The Wishbone]
    als je alleen kijk naar de mogelijkheden van M.093
    Die ontwikkeld word voor een zeer grote markt potentie dan kan je wel degelijk praten van een blockbuster.
    [/quote]
    Hier moet ik wish bijtreden.
    Als we daar eens het potentiële van gaan bekijken:
    www.merrimackpharma.com/pipeline/inde...
    MM-093 RA en Psoriasis met naar alle waarschijnlijkheid phase III
    dan nog Uveitis en MS

    En schrijf het maar al op,
    MM-101 / MM-111 / MM-121 van development naar Phase I

    Postief is alvast, dat het lijstje steeds langer aan het worden is:
    LEO / Merrimack Pharma / LFB / PharmAthene, Inc. / ....
    Nu nog eens een héle, héle grote die de GTCb-burelen binenstapt,
    en droogweg zegt, met jullie wil ik verder in zee !

    Botste op I-hub ook nog op deze:
    EU sales projections for ATryn in HD:

    >While Dr. Cox couldn't yet provide sales/revenue estimates for Atryn in the recent conf call, I was wondering if you guys have any ballpark guestimates?<

    $25M during the first twelve months after the establishment of reimbursement in the major EU countries is a reasonable projection.

    Dit zou toch een omzet van 0.25 $ per aandeel betekenen

    [quote=ramon72]
    Dat is lekker thuiskomen,moet het nog doorlezen.Maar zo naar de reacties kijkend is het dus positief.
    Amai, nu nog maar thuis van een avondje stappen.
    -):O
  8. [verwijderd] 3 maart 2007 13:33
    Japan hoeveel brengt dit op?
    Azie en Australië misschien ook China India Irak Iran enz
    Goudmijntje atryne of doel ik nu op een olie aanboring
    Ik vind het best, dromen mag toch wel!
    Als dit in de koers verwerkt is dan is de aandeel waarde?
    Huh ik schrik wakker en wat zie ik
    0,76 euro centjes is de koers koerswaarde

    Ik denk dat alles zijn tijd nodig heeft.

    quote:

    rschilders schreef:

    Als ik me niet vergis zit er ook nog geld van LEO aan te komen bij verkoop van ATryn? Was er niet toen een deal van 73 miljoen dollar uitgesmeerd over een aantal jaren....?
  9. [verwijderd] 3 maart 2007 13:43
    ramon72 schreef:

    Dat is lekker thuiskomen,moet het nog doorlezen.Maar zo naar de reacties kijkend is het dus positief.

    Amai, nu nog maar thuis van een avondje stappen.
    -):O

    Hehe tja sluitingstijden kennen we hier niet.Het begint pas enigszins gezellig te worden zo rond de klok van drieen,dan weet jij genoeg.

  10. [verwijderd] 3 maart 2007 13:48
    quote:

    SkySpam1 schreef:

    Botste op I-hub ook nog op deze:
    EU sales projections for ATryn in HD:

    >While Dr. Cox couldn't yet provide sales/revenue estimates for Atryn in the recent conf call, I was wondering if you guys have any ballpark guestimates?<

    $25M during the first twelve months after the establishment of reimbursement in the major EU countries is a reasonable projection.

    Dit zou toch een omzet van 0.25 $ per aandeel betekenen

    Plus daarbij de cashpositie en wat omzet hier en daar...nou, dan is de k/w verhouding nu wel heel errug laag.
  11. [verwijderd] 3 maart 2007 14:27
    Dew schreef op 26.10.2006:
    GTC will receive royalties is this product ever goes anywhere.

    Posted by: DewDiligence
    Date:10/18/2006 4:03:00 PM

    PharmAthene Awarded $1.7 Million NIH Grant for Protexia

    [GTC will receive royalties is this product ever goes anywhere.]

    biz.yahoo.com/prnews/061018/dcw010.ht...

