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Chimerix Completes Phase I Study and Initiates a Phase II Multi-dose Clinical Trial for CMX001
Chimerix, Inc., a biotechnology company developing orally available antiviral therapeutics, announced today that the Company has completed a single and multi-dose Phase I study of CMX001 in healthy volunteers.
Chimerix Completes Phase I Study and Initiates a Phase II Multi-dose Clinical Trial for CMX001...

Sequella Lead Drug Compound SQ109 Selected for Phase 1B Clinical Trial Program
Sequella, Inc., a clinical-stage biopharmaceutical company focused on diseases of epidemic potential, announced today that SQ109, its lead drug candidate for the treatment of tuberculosis (TB), was the first drug approved for evaluation in a newly awarded clinical program contract to Dynport Vaccine Company LLC and Quintiles
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Enhanced interferon-g gene expression in t cells and reduced ovalbumin-dependent lung eosinophilia in hypoxia-inducible factor-1-a-deficient mice
Int Arch Allergy Immunol 2009;149:98-102 (DOI:10.1159/000189191) (Source: Karger Publishers)
Enhanced interferon-g gene expression in t cells and reduced ovalbumin-dependent lung eosinophilia in hypoxia-inducible factor-1-a-deficient mice...

Co-delivery of ovalbumin and cpg motifs into microparticles protected sensitized mice from anaphylaxis
Int Arch Allergy Immunol 2009;149:111-118 (DOI:10.1159/000189193) (Source: Karger Publishers)
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Kaiser Daily Health Policy Report Highlights Budget News In Eight States
Summaries about recent news involving health care in the state budgets of California, Iowa, Kentucky, Louisiana, New York, South Carolina, Virginia and Washington state appear below.California: Gov. Arnold Schwarzenegger (R) on Thursday said he would veto an $18 billion plan by state Democrats that aims to
Kaiser Daily Health Policy Report Highlights Budget News In Eight States...

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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