Claritas Pharmaceuticals, Inc. (TSX VENTURE: KLY and OTC: KALTF)
(the "
Company" or "
Claritas")
today announced that it has signed a Letter of Intent dated January
17, 2022 (the
“LOI”) with Salzman Group, Inc. (a
Delaware corporation), Salzman Group, Ltd. (an Israeli
corporation), and Salzman Group Pty. Ltd. (an Australian
corporation), (collectively, the
“Salzman
Group”), under which Salzman Group will grant to Claritas
an exclusive, worldwide license to develop and commercialize R-107
for the treatment of skin ulceration and wound healing, including
the treatment of severe burns.
Highlights
- R-107 has
potential to be a revolutionary new treatment for severe
burns
- Claritas
will apply for Orphan Drug Designation for R-107 in treatment of
severe burns in pediatric patients
- Claritas
expects to commence a Phase 2a Clinical Study of
R-107 in pediatric patients with severe burns in
2H 2022
- The
worldwide market for an effective treatment for severe burns could
exceed $1 billion annually
R-107 is a liquid, nitric oxide-releasing
molecule with issued and pending composition of matter and method
of use patents in approximately 40 countries, including the U.S.,
Australia, Brazil, China, Europe, India, Japan, Russia and South
Korea.
Claritas previously licensed R-107 from Salzman
Group for the treatment of both COVID-related lung disease and
non-COVID pulmonary diseases. In accordance with the LOI, and
subject to the approval of the TSX Venture Exchange, Claritas will
enter into a new license agreement with Salzman Group for the
development and commercialization of R-107 for the treatment of
skin ulceration and wound healing, including the treatment of
severe burns (the “License”). The Company expects
to enter into the License by mid-February 2022.
Naturally produced nitric oxide participates in
the wound healing process by stimulating the synthesis of collagen,
triggering the release of chemotactic cytokines, increasing blood
vessels permeability, promoting angiogenic activity, stimulating
the release of epidermal growth factors, and by interfering with
the bacterial mitochondrial respiratory chain.
“Based on extensive research with nitric oxide
in treatment of burn wounds, we believe that R-107 is an
extraordinary product candidate for the treatment of severe burns,"
said Robert Farrell, President and CEO of Claritas. “There is an
important unmet medical need for a viable treatment to help
patients heal from life-threatening severe burns, and we believe
that R-107 will address this unmet need."
"Severe burns represent some of the most
horrific injuries a human can endure," said
Perenlei Enkhbaatar, MD, PhD., FAHA, a member of Claritas’
board of directors and an internationally renowned authority and
leader on the biology and pathophysiology of nitric oxide. "In
spite of major advances in burn care, we have reached a limit in
our ability to heal severe burns with currently available products.
Nitric oxide has been shown to promote tissue repair and healing in
animal models of acute burn wounds, and nitric oxide-releasing
R-107 may overcome the difficulties and limitations encountered
with direct administration of nitric oxide itself.”
Nitric Oxide
Nitric oxide is produced by virtually
every cell type in the body and plays an important
role in controlling the normal function of cells. It has been
demonstrated that this ubiquitous, naturally occurring molecule
plays an important role throughout the body. Recent studies have
demonstrated the effectiveness of nitric oxide as a potential
therapy in the treatment of skin ulceration and burn wounds,
including the treatment of severe burns.
Nitric Oxide-Releasing
R-107 in Treatment of Severe
Burns
Nitric oxide gas has been shown to play a
significant role in the promotion and regulation of diverse wound
healing processes, including burn wounds.1 For example, nitric
oxide has been shown to enhance angiogenesis, epithelial cell
migration, collagen synthesis, and wound closure.2 These cellular
and physiological responses all suggest that nitric oxide plays a
critical role in the overall wound healing process; and studies
involving the application of nitric oxide further support its
potential utility for wound healing and tissue repair and
regeneration.3 4
Nitric oxide has also been shown to promote tissue repair and
healing in animal models of diabetic ulcers and skin lacerations,
as well as in acute burn wound models.5 6 For example, the
application of a nitric oxide containing gel to full thickness
burns in a rodent model has shown significant improvements in the
rate of healing (wound closure) and re-epithelization.7 8Wound
closure is of critical importance in this setting to promote
healing and to reduce the risk of a variety of infections,
including sepsis.910
However, most studies of nitric oxide in wound
healing have involved topical application of gels designed to
stimulate the body’s own natural production of nitric oxide, and
thus generate only minute amounts of nitric oxide locally.
