Full Press Release Details
MindMed Provides Corporate Update and 2023 Outlook
- Company positioned for key MM-120 Phase 2b data readout in GAD and Phase 2a data readout in ADHD
- Company to initiate first clinical trial of MM-402 in 2023
- Cash runway to fund current operating plan into first half of 2025
- Company to host a virtual analyst and investor day in the first half of 2023
NEW YORK, January 9, 2023 Mind Medicine (MindMed) Inc. (NASDAQ: MNMD), (NEO: MMED), (the Company or MindMed ), a clinical
stage biopharmaceutical company developing novel product candidates to treat brain health disorders, today provided a corporate update and outlook for 2023.
Following a year of continued strong execution, our progress in 2022 has set the stage for a meaningful 2023, a year in which we plan to further
elucidate the potential of our MM-120 product candidate in generalized anxiety disorder (GAD) and initiate the first clinical trial for our MM-402 program, stated
Rob Barrow, Chief Executive Officer. Our focus remains on advancing and unlocking the value of our proprietary product candidates, which we believe have the potential to deliver new, life-changing therapies to people living with brain health
disorders. There are several key milestones over the next twelve months that can be used to measure our progress. This year we expect key data readouts from our Phase 2b study of MM-120 for the treatment of
generalized anxiety disorder, as well as from our Phase 2a proof-of-concept trial of repeated low-dose MM-120 in attention-deficit/hyperactivity disorder (ADHD). Additionally, we expect to initiate the first clinical trial of MM-402 later in the year. Importantly, we believe
our strong financial position provides us with the ability to fund our programs well beyond these key milestones and into the first half of 2025.
Development Program Updates and Anticipated Milestones:
Phase 2b study evaluating MM-120 for generalized anxiety disorder (GAD) remains on track
Phase 2a study evaluating MM-120 for ADHD remains on track
Advancing development of MM-402 into first clinical trial in 2023
clinical stage biopharmaceutical company developing novel product candidates to treat brain health disorders. Our mission is to be the global leader in the development and delivery of treatments that unlock new opportunities to improve patient
outcomes. We are developing a pipeline of innovative drug candidates, with and without acute perceptual effects, targeting the serotonin, dopamine, and acetylcholine systems.
MindMed trades on NASDAQ under the symbol MNMD and on the Canadian NEO Exchange under the symbol MMED.
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, but are not limited to, statements regarding anticipated upcoming milestones, trials and studies, results and timing of clinical studies, and the Company s cash runway
funding its operations into the first half of 2025. 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 in the Company s Annual Report on Form 10-K for the fiscal year ended December 31, 2021 and its Quarterly Report on Form 10-Q for the period ended September 30, 2022 under headings such as Special Note Regarding Forward-Looking Statements, and Risk Factors and Management s Discussion and
Analysis of Financial Condition and Results of Operations and other filings and furnishings made by the Company with the securities regulatory authorities in all provinces and territories of Canada which are 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. Except as required by law, the Company undertakes no duty or obligation to update any forward-looking statements contained in this
release as a result of new information, future events, changes in expectations or otherwise.
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