| FDA Calendar Updates: CTIC, ALKS, AMLN, LLY | | Print | |
| Written by Mike Havrilla |
| Tuesday, 05 May 2009 11:36 |
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Amylin Pharma (NASDAQ:AMLN), Eli Lilly (NYSE:LLY), and Alkermes (NASDAQ:ALKS) announced today that a NDA was filed for FDA approval of a once-weekly version of exenatide (Byetta LAR) as once weekly formulation for type 2 diabetes which is administered by subcutaneous injection. The companies previously announced that an analysis of clinical trial databases showed no increased risk of heart-related side effects in patients taking standard Byetta as new diabetes treatments have come under closer scrutiny by the FDA recently. Cell Therapeutics (NASDAQ:CTIC) announced today that pixantrone is available on a named-patient basis for use in Europe to treat patients with aggressive non-Hodgkin's lymphoma (NHL) that has either relapsed or is refractory to standard treatment options. On 4/14/09, CTIC began a rolling submission of a NDA to the FDA for pixantrone to treat relapsed or refractory aggressive non-Hodgkin's lymphoma (NHL). CTI expects to complete the submission during 2Q09 and will request priority review (six month) which if granted could lead to an approval decision from the agency during 4Q09. Disclosure: No positions. BiomedReports is not paid or compensated to report news and developments about publicly traded companies. Full disclosure can be read at the bottom of / About Us / Section Add this page to your favorite Social Bookmarking websites
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| Last Updated on Wednesday, 06 May 2009 06:50 |
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