Direct delivery of therapeutically relevant
doses of nitric oxide gas to the wound site has been accomplished,
although this method is complicated by nitric oxide’s instability
in air and the difficulty of delivering it in a clinical
setting.
R-107 potentially provides a more rational
approach to nitric oxide-based wound healing treatment:
- Unlike gels that stimulate the
body’s own natural production of nitric oxide, and thus generate
only minute amounts of nitric oxide locally, R-107 is a nitric
oxide-releasing molecule that delivers sustained and sufficiently
high levels nitric oxide.
- Unlike direct delivery of nitric
oxide gas to the wound site, which is complex and difficult to
accomplish in a clinical setting, R-107 can be formulated as a
topical liquid or gel that will provide a means for convenient,
practical, sustained, and safe administration.
- R-107 has a major effect on
vasodilation, and thus increases perfusion and microcirculatory
blood flow into the wound site.11 12This is crucial because wounds
have a nitric oxide deficiency, and blood flow is impaired. R-107
will greatly increase perfusion and this will help speed up the
healing process.
- R-107 is a potent antioxidant.
Specifically, it degrades superoxide, hydrogen peroxide, and
peroxynitrite. These are formed in abundance in wounds and are a
major reason for poor epithelialization and wound closure. Standard
nitric oxide donors are helpful, but they also result in production
of peroxynitrite when the nitric oxide that they deliver reacts
with superoxide in the wound. R-107 uniquely does not form
peroxynitrite. Hence its advantage over all other nitric oxide
donor molecules.
- R-107 releases nitric oxide that is
a potent antibacterial and is expected to reduce wound site
bacterial colonization, which is currently a major impediment to
timely wound healing and closure.
- R-107 does not develop tolerance,
like other organic nitrates. This is a unique attribute of R-107
and it is crucial because the drug must be given repeatedly for at
least 3 weeks.
- R-107 is expected to be safe if it
is absorbed at the wound and enters the systemic circulation. This
is important because other agents used to treat wounds (such as
silver nitrate) are toxic if absorbed into the circulation.
- It is common for severe burn
patients to receive autologous skin grafts, wherein healthy skin is
removed from a donor site on the patient’s body, and is used to
help close the wound at the site of the burn injury. R-107 will
play an important role in this setting, as it is expected to speed
up wound healing at both the site of the burn injury as well as at
the donor site.
To promote more rapid wound closure and prevent
infection at the burn wound site and at the donor skin graft site,
Claritas will develop R-107 for administration in both a liquid
solution formulation and in an ointment formulation. The R-107
liquid formulation will be a 10% solution of R-107 in PEG400 for
14-day irrigation of wound dressings for: (1) administration to
skin grafts after excision of full thickness burns; and (2)
administration to split-thickness skin donor sites. The R-107
ointment formulation will be a 10% solution of R-107 in PEG400/3500
ointment for subacute and chronic therapy of skin grafts after
excision of full thickness burns.
One of the most difficult long term-effects of a
severe burn is the hypertrophic scarring that occurs at the burn
wound site. Scarring is not only a cosmetic issue. Scarring also
causes contractures around joints, so that limbs and fingers can
become difficult or impossible to move, requiring surgery to
release such contractures. Burn wound site scarring is caused by
over-expression of collagen. Normally, nitric oxide suppresses
TGF-beta mediated stimulation of collagen expression. However, in a
burn wound, TGF beta is up-regulated, and causes over expression of
collage. Studies have demonstrated that nitric oxide suppresses
TGF-beta and thereby reduces the over-expression of collagen. For
example, when sodium nitroprusside, a nitric oxide donor, was
given, collagen expression was very strongly inhibited.R-107 in a
topical liquid or gel format has the potential to be used as a
first-line therapeutic for partial thickness burns, and also
potentially in wound healing for full thickness burns after
debridement and prior to skin grafting.
- Approximately 2.4 million people
per year in the United States are treated for burn injuries, with
650,000 of these cases requiring care by a medical professional and
75,000 requiring hospitalization.
- These patients represent one of the
most expensive catastrophic injuries to treat; a patient sustaining
burns over 30% of their total body surface may require upwards of
$200,000 in hospital, pharmaceutical, and primary care costs.
- By reducing the time to heal a burn
wound and protect against infection by using a single, inexpensive
and safe topical gel, patients can expect better healing outcomes,
shortened hospital stays and medical care duration, and reduced
cost for that care.
Claritas believes that nitric-oxide releasing
R-107 may provide significant improvements in the rate of burn
healing (wound closure) and re-epithelization, and a concomitant
reduction in hypertrophic scarring, leading to better patient
outcomes, reduced hospital stays, and diminished healthcare
costs.
