Breast Cancer

U.S. FDA approves Aromasin for adjuvant treatment of early breast cancer in postmenopausal women

Published in Cancer Weekly, November 1st, 2005

Pfizer, Inc., has received approval from the U.S. Food & Drug Administration (FDA) to market Aromasin (exemestane tablets) for adjuvant treatment of postmenopausal women with estrogen-receptor positive early breast cancer following 2-3 years of tamoxifen for a completion of 5 consecutive years of adjuvant hormonal therapy.

The approval was based on the Intergroup Exemestane Study (IES) which showed that patients who switched to Aromasin after 2-3 years of tamoxifen, for a combined total of 5 years of therapy, had 31% more protection from cancer recurrence than those who remained on 5 years of tamoxifen therapy.

This landmark study, published in the...

Want to see the full article?

Purchase this article for only $3.00

We're a pay-per-view site for premium content. If you'd like to purchase this article, it's only $3.00.

Welcome to NewsRx!

Learn more about a six-week, no-risk free trial of Cancer Weekly

Source: Cancer Weekly (2005-11-01)

NewsRx is Social

Top Medical Newsletters

Awards

Best Health/Healthcare Content, 2012
Best Health/Healthcare Content, 2011
Best e-Business Site, 2010
Best e-Business Site, 2009
Best e-Business Site, 2008
Best e-Business Site, 2007
Best e-Business Site, 2006
Best Healthcare Content, 2005
Best Overall Internet Site, 2005
Best Interactive Site, 2005

Facts & Stats

NewsRx also is available at LexisNexis, Gale, ProQuest, Factiva, Dialog, Thomson Reuters, NewsEdge, and Dow Jones.

Google 2010 PageRank: #2 Among Top Health News and Media Publications
Google 2010 PageRank: #2 Among Top Science Publications in Biology/Physiology
Google 2010 PageRank: #2 Among Top News and Media for the Business of Pharmaceuticals
Amazon's Alexa 2010 PageRank: #2 News and Media Site for the Pharmaceutical Industry