Vireo Announces Free Medical Marijuana Home Delivery

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ABC Life Literacy Canada engages Canadians to increase their health literacy with ABC Health Matters

(Toronto, ON – June 7, 2017) – ABC Life Literacy Canada (ABC) is proud to announce the second year of ABC Health Matters, a health literacy program developed to help Canadians increase their confidence when talking about and making decisions regarding health issues with family, friends, and health care professionals. With the support of AbbVie Corporation and McKesson Canada, and through delivery partner University Health Network (UHN), ABC Health Matters will reach patient groups with this health care provider-led program. The ambition of ABC Health Matters is to create a healthier and more confident Canada by increasing the health literacy of all Canadians.

 

“ABC is pleased to launch the second year of ABC Health Matters to help Canadians build their confidence and knowledge to navigate the health care system,” said Mack Rogers, Executive Director, ABC Life Literacy Canada. “With the support of AbbVie, McKesson, and delivery partner UHN, we are helping learners to be more comfortable talking about their health and to become advocates for

themselves and their family to make informed decisions about their health care for an improved quality of life.”

 

An alarming 60 percent of adults and 88 percent of seniors have low health literacy (Public Health Agency of Canada). Our ability to thrive—as individuals, families, communities, and as a country—relies on good health, yet those with low health literacy are more likely to be sick, ill, or injured and have difficulty understanding and following a treatment plan. ABC Health Matters targets adults who struggle to manage their health and arms them with the knowledge to better access health care to live a more healthy life.

 

The program was piloted across Ontario last year to adult literacy programs with very positive results. Learners reported an increase in confidence to manage their own health and the health of those they care for and an increase in knowledge of their rights and responsibilities as a patient. Ninety-three percent of participants indicated they intended to be more proactive about their health and intend to ask more questions of their health care professionals going forward.

 

“We are very excited to continue our partnership with ABC and evolve our workshops to be leveraged in hospitals. We strongly believe that improving health literacy is vital to a healthier Canada.

It is through supporting such initiatives as ABC Health Matters that we are taking a step forward in making a positive impact in healthcare sustainability,” said Stéphane Lassignardie, General Manager, AbbVie.

 

ABC Health Matters program includes two workbooks, which are delivered in two, two-hour workshops. The workbooks can also be downloaded for free from our website for use at home by learners. The first workbook includes information such as how to talk about your health with your family and with your health care provider and includes practice activities and helpful sample scripts. The second workbook

 

includes information specific to the Ontario health care system and UHN network with details about services from your local pharmacist and doctor, Telehealth, and how to create a medical history card.

 

“Increasing the health literacy of patients makes them full partners in their care. ABC Health Matters is an innovative example that demonstrates how pharmacists can be a key resource in health literacy and how active participation can increase positive outcomes and improve adherence for individuals, families and communities. McKesson Canada is proud to continue to partner with ABC Health Matters to support this important initiative,” said Paula Keays, President, McKesson Canada.

 

ABC Health Matters will be delivered at three UHN locations across Toronto in workshops held during May and June. Led by McKesson pharmacist volunteers and the UHN health care team, the program will reach 150 patient-learners as well as learners across Canada accessing the program through self-led delivery. To register for a workshop or download the program workbooks for free, visit ABCHealthMatters.ca.

 

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About ABC Life Literacy Canada

ABC Life Literacy Canada is a non-profit organization that inspires Canadians to increase their literacy and essential skills. We mobilize business, government and communities to support lifelong learning and achieve our goals through leadership in programs, communications and partnerships. We envision a Canada where everyone has the skills they need to live a fully engaged life. For the latest news and information on adult literacy please visit www.abclifeliteracy.ca. Follow us on Twitter (@abclifeliteracy). For more information about ABC Health Matters visit ABCHealthMatters.ca.

 

About AbbVie Corporation

AbbVie is a global, research-based biopharmaceutical company formed in 2013 following separation from Abbott Laboratories. The company’s mission is to use its expertise, dedicated people and unique approach to innovation to develop and market advanced therapies that address some of the world’s most complex and serious diseases. Together with its wholly-owned subsidiary, Pharmacyclics, AbbVie employs more than 29,000 people worldwide and markets medicines in more than 170 countries. For more information: www.abbvie.ca on Twitter at @abbviecanada.

