Wednesday, July 2, 2014

Fwd: Nanoparticles Prevent Bone Cancer, Strengthen Bones; Actavis Closes $28B Forest Deal



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Begin forwarded message:

From: Kent Castle <kent.d.castle@hotmail.com>
Date: July 1, 2014 3:36:11 PM CDT
To: Patterson James <w8ljz@aol.com>, Bogan Carole <bcbogan@earthlink.net>, Chamberlain Sharon <sharon.m.chamberlain@saic.com>, Astrology Valkyrie <astrogoddess@valkyrieastrology.com>, Madsen Ron <ronstar@pdq.net>, Martin Bobby <bobbygmartin1938@gmail.com>, Lozano Marianne <kemahsabe@comcast.net>, Matthews-Schmidt Linda <linda.j.matthews-schmidt@nasa.gov>, Kelley Mary <mary.n.kelley@nasa.gov>
Subject: FW: Nanoparticles Prevent Bone Cancer, Strengthen Bones; Actavis Closes $28B Forest Deal


 

From: reply@mail.dddmag.com
To: KENT.D.CASTLE@HOTMAIL.COM
Subject: Nanoparticles Prevent Bone Cancer, Strengthen Bones; Actavis Closes $28B Forest Deal
Date: Tue, 1 Jul 2014 09:46:08 -0600

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JULY
01
 
IN THIS ISSUE
  NEWS  
  Actavis Closes $28B Forest Deal  
  NEWS  
  Amgen's Leukemia Drug Gets FDA Breakthrough Designation  
  NEWS  
  GlycoVaxyn Kicks Off Trial of UTI Vaccine  
  NEWS  
  Ipsen Applies for US, EU GEP-NET Drug Marketing Authorizations  
  NEWS  
  CTI BioPharma Wraps Up Recruitment in Pivotal Trial of Myelofibrosis Drug  

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  FEATURED STORY

Nanoparticles Prevent Bone Cancer, Strengthen Bones

 
 
Featured Story
A research collaboration between Dana-Farber Cancer Institute and Brigham and Women's Hospital and has utilized nanomedicine technologies to develop a drug-delivery system that can precisely target and attack cancer cells in the bone, as well as increase bone strength and volume to prevent bone cancer progression. Read more...

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FULL STORY
 
 
NEWS

Actavis Closes $28B Forest Deal

Thumbnail
Actavis has completed its $28 billion acquisition of fellow drugmaker Forest Laboratories, and the leader of the acquired company - Brenton Saunders - is now the CEO of Actavis, and former Actavis Chairman and CEO Paul Bisaro will become executive chairman. Read more...

FULL STORY
 
 
NEWS

Amgen's Leukemia Drug Gets FDA Breakthrough Designation

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Amgen announced that the U.S. Food and Drug Administration has granted Breakthrough Therapy Designation to investigational bispecific T cell engager antibody blinatumomab, for adults with Philadelphia-negative relapsed/refractory B-precursor acute lymphoblastic leukemia, a rapidly progressing cancer of the blood and bone marrow. Read more...

FULL STORY
 
 
NEWS

GlycoVaxyn Kicks Off Trial of UTI Vaccine

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GlycoVaxyn AG, a leader in the development of innovative conjugate vaccines, announced the initiation of a Phase 1 clinical trial of a candidate vaccine to prevent infections caused by Extra-intestinal Pathogenic Escherichia coli (ExPEC), such as urinary tract infections (UTIs). Read more...

FULL STORY
 
 
NEWS

Ipsen Applies for US, EU GEP-NET Drug Marketing Authorizations

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Ipsen announced that it has submitted a Supplemental New Drug Application to the U.S. Food and Drug Administration (FDA) for Somatuline Depot 120 mg injection for the treatment of gastroenteropancreatic neuroendocrine tumors (GEP-NETs). Read more...

FULL STORY
 
 
NEWS

CTI BioPharma Wraps Up Recruitment in Pivotal Trial of Myelofibrosis Drug

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CTI BioPharma Corp. announced that it has completed recruitment in the PERSIST-1 pivotal Phase 3 clinical trial of pacritinib, a novel oral JAK2/FLT3 inhibitor that is being evaluated for the treatment of primary myelofibrosis, post-polycythemia vera myelofibrosis or post-essential thrombocythemia myelofibrosis, without exclusion for low platelet counts . Read more...

FULL STORY
 
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