Signum Surgical Granted FDA De Novo Clearance for BioHealx™
July 08 2024 - 1:00AM
Business Wire
- Novel surgical option for the treatment of anal fistula, a
painful and debilitating colorectal condition
- Milestone follows recent completion of clinical trial
evaluating the safety and efficacy of the device
- FDA clearance paves the way for BioHealx™
commercialization
Signum Surgical (‘Signum’ or ‘the Company’), a medical
technology company developing innovative solutions to treat
colorectal diseases, is pleased to announce that its BioHealx™
technology has been granted marketing clearance by the U.S. Food
and Drug Administration (FDA), as a first-of-its-kind medical
device for the treatment of anal fistula.
Anal fistulas are a painful colorectal condition affecting one
in 5,000 people worldwide1. In the United States, over 90,000
surgeries are performed annually to treat anal fistulas2. Current
treatment options are often unsuccessful, which frequently result
in inadequate or slow healing, a high risk of incontinence, and
repeat procedures. Developed in collaboration with expert
colorectal surgeons, BioHealx™ is a single use, bioabsorbable
implant used to treat anal fistula in a minimally invasive
procedure. BioHealx™ is designed to close the internal opening of
the fistula tract via tissue apposition and dissolve in the body
after treatment. The single-operation approach is designed to
promote healing, prevent fistula recurrence, and protect patient
continence.
The De Novo classification and clearance by the FDA, represents
a significant milestone for Signum and follows the completion of a
single-arm, non-randomized, clinical trial in 2023 designed to
evaluate the safety and efficacy of BioHealx™. The multi-centre
clinical trial, led by four investigators in Hungary, treated a
total of 32 patients (both male and female adults) who had
experienced recurrent anal fistula from at least one previous
failed treatment. Final follow up assessments have been completed
on the 32 patients over a period ranging from 13 to 40 months.
Peter Ónody, Colorectal Surgeon and Principal Investigator of
the clinical trial, commented: “I am excited at the potential
of BioHealx as a novel surgical option for the treatment of anal
fistula and, in particular, its ease of use for physicians. This
treatment has the potential to eliminate the need for multiple
surgeries and substantially reduce surgical trauma and the rate of
fistula recurrence, while reducing costs for patients and the
overall health care system.”
Moshe Zilversmit, Co-Founder and CEO of Signum Surgical,
commented: “We are proud to develop BioHealx, now an FDA De
Novo cleared medical device for the treatment of anal fistula. This
is a significant milestone for our business and an important step
to bring this novel treatment to market for the benefit of
patients, surgeons, and the healthcare system. We are currently in
discussions with potential strategic commercialization partners to
explore how to rapidly and efficiently make the BioHealx solution
available to patients. FDA clearance for BioHealx™, which is
protected by our growing intellectual property portfolio, continues
our strong momentum in addressing the unmet clinical need for the
treatment of anal fistula.”
Dr Bernard Collins, Investor Director, commented: “Signum
Surgical’s innovative BioHealx technology addresses a major unmet
clinical need in colorectal care and specifically for the
significant patient population suffering with anal fistula. In
excess of 90,000 surgeries are performed annually in the United
States alone to treat this debilitating condition, however current
treatment options are often unsuccessful and there is a high risk
of repeat procedures. With strong investor interest in Signum
Surgical, FDA De Novo clearance is another transformative step for
Moshe, Eoin and the team, and marks further progress towards
bringing BioHealx to market in the near future for the benefit of
patients and physicians.”
About Signum Surgical
Headquartered in Galway, Ireland, Signum Surgical is an ISO
13485 certified medical technology company focused on developing
innovative solutions to treat colorectal diseases, starting with
anal fistula, a painful and debilitating condition that severely
affects patients’ quality of life. Current treatments often fail to
successfully address this condition. With its BioHealx™ device,
Signum Surgical has developed a minimally invasive technology that
offers a breakthrough for these patients. Having explored
gastrointestinal and colorectal care, and identified an unmet need
of this patient population, Eoin Bambury and Moshe Zilversmit
founded Signum Surgical in 2016 as a spin-out of the National
University of Ireland BioInnovate programme.
Signum Surgical successfully raised €5.5 million in equity in
two investment rounds to support its clinical and regulatory
programs. In addition, Signum received €3.6 million in 2019 through
two non-dilutive grant funding awards from the European Union
Horizon 2020 SME Instrument and Ireland’s Disruptive Technologies
Innovation Fund (DTIF). The Company’s equity shareholders include
Halo Business Angel Network’s MedTech Syndicate who served as lead
investor in both funding rounds, as well as Enterprise Ireland, the
Western Development Commission, Rising Tide Europe and other
medical device industry angel investors.
For more information, please visit
https://www.signumsurgical.com
About Anal Fistula
Anal fistula is a painful colorectal condition that affects one
in 5,000 people.1 In most cases, patients will develop an anal
fistula, due to an infected anal gland that, when left untreated
will abscess and burrow through the patient’s sphincter muscle.
Anal fistulas cause a host of unpleasant symptoms that hamper
patients’ quality of life, such as swelling and discharge of blood
or pus from the anus. Current standard of care treatments,
including seton placement or fistulotomy surgery, involve the
opening or cutting of the channel to reach the fistula, followed by
draining or scraping and flushing out the infected tissue. These
treatments are often unsuccessful and can result in inadequate or
slow healing, a high risk of incontinence, and repeat
procedures.
1 Ommer A et al: Clinical practice guideline: Cryptoglandular
anal fistula Deutsches Arzteblatt International 2011; 108(42):
707–13.
https://www.researchgate.net/publication/51826318_Cryptoglandular_Anal_Fistulas
2 Zanotti, C., Martinez-Puente, C., Pascual, I. et al. Int J
Colorectal Dis (2007) 22: 1459
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FTI Consulting Paddy Berkery / Rugile Nenortaite Tel:
+353 86 602 5988 / +353 86 277 9905 Email:
signumsurgical@fticonsulting.com