    >>
    Wednesday October 18, 9:00 am ET

    Funding Supports Evaluation of Protexia for Use as a Therapeutic Medical Countermeasure Against Nerve Agent Toxicity

    ANNAPOLIS, Md., Oct. 18 /PRNewswire/ -- PharmAthene, Inc., a leading biodefense company specializing in the development and commercialization of medical countermeasures against chemical and biological terrorism, announced today that it has been awarded a grant from the National Institutes of Health (NIH) Countermeasures Against Chemical Threats (CounterACT) Research Network totaling approximately $1.7 million to support continued development of the Company's broad spectrum chemical nerve agent therapy, Protexia®.

    Protexia is a recombinant form of human butyrylcholinesterase (BChE), a naturally occurring protein found in minute quantities in blood. BChE functions as a natural bioscavenger, like a sponge, to absorb toxins such as organophosphorous (OP), nerve agents (sarin, soman, tabun, VX) and certain pesticides, before they can cause irreversible neurological damage and death. Protexia is being developed by PharmAthene as a pre and post-exposure therapy for military and civilian victims of a chemical nerve agent attack.

    "Based on an impressive collection of preclinical animal efficacy data, which demonstrate that Protexia provides enhanced survival after exposure to nerve agents without neurological impairment, we believe it has excellent potential to become the superior choice for military and civilian protection against nerve agent toxicity," commented David P. Wright, President and Chief Executive Officer of PharmAthene. "The funding announced today from the NIH, in addition to a recently announced contract from the Department of Defense, which provides up to $213 million in funding for advanced development of Protexia across multiple indications, offers important validation for Protexia and our Company's biodefense capabilities. We look forward to rapidly advancing the development of Protexia to meet the urgent biosecurity needs of our Nation and Allies."

    Preclinical research conducted by PharmAthene's development partners, the US Army Medical Research Institute of Chemical Defence (USAMRICD) and DRDC Suffield, Defence Research and Development Canada, have demonstrated the capability of Protexia to protect laboratory animals from the toxic effects of chemical nerve agents.

    In these studies, pre-treatment with rBChE provided 100% survival against the nerve agents VX and soman. In post-exposure therapeutic studies, administration of rBChE following nerve agent exposure resulted in enhanced survival compared to control animals. Results from several of these studies were recently reported by USAMRICD and DRDC at the 2006 Bioscience Review meeting.

    While the utility of BChE to protect against nerve agent exposure is well documented, a major limitation in its development has been the inability to produce it in commercial volumes due to limited raw material availability, low levels of the enzyme in blood, and low production yields using traditional biotechnology methods. To overcome these limitations, PharmAthene has developed a recombinant form of human BChE, (rBChE), utilizing transgenic expression in goats which enables substantially higher production yields. PharmAthene believes that its transgenic technology will have the capacity to produce sufficient rBChE for both military and civilian defence.

    The goal of the CounterACT program is to develop novel therapeutic agents to treat large numbers of persons exposed to nerve agents as a result of a mass civilian terrorist attack. Funding provided to PharmAthene under the grant will be used to conduct additional preclinical studies to evaluate the efficacy of Protexia as a post-exposure therapy for lethal exposure to nerve agents.

    About Protexia®: Recombinant Human Butyrylcholinesterase (rBChE)

    Protexia is a form of recombinant human butyrylcholinesterase (rBChE), a potent organophosphorus (OP) scavenger protein produced in the milk of transgenic goats, which is being developed for use as a prophylactic against acute organophosphorus (OP) nerve agent toxicity.

    About Chemical Weapons

    Organophosphorus nerve agents, or anti-cholinesterase agents, were discovered in the 1930s following intensive research into new insecticides. Their discovery represents the beginning of modern chemical warfare. These agents cause toxicity by binding to and inhibiting acetylcholinesterase, an enzyme in the body that is essential for nervous system function, leading to increases in acetylcholine and "cholinergic crisis" that can cause loss of muscle control, respiratory failure, paralysis, convulsions, permanent brain damage and eventually death.

    These so-called nerve gases, which are actually all liquids at room temperature, are lethal far more quickly and in far lower concentrations than other classical chemical warfare agents such as vesicants, choking agents and blood agents, and are effective both when inhaled and when absorbed through the skin. Nerve agents can be classified as either G-agents (sarin, soman, tabun) or V-agents (VX), both of which are exceedingly toxic.

