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Sinovac Biotech Ltd.(Public, AMEX:SVA)

32 Posts
Pagina: «« 1 2 | Laatste | Omlaag ↓
  1. [verwijderd] 3 september 2009 15:43
    quote:

    d invests. schreef:

    Ze hebben het er doorheen vannacht, 10+ nu v.b.
    Gisteren nog -18% en afgesloten op $8.53(winstnemingen) om dan nabeurs weer met wat nieuws af te komen die de stock toen al terug de hoogte in stuurde.Deze trend zette zich voorbeurs lekker voort.

    After Hours
    Last: $ 8.95
    High: $ 9.07
    After Hours
    Volume: 406,493
    Low: $ 8.61

    Pre-Market
    Last: $ 10.26
    High: $ 10.64
    Volume: 2,140,172
    Low: $ 9.60

    Real-Time: 10.36 1.83 (+21.45%)

    Sinovac Obtains Production License for H1N1 Vaccine.

    September 3, 2009 9:07 AM EDT

    Sinovac Biotech Ltd. (NYSE: SVA) announced today that the State Food and Drug Administration has approved the registration application for PANFLU.1, Sinovac's H1N1 vaccine, and has issued Sinovac a production license for this vaccine.

    Following top-line results which showed that PANFLU.1, Sinovac's H1N1 vaccine, has a good safety and immunogenicity profile, the Company announced the findings of an experts' evaluation conference organized by the SFDA on August 30 and 31. The experts unanimously agreed that Sinovac's H1N1 vaccine is suitable for all people from three to 60 years old on a single shot vaccination schedule.

    Mr. Weidong Yin, Chairman, President and CEO of Sinovac, commented, "The approval of PANFLU.1, Sinovac's H1N1 vaccine, is a significant milestone in the campaign for the prevention and control of the H1N1 virus. With the support of the Ministry of Health, State SFDA, Chinese Center for Disease Control and Prevention, Sinovac was able to successfully and rapidly complete the clinical trials and registration process for the H1N1 vaccine. By leveraging our expertise in R&D, production and commercialization of human vaccines, we continue to execute our mission to provide top-quality vaccines to eliminate human diseases."

    finance.aol.com/quotes/sinovac-biotec...

    finviz.com/screener.ashx?v=341&f=ind_...
    --------------------------------------------------------------------------------------------------------
    En voor wie de grafieken hunne dada is.

    www.windchart.com/stockta/analysis?sy...

    www.stockta.com/cgi-bin/analysis.pl?s...

    www.americanbulls.com/StockPage.asp?C...

    Gr, Skip

  2. [verwijderd] 9 november 2009 15:27
    Sinovac Biotech (NYSE Amex: SVA: 8.17, -0.12) will move the home for its stock listing from the NYSE Amex to the NASDAQ Global Market (see story). The reason given for the change was "greater liquidity." Target day for the transfer is November 16. Although most NASDAQ companies use a four-letter symbol, Sinovac will be allowed to keep its current three-letter identifier, SVA, so the new listing will not have much effect on most investors.
  3. [verwijderd] 28 december 2009 14:40
    Sinovac Files Clinical Trial Application with SFDA for Vaccine Against Hand, Foot, and Mouth Disease

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

    BEIJING, Dec. 28 /PRNewswire-Asia/ -- Sinovac Biotech Ltd. ( SVA), a leading provider of biopharmaceutical products in China, announced today that it has filed the application with China's State Food and Drug Administration (SFDA) to commence a human clinical trial for its vaccine against human enterovirus 71 (EV 71), which causes hand, foot, and mouth disease (HFMD). This is the first clinical trial application for HFMD vaccine submitted in China.

    No vaccine or antiviral treatment is currently available for HFMD worldwide, though it has become a very serious problem in Asia in recent years. The disease is highly contagious and a growing number of HFMD cases have been reported in parts of Asia, including Mainland China, Hong Kong, Singapore, Korea, and Taiwan. According to China's Center for Disease Control (CDC) between January 1 and November 30 of this year, the disease has caused more than 400 deaths in China, where health authorities reported over 1.1 million HFMD infections, compared to about 200 reported H1N1 deaths. HFMD is common among infants and children, as most of the recently reported cases have occurred in children. Due to the severity of the disease epidemic, China authorities recognize the unmet medical need and are expected to support the launch of a HFMD vaccine as soon as possible. Therefore, Sinovac believes that fast track status for the reviewing process and approval may be granted.

    As previously announced, the Company began preclinical development in 2008. Sinovac is independently developing the EV 71 vaccine and will retain full commercialization rights of the vaccine upon approval. Created by Sydney University, the animal model showed cross protection and demonstrated that the vaccine is effective in animals. In addition, Sinovac is preparing to file a patent application covering the EV 71 vaccine.

    Weidong Yin, Chairman, President & CEO, stated, "We are very pleased to submit the clinical trial application for the EV 71 vaccine to the SFDA. Our ability to submit the application ahead of the projected 2010 timeline is a validation of the R&D capabilities of the team developing this vaccine. A vaccine against EV 71 represents a significant unmet medical need, given that there are not effective preventive therapeutic alternatives for this life threatening viral illness affecting infants and children. Based on current expectations, we anticipate that the EV 71 vaccine, subject to positive human clinical trial results and commercialization, represents a significant flagship product opportunity for the Company as well as an opportunity to improve the lives of children around the world."

