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Sectornieuws - Biotech en Pharma

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Pfizer Reports Third-Quarter 2009 Results
Last update: 10/20/2009 7:00:05 AM

Third-Quarter 2009 Revenues of $11.6 Billion NEW YORK, Oct 20, 2009 (BUSINESS WIRE) --

--Third-Quarter 2009 Reported Diluted EPS(1) of $0.43, Adjusted Diluted EPS(2) of $0.51 --Continues to Execute on Financial and Strategic Commitments; Commenced Wyeth Integration on October 16, 2009 Following Completion of the Acquisition --Updates Full-Year 2009 Revenue, Reported Diluted EPS(1) and Adjusted Diluted EPS

DRW

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EU Clears Merck & Co To Buy Schering-Plough
Last update: 10/23/2009 3:50:00 AM

BRUSSELS (Dow Jones)--The European Commission Friday cleared pharmaceuticals company Merck & Co. (MRK) to buy Schering-Plough Corp. (SGP).

Merck is paying $41.1 billion in cash and stock for Schering. To avoid antitrust problems, Merck has sold its 50% stake in animal-health company Merial Limited to Sanofi-Aventis SA (SNY), its partner in the joint venture.

-By Adam Cohen, Dow Jones Newswires; +322 741 1486; adam.cohen@dowjones.com (END) Dow Jones NewswiresOctober 23, 2009 03:50 ET (07:50 GMT)
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Grassley Probe Of Health Group May Show Deeper Pharma Ties
Last update: 10/22/2009 6:33:07 PM

By Jared A. Favole
Of DOW JONES NEWSWIRES
WASHINGTON (Dow Jones)--A probe by Sen. Charles Grassley, R.-Iowa, into the ties between pharmaceutical companies and a leading patient advocacy group, the National Alliance on Mental Illness, may show their relationship goes deeper than previous thought.

Grassley's investigation shows the national group has received more than $28 million from pharmaceutical companies in the last four years. However, that number doesn't include pharmaceutical contributions given to NAMI's 50 state chapters or related foundations.

Grassley is now demanding that information, according to documents obtained by Dow Jones Newswires. Earlier this month, Grassley staffers wrote letters to the state chapters of the group demanding they turn over financial information detailing how much they receive from pharmaceutical companies.

The investigation is part of a broad look into conflict of interests and how industry influence might be driving prescription drug use. But more than conflict of interests are at stake.

Pfizer Inc. (PFE) is facing a whistleblower lawsuit in federal court in Massachusetts where a former employee alleges the company used NAMI to illegally promote its schizophrenia drug Geodon off label.

A company representative wasn't immediately available to comment. Since the beginning of 2009, Pfizer has given more than $60,000 to NAMI for fundraisers in Boston and New York and for general operational support, according to documents the company posted online.

Michael Fitzpatrick, executive director of NAMI's national office, said the state chapters operate independently of the national organization. Still, he said he has "encouraged" the state chapters to respond to Grassley's request.

Though funding varies from chapter to chapter, Fitzpatrick said pharmaceutical funding at some of the group's larger state organization makes up about 5% of their budget. He said he doesn't know if pharmaceutical money given to state chapters, once added up, will outpace the money given to the national organization.

At the national group, pharmaceutical funding makes up about 50% of its annual $10 million to $13 million budget. Grassley's probe of NAMI was first reported by The New York Times.

Fitzpatrick said the group is committed to transparency and notes that starting this year it posts all contributions over $5,000 online. Pharmaceutical money, he said, has been essential in underwriting various programs that NAMI couldn't do alone.

For instance, the money has helped the group fund weekly meetings in 300 locations to allow people suffering from mental illnesses to come together and discuss their problems.

AstraZeneca (AZN) has given more than $250,000 to a variety of NAMI chapters from January to June 2009, according to information the company posted online. The money goes to fund NAMI fundraising walks and educational outreach efforts.

-By Jared A. Favole, Dow Jones Newswires; 202-862-9207; jared.favole@dowjones.com (END) Dow Jones NewswiresOctober 22, 2009 18:33 ET (22:33 GMT
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GlaxoSmithKline boekt winststijging 30% in derde kwartaal
28-10-2009 13:55:00
LONDEN (Dow Jones)--GlaxoSmithKline Plc heeft in het derde kwartaal van 2009 de nettowinst met 30% zien stijgen, dankzij de toenemende focus van het bedrijf op de opkomende markten, Japan en consumentengezondheidsproducten. Daarnaast verwacht het grootste farmaceutische concern van Europa een significante omzet te boeken op de griepvaccins in het vierde kwartaal van 2009, als gevolg van de voorbereidingen op de massale inentingsprogramma's van overheden. De orders voor Glaxo's varkensgriepvaccin Pandemrix bedroegen volgens het bedrijf per 6 oktober 440 miljoen dosissen.