    About PharmAthene, Inc.

    PharmAthene, a privately-held biotechnology company, is dedicated to the rapid development of important and novel medical countermeasures to address biological pathogens and chemicals that may be used as weapons of bioterror. PharmAthene's lead programs include Valortim(TM), intended for the prevention and treatment of anthrax, which is being co-developed with Medarex, Inc., and Protexia®, intended to prevent and treat nerve agent toxicity. PharmAthene is located in the Chesapeake Innovation Center in Annapolis, MD, America's first business accelerator for the homeland and national security sectors. PharmAthene has been successful in obtaining U.S. Government and Venture Capital funding to finance the development of its portfolio products. For more information on PharmAthene, please visit www.PharmAthene.com.


    Nexia Biotechnologies Inc.

    Nexia Biotechnologies Inc. uit Montreal heeft een overeenkomst met het Canadese leger en met het Amerikaanse leger gesloten waaronder het bedrijf toestemming heeft om om het product Protexia™, een eiwit dat zonder bijwerkingen beschermt tegen zenuwgasgiften en andere organische fosphaten, te onderzoeken en te ontwikkelen.

    Protexia™ is Nexia´s recombinante versie van butyrylcholinesterase (BChE), dat in het menselijk bloed aanwezig is maar niet bestand is tegen aanvallen met zenuwagentia. Nexia maakt gebruik van genetisch gemanipuleerde geiten voor de massa-productie van Protexia™.
    www.investincanada.com/ng/945/Succesv...

  12. [verwijderd] 3 maart 2007 14:49
    PharmAthene, Inc.

    About us

    The development of effective countermeasures to a range of potential biological and chemical weapons is PharmAthene’s primary objective. PharmAthene has recruited exceptional scientists and management to lead its programs and oversee the outsourcing of various program activities with an urgency to develop these countermeasures as rapidly as possible. In any organization, it is the people who make it all happen and that is especially true at PharmAthene. We have a unique group of seasoned, talented pharmaceutical and biotechnology professionals—each an expert in his or her respective field. Ranging from expertise in infectious diseases and genome science across the spectrum to pharmaceutical marketing and management, the depth of knowledge and collective accomplishments of our PharmAthene team is extremely impressive.
    www.pharmathene.com/about_us.html

    Biological Defense

    Biological weapons are used to intentionally disseminate infectious agents or toxins that would otherwise appear only naturally or not at all. Such agents can be divided into bacteria, viruses, rickettsiae, fungi or toxins. These cause a wide range of diseases including anthrax, smallpox, Q fever, or generalized toxicity throughout the body. The features that influence a biologic agent’s potential for use as a weapon includes infectivity, virulence, toxicity, pathogenicity, incubation period, transmissibility, lethality and stability.

    The advent of genetic engineering has had a profound impact on the threat from biological weapons. Agents that are extremely harmful in nature can be modified to: (a) increase virulence, (b) increase the production rate per cell, (c) enhance survivability under environmental stress, and (d) improve the ability to escape detection by the host immune system. Since most agents are living organisms, their natural replication after dissemination increases the potential impact of a strike, making such bioweapons even more attractive. Any country possessing a pharmaceutical or food storage infrastructure already has an inherent stabilization and storage system for biological agents.
    www.pharmathene.com/biological_defens...

    News Releases
    www.pharmathene.com/news_releases.html

    Ter info:
    tinyurl.com/kwt6o
    Zegt niet veel, de reeële impact zal pas maandag tezien zijn !!

    Zoals ik gisteren (voor 22u00) reeds schreef,
    wanneer de nood het hoogst is, de redding nabij !!!?

  13. [verwijderd] 3 maart 2007 15:45

    Kort, maar hier zit véél waarheid in !!

    Lefty Lefty

    Its not management that has the credibility problem, its
    the investors who jump and run at every shadow.

    We live in a world of blame, but don't blame me. It goes
    like this, I bought the stock I'm brilliant, oh its
    going down, well its not me it must be someone else, after
    all I'm brilliant, its them, its management, if Cox only..

