Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

EMA Recommends Granting a Marketing Authorisation for Ribociclib

In combination with letrozole, it is intended as initial endocrine based treatment of postmenopausal women with HR-positive, HER2-negative locally advanced or metastatic breast cancer
26 Jun 2017
Breast cancer;  Anticancer agents & Biologic therapy

On 22 June 2017, the European Medicines Agency’s (EMA’s) Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion, recommending granting a marketing authorisation for the medicinal product ribociclib (Kisqali), intended for the treatment of locally advanced or metastatic breast cancer. The applicant for this medicinal product is Novartis Europharm Ltd.

Kisqali will be available as 200-mg film-coated tablets.

The active substance of Kisqali is ribociclib, a protein kinase inhibitor (ATC code: L01XE42) that selectively inhibits cyclin-dependent kinase (CDK) 4 and 6. CDK4 and 6 are downstream of multiple signalling pathways which lead to cellular proliferation. 

The approval was based on a study showing that Kisqali in combination with letrozole (an aromatase inhibitor) significantly improves progression-free survival.

The most common side effects are neutropenia, leukopenia, headache, back pain, nausea, fatigue, diarrhoea, vomiting, constipation, alopecia and rash.

The full indication is: "Kisqali in combination with an aromatase inhibitor is indicated for the treatment of postmenopausal women with hormone receptor (HR) positive, human epidermal growth factor receptor 2 (HER2) negative locally advanced or metastatic breast cancer as initial endocrine based therapy".

It is proposed that Kisqali be prescribed by physicians experienced in the use of anticancer therapies.

Detailed recommendations for the use of this product will be described in the summary of product characteristics, which will be published in the European public assessment report and made available in all official European Union languages after the marketing authorisation has been granted by the European Commission.

Summaries of positive opinion are published without prejudice to the European Commission decision, which will normally be issued 67 days from adoption of the opinion.

Last update: 26 Jun 2017

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.