Het Britse concern rapporteerde woensdagmiddag een nettowinst over het afgelopen kwartaal van GBP1,34 miljard, vergeleken met GBP1,03 miljard een jaar geleden. De omzet klom met 15% tot GBP6,76 miljard. Tegen constante wisselkoersen bedroeg de omzetstijging 3%. Analisten gepolst door Thomson Reuters hadden gerekend op een omzet van GBP6,81 miljard.

De omzet uit opkomende markten nam toe met 25%, terwijl de omzet uit Japan met 19% klom. De consumentengezondheidsproducten lieten een omzetgroei zien van 8%. In de Verenigde Staten, waar Glaxo te kampen heeft met de concurrentie van goedkopere generieke medicijnen, daalde de omzet met 12%.

Het aandeel GlaxoSmithKline noteert woensdag rond 13.45 uur in Londen zo'n 0,8% lager op 1.246,5 pence na publicatie van de kwartaalcijfers.

- Door Martijn Mom; Dow Jones Nieuwsdienst; +31-20-5715 201; martijn.mom@dowjones.com

DRW
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PRESS RELEASE: Fitch: European Pharma Faces Declining Profitability on Diversification Pressures
Last update: 10/29/2009 5:47:07 AM

The following is a press release from Fitch Ratings:

Fitch Ratings-London/Chicago-29 October 2009: Fitch Ratings says today that major European pharmaceutical companies will likely face profitability declines over the medium-to long- term, due to their risk-diversifying and -sharing strategies, which are designed to combat challenges in their traditional drug markets.

"The risk diversification and risk sharing strategies, emphasized also by GlaxoSmithKline yesterday, are aimed at addressing declining R&D productivity, looming patent expiries and governments' continuing cost containment policies, which are putting profits under pressure," says Britta Holt, Director in Fitch's European Corporates team.

"These strategies are expected to lead to a decline in profitability over time, notwithstanding the industry's restructuring and efficiency programmes implemented over the past two years." Financed by cuts in share buybacks, European pharmaceutical companies have been expanding into other healthcare areas to diversify away from pure pharmaceuticals (AstraZeneca Plc, 'AA-'/Stable, is the only pure pharma company among Fitch-rated major European pharmas).

The sectors that companies have been expanding into typically bear lower risks, but also lower profitability and cash flow generation capability. Recent examples include Novartis AG's ('AA'/Stable) USD10.4bn acquisition of a 25% stake in Alcon from Nestle SA ('AA+'/Stable) which was completed in July 2008, and Sanofi-Aventis SA's ('AA-'/Stable) USD4bn acquisition of the 50% interest in animal health company Merial, that it did not already own, which closed in September 2009.

In an effort to further diversify their businesses, large European pharmaceutical companies are also rapidly increasing their small footprint in emerging markets. Companies such as GlaxoSmithKline Plc ('A+'/Stable), which generated 9% of 2008 group sales in emerging markets, are expected to catch-up rapidly with peers having a higher presence in these markets.

A significant number of transactions in emerging markets have occurred in the past 18 months, including GlaxoSmithKline's "transformational agreement" with the South African pharmaceutical company Aspen Pharmacare Holdings Limited (announced in July 2008), and Sanofi-Aventis' acquisition of the Czech generic drugs company Zentiva N.V. for USD2.6bn which closed in February 2009.

However, the agency believes that unless companies achieve critical mass in terms of marketing and drug distribution in emerging markets, profitability will typically lag behind that seen in developed markets. Further operating margin pressure stems from risk-sharing deals with government authorities, such as the National Institute of Clinical Excellence (NICE) in the UK, for new drug launches.

UK drug manufacturer Celgene, for example, agreed in 2009 to meet the drug costs of the multiple myeloma treatment Revlimid for patients who remain on treatment for more than 26 cycles, normally a period of two years. In another example, Roche Ltd ('AA-'/Negative) agreed in 2008 to match the price of the older, less expensive drug Taxoterre, when entering the UK market with its new lung-cancer treatment, Tarceva.

