Clovis’ PARP Drug Gets New US Ovarian Cancer Use
The FDA has granted Clovis Oncology’s rucaparib a new use in ovarian cancer, approving the PARP inhibitor as a maintenance therapy for women with recurrent disease.
This puts it on an even footing with rivals from AstraZeneca and Tesaro which already have this use approved.
Rubraca’s approval in the new indication, for women whose cancer has returned after responding to chemotherapy regardless of BRCA mutation status, comes weeks before a likely first approval in Europe.
The approval from the FDA and the likely EU approval following a backing from the European Medicines Agency’s CHMP regulatory committee point to a strong 2018 for Rubraca (rucaparib), which is the biotech’s only approved drug.
In the maintenance therapy indication Rubraca will be able to prescribed without need for a biomarker test, cutting costs and allowing its use in a wider patient group.
Rival poly (ADP-Ribose) polymerase (PARP) Inhibitor Drugs from AstraZeneca and Tesaro – Lynparza and Zejula – are already approved in the maintenance indication.
Both are approved without need for BRCA tests, although patients may find Zejula the more convenient of the three options as it is taken as a once daily pill, instead of twice daily like Lynparza and Rubraca.
Clovis added that on the basis of data from the ARIEL 3 trial, the FDA has also granted Rubraca regular approval in its existing use in advanced ovarian cancer, after two or more previous therapies.
Clovis CEO Patrick Mahaffy said: “This FDA approval provides a meaningful advancement for the treatment of women with recurrent ovarian cancer, offering them the potential to reduce their risk of disease progression following platinum-based chemotherapy.”
“We are grateful that the FDA expedited review of this maintenance treatment indication, so that physicians can begin offering it to appropriate patients.”
The drug has also been added to independent US national guidelines for treatment of ovarian cancer, drawn up by the National Comprehensive Cancer Network (NCCN) – giving doctors further reassurance about its use in advanced disease.
2026-07-21
Trade Alert
Delivering the latest product trends and industry news straight to your inbox.
(We'll never share your email address with a third-party.)
Related News
-
China’s Hybio Takes Generic Tirzepatide to FDA: Lilly’s GLP-1 Fortress Gets a Warning Shot
-
FDA approves bemotrizinol, a long-used UV filter, for U.S. sunscreens
-
FDA delays proposal to ban formaldehyde in hair straighteners
-
Can Florida's Authorization to Import Prescription Drugs from Canada Lower Medication Prices?
-
FDA Releases New Resources for Food Traceability Final Rule Compliance
-
IFSAC Unveils 2021 Report: Diverse Food Sources Linked to Salmonellosis Cases
-
FDA to Nationwide Ban Brominated Vegetable Oil (BVO) in Food
-
FDA Issues Warning to Produce Importer for Non-Compliance
-
FDA Proposes Ban on Hair Relaxers Containing Formaldehyde
-
US FDA Issues Alert: High Lead Levels Detected in Baby Fruit Puree
Recommend Reading
-
Weak Cost Support for Melamine, This Round of Minor Price Increase May Not Last
-
Costs Rise, Demand Increases—January Isooctanol Prices Surge
-
Supply Decreases and Demand Increases, DOP Prices Surge Significantly in January
-
Ammonium Sulfate Market Prices Steadily Rise (2.1-2.5)
-
Supply and Demand Loosening: Butyl Alcohol Prices Weaken in the First Week of February
-
Premium Global Chemical Sourcing Requests (31 Jan - 4 Feb, 2026)
-
Bullish Factors Support Continued Rise in Adipic Acid Prices in China
-
Costs Decline, Phthalic Anhydride Prices Soar and Then Plunge
-
A New Weapon Against Spider Mites: Canada Moves to Approve Novel Miticide for Greenhouse Growers
-
Raw material prices rise, this week phthalic anhydride prices in China have significantly increased