 

About McKesson Canada

Founded more than 100 years ago, McKesson Canada is dedicated to delivering vital medicines, supplies and information technologies that enable the healthcare industry to provide patients better, safer care. Our solutions empower pharmacies, manufacturers, hospitals and other healthcare institutions by enabling them to get closer to the millions of patients they serve every single day, while contributing to the quality and safety of care in Canada. For more information, visit www.mckesson.ca.

 

For more information, please contact:

Milena Stanoeva

Marketing and Communications Coordinator ABC Life Literacy Canada

416-218-0010 x122

mstanoeva@abclifeliteracy.ca

Vireo launches first marijuana ad campaign in nyc subway history

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Vireo to Expand Home Delivery of Medical Marijuana to Bronx, Staten Island and Westchester

Vireo to Expand Home Delivery of
Medical Marijuana to Bronx, Staten Island and Westchester

Delivery currently exists in Brooklyn, Queens, Nassau and parts of Suffolk County

New York, NY –Vireo Health of New York (“Vireo”), one of only five companies licensed by New York State to cultivate, manufacture and dispense medical marijuana, will expand its groundbreaking medical marijuana home delivery program to the Bronx, Staten Island and Westchester County beginning on Saturday, May 6.

“We are rapidly expanding our delivery capabilities to reach more of the New York City metro area,” said Ari Hoffnung, CEO of Vireo Health of New York. “Our delivery program has seen great success over the last few weeks, serving not only those patients who are home-bound or have trouble visiting a dispensary but also those who appreciate its convenience.”

Last month, medical marijuana home deliveries started in Brooklyn, Queens, Nassau and parts of Suffolk County. The delivery zone will then expand into Manhattan. Over time, Vireo hopes to cover other areas throughout New York State, particularly in the Capital Region and Southern Tier.

The medical marijuana ‘from our greenhouse to your front door’ home delivery program was designed by a team of security experts, pharmacists and physicians to serve homebound patients with life-threatening and debilitating diseases, like Cancer, ALS and chronic pain.

Numerous measures have been taken to ensure the safety of patients and the delivery staff. In accordance with State regulations that prohibit outsourcing in New York’s ‘seed-to-sale’ medical marijuana industry, all deliveries will be handled exclusively by Vireo employees. The deliveries will be made by at least two employees, and company-owned delivery vehicles are outfitted with cutting-edge safety features, including GPS tracking devices.

Qualifying patients can register for the home delivery program online and use coupon code REGONLINE to receive a $10 discount off their first online order.

Additional information about the home delivery program is available at vireohealth.com/ny/delivery.

###

 

About Vireo Health of New York
Vireo Health of New York is a physician-led company dedicated to providing best-in-class cannabis-based medications and top quality patient care. The company provides a wide array of pharmaceutical grade cannabis-based products formulated from the highest quality plants and utilizes its separation chemistry capabilities to create products with novel cannabinoid combinations. Vireo Health of New York is a wholly owned subsidiary of Vireo Health, LLC. For more information, visit http:/www.vireohealth.com/ny.

Vireo Launches New York City & Long Island’s First-Ever Medical Marijuana Home Delivery Program

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Vireo approved for ny’s first-ever medical marijuana home delivery

Vireo Approved for NY’s First-Ever Medical Marijuana Home Delivery Program

Eight County Delivery Zone to include all Five New York City Boroughs, Long Island and Westchester

New York, NY – Today, Vireo Health of New York (“Vireo”), one of only five companies licensed by New York State to cultivate, manufacture and dispense medical marijuana, announced that it received approval from the New York State Department of Health to launch a medical marijuana home delivery program.

The medical marijuana ‘from our greenhouse to your front door’ home delivery program was designed by a team of security experts, pharmacists and physicians to serve homebound patients with life-threatening and debilitating diseases, like Cancer and ALS. Initially, deliveries will cover an eight-county zone, including all five New York City Boroughs, Long Island and Westchester.