Other risk-sharing deals include in-licensing and out-licensing agreements, as well as accords with authorized generic drug makers, where companies compromise on profitability to reduce R&D risks.

For more information on the pharmaceutical industry, see the Fitch report, entitled "Global Quarterly R&D Pipeline Report - Second Quarter 2009", which is available on the agency's public website, www.fitchratings.com. Contacts: Britta Holt, London, +44 (0) 20 7862 4022; Michael Zbinovec, Chicago, Tel: +1-312-368-3164.

DRW
aossa
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Lonza koopt Belgische biotechtoeleverancier Algonomics

De Gentse toeleverancier aan de biotechsector Algonomics is overgenomen door de Zwitserse farmagroep Lonza. Algonomics voert voor rekening van biotechnologiebedrijven computer- en labotesten uit om nieuwe medicijnen te ontwikkelen.
(tijd) - 'Met de overname kunnen we onze diensten aan onze klanten flink uitbreiden', zegt Janet White, directielid van Lonza. De overnameprijs werd niet bekend gemaakt.

De huidige CEO van Algonomics, Philippe Stas, zal het Gentse team van 12 werknemers ook na de overname blijven leiden.

Het bedrijf was in handen van het Vlaams Interuniversitair Instituut voor Biotechnologie (VIB) en durfkapitaalverschaffers als Baekeland II en Gemma Frisius en Trustcapital.

DA
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Was net op het nieuws , er zou een belangrijke doorbraak inzake malaria zijn, was te laat.

Iemand anders al op de hoogte?
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quote:

wildspieker schreef:

Was net op het nieuws , er zou een belangrijke doorbraak inzake malaria zijn, was te laat.

Iemand anders al op de hoogte?
Joe Cohen vertelde dat er een belangrijke doorbraak was in de ontwikkeling van een vaccin tegen Malaria.
Het ging de laatste testfase in en over drie jaar kon het in productie genomen worden.
Amerikaanse onderzoekers voerden de testen in afrika uit.

RTL 4 nieuws.
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quote:

dedokter schreef:

Fase 3 GSK
Thnkx, dus loop Crucell weer achter de feiten aan hiermee?
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quote:

wildspieker schreef:

[quote=dedokter]
Fase 3 GSK
[/quote]

Thnkx, dus loop Crucell weer achter de feiten aan hiermee?
Zal wel tzt via de WHO gaan. Die willen altijd meerdere leveranciers. Markt groot genoeg voor meerdere spelers.
flosz
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quote:

z0n0p schreef:

Zal wel tzt via de WHO gaan. Die willen altijd meerdere leveranciers. Markt groot genoeg voor meerdere spelers.
Voor nu (en de volgende 20 jaar) eerst maar eens één effectief & veilig malariavaccin op de wereld proberen te zetten.

www.iex.nl/forum/topic.asp?forum=228&...
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FDA Grants Orphan Drug Designation for TNFerade(TM)

Last update: 11/4/2009 7:44:00 AM

GAITHERSBURG, Md., Nov 04, 2009 /PRNewswire-FirstCall via COMTEX/

-- GenVec, Inc. (GNVC) announced today that the U.S. Food and Drug Administration (FDA) has granted orphan drug designation to TNFerade(TM) for the treatment of pancreatic cancer. The FDA grants orphan drug designation to drugs that may provide a significant therapeutic advantage over existing treatments and target conditions affecting 200,000 or fewer U.S. patients per year. Orphan drug designation provides potential financial and regulatory incentives including study design assistance, waiver of FDA user fees, tax credits, and up to seven years of market exclusivity upon marketing approval.

"Orphan drug designation is a critical step for the development of TNFerade and will strengthen the TNFerade program at GenVec by offering potential clinical development and commercialization benefits," stated Dr. Paul Fischer, GenVec's President and CEO.

About TNFerade(TM) TNFerade, which has not yet been approved for use, is an adenovector, or DNA carrier, which contains the gene for tumor necrosis factor-alpha (TNF-alpha), an immune system protein with potent and well-documented anti-cancer effects, for direct injection into tumors. After administration, TNFerade stimulates the production of TNF-alpha in the tumor. TNFerade has been granted Fast Track product designation by the U.S. Food and Drug Administration (FDA) for its proposed use in the treatment of locally advanced pancreatic cancer.

