UPDATE 2-FDA approves J&J advanced prostate cancer drug | Reuters

Links shared publicly online about this topic.

  • 331
    total visits

UPDATE 2-FDA approves J&J advanced prostate cancer drug | Reuters

reuters.com

* To be sold under brand name Zytiga * Prolonged survival by 4 months in pivotal trial * Sales expected to exceed $1 billion (Adds sales projection, approval details, background) NEW YORK, April

View full resource at reuters.com

Tags: Cancer, Cancer Medication, Prostate Cancer, Prostate Cancer Medication, Prostate, Men's Health, FDA, Johnson & Johnson

  • Share

Most Recently Shared on April 29, 2011 at 11:51 pm By:

JanCernyMDPhD JanCerny, MD, PhD

FDA approves J&J advanced prostate cancer drug abiraterone. http://ow.ly/4K7F4

1 year ago...

Also Shared By:

Prostate Cancer Prostate Cancer

H. Jack West, MD H. Jack West, MD

RT @AIDSmeds Just Updated : A printable drug chart of all approved #HIV medication http://t.co/tuF9HTUO #AIDS

aidsmeds.com — “RT @AIDSmeds Just Updated : A printable drug chart of all approved #HIV medication http://t.co/tuF9HTUO #AIDSView full resource at aidsmeds.com

  • View Related
  • Share

Most Recently Shared on May 1, 2012 at 2:25 pm By:

pozmagazine POZ Magazine Health Magazine

RT @AIDSmeds Just Updated : A printable drug chart of all approved #HIV medication http://t.co/tuF9HTUO #AIDS

1 month ago...

Roche - Media: News and Press Releases

roche.com — “Press releases, media archive with backgrounders, photo and video material. Subscribe to our events podcast and regular updates via RSS-feed.View full resource at roche.com

  • View Related
  • Share

Most Recently Shared on September 1, 2011 at 8:58 am By:

Roche_com Roche Pharma

For journalists: EU approval of medicine for first-line use in a genetically distinct type of #lungcancer http://t.co/wW6J6n8

9 months ago...

UPDATE 1-J&J pain drug Nucynta ER gets FDA nod | Reuters

reuters.com — “* Nucynta ER is the extended release version of Nucynta * Approved with a risk evaluation and mitigation strategy (Follows alerts) Aug 26 (Reuters) - Johnson and Johnson unit JanssenPharmaceuticalsView full resource at reuters.com

  • View Related
  • Share

Most Recently Shared on August 29, 2011 at 7:46 pm By:

forgrace Women In Pain Health Organization

Janssen's extended-release Nucynta is approved by FDA... http://t.co/jXqFTXY

9 months ago...

NCI Cancer Bulletin for July 26, 2011 - National Cancer Institute

cancer.gov — “NCI Cancer Bulletin for July 26, 2011 - National Cancer InstituteView full resource at cancer.gov

  • View Related
  • Share

Most Recently Shared on July 27, 2011 at 9:15 pm By:

NCIBulletin NCI Cancer Bulletin Health News

FDA Update: Advisory panel recommends accelerated approval for brentuximab for 2 types of lymphoma http://j.mp/r6vRw6

11 months ago...

FDA Approves Genetically Modified Grass: A Blow to the Organic Movement - Fort Lauderdale Organic Food | Examiner.com

examiner.com — “Just as sneakily as it approved genetically modified corn, soy, and various other plants, the FDA cleared the way for genetically modified Kentucky bluegrass maView full resource at examiner.com

  • View Related
  • Share

Most Recently Shared on July 10, 2011 at 6:51 pm By:

organic_beauty_ Shalona Anuj, PhD PhD, Doctor, Organic Advocate, and Skin and Beauty

FDA Approves Genetically Modified Grass: A Blow to the Organic Movement http://bit.ly/mW69j2

11 months ago...

UPDATE 2-U.S. advisers back Shire drug for rare disease | Reuters

reuters.com — “* Shire drug safe, effective for angioedema - FDA panel * Panel also says drug, Firazyr, safe for self-injection * FDA to decide on drug approval by Aug. 25 (Adds company, panelist comment, shareView full resource at reuters.com

  • View Related
  • Share

Most Recently Shared on June 24, 2011 at 12:18 pm By:

wheezemd Michael Blaiss, MD Doctor, Allergist, and Physician

U.S. advisers back Shire drug, Firazyr for hereditary angioneurotic edema (HAE) http://goo.gl/jIIfN

12 months ago...

