FDA approves Gleevec for expanded use in patients with rare gastrointestinal cancer

The U.S. Food and Drug Administration today granted Gleevec (imatinib) regular approval for use in adult patients following surgical removal of CD117-positive gastrointestinal stromal tumors (GIST). Today’s action also highlights an increase in overall patient survival when the drug is taken for 36 months rather than the standard 12 months of treatment.
Read More

Related News:

  1. FDA approves Sutent for rare type of pancreatic cancer
  2. FDA approves Inlyta to treat patients with a type of advanced kidney cancer
  3. FDA approves new test to help determine if breast cancer patients are candidates for Herceptin treatment
  4. NIH study finds experimental drug benefits patients with rare type of cancer
  5. FDA approves new treatment for rare type of pancreatic cancer

Leave a Reply

Your email address will not be published. Required fields are marked *

*

*

You may use these HTML tags and attributes: <a href="" title=""> <abbr title=""> <acronym title=""> <b> <blockquote cite=""> <cite> <code> <del datetime=""> <em> <i> <q cite=""> <strike> <strong>