DRW
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New Merck Begins Operations
Last update: 11/4/2009 8:00:05 AM

With Robust Pipeline, Broader Product Portfolio and Expanded Global Presence WHITEHOUSE STATION, N.J., Nov 04, 2009 (BUSINESS WIRE)

-- Merck & Co., Inc. (MRK) today outlined its global plans following the completion of Merck's merger with Schering-Plough Corporation announced yesterday. The new Merck is a global health care leader aimed at providing innovative, distinctive products and services that save and improve lives, while satisfying customer needs and creating long term shareholder value.

"With our merger now complete, we are ready to deliver on the promise of a new Merck built on a foundation of scientific innovation and dedication to the well-being of patients around the world," said Richard T. Clark, chairman, president and chief executive officer of Merck. "On 'Day One' for the new Merck, we are stronger and better equipped to make a difference in the lives of people globally through our broadened, diversified portfolio of innovative medicines and vaccines, and products for consumer and animal health.

"Our integration teams prepared us well for a strong start today, with thorough plans designed to ensure a seamless transition for our customers and employees," added Mr. Clark. "The combination of the considerable talents of Schering-Plough and Merck employees across the globe positions Merck to move through this dynamic time for our industry with a clear vision for the future."

From the outset, Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal and consumer health products. This portfolio is complemented by a robust pipeline with more than 15 promising late-stage candidates spanning critical therapeutic categories.

Merck now has approximately 106,000 employees and operates in more than 140 countries around the world, including emerging markets. The company expects to generate more than 50 percent of its revenue outside the United States.

"The people of the new Merck share a passion for the good our medicines and vaccines can do for patients and a commitment to pursuing high-quality results with our customers and partners," Mr. Clark said.

"Thanks to the talent and dedication of scientists at both companies, the combined company offers an outstanding clinical development pipeline that will greatly increase our ability to deliver important new medicines to patients."

The company's corporate headquarters will be in Whitehouse Station, NJ, as previously indicated. In addition, the company's U.S. organization for the Global Human Health division and Merck Research Laboratories will be headquartered in Upper Gwynedd, PA.

The former Schering-Plough headquarters in Kenilworth, NJ and Merck's operations in Rahway, NJ, will continue to be important sites, with large and diverse operations encompassing marketing, manufacturing and research.

At this time, all other sites will continue to operate as they did before the merger. Key Therapeutic Areas The new Merck has a broad portfolio of medicines -- an engine for consistent, sustainable growth -- driven in part by the addition of valuable products with long periods of exclusivity.

By leveraging Merck's expanded product offerings, the company expects to benefit from additional revenue growth opportunities. For example, Merck will pursue expanded life-cycle management through the introduction of potential new combinations and formulations of existing products.

The company's diverse portfolio of adult, adolescent and pediatric vaccines and medicines spans important therapeutic areas, including cardiovascular, diabetes, obesity, bone, respiratory, immunology, dermatology, infectious disease, oncology, neurosciences, ophthalmology, women's health and endocrinology. Diversified Businesses The new Merck's expanded portfolio also includes leading products from its Animal Health and Consumer Health Care business units. Merck's Animal Health business is a world leader with market-leading products for a broad range of species and strong growth potential. The division has more than 1,000 marketed products and generates approximately $3 billion in revenues.

The company's Consumer Health Care business has a number of attractive brands such as CLARITIN, COPPERTONE, DR. SCHOLL'S and MIRALAX. Financial Highlights Merck is targeting a high single digit non-GAAP EPS compound annual growth rate from 2009 to 2013 (with the 2009 base representing Merck's previous stand-alone non-GAAP EPS guidance of $3.20 - $3.30). Additionally, in 2013, Merck is targeting free cash flow to be approximately $15 billion.

The combined company will have a strong balance sheet with cash and investments of approximately $8 billion at the time of the closing. As previously indicated, Merck expects the transaction to be modestly accretive in 2010. Merck also continues to expect to achieve substantial incremental cost savings of approximately $3.5 billion annually beyond 2011 which are expected to come from all areas across the combined company.

The strong cash flow and substantial cost savings will enable the company to continue to invest in some of the best investment opportunities, including pipeline candidates with the greatest probability of success, as well as licensing opportunities. By optimizing its investments, the new Merck will maximize the benefits of strategic growth initiatives and R&D efforts to solidify its position at the forefront of innovation and enhance its scientific and technological leadership. Additionally, Merck's Board of Directors continues to be committed to maintaining the dividend at the current level. Organizational Structure During the past six months, Merck and Schering-Plough merger integration teams worked hard to successfully maintain the business momentum of the two companies while ensuring operational readiness and business continuity for the merged company.

