LAVAL, Québec, June 11, 2018 (GLOBE NEWSWIRE) -- Acasti Pharma Inc. (NASDAQ:ACST) (TSX-V:ACST) (the
“Company” or “Acasti Pharma”), a biopharmaceutical innovator focused on the research, development
and commercialization of its prescription drug candidate CaPre® (omega-3 phospholipid) for the treatment of severe
hypertriglyceridemia, reported on the Company’s presentation earlier today at the XVIIIth International Symposium on
Atherosclerosis (ISA2018), the premier conference for international atherosclerosis research.
CaPre was featured in an industry breakfast symposium, entitled “Omega-3, Triglycerides, and CVD: Current Status
and Future Directions,” presented by Dr. Harold Bays, an investigator in the Company’s phase 3 TRILOGY clinical trials for CaPre,
on June 11, 2018 at 7:00 a.m. to 8:30 a.m. Eastern time. Dr. Bays, MD, FOMA, FTOS, FACC, FACE, FNLA is the Medical Director /
President of the Louisville Metabolic and Atherosclerosis Research Center, in Louisville, KY, USA. The breakfast symposium
highlighted recent developments in the field of hypertriglyceridemia. Pierre Lemieux, Ph.D., COO and CSO of Acasti Pharma,
followed Dr. Bays’ presentation with a brief corporate presentation on Acasti Pharma, including an update on the progress of the
phase 3 TRILOGY clinical trials for CaPre. The objective of this symposium was to provide physicians with an overview on why CaPre
has the potential to become the “best-in-class” for treating hypertriglyceridemia if the Phase 3 studies reproduce the results
observed in Phase 2.
Pierre Lemieux, Ph.D., COO and CSO of Acasti Pharma, commented, “We are extremely pleased with the turnout at
our presentation, which included over 100 participants including key opinion leaders and top experts in the field of
atherosclerosis and lipid management. The feedback we received is further validation of the need for a prescription omega-3
that has the potential to not only lower triglyceride levels (TGs) in patients with severe hypertriglyceridemia (HTG), but also
improve these patients’ broader lipid profile (“trifecta effect”). Moreover, it was clear from the event there is a strong
interest in the market for a prescription omega-3 like CaPre that does not have the food effect associated with other prescription
products in the market. We are truly honored to have had Dr. Bays participate in our presentation, as he is one of the foremost
experts in the field.”
The International Symposium on Atherosclerosis provides extensive marketing and networking opportunities with an
anticipated attendance of 1,200 experts and professionals. The ISA2018 will focus on cutting-edge research and brings together
leading atherosclerosis researchers, top clinicians, health practitioners and leading scientists from around the world. Along with
top professionals, ISA2018 provides an opportunity for its attendees to participate in public health awareness and innovation
forums. The symposium was held on June 9th through the 12th at the Metro Toronto Convention Centre in
Toronto, Canada.
The Company also announced that on June 5, 2018, it received written notification from the Nasdaq Listing
Qualifications Department (“Nasdaq”) for failing to maintain a minimum bid price of U.S.$1.00 per share for the last 30 consecutive
business days, as required by Nasdaq Listing Rule 5550(a)(2) – bid price (the “Minimum Bid Price Rule”).
The Nasdaq notification has no immediate effect on the listing of Acasti Pharma’s shares. Under Nasdaq Listing
Rule 5810(c)(3)(A) – compliance period, Acasti Pharma has 180 calendar days, or until December 3, 2018, to regain compliance. If at
any time over this period the bid price of Acasti Pharma’s shares closes at U.S.$1.00 per share or more for a minimum of ten (10)
consecutive business days, Nasdaq will provide written confirmation of compliance and the matter will be closed.
If Acasti Pharma does not regain compliance within the initial 180-day period, but otherwise meets the continued
listing requirements for market value of publicly-held shares and all other initial listing standards for the Nasdaq Listing Rule
5505 – Capital Market criteria, except for the Minimum Bid Price Rule, Acasti Pharma may be eligible for an additional 180 calendar
days to regain compliance. If Acasti Pharma is not granted additional time, then its shares will be subject to delisting, at which
time Acasti Pharma may appeal the delisting determination to a Nasdaq Hearings Panel.
Acasti Pharma intends to evaluate all available options to resolve the deficiency and regain compliance with the
Minimum Bid Price Rule.