    About EV 71

    Enterovirus 71, or EV 71, causes Hand, Foot, and Mouth Disease (or HFMD). More than 90% of the reported cases occur in children under five years old. HFMD is a common and usually mild childhood disease. EV 71 is a frequent cause of HFMD epidemics associated with neurological disease in a small proportion of cases. A number of outbreaks of EV 71 HFMD in the Asia-Pacific region have been reported since 1997. Outbreaks have been reported in Malaysia (1997), Taiwan (1998, 2000 & 2001), Mainland China (1998-2008), Australia (1999) and

    Singapore (2000) among other areas in the region. There is no specific treatment for enterovirus infections and a vaccine is not currently available.

    In 2008, 489,073 cases were reported in China with 126 reported fatalities. For the first 11 months of 2009, over 1.1 million cases were reported in China, with over 400 reported fatalities.

    About Sinovac

    Sinovac Biotech Ltd. is a China-based biopharmaceutical company that focuses on the research, development, manufacture and commercialization of vaccines that protect against human infectious diseases. Sinovac's vaccine products include Healive(R) (hepatitis A), Bilive(R) (combined hepatitis A and B), and Anflu(R) (influenza). Panflu(R) and PANFLU.1(TM), Sinovac's pandemic influenza vaccine (H5N1) and H1N1 vaccine, have already been approved for government stockpiling. Sinovac is developing vaccines for enterovirus 71, universal pandemic influenza, Japanese encephalitis, and human rabies. Its wholly owned subsidiary, Tangshan Yian, is conducting field trials for independently developed inactivated animal rabies vaccine.

    Safe Harbor Statement

    This announcement contains forward-looking statements. These statements are made under the "safe harbor" provisions of the U.S. Private Securities Litigation Reform Act of 1995. These forward-looking statements can be identified by words or phrases such as "will," "expects," "anticipates," "future," "intends," "plans," "believes," "estimates" and similar statements. Among other things, the business outlook and quotations from management in this press release contain forward-looking statements. Statements that are not historical facts, including statements about Sinovac's beliefs and expectations, are forward-looking statements. Forward-looking statements involve inherent risks and uncertainties. A number of important factors could cause actual results to differ materially from those contained in any forward-looking statement. Sinovac does not undertake any obligation to update any forward-looking statement, except as required under applicable law.

    www.istockanalyst.com/article/viewiSt...

    vaccinenewsdaily.com/news/211400-sino...
  4. [verwijderd] 5 april 2010 17:45
    Morgen jaarcijfers, zou weleens wat beweging in koers kunnen geven. Zijn laatste tijd behoorlijk weggezakt naar nu 5,90 (geloof dat year high 12,50 was). Cijfers morgen zullen goed zijn, ze hebben met voorbehoud al de range aangegeven. Revenues voor kwartaal 4 liggen rond de 35-37 miljoen +170% tov kwartaal 4 vorig jaar. Revenues voor 2009 zouden uit moeten komen tussen 81-85 miljoen wat ongeveer +70% betekent t.o.v vorig jaar. Een en ander zal afhangen hoeveel H1N1 orders in de boeken gaan. Zal rond 9-10 miljoen stuks zijn van de in totaal nu 21 miljoen bestelde stuks. Volgens mij ligt de verkoopprijs rond de euro 3 p/dosis. Betekent dus dat er in 2010 zo en zo al 33 miljoen op de teller staat. Zal niet allemaal in de boeken komen in kwartaal 1 maar dat veel meer is dan vorig jaar (6.6 miljoen) is wel duidelijk. Bij het bekend maken van de outlook reageerde de koers negatief, denk voornamelijk omdat tegelijkertijd een aandelenemissie aangekondigd werd. Aandelen zijn inmiddels uitgegeven tegen 5,75 met over-allotment, dus ik denk dat dat wel een goede bodem zou moeten geven. Enige kanttekening is wel dat de grootste omzet van H1N1, stockpiling, non recurring omzet is en dus op een gegeven moment wegvalt. De vraag is in hoeverre ze dit op kunnen vangen met andere vaccins..
  5. [verwijderd] 6 april 2010 15:34
    cijfers bekend, gelijk aan de range eerder voorpeld. revenues Q4 36,2 miljoen (+193%) en full 2009 84,2 miljoen (+80%). Ze geven ook gelijk prognose af voor volgend jaar, tussen de 67 en 72 miljoen wat dus lager is.

    Aantal punten die wat negatief klinken in het pb:
    -in 2010 nemen ze geen omzet van H1N1 mee in prognose. Van merendeel al bestelde dosis zal meer als 8 miljoen pas in 2011 de boeken in gaan als de shelflife van de dosis vervalt.. zeggen niets over eventuele vervolgorders uit China
    -revenues voor H1N1 uit andere landen worden pas in 2011 verwacht
    -op korte termijn verwachten ze dat sales worden gedrukt door 2 vaccin schandalen in China (waar SVA niets mee te maken heeft)

    Jammer, op fancy cijfers en zonder negatieve klanken had er denk best een koersstijging in kunnen zitten, nu niet. Met wpa die in 2010 zal gaan dalen door lagere omzet en meer uitstaande aandelen, verwacht ik EPS van 0,34 voor full 2010 (tegenover 0.46 nu). wat betekent een K/W nu op koers van bijna 6 ongeveer 18. Denk dat deze dus nog wel kan zakken de komende tijd. Vandaag gelukkig zonder veel schade eruit en maar weer op de watchlist voor ik denk 3-4.
32 Posts
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