The integration plans are focused on these priorities: an effective transition for customers and employees; putting the right people in the right jobs; realizing projected merger synergies in the form of cost savings and revenue growth opportunities; and maintaining momentum in the company's late stage pipeline. The company took significant steps prior to the merger's completion to advance its integration planning objectives. In August, Merck announced the new organizational structure and top leadership team for the combined company. Last month, approximately 300 executives from Merck and Schering-Plough were named to key country leadership positions to ensure that all markets around the world would be ready for business on the first day of operations for the new Merck. The company's previously announced organizational structure takes advantage of the combined strengths of Merck and Schering-Plough to create a more customer-focused, innovative, and diversified global health care company positioned to capitalize on the company's greatest opportunities for growth, particularly in emerging markets, biologics and vaccines. Merck has five primary divisions: Global Human Health, Animal Health, Consumer Health Care, Merck Research Laboratories and Merck Manufacturing. Leadership The new Merck will benefit from the unparalleled industry experience of senior leaders from both Schering-Plough and Merck, with approximately 40 percent of Schering-Plough's senior leaders joining the com
flosz
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quote:

Dirk R. Wijnen schreef:

FDA Grants Orphan Drug Designation for TNFerade(TM)
Ha, dank Dirk…eens kijken of ik zometeen de GNVC’s eindelijk kan dumpen….30+ pre-market ziet er goed uit.
aossa
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GenVec shares soar on orphan cancer drug designation

By John Carroll Comment | Forward

Regulators at the FDA have presented GenVec with orphan drug status for TNFerade, an experimental therapy that spurs development of an immune system protein which helps fight advanced pancreatic cancer. And investors swiftly bid up the company's stock (GNVC) by 35 percent in premarket trading.

GenVec started out the year with a restructuring that claimed the jobs of 22 employees. Nine months ago the developer said that the cutbacks would leave enough money to operate for 18 to 24 months as it pushed ahead with its late-stage program for TNFerade and pursued talks with a partner. And since then it's received new grant money and completed two stock offerings.

Last summer Gaithersburg, MD-based GenVec unveiled interim Phase III survival data for TNFerade, demonstrating a 25 percent reduction in the risk of death when combined with standard treatment. In the standard of care arm, 75 percent of the patients died within 11.8 months, but that mortality rate wasn't hit in the combination arm until 19.4 months.

GenVec CFO Douglas Swirsky tells FierceBiotech this morning that finding a partner for the drug remains a "top priority," but he isn't providing any clues on when a deal can be wrapped. The next key event for the company, he adds, will come later this quarter when researchers expect to see its pivotal trial hit a key point on overall survival. The trial recruited 330 patients and will conclude on the death of the 276th patient. The 184th death, two thirds of the total, should occur before the end of the year, with new data out in the first quarter. GenVec comes out with its quarterly numbers tomorrow and is keeping its financial cards close to its vest until then.

www.fiercebiotech.com/story/genvec-sh...
voda
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UPDATE: OncoMethylome focust op drie soorten kanker
(Update van eerder gepubliceerd bericht 'OncoMethylome focust op drie soorten kanker', om extra informatie en actuele koers toe te voegen.)



Archie van Riemsdijk

Van DOW JONES NIEUWSDIENST



AMSTERDAM (Dow Jones)--OncoMethylome Sciences nv gaat zich concentreren op zijn diagnostische producten voor drie soorten kanker, en op de Verenigde Staten als primaire afzetmarkt, meldt het biotechbedrijf donderdag.

Door de focus aan te brengen verwacht het bedrijf het nettoverlies in de 2010 terug te dringen, bij een stabiele omzet.

OncoMethylome ontwikkelt tests om diverse soorten kanker effectief en efficient te kunnen opsporen. Het bedrijf wil zich nu richten op het naar de markt brengen van zijn meest vergevorderde tests, voor darmkanker, prostaatkanker en blaaskanker.

De focus op introductie van producten in de VS, in samenwerking met grote distributeurs, betekent dat OncoMethylome voorlopig geen verkooporganisatie in Europa zal opzetten.