About CaPre®
CaPre is a krill oil derived mixture containing polyunsaturated fatty acids (PUFAs), primarily composed of
omega-3 fatty acids, principally eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). EPA and DHA are well known to be
beneficial for human health, and may promote healthy heart, brain and visual function¹, and may contribute to reducing
inflammation, and blood triglycerides.² Krill is a natural source of phospholipids and omega-3 fatty acids. The EPA and DHA
contained in CaPre are delivered as free fatty acids or bound to phospholipid esters, allowing these PUFAs to reach the small
intestine where they undergo rapid absorption and transformation into complex fat molecules that are required for transport in the
bloodstream. Acasti believes that EPA and DHA are more efficiently transported by phospholipids sourced from krill oil than the EPA
and DHA contained in fish oil that are transported either by triglycerides (as in dietary supplements) or as ethyl esters in other
prescription omega-3 drugs, which must then undergo additional digestion before they are ready for transport in the bloodstream.
CaPre is intended to be used as a therapy in conjunction with positive lifestyle changes including diet, and is to be administered
either alone or with other drug treatment regimens such as statins (a class of drug used to reduce cholesterol levels). CaPre is
intended to be taken orally once per day in capsule form.
1Sources: Kwantes and Grundmann, Journal of Dietary Supplements, 2014.
2Source: Ulven and Holven, Vascular health and risk management, 2015.
About Acasti Pharma
Acasti Pharma is a biopharmaceutical innovator advancing a potentially best-in-class cardiovascular drug, CaPre®
(omega-3 phospholipid), for the treatment of hypertriglyceridemia, a chronic condition affecting an estimated one third of the U.S.
population. Since its founding in 2008, Acasti Pharma has focused on addressing a critical market need for an effective, safe and
well-absorbing omega-3 therapeutic that can make a positive impact on the major blood lipids associated with
cardiovascular disease risk. CaPre is being evaluated in a Phase 3 clinical program in patients with severe
hypertriglyceridemia, a market that includes 3 to 4 million patients in the U.S. and may expand significantly if omega-3s
demonstrate long-term cardiovascular benefits in on-going outcomes studies. Acasti Pharma’s strategy is to commercialize CaPre in
the U.S. and the company is pursuing partnerships to market CaPre in major countries around the world. For more information, visit
www.acastipharma.com.
Forward Looking Statements
Statements in this press release that are not statements of historical or current fact constitute
“forward-looking information” within the meaning of Canadian securities laws and “forward-looking statements” within the meaning of
U.S. federal securities laws (collectively, “forward-looking statements”). Such forward-looking statements involve known and
unknown risks, uncertainties, and other unknown factors that could cause the actual results of Acasti Pharma to be materially
different from historical results or from any future results expressed or implied by such forward-looking statements. In addition
to statements which explicitly describe such risks and uncertainties, readers are urged to consider statements labeled with the
terms “may,” “believes,” “belief,” “expects,” “intends,” “anticipates,” “potential,” “will,” or “plans” to be uncertain and
forward-looking. Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the
date of this press release. Forward-looking statements in this press release include, but are not limited to, CaPre’s potential to
become the “best-in-class” cardiovascular drug for treating severe Hypertriglyceridemia (HTG).
The forward-looking statements contained in this press release are expressly qualified in their entirety by this
cautionary statement and the “Cautionary Note Regarding Forward-Looking Information” section contained in Acasti Pharma’s latest
annual report on Form 20-F (the “Annual Report”) and most recent management’s discussion and analysis (“MD&A”), which are
available on SEDAR at www.sedar.com, on EDGAR at www.sec.gov/edgar/shtml, and on the investor section of Acasti Pharma’s website at www.acastipharma.com. All forward-looking statements in this press release are made as of the
date of this press release. Acasti Pharma does not undertake to update any such forward-looking statements whether as a result of
new information, future events or otherwise, except as required by law. The forward-looking statements contained herein are also
subject generally to other assumptions, risks and uncertainties that are described from time to time in Acasti Pharma’s public
securities filings with the Securities and Exchange Commission and the Canadian securities regulators, including Acasti Pharma’s
Annual Report and MD&A.
Neither NASDAQ, the 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.
Acasti Contact:
Jan D’Alvise, President and Chief Executive Officer
Tel: 450-686-4555
Email: info@acastipharma.com
www.acastipharma.com
U.S. Contact:
Crescendo Communications, LLC
Tel: 212-671-1020
Email: ACST@crescendo-ir.com
Canada Contact:
Glen Akselrod Bristol Capital Ltd.
Tel: (905) 326-1888 ext 10
Email: glen@bristolir.com
