The world's largest RCT investigating use of MagicTouch PTA Sirolimus Coated balloon for peripheral artery disease kicks off to a flying start
PR86498
ZURICH, Nov. 9, 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 SirPAD (Sirolimus in Peripheral Artery Disease) trial.
is the first All-Comer randomized controlled clinical trial (RCT) investigating major
adverse limb events in PAD patients with lesions below the inguinal ligament.
SirPAD (https://www.conceptmedical.com/press-release/the-worlds-largest-rct-investigating-use-of-magictouch-pta-sirolimus-coated-balloon-for-peripheral-artery-disease-kicks-off-to-a-flying-start/ ) is investigator-initiated, single-center, randomized, non-inferiority, open-label clinical
trial investigating whether the use of MagicTouch PTA (https://www.conceptmedical.com/product/magic-touch-pta/ )
sirolimus-coated balloon catheters in patients with peripheral artery disease of the
femoro-popliteal or below-the-knee segment is not inferior to that of uncoated
balloon catheters for major clinical outcomes (unplanned major amputation,
target limb re-vascularization). Total of 1200 patients are to be randomized
1:1 (600 patients per treatment group).
The primary objective is to evaluate whether the use of sirolimus-coated
balloon catheters (MagicTouch PTA) (https://www.conceptmedical.com/product/magic-touch-pta/ )
is non-inferior touncoated balloon catheters in infra-inguinal angioplasty to prevent one-year
major adverse limb events (MALE), including unplanned major amputation of the
target limb and target lesion re-vascularization for critical limb ischemia, in a representative
population of patients with PAD (`all-comers`). If the criterion for non-inferiority is confirmed,
the study will test whether sirolimus-coated catheters (MagicTouch PTA)
(https://www.conceptmedical.com/product/magic-touch-pta/ ) are superior to
uncoated catheters for important secondary outcomes and for the primary outcome
itself according to pre-specified criteria for hierarchical analysis.
The index patient was successfully enrolled on 3rd November 2020 in
University Hospital Zurich.
The study is initiated by Prof. Dr. med Nils Kucher (also the Principal Investigator)
in charge of the Clinic of Angiology at the University Hospital Zurich, Switzerland.
Prof. Dr. med Nils Kucher was excited to initiate the study and said, "Over
the past decade, a few RCTs have compared the efficacy and safety of
drug-coated (mainly paclitaxel-coated) devices vs. that of uncoated ones, and
demonstrated a significant reduction in restenosis rates, late lumen loss, and
incidence of target lesion re-vascularization. However, the size of these
trials was often too small to draw firm conclusions concerning major clinical
outcomes. Moreover, substantial heterogeneity of the study populations and too
restrictive eligibility criteria limited their external validity, leading to a
difficult interpretation of the results of meta-analyses. Indeed, these trials
adopted surrogate (and rather subjective) outcomes as the primary outcome, such
as vessel patency and target limb re-vascularization, which may be difficult to
objectively judge in the setting of an open-label trial, rather than ´hard´
objective clinical endpoints, such as major amputation or urgent
revascularization due to critical limb ischemia. The aim of the SirPAD trial is
to compare the efficacy, as defined by a composite of clinically relevant
non-subjective 'hard' outcomes (major amputation and target lesion
re-vascularization for critical limb ischemia), of sirolimus-coated vs.
uncoated balloon angioplasty for peripheral artery disease in patients."
Photo:
https://mma.prnewswire.com/media/1329810/Enrolment_of_the_first_patient_in_the_SirPAD.jpg
Logo: https://mma.prnewswire.com/media/1244676/Concept_Medical_Logo.jpg
Source: Concept Medical Inc.
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