Upcoming Login Downtime

We're updating the Biocentury.com platform login experience to make access more secure and reliable. As part of this update, logins will be temporarily unavailable on Sunday, March 16, from 4:00AM to 4:00PM GMT. We recognize the inconvenience and appreciate your understanding. Please check back after the maintenance period.

For updates, questions, or issues, please call us at +1 650-552-4224 or email us at support@biocentury.com.

BioCentury
ARTICLE | Product Development

March 23 Quick Takes: Venclexta combo hits in AML; plus Jardiance rebuffed, Zolgensma approved in Japan and Zealand-Boehringer

March 23, 2020 11:14 PM UTC

Partners Roche (SIX:ROG; OTCQX:RHHBY) and AbbVie Inc. (NYSE:ABBV) said Venclexta venetoclax plus azacitidine significantly improved overall survival and composite complete remission rate among acute myelogenous leukemia (AML) patients in the Phase III VIALE-A trial, compared with placebo plus azacitidine. Venclexta has accelerated approval from FDA in combination with azacitidine, decitabine or low-dose cytarabine to treat AML; a Venclexta/cytarabine combination failed to significantly improve OS in the Phase III VIALE-C trial, AbbVie announced Feb. 28. Venclexta is a small molecule inhibitor of BCL-2 (see “Growing Options”).

FDA has issued a complete response letter for an sNDA for Jardiance empagliflozin from Boehringer Ingelheim GmbH and Eli Lilly and Co. (NYSE:LLY) to treat Type I diabetes as an adjunct to insulin. In November, FDA’s Endocrinologic and Metabolic Drugs Advisory Committee voted 14-2 that available data do not support approval of the SGLT2 inhibitor. The drug is approved in Type II diabetes...

Get Unlimited Access
Continue reading with a free trial.
Or Purchase This Article