    Look Cox and the boys are not the best, but they are far
    far from the worst. They bring a new technology. They
    keep the company up 14 hard years. Its not him its
    us.

    If the MM play every game in the book if we dont
    sell what could they do. They are not bad management,
    we are bad investors.

    OKY
  14. [verwijderd] 3 maart 2007 17:28
    quote:

    jve72 schreef:

    Vergeet niet dat er maandag wel eens iets onverwachts naar buiten kan komen,mischien proberen ze er nog snel een aantal hiermee bang te maken en lekker goedkoop op te rapen voor het goede nieuws!
    Wat loop je nou allemaal weer te zeiken skyspam!,een paar postings terug dat ik alleen maar onzin post met:"zoek de verschillen jve!",ik zat dus gisteravond wel goed dacht ik zo met deze post waar je ook om moest lachen!
  15. [verwijderd] 3 maart 2007 17:40
    Nee,nu heeft mijnheer geen antwoord meer,hij was deze post van mij gisteravond voor het gemak maar even vergeten.Ik denk zelfs dat dit precies is wat er gebeurd is de laatste dagen!
  16. [verwijderd] 3 maart 2007 17:41
    jve

    Ik ben bang dat je te laat bent om te kopen.
    De koers laat nu al een winst zien.

    De uptrend is gezet

    En nu hoe verder
    Heb je al een scenario voor deze positie wat betreft de gang van zaken.

  17. [verwijderd] 3 maart 2007 17:50
    quote:

    jve72 schreef:

    [quote=jve72]
    Vergeet niet dat er maandag wel eens iets onverwachts naar buiten kan komen,mischien proberen ze er nog snel een aantal hiermee bang te maken en lekker goedkoop op te rapen voor het goede nieuws!
    [/quote]
    Wat loop je nou allemaal weer te zeiken skyspam!,een paar postings terug dat ik alleen maar onzin post met:"zoek de verschillen jve!",ik zat dus gisteravond wel goed dacht ik zo met deze post waar je ook om moest lachen!
    [/quote]

    [quote=jve72]
    Nee,nu heeft mijnheer geen antwoord meer,hij was deze post van mij gisteravond voor het gemak maar even vergeten.Ik denk zelfs dat dit precies is wat er gebeurd is de laatste dagen!
    Wat ik bedoel, dat je op dergelijke uitspraken géén pijl kunt trekken, en qua inhoud niks informatiefs bevat !!!!!
    Dus met desbetreffende citaat heb je 50 % kans,
    of het klopt, of het klopt niet !!
    Uw JA/NEE-opmerking is voor alles toepasbaar, een mooi voorbeeld hiervan is:
    "Deze avond win ik de lotto", en achteraf zal blijken of mijn stelling klopte, dus quasi inhoud en informatie: 0,0000000000000.
    Ik bedoel hier niks slecht mee, en je moet je ook niet steeds zo aangevallen voelen !! Ik stel alleen vast.
    Voor iemand van 35 kom je toch maar puberaal uit de hoek !!!

    Dit gezegd zijnde !
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Amarin Corporation 1 133
Amerikaanse aandelen 3.836 242.925
AMG 971 133.200
AMS 3 73
Amsterdam Commodities 305 6.687
AMT Holding 199 7.047
Anavex Life Sciences Corp 2 490
Antonov 22.632 153.605
Aperam 92 14.975
Apollo Alternative Assets 1 17
Apple 5 381
Arcadis 252 8.767
Arcelor Mittal 2.033 320.659
Archos 1 1
Arcona Property Fund 1 286
arGEN-X 17 10.293
Aroundtown SA 1 219
Arrowhead Research 5 9.729
Ascencio 1 26
ASIT biotech 2 697
ASMI 4.108 39.089
ASML 1.766 106.426
ASR Nederland 21 4.452
ATAI Life Sciences 1 7
Atenor Group 1 485
Athlon Group 121 176
Atrium European Real Estate 2 199
Auplata 1 55
Avantium 32 13.647
Axsome Therapeutics 1 177
Azelis Group 1 64
Azerion 7 3.392