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VVUS - Vivus

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  1. [verwijderd] 6 oktober 2008 22:09
    Vivus announces weight loss effects of Qnexa

    Oct 6 (Reuters) - Vivus Inc : * Announces the weight loss effects of Qnexa in type 2 diabetes * Says on intent-to-treat basis subjects treated with Qnexa for 28 weeks had mean weight loss of about 17 pounds or 8 percent of starting body weight

    vorige week concurrent merxk ermee gestopt ivm side effects

    positie genomen, grote markt en dit is een sterk aandeel, afgelopen jaren strak boven 100MA, goede business deals en nu dus goede resultaten
  2. [verwijderd] 7 oktober 2008 20:38
    chartwise interessant

    op weekly chart ema 62 rond 6,50
    is een steunniveau

    en een zeer sterke daaronder is de 100 MA op de weekly op 5,66

    heb rond 7 wat bijgekocht en kijk verloop even aan

    uptrend nog intact
    veel cash in huis
    emissie al achter de rug
    goede resultaten en ze gebruiken nieuwe combinate van al bestaande medicijnen
    vrij sterke institutional ownership
  3. [verwijderd] 21 oktober 2008 13:29
    VVUS' most recent profitability was/is temporary due to the sale of Evamist for $150M up front, and possibly $30M more in milestones. That money has been amortized out over several quarters. Qnexa is indeed a high prospect for the company - which is why just about anyone invested is still here. Obesity and Type 2 Diabetes are both billion dollar markets - I have no doubt they will partner this with a nice split once Phase III results are in. December will have the first of the 3 Phase III's reporting data (6 month study - Equate). The 2 year-long studies complete on/around May 2009 - data should be out late summer. If things are positive as everyone believes they will be, NDA should be submitted late Q3 or Q4 with approval approx. 10-11 months following. Qnexa Diabetes trial is to begin ASAP (according to VVUS) following a post-Phase II meeting. I would anticipate trial data from that one due out sometime during NDA review for the obesity indication based on current timelines.

    Qnexa partner talks will not begin until all obesity Phase III's are complete according to VVUS.

    At this point, the main catalysts are the release of data for each of the 3 Phase III obesity studies.

    Summary of remaining pipeline:

    Avanafil: Yawn - financing arranged, waiting on word of Phase III start. No marketing partner announced - IMO, this is best marketed as a psuedo-generic and priced less than current solutions with higher safety. Stretch: Partner with Pfizer under the Viagra 2 label as a faster and safer formulation of Viagra.

    Luramist: Phase III on hold pending partnership to fund trial. Large market potential, not sure why partnering this has taken so long.

    Phase II drug: Mentioned in a prior call, they have some Phase II drug(s) they are tinkering with but nothing more said than that yet.

    Vivus is in a great cash position with nearly $200M to see them through to Qnexa partnering and/or product launch. The only Phase III not funded at this point is Luramist.

    HTH,

    HAB
  4. [verwijderd] 4 november 2008 13:58
    MOUNTAIN VIEW, Calif.--(BUSINESS WIRE)--VIVUS, Inc. (NASDAQ: VVUS - News), a pharmaceutical company dedicated to the development and commercialization of novel therapeutic products, today announced that they will attend and present an overview of the company at the following conferences in November. Barclays Capital Small & Mid-Cap Healthcare Forum
    Barclays Capital, 745 Seventh Avenue, New York
    Presenter: Timothy Morris, CFO
    Presentation date: Thursday, November 6, 2008
    Presentation time: 3:00pm ET

    Rodman & Renshaw Annual Global Investor Conference
    The Palace Hotel, New York
    Presenter: Leland Wilson, President and CEO
    Presentation date: Tuesday November 11, 2008
    Presentation time: 12:15pm. ET

    Credit Suisse Healthcare Conference
    Arizona Biltmore, Phoenix
    Presenter: Leland Wilson, President and CEO
    Presentation date: Friday, November 14, 2008
    Presentation time: 10:30am MT

    ------------------

    met de quarterly CC vandaag nov 5th nabeurs 4.30pm
  5. [verwijderd] 12 november 2008 21:21
    Obesity ... the final frontier. These are the voyages of the drug companies. Their mission: to help patients shed the pounds, to boldly go where no company has successfully gone before.