Numerous measures have been taken to ensure the safety of patients and the delivery staff. In accordance with State regulations that prohibit outsourcing in New York’s ‘seed-to-sale’ medical marijuana industry, all deliveries will be handled exclusively by Vireo employees. The deliveries will be handled by at least two employees, and company-owned delivery vehicles will be outfitted with cutting-edge safety features, including GPS tracking devices.

“New Yorkers have increasingly come to expect home delivery and we plan on leveraging ‘last mile’ supply chain technologies to meet and exceed patient expectations,” said Ari Hoffnung, CEO of Vireo Health of New York. “We are grateful to the State’s public health and safety officials for their help making this Compassion Care Act program a reality.”

“Day-in and day-out our goal at Vireo Health of New York is to provide the best possible care and service to our patients,” said Dr. Stephen Dahmer, Vireo Health’s Chief Medical Officer. “Home delivery will not only help us to improve upon current services, but also expand our reach to those patients who are unable to travel. Our team is excited to provide this service to all of our existing patients, and to have the opportunity to meet new patients in other parts of the state.”

The Company plans to launch the program within 90 days. Delivery pricing and other details will be released over the coming weeks. Certified patients or family members of patients interested in receiving more information can sign-up for home delivery program updates by visiting: www.vireohealth.com/ny/delivery.

###

About Vireo Health of New York
Vireo Health of New York is a physician-led company dedicated to providing best-in-class cannabis-based medications and top quality patient care. The company provides a wide array of pharmaceutical grade cannabis-based products formulated from the highest quality plants and utilizes its separation chemistry capabilities to create products with novel cannabinoid combinations. Vireo Health of New York is a wholly owned subsidiary of Vireo Health, LLC. For more information, visit http:/www.vireohealth.com/ny.

Health Canada Grants Priority Review to AbbVie’s Investigational Regimen of Glecaprevir/Pibrentasvir (G/P) for the Treatment of Chronic Hepatitis C in All Major Genotypes (GT1-6)

 

  • If approved, G/P may provide a shorter, eight week, once-daily, ribavirin-free treatment option for the majority of HCV patients without cirrhosis
  • AbbVie’s New Drug Submission is supported by data from its global registrational clinical development program across all major HCV genotypes and in patients with specific treatment challenges

 

Montreal, QC, February 1, 2017 – AbbVie, a global biopharmaceutical company, today announced it has submitted a New Drug Submission (NDS), and received priority review from Health Canada, for its investigational, pan-genotypic regimen of glecaprevir (ABT-493)/pibrentasvir (ABT-530) (G/P) for the treatment of all major chronic hepatitis C virus (HCV) genotypes.

 

If approved, G/P may provide a shorter treatment duration for genotypes 1-6 (GT1-6) in patients without cirrhosis, who make up a large portion of HCV patients in Canada, and an additional treatment option to patients with compensated cirrhosis (Child-Pugh A). G/P is also intended to address the unmet medical needs of patients with specific treatment challenges, including those with severe chronic kidney disease (CKD) and those not cured with previous direct acting antiviral (DAA) treatment.

 

“HCV patients with severe chronic kidney disease present a complex challenge for physicians to treat. This is particularly true in those with genotype 2 and 3 infection, and those with cirrhosis,” said

Curtis Cooper, Director of the Regional Hepatitis Program at the Ottawa Hospital. “Recent clinical trial

results are a positive development in AbbVie’s investigation of the G/P regimen for patients with chronic kidney disease, who currently have limited HCV treatment options.”

 

“At no other time in history has the goal of eliminating hepatitis C in Canada been within reach like it is now, said Stéphane Lassignardie, General Manager, AbbVie Canada. “We are firmly committed to seeing this goal accomplished. As such, we have invested significantly in recent years in clinical trials in Canada for our investigational, pan-genotypic G/P regimen and will continue collaborating with Health Canada to help provide a cure for as many Canadians as possible living with HCV.”

 

AbbVie’s NDS is supported by data from eight registrational studies in AbbVie’s G/P clinical development program, which evaluated more than 2,300 patients in 27 countries, including 174 patients in Canada, across all major HCV genotypes and special populations. Patient populations studied included GT1-6, those new and experienced to antiviral treatment, those with compensated cirrhosis and without cirrhosis, and patients with specific treatment challenges, including those with severe CKD, and those not cured with a prior DAA-containing regimen. The registrational program for G/P was designed to

 

investigate a faster path to virologic cure* for all major HCV genotypes (GT1-6) and with the goal of addressing areas of continued unmet need.

