Jump to content
RemedySpot.com

Tasigna approved by FDA

Rate this topic


Guest guest

Recommended Posts

WASHINGTON - A second-line drug to treat a life-threatening form of

leukemia has won federal approval, the Food and Drug Administration

said Monday.

Tasigna, known generically as nilotinib, won approval to treat chronic

and accelerated phase Philadelphia chromosome-positive, chronic

myeloid leukemia. The form of the blood cancer affects about 4,500

Americans a year.

FDA approval is specifically for use in patients who are resistant or

intolerant to previous treatment, including with another drug called

Gleevec also made by the Swiss pharmaceutical company Novartis AG.

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...