    Unfortunately, two more drugs got assimilated by the Borg on Wednesday.

    Sanofi-Aventis (NYSE: SNY) is stopping research on Acomplia, its diet drug that was sold in Europe until it was pulled from the market two weeks ago as officials became increasingly worried about side effects -- depression, anxiety, and stress disorders. The drug never made it past the Food and Drug Administration for the same reasons.

    Farther back in the drug development process, Pfizer (NYSE: PFE) could see the writing on the walls of the FDA and scrapped its CP-945,598, which was designed to target the same cannabinoid receptors in the brain -- the ones that give the "munchies" to smokers of marijuana.

    The two companies join Merck (NYSE: MRK), which ended development of its cannabinoid receptor inhibitor, taranabant, after a lackluster phase 3 trial earlier this month. The drug didn't work too well at the low dose, and the high dose caused the same sort of side effects seen in Acomplia.

    You'd think the news that three large pharmaceutical companies were abandoning the market would help smaller companies developing anti-obesity drugs like Arena's (Nasdaq: ARNA) Lorcaserin and VIVUS' (Nasdaq: VVUS) Qnexa that don't have the same mechanism of action, but anti-obesity drugs are the final frontier for a reason. It's a major potential market, but there's also a lot of risk in developing drugs. For whatever reasons, drugs that do make it past the FDA -- like Abbott Laboratories' (NYSE: ABT) prescription drug called Meridia or GlaxoSmithKline (NYSE: GSK) over-the-counter drug alli -- either don't work all that well or have unpleasant side effects … or sometimes both.

    The anti-obesity market may be a potential supernova for a drugmaker's revenue, but for now, it remains a black hole sucking up drugs and making pipelines thinner
  6. [verwijderd] 4 december 2008 17:46
    VIVUS to Host R&D Day Event and Live Webcast December 12, 2008
    Event to Feature Update on Qnexa and Avanafil Clinical Programs

    MOUNTAIN VIEW, Calif.--(BUSINESS WIRE)--Dec. 4, 2008--VIVUS, Inc. (NASDAQ: VVUS), a pharmaceutical company dedicated to the development and commercialization of novel therapeutic products, today announced that it will host a Research and Development Day Event on Friday, December 12, 2008 at 8:00 a.m. ET in New York City, New York.

    Leland Wilson, president and chief executive officer of VIVUS, along with other members of the VIVUS management team and leading obesity, diabetes and sexual health practitioners will present a detailed update on the status of the Qnexa(TM) and avanafil clinical programs. Presentations will include:

    -- Qnexa for obesity - six-month data - a review of the results of the
    first of three phase 3 Qnexa studies, the EQUATE (OB-301) study, a
    28-week, confirmatory factorial study in obese subjects. The EQUATE
    study enrolled over 700 subjects and was designed to evaluate two dosage
    strengths of Qnexa: full-strength that contains 15mg phentermine and
    92mg topiramate controlled-release (CR) and a mid-dose that contains
    7.5mg phentermine and 46mg topiramate CR. The co-primary endpoints of
    the study are weight loss and percent of patients achieving a 5% weight
    loss over 28 weeks.
    -- Qnexa for diabetes - one-year data - a review of the results of the
    DM-230 study, a phase 2, 56-week, double-blind, placebo-controlled study
    in subjects with type 2 diabetes. The DM-230 study included 130 subjects
    that had completed the OB-202 study. The primary endpoint of the study
    is glycemic control as measured by a reduction in HbA1c.
    -- Avanafil for erectile dysfunction - an overview of the phase 3 clinical
    development plans for avanafil, an oral treatment for erectile
    dysfunction (ED). VIVUS has successfully completed the phase 2 studies
    for avanafil. VIVUS is preparing to initiate the pivotal phase 3 studies
    and will discuss the design and objectives of the phase 3 program.