 

On January 24, AbbVie announced its marketing authorization application (MAA) for G/P has been validated and is now under accelerated assessment by the European Medicines Agency (EMA). On December 19, 2016, AbbVie submitted its New Drug Application (NDA) for G/P to the U.S. Food and Drug Administration (FDA) for the treatment of GT1-6 chronic HCV. And on September 30, 2016, AbbVie announced that G/P was granted Breakthrough Therapy Designation by the FDA for genotype 1 patients not cured with prior direct-acting antivirals.

 

G/P is an investigational product and its safety and efficacy have not been established. Additional information on the clinical trials for G/P is available at www.clinicaltrials.gov.

 

About AbbVie’s HCV Clinical Development Program

AbbVie’s Glecaprevir/Pibrentasvir (G/P) clinical development program was designed to investigate a faster path to virologic cure* for all major HCV genotypes (GT1-6) and with the goal of addressing treatment areas of continued unmet need.

 

G/P is an investigational, pan-genotypic regimen being evaluated as a potential cure in 8 weeks for HCV patients without cirrhosis and who are new to treatment with direct-acting antivirals (DAA)**, who make up the majority of HCV patients. AbbVie is also studying G/P in patients with specific treatment challenges, such as genotype 3 patients who were not cured with previous DAA treatment, and those with CKD, including patients on dialysis.

 

G/P is a once-daily regimen that combines two distinct antiviral agents. G/P is a fixed-dose combination of glecaprevir (300mg), an NS3/4A protease inhibitor, and pibrentasvir (120mg), an NS5A inhibitor, dosed once-daily as three oral tablets. Glecaprevir (GLE) was discovered during the ongoing collaboration between AbbVie and Enanta Pharmaceuticals for HCV protease inhibitors and regimens that include protease inhibitors.

 

*Patients who achieve a sustained virologic response at 12 weeks post treatment (SVR12) are considered cured of hepatitis C.

**Patients who are treatment-naive or not cured with previous IFN-based treatments ([peg]IFN +/- RBV or SOF/RBV +/- pegIFN).

 

About AbbVie Canada

AbbVie is a global, research-based biopharmaceutical company formed in 2013 following separation from Abbott Laboratories. The company’s mission is to use its expertise, dedicated people and unique approach to innovation to develop and market advanced therapies that address some of the world’s most complex and serious diseases. Together with its wholly-owned subsidiary, Pharmacyclics, AbbVie employs more than 28,000 people worldwide and markets medicines in more than 170 countries. For further information on the company and its people, portfolio and commitments, please visit www.abbvie.ca and www.abbvie.com. Follow @abbviecanada on Twitter or view careers on our Facebook or LinkedIn page.

xxx

For further information:

Eileen Murphy AbbVie Canada

 

(514) 832-7788

Eileen.murphy@abbvie.com

AIkido Pharma Inc. Announces Participation at the H.C. Wainwright 22nd Annual Global Investment Conference on September 14-16, 2020 (Virtual Conference)

NEW YORKSept. 11, 2020 /PRNewswire/ — AIkido Pharma Inc. (Nasdaq: AIKI) (“AIkido” or the “Company”) today announced it will be featured as a presenting company at the H.C. Wainwright 22nd Annual Global Investment Conference.  The conference is being held on September 14-16, 2020 virtually.

(PRNewsfoto/AIkido Pharma Incorporated)

Darrell Dotson, Vice President and General Counsel, of AIkido Pharma Inc. will provide an overview of the Company’s business during the live presentation.

If you are an institutional investor, and would like to attend the Company’s presentation, please click on the following link (www.hcwevents.com ) to register for the conference.

Event:  H.C. Wainwright 22nd Annual Global Investment Conference (Virtual Conference)
Date:  Tuesday, September 15, 2020
Time:  3:00 p.m. (Eastern Time)
Location:  Virtual Conference
Webcast:  https://wsw.com/webcast/hcw7/aiki/1585998

The presentation will be webcast live.  To access the webcast, please visit www.hcwevents.com .  The webcast replay will remain available for 90 days following the live presentation.

