Silver Spring, Maryland–(ENEWSPF)–December 22, 2016. The U.S. Food and Drug Administration has granted accelerated approval to Rubraca (rucaparib) to treat women with a certain type of ovarian cancer. Rubraca is approved for women with advanced ovarian cancer who have been treated with two or more chemotherapies and whose tumors have a specific gene mutation (deleterious BRCA) as identified by an FDA-approved companion diagnostic test.
“Today’s approval is another example of the trend we are seeing…