    In addition to VIVUS management, presenters will include:

    -- Louis J. Aronne, M.D., FACP - Clinical Professor of Medicine at
    Weill-Cornell Medical College
    -- W. Timothy Garvey, M.D. - Professor of Medicine and Chair of the
    Department of Nutrition Sciences at the University of Alabama at
    Birmingham
    -- Andrew McCullough, M.D. - Director, Sexual Health Program; Director,
    Male Fertility and Microsurgery at NYU Langone Medical Center

    To access the webcast of this event, please visit: phx.corporate-ir.net/phoenix.zhtml?p=... or VIVUS' Investors site at www.vivus.com. Replay will also be available on demand from the website at the conclusion of the program and will run through December 31, 2008.

    If you are interested in attending or would like more information on the company, please contact Brian Korb at The Trout Group at 646 378 2923 or bkorb@troutgroup.com.

    About VIVUS

    VIVUS, Inc. is a pharmaceutical company dedicated to the development and commercialization of novel therapeutic products. The current portfolio includes investigational products addressing obesity, diabetes and sexual health. The pipeline includes: Qnexa(TM), which is in phase 3 for the treatment of obesity; Qnexa(TM), for which a phase 2 study has been completed for the treatment of type 2 diabetes; avanafil, for which a phase 2 study has been completed for the treatment of erectile dysfunction (ED) and testosterone MDTS(R), for which a phase 2 study has been completed for the treatment of Hypoactive Sexual Desire Disorder (HSDD). For more information on clinical trials and products, please visit the company's web site at www.vivus.com.
  7. [verwijderd] 28 mei 2009 15:37
    Na vijf jaar uit Vivus te zijn geweest zit ik er sterk over te denken weer eens een positie in te nemen. Zijn er nog meer mensen die nog steeds met een schuin oog naar Vivus kijken?

    Groetjes, Saffi

    finance.yahoo.com/news/Vivus-Qnexa-in...

    We view Qnexa as the leading phase III obesity candidate under development today. Vivus, Inc. (NasdaqGM: VVUS - News) has shown that Qnexa offers a synergistic benefit off added weight loss to patients beyond what can be achieved with phentermine or topiramate alone.

    Related Quotes
    Symbol Price Change
    VVUS 4.93 0.00


    {"s" : "vvus","k" : "c10,l10,p20,t10","o" : "","j" : ""} Phase III data released by the company from the EQUATE program in December 2008 demonstrated the drug to be both highly efficacious and well tolerated. Patients on the full commercial dose of Qnexa lost a placebo-adjusted 16.5 lbs, or 7.5% of their body weight, after only 28 weeks of treatment. Additionally, we are less concerned with the safety, specifically the cardiovascular or psychiatric side effects, of the drug compared to recently rejected and discontinued cannabinoid type 1 receptor molecules at several large pharmaceutical companies.

    Our trepidation at this point stems from the lack of long-term safety data -- currently being conducted -- and a lack of confidence in the FDA. That being said, if approved for obesity, Qnexa has blockbuster ($1 billion plus) potential. Vivus is also developing the drug for type 2 diabetes, an enormous problem with significant co-morbidity in the obesity population (and vice versa). Mid-stage diabetes data has been outstanding. Full approval in both obesity and type 2 diabetes, along with a strong worldwide commercialization partner to market it, makes Qnexa a multi-billion dollar drug.

    Vivus current trades with a market capitalization of only $310 million. Management exited the first quarter 2009 with $165 million in cash on hand, positive initial phase III data on a potential blockbuster multi-billion dollar drug, and two additional niche multi-hundred million dollar phase III drugs in sexual dysfunction.

    By almost all calculations, the stock looks significantly undervalued. However, the risks of clinical development are high and getting drugs past the U.S. FDA, specifically in the area of behaviorally modification such as obesity, has been difficult.