Terms of the LOI
The LOI which Claritas has entered into with the
Salzman Group provides that Salzman Group will grant to Claritas an
exclusive, worldwide license (the “License”) to develop,
manufacture and commercialize R-107 for the treatment of skin
ulceration and wound healing, including the treatment of severe
burns (“Skin Ulcers and Wound Healing
Indications”).
Under the terms of the LOI, Claritas has agreed
to provide the following compensation to Salzman Group in
consideration for the License:
- Upon execution of the definitive License
agreement, Claritas will issue
1.2 million shares of
Claritas’ common stock to Salzman Group, Inc. Provided, however,
that Claritas will not issue any common shares to Salzman Group,
Inc. unless Salzman Group, Inc. and all affiliates certify that the
issuance of such common shares will not cause Salzman Group, Inc.
and its affiliates to beneficially own in excess
of 19.99% of the Company’s outstanding shares of common
stock;
- Claritas will pay cash license fees of
USD $12,300 to Salzman Group Pty. Ltd. and USD
$187,700
to Salzman Group Ltd. within 90 days of the execution of the
definitive License
agreement;
- Claritas will also pay to Salzman
Group, Inc. the following cash milestone payments
and royalties on net sales for Skin Ulcers and
Wound Healing Indications:
- USD $1 million
on successful completion
of a Phase
2 clinical study
of R-107 in the treatment of either
skin
ulcers or
wound
healing, including the
treatment of severe burns;
- USD $1.5 million
on successful completion
of a pivotal Phase
3 registration clinical
study of R-107 in the treatment of either
skin ulcers or wound healing, including the treatment of severe
burns;
- USD $5 million on FDA approval of
R-107 for the treatment of any one Skin Ulcer and
Wound Healing Indication;
- USD $5 million on EMEA
or MHRA approval of R-107
for the treatment of any one Skin Ulcer and Wound
Healing Indication;
- USD $5 million on Japanese
approval of R-107 for the treatment of any
one Skin Ulcer and Wound Healing
Indication;
- During the applicable term of any patent covering R-107
in the treatment of Skin Ulcer and Wound Healing
Indications, Claritas will pay to Salzman Group,
Inc. a royalty of five percent
(5%) of the net sales for all
R-107 products for the treatment of Skin Ulcers
and Wound Healing Indications
About Claritas
PharmaceuticalsClaritas Pharmaceuticals, Inc. is a
clinical stage biopharmaceutical company focused on developing and
commercializing therapies for patients with significant unmet
medical needs. Claritas focuses on areas of unmet medical need, and
leverages its expertise to find solutions that will improve health
outcomes and dramatically improve people's lives.
- Website
Home: https://claritaspharma.com/
- News and
Insights: https://claritaspharma.com/news/
-
Investors: https://claritaspharma.com/investors
Cautionary StatementsNeither
TSX Venture Exchange nor its Regulation Services Provider (as that
term is defined in the policies of the TSX Venture Exchange)
accepts responsibility for the adequacy or accuracy of this
release.
This press release may contain certain
forward-looking information and statements ("forward-looking
information") within the meaning of applicable Canadian securities
legislation, that are not based on historical fact, including
without limitation in respect of its product candidate pipeline,
planned clinical trials, regulatory approval prospects,
intellectual property objectives, and other statements containing
the words "believes", "anticipates", "plans", "intends", "will",
"should", "expects", "continue", "estimate", "forecasts" and other
similar expressions. Readers are cautioned to not place undue
reliance on forward-looking information. Actual results and
developments may differ materially from those contemplated by these
statements depending on, among other things, the risk that future
clinical studies may not proceed as expected or may produce
unfavorable results. Claritas undertakes no obligation to comment
on analyses, expectations or statements made by third parties, its
securities, or financial or operating results (as applicable).
Although Claritas believes that the expectations reflected in
forward-looking information in this press release are reasonable,
such forward-looking information has been based on expectations,
factors and assumptions concerning future events which may prove to
be inaccurate and are subject to numerous risks and uncertainties,
certain of which are beyond Claritas’ control. The forward-looking
information contained in this press release is expressly qualified
by this cautionary statement and is made as of the date hereof.
Claritas disclaims any intention and has no obligation or
responsibility, except as required by law, to update or revise any
forward-looking information, whether as a result of new
information, future events or otherwise.
Contact InformationRobert
FarrellPresident, CEO(888) 861-2008info@claritaspharma.com
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