Eli Lilly and Company - FDA Approves Updates to Lilly's Humalog® (insulin lispro injection [rDNA origin]) Label

newsroom.lilly.com — “Eli Lilly and Company - FDA Approves Updates to Lilly's Humalog® (insulin lispro injection [rDNA origin]) LabelView full resource at newsroom.lilly.com

  • View Related
  • Share

Most Recently Shared on June 8, 2011 at 10:31 pm By:

Glycosmedia Jim Health News

FDA Approves Updates to Lilly's Humalog® (insulin lispro injection [rDNA origin]) Label http://bit.ly/jZ4a7v

1 year ago...

UPDATE 4-J&J to seek approval for 11 new drugs by 2015 | Reuters

reuters.com — “* Aims to seek approval of Alzheimer's drug in 2012-2013 * To boost investments in emerging markets * 7 launches seen in Japan this year * Shares fall 0.4 percent (Adds analyst comment, detailsView full resource at reuters.com

  • View Related
  • Share

Most Recently Shared on May 26, 2011 at 1:30 pm By:

JohnCFierce John Carroll Health Communicator

J&J plans to introduce 11 new drugs by 2015. J&J has real skill at buying companies and programs.Will that get harder? http://reut.rs/jEBjI3

1 year ago...

UPDATED: J&J is on a roll as drug deals deliver blockbuster approvals - FierceBiotech

fiercebiotech.com — “J&J never has won much praise for its science. The pharma giant, though, can spot a promising treatment in the pipeline, which it proved two years ago when it paid a billion dollars to buy up Read more...View full resource at fiercebiotech.com

  • View Related
  • Share

Most Recently Shared on May 23, 2011 at 1:06 pm By:

JohnCFierce John Carroll Health Communicator

J&J is on a roll as drug deals deliver blockbuster approvals http://bit.ly/kMEhCp

1 year ago...

Update to Fuzeon (Enfuvirtide) Label Regarding Incidence of Bacterial Pneumonia - The Body

thebody.com — “Updates to the Warnings and Precautions, Pneumonia subsection of the Fuzeon (enfuvirtide) package insert were approved on April 28, 2011 in response to ...View full resource at thebody.com

  • View Related
  • Share

Most Recently Shared on May 9, 2011 at 1:01 pm By:

TheBodyDotCom The Body Health Site

Update to Fuzeon (Enfuvirtide) Label Regarding Incidence of Bacterial Pneumonia http://bit.ly/j6NiEU #hiv #aids #t-20 #fda

1 year ago...

UPDATE 1-Vivus to submit Qnexa application as limited indication, shares up | Reuters

reuters.com — “* Says decided goals of Qnexa study with FDA * Plans to resubmit Qnexa marketing approval in Q4 as lmtdindication * Q1 loss per shr $0.12 vs est $0.15 * Shares up 6 pct after-market (Follows alerts)View full resource at reuters.com

  • View Related
  • Share

Most Recently Shared on May 3, 2011 at 11:19 am By:

JohnCFierce John Carroll Health Communicator

Vivus shares got a little boost with its plan to submit a new, much more narrowly defined app for its obesity drug. http://reut.rs/j4eUxT

1 year ago...

Medical News: FDA Updates PML Risk Info for Natalizumab - in Neurology, Multiple Sclerosis from MedPage Today

medpagetoday.com — “As expected, the FDA has approved new label language for the multiple sclerosis drug natalizumab (Tysabri) with additional detail on the risks of progressive multifocal leukoencephalopathy (PML).View full resource at medpagetoday.com

  • View Related
  • Share

Most Recently Shared on April 22, 2011 at 8:31 pm By:

CMS Wants To 'Refresh' Health Plan Information on Healthcare.gov - iHealthBeat

ihealthbeat.org — “CMS is asking the White House Office of Management and Budget to quickly review its plan to collect updated information from health insurance companiesfor the Healthcare.gov website. The website, mandated by the federal health reform law, aims to provide consumers with information about their health plan options. Modern Healthcare.View full resource at ihealthbeat.org

  • View Related
  • Share

Most Recently Shared on March 28, 2011 at 7:04 pm By:

iHealthBeat iHealthBeat.org Health Organization

CMS Wants To 'Refresh' Health Plan Information on Healthcare.gov - http://bit.ly/hGI0jM

1 year ago...

Radient Pharmaceuticals Receives Update EU Certification | IVD Technology

ivdtechnology.com — “Radient Pharmaceuticals Corp. (RPC) has received CE Mark approval from the European Union (EU) for the use of its Onko-Sure IVD cancer test as a pan tumor marker for cancer.View full resource at ivdtechnology.com

  • View Related
  • Share

Most Recently Shared on January 20, 2011 at 6:55 pm By:

ivdtechnology IVD Technology Health Magazine

Radient Pharmaceuticals Receives Update EU Certification http://tinyurl.com/4z68j54

1 year ago...

Advertisement