    The key wildcard events over the next few quarters include the 56-week phase III data on Qnexa from the EQUIP and CONQUER clinical trials -- expected in the third quarter 2009, and the initial phase III data on avanafil -- expected in the fourth quarter of 2009. Additionally, management is likely to start entertaining partnership discussions on Qnexa, and potentially even avanafil and Luramist, later in 2009.

    Vivus would be an extremely attractive acquisition target for a larger pharmaceutical company. Obesity is a highly coveted and wide-open market. Big pharma managements are clearly interested in obesity, as well as sexual dysfunction. The acquisition of Vivus brings in three phase III candidates -- something most big pharma companies are in desperate need of. As visibility on Qnexa and avanafil improve, we would not be surprised to see interest from potential suitors soar.

    Read the full analyst report on VVUS

  8. [verwijderd] 1 juni 2009 07:59
    quote:

    saffi2002 schreef:

    Na vijf jaar uit Vivus te zijn geweest zit ik er sterk over te denken weer eens een positie in te nemen. Zijn er nog meer mensen die nog steeds met een schuin oog naar Vivus kijken?

    Groetjes, Saffi

    finance.yahoo.com/news/Vivus-Qnexa-in...

    We view Qnexa as the leading phase III obesity candidate under development today. Vivus, Inc. (NasdaqGM: VVUS - News) has shown that Qnexa offers a synergistic benefit off added weight loss to patients beyond what can be achieved with phentermine or topiramate alone.

    Related Quotes
    Symbol Price Change
    VVUS 4.93 0.00


    {"s" : "vvus","k" : "c10,l10,p20,t10","o" : "","j" : ""} Phase III data released by the company from the EQUATE program in December 2008 demonstrated the drug to be both highly efficacious and well tolerated. Patients on the full commercial dose of Qnexa lost a placebo-adjusted 16.5 lbs, or 7.5% of their body weight, after only 28 weeks of treatment. Additionally, we are less concerned with the safety, specifically the cardiovascular or psychiatric side effects, of the drug compared to recently rejected and discontinued cannabinoid type 1 receptor molecules at several large pharmaceutical companies.

    Our trepidation at this point stems from the lack of long-term safety data -- currently being conducted -- and a lack of confidence in the FDA. That being said, if approved for obesity, Qnexa has blockbuster ($1 billion plus) potential. Vivus is also developing the drug for type 2 diabetes, an enormous problem with significant co-morbidity in the obesity population (and vice versa). Mid-stage diabetes data has been outstanding. Full approval in both obesity and type 2 diabetes, along with a strong worldwide commercialization partner to market it, makes Qnexa a multi-billion dollar drug.

    Vivus current trades with a market capitalization of only $310 million. Management exited the first quarter 2009 with $165 million in cash on hand, positive initial phase III data on a potential blockbuster multi-billion dollar drug, and two additional niche multi-hundred million dollar phase III drugs in sexual dysfunction.

    By almost all calculations, the stock looks significantly undervalued. However, the risks of clinical development are high and getting drugs past the U.S. FDA, specifically in the area of behaviorally modification such as obesity, has been difficult.

    The key wildcard events over the next few quarters include the 56-week phase III data on Qnexa from the EQUIP and CONQUER clinical trials -- expected in the third quarter 2009, and the initial phase III data on avanafil -- expected in the fourth quarter of 2009. Additionally, management is likely to start entertaining partnership discussions on Qnexa, and potentially even avanafil and Luramist, later in 2009.

    Vivus would be an extremely attractive acquisition target for a larger pharmaceutical company. Obesity is a highly coveted and wide-open market. Big pharma managements are clearly interested in obesity, as well as sexual dysfunction. The acquisition of Vivus brings in three phase III candidates -- something most big pharma companies are in desperate need of. As visibility on Qnexa and avanafil improve, we would not be surprised to see interest from potential suitors soar.

