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Final FDA approval for generic version of antiretroviral Zerit capsules
Mylan Inc. has announced that Matrix Laboratories Limited, its India-based subsidiary in which it holds a 71.5% controlling interest, received final approval from the U.S. Food and Drug Administration (FDA) on December 29, for its Abbreviated New Drug Application (ANDA) for Stavudine Capsules USP, 15 mg, 20
Final FDA approval for generic version of antiretroviral Zerit capsules...

Enhancement of mucosal and cellular immune response in mice by vaccination with respiratory syncytial virus dna encapsulated with transfersome
Viral Immunology Dec 2008, Vol. 21, No. 4: 483-490. Respiratory syncytial virus (RSV) is one of the principal causes of bronchiolitis and pneumonia in young children, and currently there is no safe and effective vaccine. DNA vaccines encoding RSV surface glycoproteins are one option being examined. We
Enhancement of mucosal and cellular immune response in mice by vaccination with respiratory syncytial virus dna encapsulated with transfersome...

Insertion of a targeting peptide on capsid surface loops of human papillomavirus type-16 virus-like particles mediate elimination of anti-dsdna abs-producing b cells with high efficiency.
Page: 36DOI: 10.1097/CJI.0b013e31818dbb8fAuthors: Wang, Huiming *; Yang, Zhao +; Li, Fan ++; He, Yani *; Wang, Shuguang [S]; Yang, Di +; Wu, Yuzhang + (Source: Journal of Immunotherapy)
Insertion of a targeting peptide on capsid surface loops of human papillomavirus type-16 virus-like particles mediate elimination of anti-dsdna abs-producing b cells with high efficiency....

Philadelphia Inquirer Series Examines Lifetime Health Insurance Caps
The Philadelphia Inquirer on Monday, as part of a continuing series called “Falling Through: Casualties of the Health Insurance Crisis,” examined how more U.S. More: continued here
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Mylan receives FDA approval for Fluoxetine capsules
Mylan Inc. has announced that its subsidiary, Mylan Pharmaceuticals Inc., received final approval from the U.S. Food and Drug Administration (FDA) for its Abbreviated New Drug Application (ANDA) for Fluoxetine Capsules USP, 10 mg and 20 mg.
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NeurogesX Submits NDA For NGX-4010 Dermal Capsaicin Patch For Treatment Of Postherpetic Neuralgia (PHN)
NeurogesX, Inc. (Nasdaq: NGSX), a biopharmaceutical company focused on developing and commercializing novel pain management therapies, announced that it has submitted a new drug application (NDA) with the U.S. Food and Drug Administration (FDA) for approval to market its investigational
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