Kane Biotech Receives Funding Support to Expand the revyve™ Antimicrobial Wound Gel Family
August 13 2024 - 8:30AM
Kane Biotech Inc. (TSX- V:KNE; OTCQB:KNBIF) (“Kane Biotech”, “Kane”
or the “Company”) announces that it is receiving advisory services
and up to $200,000 in research and development funding from the
National Research Council of Canada Industrial Research Assistance
Program (“NRC IRAP”).
The funding will be received over a period of 20 months and will
support the development of three additional products to build on
Kane Biotech’s revyveTM Antimicrobial Wound Gel technology. The
Company expects to be able to leverage its newly expanded US Food
and Drug Administration (“FDA”) 510(k) clearance for its revyveTM
Antimicrobial Wound Gel.
(1) |
revyveTM Antimicrobial Wound Gel Spray: Will provide ease of use
and is optimized for sensitive wounds like first-second degree
burns and venous leg ulcers (VLU). The patent pending Gel Spray
will allow for contact-free application and removal and will
command a higher price per ounce. |
(2) |
revyveTM Antimicrobial Wound
Cleanser: Intended for mechanical cleansing and removal of debris
and foreign material from diabetic foot ulcers (DFU), venous leg
ulcers (VLU), pressure ulcers (PU), first-second degree burns, skin
grafts, and donor sites. Sales targets will be hospitals, ASC,
(ambulatory surgery centers), physician offices and HOPD settings
where these types of cleansers are used every day. The Wound Rinse
has the potential to become Kane’s highest volume product in the
revyveTM Antimicrobial Wound Care family. |
(3) |
Antimicrobial Surgical Gel: A
sterilized version of the revyve™ gel for surgical/acute wounds.
The product will be applied to all types of surgical wounds and can
be used prophylactically on post-surgical incisions as well.
Although hospital operating room settings are the initial target
for this application, ASC (ambulatory surgery centers), physician
offices and HOPD settings are also potential markets. Being
sterile, the Surgical Gel will command a significant higher price
per ounce. |
“We made the strategic decision to ensure that revyveTM fits
within reimbursement as the products are being delivered to
patients. These product line extensions will provide either higher
price points or higher volumes which will drive our ability to
rapidly scale our revenues,” said Marc Edwards, President &
CEO. “I would like to thank NRC IRAP for their past and ongoing
support of Kane’s research and development.”
Prior support from NRC IRAP has significantly contributed toward
the development of Kane Biotech’s quality program infrastructure
which led to the Company reaching key milestones in its domestic
and global commercialization strategy including ISO 13485:2016
certification, US FDA 510(k) clearance of revyveTM and most
recently its ISO 13485:2016 Medical Device Single Audit Program
(MDSAP) Quality Certification.
About Kane Biotech
Kane Biotech Inc. is a biotechnology company
engaged in the research, development and commercialization of
technologies and products that prevent and remove microbial
biofilms. Kane has a portfolio of biotechnologies, intellectual
property (68 patents and patents pending, trade secrets and
trademarks) and products developed by Kane's own biofilm research
expertise and acquired from leading research institutions.
DispersinB®, coactiv+™, coactiv+®, DermaKB™, DermaKB Biofilm™, and
revyve™ are trademarks of Kane Biotech Inc. Kane is listed on the
TSX Venture Exchange under the symbol "KNE" and on the OTCQB
Venture Market under the symbol “KNBIF”.
For more information:
|
|
Marc
Edwards |
Ray Dupuis |
Chief Executive Officer |
Chief Financial Officer |
Kane Biotech Inc |
Kane Biotech Inc |
medwards@kanebiotech.com |
rdupuis@kanebiotech.com |
Neither TSX Venture Exchange nor its Regulation
Services Provider (as that term is defined in policies of the TSX
Venture Exchange) accepts responsibility for the adequacy or
accuracy of this release.
Caution Regarding Forward-Looking
InformationThis press release contains certain statements regarding
Kane Biotech Inc. that constitute forward-looking information under
applicable securities law. These statements reflect
management’s current beliefs and are based on information currently
available to management. Certain material factors or assumptions
are applied in making forward-looking statements, and actual
results may differ materially from those expressed or implied in
such statements. These risks and uncertainties include, but are not
limited to, risks relating to Kane’s: (a) financial condition,
including lack of significant revenues to date and reliance on
equity and other financing; (b) business, including its early stage
of development, government regulation, market acceptance for its
products, rapid technological change and dependence on key
personnel; (c) intellectual property including the ability of Kane
to protect its intellectual property and dependence on its
strategic partners; and (d) capital structure, including its lack
of dividends on its common shares, volatility of the market price
of its common shares and public company costs. Further information
about these and other risks and uncertainties can be found in the
disclosure documents filed by Kane with applicable securities
regulatory authorities, available at www.sedarplus.ca. Kane
cautions that the foregoing list of factors that may affect future
results is not exhaustive.
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