    Read the full analyst report on VVUS

    Ik heb een positie ingenomen op 4,65. Lijkt me LT een mooi aandeel, goed gepositioneerd.
  9. [verwijderd] 20 juli 2009 16:24
    quote:

    Eisbear schreef:

    Ik heb een positie ingenomen op 4,65. Lijkt me LT een mooi aandeel, goed gepositioneerd.
    Ik zit er sinds mei ook weer in.

    Vandaag de resultaten van de concurrentie, Orexigen Therapeutics Inc.: finance.yahoo.com/news/Orexigen-obesi...

    De resultaten van VIVUS worden op korte termijn verwacht. ik denk/hoop dat ze iets beter zullen zijn.

    "Orexigen said the data show Contrave is safe. The most serious side effects in the trial included a gallbladder infection and seizure, which affected two patients each. One patient reported heart palpitations, while another experienced poor circulation in the limbs and one had vertigo. The most common side effects were nausea, constipation and headache."

    Qua bijwerkingen lijkt Qnexa beter te scoren:

    "Qnexa was well-tolerated, with no drug-related serious adverse events. The most common drug-related adverse events reported over the 56 weeks for the treatment and placebo groups, respectively, were tingling, nausea, dry mouth, dizziness, insomnia and constipation. Patients were monitored for depression and suicidality using the PHQ-9 questionnaire, the FDA's preferred mental health assessment tool. Patients treated with Qnexa demonstrated greater improvements in PHQ-9 scores from baseline to the end of the study than the placebo group, providing further assurance that Qnexa treatment does not produce significant adverse mood changes or suicidality."

    De data voor Qnexa komt uit een trial met 130 type 2 diabetici. Bij Contrave waren het er 505. Nog even geduld en we weten het..

    Ik vond het ook wel vreemd dat Orexigen geen "drop-out rate" heeft opgegeven vanwege bijwerkingen. vivus noemde die wel (minder dan 10%).

    Groeten, Saffi.
  10. leo s 25 juli 2009 23:33
    Van de drie obesity fondsen is Arena (ARNA) de meest veelbelovende, ten minste als de resultaten van fase 3 in september geplubiceerd zullen worden volgens verwachting in lijn met eerdere resultaten. VIVUS en Orexigen hebbe allerlei bijkomende problemen, als het verplicht aanhouden van strenge dieeten, bijwerkingen en onduidelijke bjkomende zaken als dropout rate en gewichtsafname na landgere tijd, ook tijdstip dat product ook echt op de markt verwacht kan worden speelt nogal mee. Arna (BLA derde kwartaal, FDA approval April,) zal de eerste zijn.
    Ik gok op ARNA, (koers nu ca $4,75) dat die in september al vier a vijf keer zo hoog zal zijn, na bekendmaking resultaten phase III.
    e.e.a volgens Murphy, een subscription site, die Dendreon ook perfect voorspeld heeft
  11. [verwijderd] 9 september 2009 19:45
    quote:

    Eisbear schreef:

    [quote=saffi2002]
    Na vijf jaar uit Vivus te zijn geweest zit ik er sterk over te denken weer eens een positie in te nemen. Zijn er nog meer mensen die nog steeds met een schuin oog naar Vivus kijken?

    Groetjes, Saffi

    finance.yahoo.com/news/Vivus-Qnexa-in...

    We view Qnexa as the leading phase III obesity candidate under development today. Vivus, Inc. (NasdaqGM: VVUS - News) has shown that Qnexa offers a synergistic benefit off added weight loss to patients beyond what can be achieved with phentermine or topiramate alone.

    Related Quotes
    Symbol Price Change
    VVUS 4.93 0.00


    {"s" : "vvus","k" : "c10,l10,p20,t10","o" : "","j" : ""} Phase III data released by the company from the EQUATE program in December 2008 demonstrated the drug to be both highly efficacious and well tolerated. Patients on the full commercial dose of Qnexa lost a placebo-adjusted 16.5 lbs, or 7.5% of their body weight, after only 28 weeks of treatment. Additionally, we are less concerned with the safety, specifically the cardiovascular or psychiatric side effects, of the drug compared to recently rejected and discontinued cannabinoid type 1 receptor molecules at several large pharmaceutical companies.