About H.C. Wainwright

H.C. Wainwright is a full–service investment bank dedicated to providing corporate finance, strategic advisory and related services to public and private companies across multiple sectors and regions.  H.C. Wainwright & Co. also provides research and sales and trading services to institutional investors.   According to Sagient Research Systems, H.C. Wainwright’s team is ranked as the #1 Placement Agent in terms of aggregate CMPO (confidentially marketed public offering), RD (registered direct offering) and PIPE (private investment in public equity) executed cumulatively since 1998.

About AIkido

AIkido was initially formed in 1967 and is a biotechnology company with a diverse portfolio of small-molecule anti-cancer therapeutics.  The Company’s platform consists of patented technology from leading universities and researchers and we are currently in the process of developing an innovative therapeutic drug platform through strong partnerships with world renowned educational institutions, including The University of Texas at Austin and Wake Forest University. Our diverse pipeline of therapeutics includes therapies for pancreatic cancer, acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL). In addition, we are constantly seeking to grow our pipeline to treat unmet medical needs in oncology.  The Company is also developing a broad spectrum antiviral platform that may potentially inhibit replication of multiple viruses including Influenza virus, SARS-CoV (coronavirus), MERS-CoV, Ebolavirus and Marburg virus.

Contact:

Investor Relations:

Hayden IR
Brett Maas, Managing Partner
Phone: (646) 536-7331
Email: brett@haydenir.com
www.haydenir.com

AIkido:

Phone: 212-745-1373
Email: investorrelations@AIkido.com
www.AIkido.com

 

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SOURCE AIkido Pharma Inc.

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BETTER PLANT’S HAND SANITIZER GEL APPROVED FOR LISTING ON AMAZON.COM

Vancouver, B.C. – October 6, 2020: Better Plant Sciences Inc. (CSE: PLNT) (OTCQB: VEGGF) (FSE: YG3) (“Better Plant”) or (the “Company”) is pleased to announce that Amazon.com has approved the listing for its hand sanitizer gel, which is manufactured by its subsidiary, Urban Juve. The hand sanitizer gel is listed with the FDA (NDC 75385-0010-1) and has received Natural Health Product Number 80098154 from Health Canada. Urban Juve’s Ultra Hydrating Hand Sanitizer Spray received Health Canada approval on March 27, 2020. The Hand Sanitizer Gel will be live on Amazon.com later this month. Both the Hand Sanitizer Gel and Spray are available for purchase on Amazon.ca and urbanjuve.com.

“The popularity of Amazon is undeniable”, says Gabe Villablanca, Better Plant’s Director of eCommerce. “During these times, it is becoming more and more simple and stress-free to shop online, so we want to expand that accessibility across the top platforms.” Earlier this year, Urban Juve’s full line went live on Amazon.ca, offering free shipping on orders over $35. Due to high demand, Urban Juve ensured the Hand Sanitizer Gel was the first product to be pushed through the approval process for Amazon.com. The Company plans to continue to use data to guide where they will make products available online for the convenience of consumers.

Based on a survey of more than 2,000 U.S.  customers, 89 percent of buyers agree that they’re more likely to buy products from Amazon than other eCommerce sites (Feedvisor, 2019).

 

About Better Plant Sciences Inc. 

Better Plant develops and acquires intellectual property and other assets related to plant-based products and therapeutics. Through its integrated business model, Better Plant develops, manufactures, markets, sells and distributes plant-based products. It has over 200 proprietary wellness formulas at various stages of commercialization.  It operates websites and sells through eCommerce, Amazon and through a retail store network over 150 plant based products for body, baby and home under the brands JUSU, Urban Juve and Wright & Well. Its majority-owned subsidiary NeonMind Biosciences Inc. is launching a line of coffees infused with health optimizing functional mushrooms including reishi, cordyceps, lion’s mane and turkey tail mushrooms. NeonMind is also engaged in research into developing a psilocybin (psychedelic mushroom) based product for weight loss and has applied for Health Canada approval to begin preclinical trials to study its pending psychedelic medicine patents.

For more information about Better Plant, visit www.betterplantsciences.com or follow @betterplantsciences on Instagram.

