Concept Medical announces index patient enrolment in world's first Randomized Controlled Trial with Sirolimus Coated Balloon for the treatment of SFA
Concept Medical announces index patient enrolment in world's first Randomized Controlled Trial with Sirolimus Coated Balloon for the treatment of Superficial Femoral Artery (SFA) in Peripheral Artery Disease
PR85583
SINGAPORE, Sept. 14, 2020 /PRNewswire=KYODO JBN/ --
Concept Medical Inc.[https://www.conceptmedical.com/ ], focused on vascular
intervention drug delivery devices, has announced the enrolment of the first
patient in the FUTURE SFA (Randomized Controlled Trial of First SirolimUs
CoaTed Balloon VersUs StandaRd Balloon Angioplasty in The TrEatment of
Superficial Femoral Artery and Popliteal Artery Disease).
The index patient was successfully enrolled on 11th September in Singapore.
FUTURE SFA [https://www.conceptmedical.com/press-release/future-sfa-enrolment/ ]
is a randomized, double blind, placebo-controlled, multi-center trial to determine
the effectiveness of MagicTouch PTA [https://www.conceptmedical.com/product/magic-touch-pta/ ]
sirolimus drug coated balloon versus standard percutaneous transluminal angioplasty for the
treatment of superficial femoral and popliteal arterial disease.
The burden of peripheral arterial disease (PAD) is high globally. Its
burden is likely to grow in the coming years given the rising trends in key
risk factors such as age and diabetes. In its most advanced stage, patients
present as critical limb ischemia (CLI) and many end up with leg amputations.
Current standard of care for severe PAD is revascularization, the majority
of which involves the use of balloon angioplasty to unblock the vessel and
restore blood flow to the leg. However, these vessels frequently become blocked
again, resulting in repeated procedures which is potentially dangerous and may
result in loss of limb or even life.
Local drug delivery using drug coated balloons (DCBs)
[https://www.conceptmedical.com/product/magic-touch-pta/ ] during
angioplasty can successfully deliver anti-proliferative drugs to the lesions in
the artery, with the aim of keeping the vessel open for longer. Sirolimus
coated balloons are considered to be the next new generation of DCBs and the
novel MagicTouch PTA[https://www.conceptmedical.com/product/magic-touch-pta/ ]
sirolimus coated balloon (SCB), has emerged as one of the most promising
transcatheter technologies in preventing restenosis for diseased arteries.
The principal investigator of FUTURE-SFA is Associate Professor Edward
Choke from the Department of General Surgery (Vascular Surgery) at the Sengkang
General Hospital, Singapore.
Associate Professor Edward Choke said, "I am inspired by the bold,
imaginative and futuristic concepts presented by the Nanolute
technology[https://www.conceptmedical.com/technology/nanolute/ ] of the
MagicTouch PTA sirolimus coated balloon. In contrast to other contemporary
technologies, MagicTouch PTA offers a solution which optimizes both the
deliverability and the absorption of sirolimus into the vessel wall."
He added, "Initial experience with the XTOSI first in man study suggested
that MagicTouch PTA can provide an effective way of revascularization for PAD
patients, by keeping the vessels open longer and reducing the need of repeated
angioplasty procedures. I look forward to the FUTURE-SFA randomized controlled
trial, which will test whether the Magic Touch PTA sirolimus coated balloon can
improve the patencies of femoral and popliteal arteries in PAD patients. We
hope to establish whether SCB will emerge as the new standard of care which
will impact the way we treat PAD."
The trial will enrol 153 patients with Rutherford class 3 to 6 PAD. These
subjects will be randomized in 2:1 fashion to receive either Magic Touch PTA or
standard balloon angioplasty.
Primary outcome will be primary patency at 6 months, defined as duplex peak
systolic velocity ratio (PSVR) of 2.4 or less.
The trial is designed to follow a rigorous blinding protocol in order to
minimise bias. Patients, care providers, investigators and outcome assessors,
including vascular technologists performing the duplex ultrasound, will be blinded
to the treatment allocations. The patients will be followed up for two years.
[NCT04511234 - Randomized Controlled Trial of First Sirolimus Coated
Balloon Versus Standard Balloon Angioplasty in The Treatment of Superficial
Femoral Artery and Popliteal Artery Disease (FUTURE-SFA)]
Photo: https://mma.prnewswire.com/media/1273493/Future_SFA_Enrollment.jpg
Caption: Enrolment of the first patient in the FUTURE SFA by Dr. Edward
Choke and his team at Sengkang General Hospital Singapore.
Logo: https://mma.prnewswire.com/media/1244676/Concept_Medical_Logo.jpg
Source: Concept Medical
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