    Our trepidation at this point stems from the lack of long-term safety data -- currently being conducted -- and a lack of confidence in the FDA. That being said, if approved for obesity, Qnexa has blockbuster ($1 billion plus) potential. Vivus is also developing the drug for type 2 diabetes, an enormous problem with significant co-morbidity in the obesity population (and vice versa). Mid-stage diabetes data has been outstanding. Full approval in both obesity and type 2 diabetes, along with a strong worldwide commercialization partner to market it, makes Qnexa a multi-billion dollar drug.

    Vivus current trades with a market capitalization of only $310 million. Management exited the first quarter 2009 with $165 million in cash on hand, positive initial phase III data on a potential blockbuster multi-billion dollar drug, and two additional niche multi-hundred million dollar phase III drugs in sexual dysfunction.

    By almost all calculations, the stock looks significantly undervalued. However, the risks of clinical development are high and getting drugs past the U.S. FDA, specifically in the area of behaviorally modification such as obesity, has been difficult.

    The key wildcard events over the next few quarters include the 56-week phase III data on Qnexa from the EQUIP and CONQUER clinical trials -- expected in the third quarter 2009, and the initial phase III data on avanafil -- expected in the fourth quarter of 2009. Additionally, management is likely to start entertaining partnership discussions on Qnexa, and potentially even avanafil and Luramist, later in 2009.

    Vivus would be an extremely attractive acquisition target for a larger pharmaceutical company. Obesity is a highly coveted and wide-open market. Big pharma managements are clearly interested in obesity, as well as sexual dysfunction. The acquisition of Vivus brings in three phase III candidates -- something most big pharma companies are in desperate need of. As visibility on Qnexa and avanafil improve, we would not be surprised to see interest from potential suitors soar.

    Read the full analyst report on VVUS

    [/quote]

    Ik heb een positie ingenomen op 4,65. Lijkt me LT een mooi aandeel, goed gepositioneerd.
    VVUS: + 72%....

    Ik hoop dat jij ook een fijne dag had ;)

    mvg, Saffi
  12. [verwijderd] 9 september 2009 20:41
    quote:

    saffi2002 schreef:

    [quote=Eisbear]
    [quote=saffi2002]
    Na vijf jaar uit Vivus te zijn geweest zit ik er sterk over te denken weer eens een positie in te nemen. Zijn er nog meer mensen die nog steeds met een schuin oog naar Vivus kijken?

    Groetjes, Saffi

    finance.yahoo.com/news/Vivus-Qnexa-in...

    We view Qnexa as the leading phase III obesity candidate under development today. Vivus, Inc. (NasdaqGM: VVUS - News) has shown that Qnexa offers a synergistic benefit off added weight loss to patients beyond what can be achieved with phentermine or topiramate alone.

    Related Quotes
    Symbol Price Change
    VVUS 4.93 0.00


    {"s" : "vvus","k" : "c10,l10,p20,t10","o" : "","j" : ""} Phase III data released by the company from the EQUATE program in December 2008 demonstrated the drug to be both highly efficacious and well tolerated. Patients on the full commercial dose of Qnexa lost a placebo-adjusted 16.5 lbs, or 7.5% of their body weight, after only 28 weeks of treatment. Additionally, we are less concerned with the safety, specifically the cardiovascular or psychiatric side effects, of the drug compared to recently rejected and discontinued cannabinoid type 1 receptor molecules at several large pharmaceutical companies.

