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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
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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
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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)
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Mylan receives FDA approval for Fluoxetine capsules
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