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FDA approves new dosing for Xarelto to reduce risk of VTE

Published 31 October 2017

Janssen Pharmaceuticals reported that 10mg once-daily dose of Xarelto (rivaroxaban) has been approved by the US Food and Drug Administration (FDA) for reducing the continued risk for recurrent venous thromboembolism (VTE) after at least six months of initial anticoagulation therapy.

This approval follows a FDA Priority Review and is based on data from EINSTEIN CHOICE, the only clinical study to find that a Factor Xa inhibitor, specifically XARELTO, demonstrates superior efficacy in reducing the continued risk of recurrent VTE and with major bleeding rates similar to aspirin.

VTE includes deep vein thrombosis (DVT), a blood clot in a deep vein (often the legs), and pulmonary embolism (PE), a clot that travels to the lung. It is the third most common cause of cardiovascular death worldwide, after heart attack and stroke.

"We believe the availability of the 10 mg XARELTO dose will change clinical practice and the management of VTE recurrence," said Paul Burton, MD, PhD, FACC, Vice President, Medical Affairs, Janssen.

"The landmark EINSTEIN program results yet again demonstrate XARELTO is a safe and highly effective option, not only for the initial treatment of a VTE, but also for the continued prevention of a recurrent event."

With this approval, the XARELTO prescribing information provides instructions for physicians to begin treatment with XARELTO 15 mg, dosed twice daily, for the first 21 days after a VTE occurrence. On day 22 through at least day 180, the daily dose decreases to XARELTO 20 mg once daily. After at least 180 days (6 months), physicians can prescribe XARELTO 10 mg once daily in patients at continued risk for DVT and/or PE.

"If anticoagulation therapy is stopped, up to 20 percent of patients will have a recurrent VTE within three years. To prevent this, physicians have long debated how best to extend anticoagulant use beyond the initial treatment window," said Jeffrey Weitz, MD, FRCP(C), FACP, Professor, Departments of Medicine and Biochemistry and Biomedical Sciences, McMaster University, and Executive Director, Thrombosis & Atherosclerosis Research Institute.

"The FDA's approval of the 10 mg dose of XARELTO for preventing recurrent VTE, along with clinical evidence confirming the superiority of XARELTO over aspirin for extended VTE prevention, means we can finally put this debate to rest."

The FDA's approval of the XARELTO 10 mg once-daily dose was based on the EINSTEIN CHOICE study results. The EINSTEIN CHOICE study evaluated patients with VTE who were already treated with six to 12 months of initial anticoagulation therapy and then received XARELTO 10 mg once daily, XARELTO 20 mg once daily or aspirin 100 mg once daily for up to an additional 12 months of treatment.

Patients taking either XARELTO dose had significantly fewer recurrent VTE compared to those taking aspirin. Specifically, XARELTO 10 mg reduced the risk of recurrent VTE by 74 percent and XARELTO 20 mg by 66 percent. All three treatment groups had low rates of major bleeding (0.4 percent with XARELTO 10 mg, 0.5 percent with XARELTO 20 mg, 0.3 percent with aspirin).

In September 2017, Janssen's development partner Bayer announced the Committee for Medicinal Products for Human Use of the European Medicines Agency granted a positive opinion to update the XARELTO label to include the 10 mg once-daily dose in the European Union; the European Commission granted approval on October 19, 2017.



Source: Company Press Release