    Our trepidation at this point stems from the lack of long-term safety data -- currently being conducted -- and a lack of confidence in the FDA. That being said, if approved for obesity, Qnexa has blockbuster ($1 billion plus) potential. Vivus is also developing the drug for type 2 diabetes, an enormous problem with significant co-morbidity in the obesity population (and vice versa). Mid-stage diabetes data has been outstanding. Full approval in both obesity and type 2 diabetes, along with a strong worldwide commercialization partner to market it, makes Qnexa a multi-billion dollar drug.

    Vivus current trades with a market capitalization of only $310 million. Management exited the first quarter 2009 with $165 million in cash on hand, positive initial phase III data on a potential blockbuster multi-billion dollar drug, and two additional niche multi-hundred million dollar phase III drugs in sexual dysfunction.

    By almost all calculations, the stock looks significantly undervalued. However, the risks of clinical development are high and getting drugs past the U.S. FDA, specifically in the area of behaviorally modification such as obesity, has been difficult.

    The key wildcard events over the next few quarters include the 56-week phase III data on Qnexa from the EQUIP and CONQUER clinical trials -- expected in the third quarter 2009, and the initial phase III data on avanafil -- expected in the fourth quarter of 2009. Additionally, management is likely to start entertaining partnership discussions on Qnexa, and potentially even avanafil and Luramist, later in 2009.

    Vivus would be an extremely attractive acquisition target for a larger pharmaceutical company. Obesity is a highly coveted and wide-open market. Big pharma managements are clearly interested in obesity, as well as sexual dysfunction. The acquisition of Vivus brings in three phase III candidates -- something most big pharma companies are in desperate need of. As visibility on Qnexa and avanafil improve, we would not be surprised to see interest from potential suitors soar.

    Read the full analyst report on VVUS

    [/quote]

    Ik heb een positie ingenomen op 4,65. Lijkt me LT een mooi aandeel, goed gepositioneerd.
    [/quote]

    VVUS: + 72%....

    Ik hoop dat jij ook een fijne dag had ;)

    mvg, Saffi
    Yep!! Ook gefeliciteerd! Had ze voor de LT! Heb vandaag 2/3 van mijn positie verkocht en nog meer SOMX aangeschaft alswel MERR. 1/3 hou ik. En jij?

    Grt
  13. [verwijderd] 9 september 2009 21:47
    Tja, zit te twijfelen, loopt iets op nu. Maar goede resultaten is iets heel anders dan een goedkeuring natuurlijk. Ik ga er even uit denk ik en kom weer terug voor de "runup" naar een eventuele goedkeuring.

    De weg is nog best lang....

    Misschien deze positie weer omruilen naar Pharming om daar mee te liften op wat koersbewegingen richting een (eventuele) goedkeuring. Eerst maar eens wachten hoe ze het "pinprobleem" gaan ondervangen.

    Cheers, Saffi
  14. [verwijderd] 9 januari 2012 15:31


    Vivus, Inc. (NASDAQ:VVUS) is up 18.11% in pre market trading at $12.00. VVUS has traded 22 thousand shares already this morning and trades 1.69 million shares a day on average. VVUS shares have jumped more than $0.50 over the past week. The company has a market cap of 903.04 million.

    www.prnewswire.com/news-releases/vivu...

    Pre-market: 11.50 +1.34 (+13.19%)

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Athlon Group 121 176
Atrium European Real Estate 2 199
Auplata 1 55
Avantium 29 10.650
Axsome Therapeutics 1 177
Azelis Group 1 49
Azerion 7 2.665

Macro & Bedrijfsagenda

  1. 29 april

    1. NL producentenvertrouwen april
    2. Philips Q1-cijfers
    3. Umicore Q1-cijfers
    4. Proximus Q1-cijfers
    5. Fra BBP eerste kwartaal (voorlopig)
    6. AkzoNobel €1,54-ex-dividend
    7. Besi €2,15 ex-dividend
    8. Fugro €0,40 ex-dividend
    9. Heineken €1,04 ex-dividend
    10. Vastned €1,28 ex-dividend
de volitaliteit verwacht indicator betekend: Market moving event/hoge(re) volatiliteit verwacht