 

Investor Relations Contact:

Penny White, President & CEO

Kevan Matheson, Investor Relations

invest@betterplantsciences.com

1-833-514-2677

The Canadian Securities Exchange has not reviewed, approved or disapproved the contents of this news release.

 

Cautionary Statement Regarding Forward-Looking Statements

This press release includes forward-looking information and statements (collectively, “forward looking statements”) under applicable Canadian securities legislation.  Forward-looking statements are necessarily based upon a number of estimates, forecasts, beliefs and assumptions that, while considered reasonable, are subject to known and unknown risks, uncertainties, and other factors which may cause actual results and future events to differ materially from those expressed or implied by such forward-looking statements.  Such risks, uncertainties and factors include, but are not limited to: risks related to the development, testing, licensing, brand development, availability of packaging, intellectual property protection, reduced global commerce and reduced access to raw materials and other supplies due to the spread of the Coronavirus, the potential for not acquiring any rights as a result of the patent  application and any products making use of the intellectual property may be ineffective or the company may be unsuccessful in commercializing them; and other approvals will be required before commercial exploitation of the intellectual property can happen.  Demand for the company’s products, general business, economic, competitive, political and social uncertainties, delay or failure to receive board or regulatory approvals where applicable, and the state of the capital markets.  Better cautions readers not to place undue reliance on forward-looking statements provided by Better, as such forward-looking statements are not a guarantee of future results or performance and actual results may differ materially. The forward-looking statements contained in this press release are made as of the date of this press release, and Better expressly disclaims any obligation to update or alter statements containing any forward-looking information, or the factors or assumptions underlying them, whether as a result of new information, future events or otherwise, except as required by law.

MindMed Appoints Pharmaceutical Veteran Peter Bergethon, M.D. to Scientific Advisory Board

MindMed (NASDAQ: MNMD) (NEO: MMED) (DE: MMQ) (the “Company”), a leading biotech company developing psychedelic-inspired therapies, has announced the addition of Dr. Peter Bergethon, a world-leading expert in neurology, digital medicine, and central nervous system (CNS) drug development to the Company’s Scientific Advisory Board.

Dr. Bergethon is the Vice President and Head of Digital and Quantitative Medicine at Biogen Inc., where he leads the effort to transform clinical trials and humanize drug discovery by encouraging the transition of clinical trial measures from a qualitative to a quantitative discipline. The Quantitative Medicine transformation has advanced Biogen’s leadership in neuroscience therapeutics and personalized medicine. Dr. Bergethon came to Biogen in 2017 from Pfizer Worldwide Research and Development where he was Vice President and Head of the Pfizer Innovation Research Lab within the Early Clinical Development group.

Before joining the biopharmaceutical industry in 2012, Dr. Bergethon spent 30 years in academic medicine as a Professor at Boston University and Tufts University in the Departments of Biochemistry, Neurology, Neurobiology & Anatomy, and Biomedical Engineering. Dr. Bergethon graduated from Williams College with honors in biology for research in neurocybernetics and then earned an M.D. from Jefferson Medical College. He is board-certified in internal medicine and neurology following dual residencies at Boston City Hospital. Dr. Bergethon received his formal science training through the National Institutes of Health’s Physician-Scientist training in biophysical chemistry at Boston University School of Medicine. He then completed a fellowship training in EEG and neurophysiology at Lahey Clinic-Hitchcock Medical Center in Burlington, MA. In 1995, Dr. Bergethon received the American Academy of Neurology’s Founders’ Award. Dr. Bergethon has written and contributed to over 130 research papers and books and is the single author of “The Physical Basis of Biochemistry: The Foundations of Molecular Biophysics”, 2nd Ed.

MindMed CEO Robert Barrow said, “We are thrilled to welcome Dr. Bergethon to our Scientific Advisory Board. As we seek to revolutionize mental health and addiction care, we continue to explore ways of leveraging innovative digital medicine approaches to facilitate broad accessibility and major public health impacts. Dr. Bergethon’s extensive experience in this field will be invaluable in progressing all of our research and development efforts.”

