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Clearmind Medicine Announces “Inside MEAI” Webinar Featuring New Insights from CMND-100 Psychedelic Clinical Trial

Rhea-AI Impact
(High)
Rhea-AI Sentiment
(Positive)

Clearmind Medicine (Nasdaq: CMND) will host a live webinar, “Inside MEAI: New Insights from the CMND-100 Psychedelic Clinical Trial,” on June 10, 2026, 4:00–5:00 PM IDT.

The event will review latest Phase I/IIa CMND-100 data in Alcohol Use Disorder, featuring investigators from Yale and Johns Hopkins, and include corporate updates and a live Q&A.

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AI-generated analysis. Not financial advice.

Positive

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Negative

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News Market Reaction – CMND

-5.56%
12 alerts
-5.56% News Effect
+6.8% Peak in 15 hr 10 min
-$51K Valuation Impact
$869,756 Market Cap
0.0x Rel. Volume

On the day this news was published, CMND declined 5.56%, reflecting a notable negative market reaction. Argus tracked a peak move of +6.8% during that session. Our momentum scanner triggered 12 alerts that day, indicating notable trading interest and price volatility. This price movement removed approximately $51K from the company's valuation, bringing the market cap to $869,756 at that time.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

Webinar date: June 10, 2026 Webinar time: 4:00 PM–5:00 PM IDT Trial phase: Phase I/IIa
3 metrics
Webinar date June 10, 2026 “Inside MEAI” CMND-100 clinical data webinar
Webinar time 4:00 PM–5:00 PM IDT Scheduled duration of CMND-100 data webinar
Trial phase Phase I/IIa Ongoing multi-center CMND-100 trial for Alcohol Use Disorder

Market Reality Check

Price: $3.17 Vol: Volume 355,449 is far bel...
low vol
$3.17 Last Close
Volume Volume 355,449 is far below 20-day average of 14,533,758 (0.02x), suggesting muted pre-news trading. low
Technical Shares at $0.5508 sit close to the 52-week low of $0.5202 and far below the 200-day MA at $16.76, signaling a heavily beaten-down trend before this update.

Peers on Argus

Multiple biotech peers showed mixed moves, with several negative. KTTA was down ...
1 Up 2 Down

Multiple biotech peers showed mixed moves, with several negative. KTTA was down 4.55%, TTNP down 3.96%, SXTP down 2.53%, while PLRZ gained 16.38%. Momentum data also flagged KTTA and SILO, indicating broader sector cross-currents rather than a purely idiosyncratic setup.

Common Catalyst No clear shared news catalyst across peers; only PLRZ reported a separate product-focused headline.

Previous Clinical trial Reports

5 past events · Latest: Apr 20 (Positive)
Same Type Pattern 5 events
Date Event Sentiment Move Catalyst
Apr 20 Safety endpoint met Positive +58.4% CMND-100 met primary safety and tolerability endpoint with no serious events.
Apr 15 DSMB safety review Positive -28.6% Independent DSMB issued positive recommendation to continue the Phase I/IIa trial.
Apr 14 Endpoint achievement Positive -36.4% CMND-100 again reported meeting primary safety and tolerability endpoint in trial.
Mar 30 Treatment completion Positive +22.7% Completed treatment and follow-up for 18 participants in Phase I/IIa trial.
Mar 19 Ongoing treatment Positive -3.1% Reported successful ongoing treatment at Yale and Johns Hopkins with no serious events.
Pattern Detected

Clinical-trial headlines for CMND-100 have produced mixed reactions, with more divergences than alignments despite generally positive safety and progress updates.

Recent Company History

Recent news for Clearmind has centered on its FDA-approved Phase I/IIa trial of CMND-100 for Alcohol Use Disorder. From Mar 19 through Apr 20, the company reported successful ongoing treatment, completion of follow-up for 18 participants, positive DSMB recommendations, and the trial meeting its primary safety and tolerability endpoint with no serious adverse events. Market reactions to these clinical updates have been volatile, with both sharp gains and steep declines, framing today’s webinar-focused announcement as part of an ongoing trial narrative.

Historical Comparison

+2.6% avg move · Past clinical-trial updates on CMND-100 produced volatile but modest average moves of 2.61%, with bo...
clinical trial
+2.6%
Average Historical Move clinical trial

Past clinical-trial updates on CMND-100 produced volatile but modest average moves of 2.61%, with both sharp rallies and notable selloffs.

Same-tag history shows steady advancement of the CMND-100 Phase I/IIa program: successful ongoing treatment at U.S. sites, completion of follow-up for 18 participants, repeated confirmation of safety with no serious adverse events, and achievement of the primary safety and tolerability endpoint, all building the backdrop for further data discussions.

