Clearmind Medicine Signs Agreement to Examine MEAI in Combination and Sequencing with Tirzepatide Against Blockbuster GLP-1 Medications
Clearmind Medicine (Nasdaq: CMND) signed a new research agreement with Yissum to fund a 12‑month preclinical study of MEAI (CMND‑100) with tirzepatide in diet‑induced obese mice.
Rhea-AI Summary
Clearmind Medicine (Nasdaq: CMND) signed a new research agreement with Yissum to fund a 12‑month preclinical study of MEAI (CMND‑100) with tirzepatide in diet‑induced obese mice.
The study will assess combination and maintenance use in the fast‑growing $50–66B incretin therapeutics market.
Positive
- New 12‑month preclinical study of MEAI with tirzepatide in obese mice
- Prior MEAI data: approximately 15–20% body weight reduction in DIO mice
- MEAI effects included increased energy expenditure and fat utilization
- MEAI preserved lean mass and improved glucose homeostasis and hepatic steatosis in mice
- Targeting incretin market projected to reach $170–185B by 2033
Negative
- Current work is preclinical and limited to diet‑induced obese mouse models
Details
News Market Reaction – CMND
On May 18, the day this news came out, CMND closed 26.90% below the previous close.
Data tracked by StockTitan Argus for the May 18 session.
Key Figures
- Prior MEAI weight loss
- 15–20% body weight reduction
- Diet-induced obese mice in prior Hebrew University study
- New study duration
- 12 months
- Preclinical MEAI–tirzepatide DIO mouse study
- Incretin market size 2025
- $50–66 billion
- Global market for incretin-based therapies and tirzepatide in 2025
- Incretin market 2033
- $170–185 billion
- Projected global incretin and tirzepatide market by 2033
- Post-therapy weight regain
- 25% or more
- Typical regain of lost weight within one year after GLP-1 discontinuation
- MEAI indication
- Alcohol Use Disorder
- Ongoing FDA-approved Phase I/IIa trial of CMND-100 (MEAI)
- Registered resale shares
- 22,626,988 common shares
- Form F-3 for resale of note-conversion shares
- Convertible facility capacity
- $10,000,000
- Remaining capacity for future convertible promissory note issuances as of 2026-04-30
Historical Context
-
Phase I/IIa MEAI trial reaches 20 treated participants with no serious AEs.
-
Announcement of “Inside MEAI” webinar to review clinical data and updates.
-
European patent filing for non-hallucinogenic compounds targeting PTSD and others.
-
Company evaluates MEAI for potential FDA Breakthrough Therapy Designation in AUD.
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Company highlights U.S. policy support for psychedelic therapies and its MEAI program.
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Key Terms
glp-1 medical
gip medical
receptor agonists medical
incretin-based therapies medical
diet-induced obese ("dio") mice medical
hepatic steatosis medical
cardiometabolic medical
maintenance therapy medical
AI-generated analysis. How Rhea-AI works. Not financial advice.
Vancouver, Canada, May 18, 2026 (GLOBE NEWSWIRE) -- Clearmind Medicine Inc. (Nasdaq: CMND) (“Clearmind” or the "Company"), a clinical-stage biotech company focused on the discovery and development of novel, non-hallucinogenic, second-generation, neuroplastogen-derived therapeutics to solve major under-treated health problems, today announced the signing of a new research agreement with Yissum Research Development Company of the Hebrew University of Jerusalem Ltd. The agreement will fund a comprehensive preclinical study evaluating the metabolic efficacy of MEAI (CMND-100), both in combination with and as a maintenance therapy following tirzepatide treatment in diet-induced obese ("DIO") mice. The research will be conducted by Professor Joseph (Yossi) Tam and his team at the Obesity and Metabolism Laboratory at the Institute for Drug Research, School of Pharmacy, Hebrew University of Jerusalem.
The global market for incretin-based therapies and tirzepatide has grown into a massive industry valued at approximately $50–66 billion in 2025, and is projected to reach
Building on positive results from its prior collaboration with Professor Yossi Tam’s laboratory at the Hebrew University, where MEAI demonstrated approximately 15–
The new 12-month study, titled “Assessing the Metabolic Efficacy of MEAI in Combination and Sequencing with Tirzepatide in Diet-Induced Obese Mice,” will examine: Additive or synergistic effects when MEAI is administered concomitantly with tirzepatide and the potential of MEAI as a maintenance therapy to attenuate post-tirzepatide weight regain and preserve metabolic benefits across multiple doses.
“MEAI is designed to offer a differentiated mechanism that potentially complements incretin therapies,” said Dr. Adi Zuloff-Shani, Ph.D., Chief Executive Officer of Clearmind Medicine. “While those drugs excel at reducing food intake, our previous preclinical data show MEAI significantly enhances energy expenditure. We believe that this combination and maintenance approach has potential to deliver more robust, durable, and clinically meaningful outcomes for patients.”
About Clearmind Medicine Inc.
Clearmind is a clinical-stage neuroplastogens pharmaceutical biotech company focused on the discovery and development of non-hallucinogenic, second generation, neuroplastogen-derived therapeutics to solve widespread and underserved health problems, including alcohol use disorder. Its primary objective is to research and develop psychedelic-based compounds and attempt to commercialize them as regulated medicines, foods, or supplements.
The Company’s intellectual portfolio currently consists of nineteen patent families, including 31 granted patents. The Company intends to seek additional patents for its compounds whenever warranted and will remain opportunistic regarding the acquisition of additional intellectual property to build its portfolio.
Shares of Clearmind are listed for trading on Nasdaq under the symbol "CMND."
For further information, visit: https://www.clearmindmedicine.com or contact:
Investor Relations
invest@clearmindmedicine.com
www.Clearmindmedicine.com
Forward-Looking Statements:
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act and other securities laws. Words such as “expects,” “anticipates,” “intends,” “plans,” “believes,” “seeks,” “estimates” and similar expressions or variations of such words are intended to identify forward-looking statements. For example, the Company is using forward-looking statements when it discusses the expected growth of the global market for incretin-based therapies, how Clearmind is advancing MEAI into combination and sequencing strategies with today’s leading incretin therapy, how MEAI is designed to offer a differentiated mechanism that potentially complements incretin therapies and its belief that the combination and maintenance approach of MEAI and incretin therapies has potential to deliver more robust, durable, and clinically meaningful outcomes for patients. Forward-looking statements are not historical facts, and are based upon management’s current expectations, beliefs and projections, many of which, by their nature, are inherently uncertain. Such expectations, beliefs and projections are expressed in good faith. However, there can be no assurance that management’s expectations, beliefs and projections will be achieved, and actual results may differ materially from what is expressed in or indicated by the forward-looking statements. Forward-looking statements are subject to risks and uncertainties that could cause actual performance or results to differ materially from those expressed in the forward-looking statements. For a more detailed description of the risks and uncertainties affecting the Company, reference is made to the Company’s reports filed from time to time with the Securities and Exchange Commission (“SEC”), including, but not limited to, the risks detailed in the Company’s annual report on Form 20-F for the fiscal year ended October 31, 2025 and subsequent filings with the SEC. Forward-looking statements speak only as of the date the statements are made. The Company assumes no obligation to update forward-looking statements to reflect actual results, subsequent events or circumstances, changes in assumptions or changes in other factors affecting forward-looking information except to the extent required by applicable securities laws. If the Company does update one or more forward-looking statements, no inference should be drawn that the Company will make additional updates with respect thereto or with respect to other forward-looking statements. References and links to websites have been provided as a convenience, and the information contained on such websites is not incorporated by reference into this press release. Clearmind is not responsible for the contents of third-party websites.
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