VANCOUVER, British Columbia, Sept. 13, 2018 (GLOBE NEWSWIRE) -- Breathtec Biomedical
Inc. (CSE: BTH) (CNSX: BTH) (FRANKFURT: BTI) (OTCQB: BTHCF) (the “Company”) is pleased to provide details on Nash Pharmaceutical’s (“Nash
Pharma”) plans for the next 12 month period. Breathtec recently announced that it has signed a letter of intent (“LOI”) to acquire
100% of the shares of Nash Pharma. Nash Pharma 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).
Through its ongoing research programs, Nash Pharma has developed data that supports the advancement of up to 7
drug candidates into Phase II studies, with a number of the candidates outperforming current standard of care therapies when tested
in animal models.
“The addition of Nash Pharma’s technology and its focus on CKD and NASH is complimentary to Breathtec’s ongoing
program to develop a device for early screening for the same disease states,” says Christopher J. Moreau, CEO of Breathtec
Biomedical Inc. “We look forward to advancing our knowledge about these diseases and to leverage our expertise to help find markers
in the breath that can help screen for these diseases.”
Nash Business Model Overview
Nash Pharma’s business model is based on a drug repurposing strategy where previously approved drug candidates
are identified and rapidly screened for use in new diseases. If the data generated from pre-clinical in vivo animal
testing shows positive results, the drugs can be moved forward into Phase II clinical studies.
As a comparison, taking a new compound from the discovery stage though pre-clinical research and into human
trials, can cost from $30M to >$50M per drug. Nash Pharma estimates that its costs will be closer to $2M per drug on average, to
identify drug candidates, screen them and complete Phase IIA trials. This is a dramatic cost and risk reduction in comparison to
the standard drug development pathway and can add as many as 8 years to the patent life of the drug.
Up to 50% of drugs, depending on the disease type, achieve positive data results in Phase II trials.
Built in Partnership Potential
Because the drugs chosen by Nash Pharma for screening have already been approved for human use, the original
manufacturer of the drug represents a natural built in partnering opportunity. Nash Pharma has already begun the process to develop
an outreach strategy to communicate with selected manufacturers of the 7 drug candidates that showed promising data in recent
animal in vivo studies.
Phase II Studies
Under the leadership of Dr. Mark Williams, who has previously brought 3 repurposed drugs through successful
Phase II trials, Nash Pharma will undertake cost effective Phase II studies in order to establish the drug’s clinical efficacy for
the new indication. Nash Pharma’s low relative overhead, use of contract research groups and well researched and planned study
designs are part of its strategic approach to drug development.
Nash Pharma’s Plans for Next Year
-
Conduct Additional Research on 7 Screened Candidates
- Nash Pharma plans to conduct additional research, on each of the 7 best preforming drugs from its in vivo
studies to determine the mechanism of action.
- Nash Pharma plans to conduct additional animal in vivo research studies combining its leading drugs in each of
the 3 diseases of, NASH, CKD and IBD with the leading drug treatments for each disease. The goal is to see if the Nash Pharma
drug candidates combined with the current standard of care drugs provide an accretive result, which would result in
additional patents being filed.
- Begin Phase IIA Study
Nash Pharma plans to begin a Phase IIA study for its leading drug candidate in IBD.
- Screen Additional Drug Candidates for Orphan Disease Applications
Based on certain performance characteristics of the leading Nash Pharma drug candidates, additional screening
studies are planned in Crohn’s disease (CD) and Idiopathic Pulmonary Fibrosis (IPF) which are orphan diseases. Orphan diseases
are attractive diseases for drug development owing to favourable regulatory conditions for drug approvals and the extended sales
exclusivity periods. In addition, the rates of successful drug approvals are historically higher for orphan diseases compared to
non-orphan diseases.
- Begin Partnering Discussions
Nash Pharma plans to begin preliminary discussions with a number of the original manufacturers of its key drug
candidates. Possible partnership deal structures include standard licensing agreements, co-development and option to license
agreements or a combination of the above.
- Publish Data From Animal Studies
Nash Pharma plans to publish the data from its 3 in vivo animal studies for NASH, CKD and IBD that resulted
in positive data from 7 screened drug candidates.
- Appoint Medical Advisory Board
Nash Pharma is planning to formalize a Medical Advisory Board (MAB) incorporating both medical and scientific
leaders. The purpose of the MAB will be to advise Nash Pharma on a variety of topics from research strategies to clinical trial
designs. The Board will also provide recommendations for the scientific and research goals and will assist in communicating Nash
Pharma’s value proposition to third parties.
ABOUT BREATHTEC BIOMEDICAL INC.
Breathtec Biomedical, Inc. (“Breathtec”) was formed to propel innovative research in the area of airborne
analysis as a medical screening tool. Our efforts are aimed at leading the development of commercially viable methods for the early
screening of certain pathogens. Our primary avenue of investigation is focused on innovation and advances in the field of
specialized mass spectrometry.
Breathtec also recently announced that it will be opening a new drug development division and has signed a
Letter of Intent (“LOI”) to acquire 100% of the shares of Nash Pharmaceuticals Inc. (“Nash Pharma”). Nash Pharma 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). For more information, visit www.breathtecbiomedical.com.
CONTACT INFORMATION
Christopher J. Moreau
CEO
Breathtec BioMedical Inc.
604.398.4175 ext 701
info@breathtechbiomedical.com
investors@breathtecbiomedical.com
www.breathtecbiomedical.com
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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,
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preparation, may prove to be incorrect and actual results may differ materially from those anticipated. Forward-looking statements
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