August 19, 2022 – BD has announced the start of enrollment in a first-in-human trial of a peripheral sirolimus drug-coated balloon (DCB).
BD is a pioneer in DCB technology as the first to gain U.S. FDA approval for a paclitaxel DCB. BD’s Lutonix™, which received FDA approval in 2014, is celebrating its 10-year anniversary globally this year. Over this time, BD has continued to innovate and lead in DCB technology with advancements such as additional indications, lower sheath profile, longer treatment lengths, and additional guidewire configurations. Today, DCBs remain a broadly accepted endovascular interventional treatment option for patients with peripheral arterial disease (PAD) of the femoropopliteal artery.
“PAD impacts more than 200 million people across the globe and is often associated with morbidity, functional declines and higher health care costs.1 BD is committed to delivering much-needed solutions to address these challenges,” said Paddy O’Brien, Worldwide President of BD Peripheral Intervention. “The launch of our PREVISION first-in-human study demonstrates our ongoing commitment to advancing the drug coated balloon category. It marks an important milestone on the path towards bringing this technology to clinicians and patients around the globe.”
The PREVISION trial is a prospective, multicenter, single arm, non-randomized study designed to evaluate the safety of the BD sirolimus DCB in the treatment of peripheral arterial disease in the femoropopliteal arteries.
BD initiated this trial to determine the viability of sirolimus as a future treatment option for patients with PAD. The first patient was successfully treated by Dr. Andrew Holden, principal investigator at Auckland City Hospital, New Zealand.
“It is an honor to enroll the first patient in the PREVISION study,” said Dr. Holden. “The burden of PAD continues to impact patients and challenge physicians around the globe. A continued focus on developing next-generation technology is important for the patients suffering from PAD.”