Nash Pharmaceuticals Announces Positive Pre-Clinical Results Showing Lead Compound NP-160 Significantly Reduces NALFD Score...
01 11월 2018 - 9:18PM
InvestorsHub NewsWire
Nash Pharmaceuticals Announces
Positive Pre-Clinical Results Showing Lead Compound NP-160
Significantly Reduces NALFD Score and Fibrosis in Non-Alcoholic
Fatty Liver Disease
Planning Phase II
Trial
Vancouver, BC -- November 01,
2018 -- InvestorsHub NewsWire -- Nash Pharmaceuticals Inc., a
wholly owned subsidiary of Breathtec Biomedical
Inc. (CSE: BTH) (CNSX: BTH) (FRANKFURT: BTI)
(OTCQB: BTHCF) (the
“Company” or “Nash Pharma”) is
pleased to announce that its lead compound for non-alcoholic
steatohepatitis (“NASH”) NP-160 showed positive results in a
recently completed study investigating its therapeutic effects in
the widely used STAM™ mouse model from SMC Laboratories. NP-160 is
one of a number of already approved compounds that Nash Pharma has
been screening for new therapeutic uses as part of its drug
repurposing strategy.
Data from this study
demonstrated statistically significant improvements in several key
measures relevant to the development and progression of NASH
including:
- A 2.0
reduction in the NAFLD/NAS score vs controls
(p<0.05)
- A 42.0%
reduction in fibrosis as measured by Sirius red staining
(p<0.01)
- In the
same study, Telmisartan (a well accepted control in NASH studies)
significantly reduced the NAS score by 2.0 points (p<0.05) and
reduced fibrosis by 19.7% (not statistically
significant)
- No
negative side effects were observed.
“The NASH market segment
represents an enormous unmet medical need globally and there is a
particular interest in compounds exhibiting anti-fibrotic
activity,” said Christopher J. Moreau CEO of Nash Pharma. “We plan
to present our preclinical in vivo NASH
results at the upcoming 2nd Global NASH Congress, in
February 2019 in London, UK and have now begun preparations to
start a Phase IIa study for our repurposed lead candidate NP-160 in
2019.”
About
NASH/NFLD
According to a new report
published by Allied Market Research, “Global Opportunity Analysis
and Industry Forecast, 2021-2025," the global NASH market was
valued at $1.17 Billion in 2017, and is expected to reach $21.4
Billion by 2025, growing at a CAGR of 58.4% from 2021 to 2025.
Currently, there are no US FDA approved treatments for NAFLD or
NASH.
About Nash
Pharmaceuticals Inc.
Nash Pharmaceuticals Inc. is
a wholly owned subsidiary of Breathtec Biomedical Inc. Nash
is a clinical stage pharmaceutical development company focused on
drug repurposing in the areas of non–alcoholic steatohepatitis
(NASH), chronic kidney disease (CKD) and inflammatory bowel disease
(IBD). Drug repurposing is the process of discovering new
therapeutic uses for existing drugs.
For more information,
visit https://nashpharmaceuticals.com/.
CONTACT
INFORMATION
Christopher J. Moreau
CEO
Nash Pharmaceuticals Inc.
604.398.4175 ext 701
info@breathtechbiomedical.com
investors@breathtecbiomedical.com
www.breathtecbiomedical.com
The CSE
does not accept responsibility for the adequacy or accuracy of this
release.
Neither the
Canadian Securities Exchange nor its Market Regulator (as that term
is defined in the policies of the Canadian Securities Exchange)
accepts responsibility for the adequacy or accuracy of this
release. The Canadian Securities Exchange has not in any way passed
upon the merits of the proposed transaction and has neither
approved nor disapproved the contents of this press
release.
CAUTIONARY DISCLAIMER
STATEMENT: No Securities Exchange has reviewed nor accepts
responsibility for the adequacy or accuracy of the content of this
news release. This news release contains forward-looking statements
relating to product development, licensing, commercialization and
regulatory compliance issues and other statements that are not
historical facts. Forward-looking statements are often identified
by terms such as “will”, “may”, “should”, “anticipate”, “expects”
and similar expressions. All statements other than statements of
historical fact, included in this release are forward-looking
statements that involve risks and uncertainties. There can be no
assurance that such statements will prove to be accurate and actual
results and future events could differ materially from those
anticipated in such statements. Important factors that could cause
actual results to differ materially from the Company’s expectations
include the failure to satisfy the conditions of the relevant
securities exchange(s) and other risks detailed from time to time
in the filings made by the Company with securities regulations. The
reader is cautioned that assumptions used in the preparation of any
forward-looking information may prove to be incorrect. Events or
circumstances may cause actual results to differ materially from
those predicted, as a result of numerous known and unknown risks,
uncertainties, and other factors, many of which are beyond the
control of the Company. The reader is cautioned not to place undue
reliance on any forward-looking information. Such information,
although considered reasonable by management at the time of
preparation, may prove to be incorrect and actual results may
differ materially from those anticipated. Forward-looking
statements contained in this news release are expressly qualified
by this cautionary statement. The forward-looking statements
contained in this news release are made as of the date of this news
release and the Company will update or revise publicly any of the
included forward-looking statements as expressly required by
applicable law.
Breathtec BioMedical Inc. (CSE:BTH)
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부터 1월(1) 2025 으로 2월(2) 2025
Breathtec BioMedical Inc. (CSE:BTH)
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부터 2월(2) 2024 으로 2월(2) 2025