Skip over navigation
Banner
Industry
Directory Facilities Technology Transfer Economic Develop. NE BioHistory (TM)
Career
Job Search Post a Job Destination NE
News/Events
Industry News Submit News Release Calendar Submit Event CEO Reading
Patient
Clinical Trials Drug Development Resources
Education
K-12 Higher Ed BioEd Reading
About
Advertising Feedback Home
 
News
 Industry News
 Submit News Release
 Calendar
 Submit Event
 CEO Reading
Quick Links
 Directory
 Job Search
 Facilities
 Calendar
 Advertising
Community Service Ad:  Every Child Deserves a Chance to Play Baseball
Facilities
 
Jobs
 

Conference on Biosimilars, University of Washington, Seattle - March 19-20. Sign up today!


Industry News

News

Submit News Release


Search Articles: 

  • ARCA announces receipt of NASDAQ notice per NASDAQ Rule 5810(b)  ARCA biopharma announced, as required by NASDAQ Marketplace Rule 5810(b), that on March 12, 2010, it received a notice from the NASDAQ Stock Market indicating that the Company's stockholders' equity as of December 31, 2009, did not meet the minimum requirement of $10,000,000 for continued listing.
    ARCA biopharma, Inc. March 17, 2010  
  • U.S. Food And Drug Administration accepts New Drug Application  Bristol-Myers Squibb and AstraZeneca announced that the FDA has accepted for review a New Drug Application (NDA) for an investigational fixed dose combination of ONGLYZA(TM) (saxagliptin), a dipeptidyl peptidase-4 (DPP4) inhibitor, and metformin HCl extended-release tablets.
    Bristol-Myers Squibb Company March 17, 2010  
  • Study shows Prevenar 13* is immunogenic in young children previously vaccinated  According to results from a Phase III safety and immunogenicity study presented today, Prevenar 13* was shown to be immunogenic and generally well tolerated in healthy young children who had received at least three prior doses of Prevenar* (Pneumococcal Saccharide Conjugated Vaccine, Adsorbed).
    Pfizer Inc. March 17, 2010  
  • Boston Scientific completes enrollment in PLATINUM trials  Boston Scientific announced completion of patient enrollment in the Small Vessel and Long Lesion trials of its PLATINUM clinical program that are designed to compare the platinum chromium PROMUS® Element Everolimus-Eluting Stent System to matched historical control groups of patients.
    Boston Scientific Corporation March 16, 2010  
  • New PLATO sub-analysis of CABG patients presented at ACC  AstraZeneca announced results of a new analysis of the PLATO study which showed there were fewer deaths in patients with acute coronary syndromes who took the investigational oral antiplatelet BRILINTA within seven days prior to having heart bypass surgery compared to those who took clopidogrel.
    AstraZeneca March 16, 2010  
  • Additional $162 million in Recovery Act investment to advance health IT  U.S. Department of Health and Human Services Secretary Kathleen Sebelius announced awards to help states facilitate health information exchange and advance health information technology (health IT).
    Dept. of Health & Human Services March 15, 2010  
  • Nebraska receives $6 million for health information projects  Gov. Dave Heineman announced that the state was awarded more than $6.8 million in American Recovery and Reinvestment Act (ARRA) grant funding for the statewide digital health information exchange known as the Nebraska Health Information Initiative (NeHII).
    Governor of Nebraska March 15, 2010  
  • Lilly to acquire global license to AXIRON testosterone solution from Acrux  Eli Lilly and Company and Acrux announced that they have entered into an exclusive worldwide license agreement for the potential commercialization of Acrux's experimental underarm testosterone solution (proposed tradename AXIRON(TM)).
    Eli Lilly and Company March 15, 2010  
  • Intensive Lipitor therapy was associated with reduced risk of cardiovascular events  Lipitor(R) (atorvastatin calcium) 80 mg was associated with a significantly reduced risk of major cardiovascular events compared with Lipitor 10 mg among patients with both coronary heart disease (CHD) and chronic kidney disease (CKD) who were obese or had metabolic syndrome.
    Pfizer Inc. March 15, 2010  
  • Mipomersen Phase 3 study in HoFH patients featured in The Lancet  Genzyme and Isis Pharmaceuticals announced that data from a phase 3 study of mipomersen in patients with homozygous familial hypercholesterolemia (hoFH) were published in The Lancet.
    Isis Pharmaceuticals, Inc. March 15, 2010  

   (next 10 articles)

Search Articles: 


Submit News Release

 
Email thie page to a friend. Email This Page
to a Friend
Print this page. Print This
Page
© 2010 Info.Resource, Inc. All rights reserved.
Privacy Policy . Terms of Use . Advisory Board . Advertising

NebraskaLifeScience.com is owned and published by Info.Resource, Inc..