Orthocell Secures New Patent for Suture-Less Repair of Soft Tissue
January 17 2018 - 7:33PM
Business Wire
- Australian patent granted for CelGro®
soft tissue reconstruction platform, which covers the method of
suture-less repair of soft tissue defects
- Suture-free repair of soft tissue has
potential to greatly improve the efficiency and efficacy of
surgical procedures such as tendon, ligament and nerve repair
- CelGro® represents a breakthrough in
soft tissue reconstruction and offers significant global commercial
potential in soft tissue and bone repair
Regenerative medicine company Orthocell Limited (ASX:OCC,
“Orthocell” or the “Company”) is pleased to announce it has been
granted a further Australian patent for its CelGro® collagen
medical device platform for soft tissue regeneration and repair
applications. The patent entitled “Suture-less repair of soft
tissue” provides additional important intellectual property to
protect the CelGro® product platform.
Orthocell Managing Director Paul Anderson said: “This is
an important addition to our current global IP portfolio. Not only
does it further strengthen our IP position in regenerative medicine
products and surgical techniques for soft tissue repair, but it
also acts to validate CelGro® as a collagen medical device
platform, for use across multiple indications including bone,
tendons, peripheral nerves and aid in the repair of spinal cord
injuries. This comes at a perfect time for the company as we move
our products through the registration processes in the US.”
The patent has an expiry date of 12 October 2035. This is the
first patent granted in the suture-less repair of tissue patent
family. Further patent applications are in progress in all major
jurisdictions including US, EU and Japan.
Suture-less repair of soft tissue refers to the method of
repairing damaged soft tissue without the use of stitches.
Suture-less repair has the potential to greatly improve the
efficiency and efficacy of surgical procedures by simplifying
techniques, reducing surgery time and reducing the risk of
additional trauma to soft tissue through the use of sutures.
Therefore, Orthocell’s patented method of suture-less repair
provides surgeons with an alternative to direct suture repair of
soft tissue defects within tendons, ligaments and nerves.
For example, in the US alone, over 20 million people suffer from
peripheral nerve injury as a result of motor vehicle, sporting or
work related incidents every year, at an annual cost of
approximately US$150 billion. Many of these injuries require
surgical nerve reconstruction involving the use of collagen
conduits that are secured in place using sutures. To address the
disadvantages of suturing, Orthocell developed the CelGro® collagen
medical device platform with handling characteristics to assist
surgeons in performing complex reconstructive surgical procedures
and enabling the suture-less repair of soft tissue defects.
CelGro®’s nerve addressable market is estimated to be worth more
than US$1.1 billion per annum, with approximately 700,000
procedures that could utilise CelGro® completed each year. Market
growth is expected to be underpinned by the surgeons’ preference
for quality and functional bio-absorbable membranes. The company
believes CelGro® represents a breakthrough in soft tissue
reconstruction and offers significant global commercial potential
in its existing addressable markets of bone, tendon, nerve and
cartilage as well as much wider applications in general surgical
and soft tissue reconstructive applications.
About CelGro®
CelGro® is a collagen medical device platform for soft tissue
regeneration and repair applications manufactured by Orthocell at
its quality controlled Good Manufacturing Practices (GMP) licensed
facility in WA.
Orthocell has received market authorisation (CE Mark) of CelGro®
collagen scaffold medical device in the EU for dental bone and soft
tissue applications. The CE Mark allows CelGro® to be sold within
EU countries, validates CelGro®’s quality manufacturing and product
performance, and provides a strong foundation for indication
expansion and regulatory approvals.
CelGro® has been shown to improve tissue in-growth and repair in
clinical studies using the collagen medical device to augment
repair of the rotator cuff tendon within the shoulder, to guide
bone regeneration within the jaw and to assist in the rejoining of
severed, or damaged peripheral nerves. CelGro® is a customisable
collagen medical device with numerous competitive advantages over
existing synthetic and biologic tissue repair devices, particularly
in the areas of cell compatibility, tensile strength and the
promotion of quality tissue in growth and repair.
Medical scaffolds are analogous to construction scaffolds in
that they provide integral support to the soft tissue whilst it
undergoes repair.
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General enquiriesOrthocell LimitedPaul
Anderson, +61 8 9360 2888Managing
Directorpaulanderson@orthocell.com.auorInvestor
enquiriesVesparum CapitalJoel Seah, +61 3 8582
4800orthocell@vesparum.comorMedia enquiriesWE
BuchanBen Walsh, +61 411 520
012bwalsh@buchanwe.com.au
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