In de VS moet het bedrijf op zoek naar een nieuwe partner voor de verdere ontwikkeling van een van zijn prostaatkankertests, nu licentiepartner Veridex heeft laten weten het product niet verder te willen ontwikkelen.

De koerswijziging van Veridex, dat onderdeel is van farmaceutisch concern Johnson & Johnson (J&J), komt als een verrassing, zegt interim-CEO Philip Devine van OncoMethylome donderdag tegen Dow Jones Nieuwsdienst. Hij merkt op dat de testresultaten voor de op urine gebaseerde test boven verwachting waren en dat J&J eerder had aangegeven dat het product in 2010 op de markt zou worden gelanceerd.

Het knelpunt was volgens Devine dan ook niet de kosten de resterende klinische tests, die voor een partij als Johnson & Johnson 'peanuts' zijn. Het farmaceutische concern heeft echter nog geen verkoopkanaal voor de urologen, die het product zouden moeten kopen. Het creeren van zo'n verkoopafdeling wordt door J&J niet haalbaar geacht, na de recente aankondiging van een reorganisatie met veel ontslagen bij het concern.

De Amerikanen gaan nu met OncoMethylome op zoek naar een andere partner om de klinische tests uit te voeren. Hij benadrukt dat alle rechten voor de betreffende prostaatkankertest nog bij J&J liggen.

Devine stelt dat er momenteel een 'scan' in de markt wordt uitgevoerd door J&J en dat er verschillende kandidaten zijn die producten aan urologen verkopen. Idealiter zou behalve de prostaatkankertest ook de blaaskankertest via dezelfde partij naar de markt kunnen worden geloodst, merkt hij op.

Voor 2009 verwacht OncoMethylome een lagere omzet dan in 2008, terwijl het nettoverlies naar verwachting toeneemt.

OncoMethylome meldt verder dat oprichter Herman Smolders van het biotechbedrijf per 1 januari 2010 terugtreedt als chief executive officer (CEO). Hij blijft in het bestuur als commissaris. Chief financial officer Philip Devine wordt interim-CEO.

In het derde kwartaal werd een nettoverlies geboekt van EUR2,9 miljoen, tegen EUR2,0 miljoen in dezelfde periode van 2008. Daarmee liep het verlies over de eerste negen maanden op tot EUR9,2 miljoen, van EUR7,8 miljoen een jaar eerder.

De omzet daalde in het derde kwartaal tot EUR0,6 miljoen van EUR0,8 miljoen.

Het aandeel OncoMethylome noteert donderdag aan het eind van de ochtendhandel 5,2% lager op EUR5,34.



Door Archie van Riemsdijk; Dow Jones Nieuwsdienst: +31-20-5715200; archie.vanriemsdijk@dowjones.com

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GenVec Signs New Contract to Support HIV and Influenza Vaccine Development

Last update: 11/5/2009 7:53:00 AM

GAITHERSBURG, Md., Nov 05, 2009 /PRNewswire-FirstCall via COMTEX/ -

- GenVec, Inc. (GNVC) announced today that SAIC-Frederick, Inc. has signed a contract with GenVec for the development of influenza and HIV vaccines in support of the Vaccine Research Center (VRC) of the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health (NIH).

This four-year contract has a total value of over $22 million if all options are exercised. Over the next year, GenVec will receive approximately $2.6 million. Under the contract, the vaccines would be comprised of genetic material supplied by the VRC and adenoviral vectors supplied by GenVec.

"This new contract supports important efforts in HIV and influenza. Given the heightened concerns about influenza, this contract is timely and we look forward to applying our novel technology to this problem," stated Dr. Paul Fischer, GenVec's President and CEO.

"In particular, we are looking forward to working on a universal flu vaccine, which has the potential to protect against seasonal and pandemic outbreaks." Work under this contract will include generation of HIV vaccine candidates, generation of a universal flu vaccine candidate, process and assay development for manufacture of vaccine candidates for clinical testing, and continued support of the HIV vaccine candidates currently in clinical testing.

DRW

custom.marketwatch.com/custom/tdameri...
voda
0
OctoPlus

Biotechnologiebedrijf OctoPlus maakte maandag bekend in het derde kwartaal een positief operationeel resultaat te hebben geboekt. Het bedrijf verwacht zoals eerder aangegeven 19 miljoen euro omzet te boeken in 2009. Beleggers reageerden zeer positief, OctoPlus noteerde 9,8 procent hoger.

Bron: ANP
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