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UPDATE: FDA Approves Vaccines for 2010-11 Flu Season

Fri, 30th Jul 2010 19:57

(Update in last paragraph with list of companies making the flu vaccine.) By Shayndi Raice Of DOW JONES NEWSWIRES WASHINGTON (Dow Jones)--The U.S. Food and Drug Administration announced Friday it has approved vaccines for the 2010-2011 flu season. The latest flu vaccine will prevent against three strains of influenza, including the H1N1 virus, or swine flu, that caused last year's pandemic. Karen Midthun, acting director of the FDA's center for biologics evaluation and research, said the best way to protect against the flu is to get vaccinated annually. "The availability of a new seasonal influenza vaccine each year is an important tool in the prevention of influenza related illnesses and death," she added. Because H1N1 developed after the flu vaccine was produced, a separate vaccine to address swine flu was needed. The FDA's approval means that only one vaccine will be required for all strains of influenza. Companies that will be producing a version of the vaccine include CSL Limited (CSL), Novartis Vaccines and Diagnostics (NOVN), GlaxoSmithKline Biologicals (GSK), ID Biomedical Corporation, MedImmune Vaccines Inc., and Sanofi Pasteur Inc. (SNY). -By Shayndi Raice, Dow Jones Newswires; 202-862-9291; shayndi.raice@dowjones.com (END) Dow Jones Newswires July 30, 2010 14:57 ET (18:57 GMT)
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(Sharecast News) - GSK unveiled promising outcomes from a phase three trial of 'Jemperli', or dostarlimab, in treating primary advanced or recurrent endometrial cancer on Monday.

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(Alliance News) - GSK PLC on Monday said a test of its Jemperli drug in combination with chemotherapy has shown it reduced the risk of death in patients with endometrial cancer by nearly a third.

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(Alliance News) - GSK PLC on Thursday announced positive results for Blenrep for the treatment of multiple myeloma.

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(Sharecast News) - GSK unveiled encouraging results from its 'DREAMM-8' phase three trial on Thursday, comparing the efficacy of 'Blenrep', or belantamab mafodotin, in combination with pomalidomide plus dexamethasone, or PomDex, against the standard treatment of bortezomib plus PomDex in relapsed or refractory multiple myeloma patients.

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GSK says ViiV's cabotegravir study supports longer HIV dose interval

(Alliance News) - GSK PLC on Tuesday celebrated study results from ViiV Healthcare Ltd, that showed an investigational formulation of cabotegravir can be dosed at four-month intervals.

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GSK's ViiV upbeat on ultra-long-acting HIV treatment study

(Sharecast News) - GSK announced on Tuesday that its specialist GIV joint venture with Pfizer and Shionogi, ViiV Healthcare, had reported encouraging results from its phase one clinical trial of an investigational formulation of cabotegravir, termed cabotegravir ultra long-acting (CAB-ULA).

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(Alliance News) - GSK PLC on Thursday emphasised its commitment to science, as it reached another settlement in ongoing litigation over alleged links between its heartburn drug and cancer.

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(Sharecast News) - GSK announced a confidential settlement with Boyd/Steenvoord, effectively resolving a case filed in California state court over its discontinued heartburn drug Zantac.

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GSK reports encouraging results for ViiV's Cabenuva HIV treatment

(Alliance News) - GSK PLC on Wednesday said that its majority-owned company ViiV Healthcare had received positive interim data from ongoing trials of its injectable HIV treatment.

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(Sharecast News) - GSK's specialist HIV unit ViiV Healthcare, which it owns in partnership with Pfizer and Shionogi, unveiled promising findings from the 'LATITUDE' phase three trial of its long-acting injectable HIV treatment Cabenuva on Wednesday.

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(Alliance News) - Supplements maker Applied Nutrition, plotting a London stock market float, is to add AJ Bell PLC founder Andy Bell as its chair, Sky News reported on Tuesday.

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