Previous Page  15 / 21 Next Page
Information
Show Menu
Previous Page 15 / 21 Next Page
Page Background

30-05-18

19 December 2016: US FDA-accelerated approval

of

rucaparib monotherapy

for the treatment of

patients with deleterious BRCA mutation (

germline

and/or somatic; as detected by an FDA-approved

companion diagnostic for RUBRACA) associated

advanced ovarian cancer

who have been treated

with ≥2 chemotherapies

2

Study 10 and ARIEL2:

Rucaparib Monotherapy in g

BRCA

/s

BRCA-

Mutated Ovarian Cancer