FDA gives fast-track review status to breast cancer drug

Organisation: Position: Deadline Date: Location:

The US Food and Drug Administration gave fast-track review status to Novartis’s medication ribociclib in first-line treatment of postmenopausal women with advanced breast cancer, as the Swiss company seeks to challenge Pfizer’s Ibrance drug.

Reuters Health reports that the company said ribociclib, or LEE011, was also accepted by the European Medicines Agency for review in use with letrozole in the same patient population.

The US priority review of LEE011 is based on data presented last month at a cancer conference. It showed patients with hormone-receptor positive, human epidermal growth factor receptor-2 negative (HR+/HER2-) advanced or metastatic breast cancer who took ribociclib with letrozole were 44% less likely to see their disease progress or to die versus those on letrozole alone.

“Priority Review allows a shorter review period compared with FDA standard review in the US, helping us to potentially bring LEE011 plus letrozole to patients more quickly,” said Bruno Strigini, the head of Novartis’s oncology business is quoted in the report as saying.

Eli Lilly’s abemaciclib is trailing in this race for new options to fight what is the most common form of breast cancer, after an independent panel in August had found the US company’s investigational medicine failed in combination with another drug to meet its interim effectiveness goal. Lilly is continuing its trial, the report said.

Reuters Health report

Receive Medical Brief's free weekly e-newsletter



Related Posts

Thank you for subscribing to MedicalBrief


MedicalBrief is Africa’s premier medical news and research weekly newsletter. MedicalBrief is published every Thursday and delivered free of charge by email to over 33 000 health professionals.

Please consider completing the form below. The information you supply is optional and will only be used to compile a demographic profile of our subscribers. Your personal details will never be shared with a third party.


Thank you for taking the time to complete the form.