Search Results for: "Other News to Note"
-
Pharma: Other News To Note
Pfizer Inc., of New York, agreed to divest its nutrition business to Nestle for $11.85 billion in cashBioWorld Today | Tuesday, April 24, 2012 -
Other News To Note
Synta Pharmaceuticals Corp., of Lexington, Mass., said a preclinical study found that ganetespib equally inhibits growth of Xalkori (crizotinib, Pfizer Inc.)-sensitive and crizotinib-resistant cancer cells driven by the EML4-ALK fusion protein, regardless of ALK mutation statusBioWorld Today | Thursday, April 19, 2012 -
Other News To Note
Formerly being developed by New York-based Pfizer Inc...Puma was founded last fall, reverse merged with a public shell and licensed clinical-stage kinase inhibitor neratinib from New York-based Pfizer IncBioWorld Today | Wednesday, April 18, 2012 -
Pharma: Other News To Note
Pfizer Inc., of New York, is facing a lawsuit alleging negligence and other allegations claiming that the firm failed to warn the medical community that antidepressant Zoloft (sertraline) carried a risk of congenital birth defects when taken during pregnancyBioWorld Today | Friday, April 13, 2012 -
Other News To Note
PolyMedix Inc., of Radnor, Pa., said lead defensing-mimetic antibiotic PMX-30063 demonstrated activity against 1,000 worldwide strains of Gram-positive staphylococci and streptococci clinical isolates, including strains resistant to Zyvox (linezolid, Pfizer Inc.), Cubicin (daptomycin, Cubist Pharmaceuticals Inc.) and methicillinBioWorld Today | Tuesday, April 3, 2012 -
Other News To Note
Biocon Ltd., of Bangalore, India, and Pfizer Inc., of New York, ended their alliance to commercialize Biocon's biosimilar versions of insulin and insulin analogue products, citing differing priorities for their respective biosimilars businessesBioWorld International | Wednesday, March 21, 2012 -
Pharma: Other News To Note
Pfizer Inc., of New York, faces a federal lawsuit filed by St. Louis-based law firm Carey, Danis & Lowe, alleging that birth defects resulted in a child after the mother was prescribed and ingested antidepressant drug Zoloft (sertraline) while pregnantBioWorld Today | Tuesday, March 20, 2012 -
Other News To Note
Results for the moderate dose level of addiction candidate EMB-001 were similar to those observed for positive control Chantix (varenicline, Pfizer Inc.), an FDA-approved smoking cessation productBioWorld Today | Monday, March 19, 2012 -
Other News To Note
Biocon Ltd., of Bangalore, India, and Pfizer Inc., of New York, ended their alliance to commercialize Biocon's biosimilar versions of insulin and insulin analogue products, citing differing priorities for their respective biosimilars businessesBioWorld Today | Wednesday, March 14, 2012 -
Pharma: Other News To Note
and Pfizer Inc., both of New York, said the FDA extended the PDUFA date for their new drug application (NDA) for Eliquis (apixaban) by three months to June 28BioWorld Today | Friday, March 2, 2012 -
Pharma: Other News To Note
Pfizer Inc., of New York, issued a statement regarding the use of Prevnar 13 (pneumococcal 13-valent conjugate vaccine [diphtheria CRM197 protein]) in adults, 50 and olderBioWorld Today | Friday, February 24, 2012 -
Pharma: Other News To Note
Pfizer Inc., of New York, said the FDA accepted for review the new drug application for tafamidis meglumine, its oral treatment for transthyretin familial amyloid polyneuropathy, a rare, progressive and fatal neurodegenerative disease that affects about 8,000 patients worldwideBioWorld Today | Thursday, February 16, 2012 -
Other News To Note
plc and Madison-N.J.-based Wyeth (now part of Pfizer Inc.), which are co-developing bapineuzumab, a Phase III-stage Alzheimer's disease candidateBioWorld Today | Wednesday, February 15, 2012 -
Other News To Note
Siemens also signed a deal with ViiV Healthcare Co., a joint venture between London-based GlaxoSmithKline plc and New York-based Pfizer Inc., for diagnostic tests related to Celsentri/Selzentry (maraviroc), a CCR5 co-receptor antagonist for CCR5-tropic HIVBioWorld Today | Wednesday, February 8, 2012 -
Other News To Note
Pfizer Inc., of New York, said the FDA approved kinase inhibitor Inlyta (axitinib) for treating patients with advanced renal cell carcinoma after failure of one prior systemic therapyBioWorld Today | Monday, January 30, 2012 -
Other News To Note
Trius Therapeutics Inc., of San Diego, said it earned a $5 million milestone payment from Bayer Pharma AG, of Leverkusen, Germany, for meeting efficacy and safety objectives in the pivotal Phase III study of the oral formulation of TR701-112 (tedizolid phosphate) compared to linezolid (Zyvox, Pfizer Inc.) in bacterial skin and skin structure infections (ABSSSIBioWorld Today | Tuesday, January 24, 2012 -
Other News To Note
II, of San Francisco, entered a collaborative development agreement with Pfizer Inc., of New York, to conduct a Phase III trial in Asia of Pfizer's investigational axitinib for the adjuvant treatment of patients at high risk of recurrent renal cell carcinoma (RCC) following nephrectomyBioWorld Today | Tuesday, January 10, 2012 -
Other News To Note
Developed by Veloxis through Phase II in the U.S., AtorFen demonstrated improvements in HDL-C, triglycerides, VLDL and fibrinogen compared with Lipitor (atorvastatin, Pfizer Inc.) alone, as well as a significantly greater effect on non-HDL-C, LDL-C, triglycerides and total cholesterol compared with Tricor (fenofibrate, Abbott) aloneBioWorld International | Wednesday, January 4, 2012 -
Other News To Note
Developed by Veloxis through Phase II in the U.S., AtorFen demonstrated improvements in HDL-C, triglycerides, VLDL and fibrinogen compared with Lipitor (atorvastatin, Pfizer Inc.) alone, as well as a significantly greater effect on non-HDL-C, LDL-C, triglycerides and total cholesterol compared with Tricor (fenofibrate, Abbott) aloneBioWorld Today | Wednesday, December 28, 2011 -
Other News To Note
Antares Pharma Inc., of Ewing, N.J., has licensed to Pfizer Inc.'s Consumer Healthcare Business Unit one of its drug delivery technologies to develop an undisclosed product on an exclusive basis for North America...Pfizer Inc., of New York, said the FDA accepted for review its new drug application seeking approval of oral JAK inhibitor tofacitinib for moderate to severe active rheumatoid arthritisBioWorld Today | Wednesday, December 21, 2011
Category
Current Filters
- xPfizer Inc
Related Keywords
Categories
- x BioWorld Today (604)
- x BioWorld International (108)
- x Bio Perspectives (1)
BioWorld | 3525 Piedmont Road
Building 6, Suite 400 | Atlanta, Georgia 30305, USA
Building 6, Suite 400 | Atlanta, Georgia 30305, USA
Part of Thompson Media Group LLC
Free Ezine
Sign up for Perspectives FREE e-mail newsletter.
Customer Service: In the U.S. and Canada: 1-800-477-6307
Outside the U.S.: 1-404-262-5476
customerservice@bioworld.com
Hours: Monday - Thursday, 8:30 am - 6:00 pm EST
Friday, 8:30am - 4:30 pm EST
Outside the U.S.: 1-404-262-5476
customerservice@bioworld.com
Hours: Monday - Thursday, 8:30 am - 6:00 pm EST
Friday, 8:30am - 4:30 pm EST
Copyright @ 2013 AHC Media. Reproduction, reposting content is strictly prohibited.