Dr. Bergethon stated, “My research and interests have always centered around a core question: ‘What are the physical and systemic bases for creativity and intelligent behavior, and how could such behavior be practically constructed or reconstructed?’ This core query continues to form the basis for the approach that digital medicine takes toward transforming neuroscience therapeutics. The ultimate thrust of my interest is the design, construction, and operation of ‘intelligent machines’ inspired by biological understanding. By any measure, I have lived a charmed scientific existence.”

MindMed’s Scientific Advisory Board is composed of a diverse group of members with expertise in psychiatry, neuroscience, and clinical development. The Scientific Advisory Board leverages decades of deep knowledge in biotech and psychiatry to guide MindMed’s development programs. Members represent institutions such as Johns HopkinsNew York University Langone Health, Duke University, National Institutes of Health (NIH), Stanford University, and Albany Medical College.

Scientific Advisory Board Chair, Dr. Robert Malenka added, “We are very excited to welcome Dr. Bergethon to the Scientific Advisory Board. He brings a wealth of experience and innovative thinking to MindMed’s digital medicine efforts and will be invaluable in helping MindMed be the world leader in developing effective new treatments based on the most rigorous science.”

About MindMed
MindMed is a clinical-stage biotech company that discovers, develops and deploys psychedelic inspired medicines and therapies to address addiction and mental health. The Company is assembling a compelling drug development pipeline of innovative treatments based on psychedelic substances including psilocybin, LSD, MDMA, DMT and an ibogaine derivative, 18-MC. The MindMed executive team brings extensive biopharmaceutical experience to MindMed’s approach of developing the next generation of psychedelic inspired medicines and therapies.

MindMed trades on the NASDAQ under the symbol MNMD and on the Canadian NEO exchange under the symbol MMED. MindMed is also traded in Germany under the symbol MMQ. For more information: www.mindmed.co

MindMed Forward-Looking Statements
Certain statements in this news release related to the Company constitute “forward-looking information” within the meaning of applicable securities laws and are prospective in nature. Forward-looking information is not based on historical facts, but rather on current expectations and projections about future events and are therefore subject to risks and uncertainties which could cause actual results to differ materially from the future results expressed or implied by the forward-looking statements. These statements generally can be identified by the use of forward-looking words such as “will”, “may”, “should”, “could”, “intend”, “estimate”, “plan”, “anticipate”, “expect”, “believe”, “potential” or “continue”, or the negative thereof or similar variations. Forward-looking information in this news release include statements regarding the expertise of the Scientific Advisory Board and ability to leverage the knowledge of the Scientific Advisory Board, the ability to develop and the potential success of using technology to improve health outcomes, the pursuit of strategic initiatives, and the Company’s intended future business plans and operations, including the development of psychedelic inspired medicines and experiential therapies. Although the Company believes that the expectations reflected in such forward-looking information are reasonable, such information involves risks and uncertainties, and undue reliance should not be placed on such information, as unknown or unpredictable factors could have material adverse effects on future results, performance or achievements of the Company. There are numerous risks and uncertainties that could cause actual results and the Company’s plans and objectives to differ materially from those expressed in the forward-looking information, including history of negative cash flows; limited operating history; incurrence of future losses; availability of additional capital; lack of product revenue; compliance with laws and regulations; difficulty associated with research and development; risks associated with clinical trials or studies; heightened regulatory scrutiny; early stage product development; clinical trial risks; regulatory approval processes; novelty of the psychedelic inspired medicines industry; as well as those risk factors discussed or referred to herein and the risks described under the headings “Risk Factors” in the Company’s filings with the securities regulatory authorities in all of the provinces and territories of Canada and available under the Company’s profile on SEDAR at www.sedar.com and with the U.S. Securities and Exchange Commission on EDGAR at www.sec.gov. Should one or more of these risks or uncertainties materialize, or should assumptions underlying the forward-looking information prove incorrect, actual results and future events could differ materially from those anticipated in such information. Although the Company has attempted to identify important risks, uncertainties and factors that could cause actual results to differ materially, there may be others that cause results not to be as anticipated, estimated or intended. These and all subsequent written and oral forward-looking information are based on estimates and opinions of management on the dates they are made and are expressly qualified in their entirety by this notice. Except as required by law, the Company does not intend and does not assume any obligation to update this forward-looking information.