Rubraca® Approved for Indications in the U.S.

If in the U.S. learn more about Rubraca by visiting the product website or by downloading prescribing information.

Rubraca Authorized for Indication in the EU

If a healthcare provider in the EU, for more information see news release. 

Medical Information - Adverse Events or Product Quality Complaints

In the U.S., to report an adverse event related to use of a Clovis product, or if you have a product quality complaint, please contact the Medical Information department at 1-415-409-7220 (US toll), 1-844-CLVS ONC (1-844-258-7662; US toll-free), by email at medinfo@clovisoncology.com, or by using our website at clovismedicalinformation.com.

In Europe, to report an adverse event related to use of a Clovis product, or if you have a product quality complaint, please contact the Medical Information department at +44 (0)3301 004723 (UK toll), +44 (0)800 0093361 (UK toll-free), by email at medinfo.GB@clovisoncology.com.