Regulatory & Risk Context

Active S-3 Shelf · $10.0M principal plus $3.576M accrued interest
Shelf Active
Active S-3 Shelf Registration 2026-04-30
$10.0M principal plus $3.576M accrued interest registered capacity

An effective Form F-3 dated Apr 30, 2026 registers up to 22,626,988 common shares for resale tied to convertible promissory notes. The registration covers conversion of up to $10.0M principal and $3.576M accrued interest at an assumed $0.60 per share, alongside additional financing capacity and VWAP-based conversion mechanics. This framework enables CLA Investors to convert debt to equity within the filing’s terms.

Market Pulse Summary

The stock moved -5.6% in the session following this news. A negative reaction despite a data-focused...
Analysis

The stock moved -5.6% in the session following this news. A negative reaction despite a data-focused webinar announcement would fit a pattern where positive CMND-100 trial updates sometimes preceded declines, including moves of -36.36% and -28.57%. Historically, an average same-tag move of only 2.61% masks wide swings in both directions. An effective F-3 registering 22,626,988 resale shares tied to convertible notes may contribute to perceived overhang and help explain investor sensitivity to new headlines.

Key Terms

phase i/iia, alcohol use disorder, aud, neuroplasticity, +4 more
8 terms
phase i/iia medical
"ongoing FDA-approved Phase I/IIa multi-center trial evaluating CMND-100"
An early-stage clinical trial program that combines Phase I (primarily testing safety and finding a tolerable dose) with Phase IIa (initial checks for whether the drug shows signs of working in patients). Think of it as trying a new product with a small group to confirm it’s safe and gives early benefits before a larger rollout. For investors, these studies are major risk/reward checkpoints: positive results can boost value, while failures are common and costly.
alcohol use disorder medical
"oral drug candidate, for the treatment of Alcohol Use Disorder (AUD)."
A chronic medical condition characterized by an inability to control or stop drinking despite negative effects on health, work, relationships or safety; it ranges from mild to severe based on frequency, loss of control, and withdrawal symptoms. Investors care because its prevalence and treatment options affect markets for pharmaceuticals, medical services and health-related productivity—think of it like a long-running equipment fault in a factory that reduces output and creates demand for repairs and preventive solutions.
aud medical
"oral drug candidate, for the treatment of Alcohol Use Disorder (AUD)."
AUD is the international currency code for the Australian dollar, the official money used in Australia and several nearby territories. Investors watch AUD because changes in its value act like a price tag or thermometer for assets and transactions denominated in that currency — affecting export revenues, import costs, commodity prices, and the value of overseas investments. Movements in AUD can change returns and risk for portfolios with exposure to Australia or Australian-dollar contracts.
neuroplasticity medical
"mechanistic studies using advanced brain imaging to explore neuroplasticity, functional connectivity"
Neuroplasticity is the brain’s ability to change its wiring and strength of connections in response to experience, injury, or treatment—like a city that reroutes and upgrades roads to handle new traffic. For investors, it matters because therapies, devices, or programs that harness or enhance this adaptability can improve patient outcomes, extend treatment markets, and influence clinical trial success, regulatory chances, and long-term revenue potential.
functional connectivity medical
"brain imaging to explore neuroplasticity, functional connectivity, and endocannabinoid system"
Functional connectivity describes how different areas of the brain show coordinated activity over time — essentially how well they "talk" to each other during tasks or at rest. Investors should care because changes in these patterns can be used as biomarkers for neurological or psychiatric conditions, to measure drug or device effects, or to support claims about a product’s impact on brain function, which affects clinical value, regulatory approval, and market potential.
endocannabinoid system medical
"explore neuroplasticity, functional connectivity, and endocannabinoid system dysregulation in addiction"
A system of receptors, signaling molecules and enzymes in the body that helps regulate appetite, mood, pain, sleep, immune response and other basic functions — acting like an internal messaging and balance system. It matters to investors because drugs, medical treatments or consumer products that safely target this system can create new markets or change competitive dynamics; research results, clinical progress and regulatory rulings can therefore have a direct impact on a company’s commercial prospects and valuation.
ptsd medical
"therapeutic potential of psychedelics and other novel compounds for alcohol use disorder, depression, and PTSD"
PTSD, or post-traumatic stress disorder, is a mental health condition that can develop after experiencing or witnessing a traumatic event, leading to ongoing feelings of fear, anxiety, or distress. For investors, understanding PTSD is important because widespread psychological impacts can influence market behavior, cause sudden shifts in confidence, or affect economic stability during times of collective trauma or crisis.
psychedelics medical
"therapeutic potential of psychedelics and other novel compounds for alcohol use disorder"
Psychedelics are a class of drugs that temporarily alter perception, mood and thought patterns, often producing vivid sensory changes or introspective experiences. Investors watch them because scientific trials, regulatory decisions and shifting laws can create or destroy markets for medical treatments, diagnostics and services—similar to how a new technology can open entirely new industries—so clinical results and approvals tend to drive company value and investor risk.

AI-generated analysis. Not financial advice.

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Registration Now Open - Join the Live Webinar on June 10, 2026

Vancouver, Canada, May 11, 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 it will host a live webinar titled “Inside MEAI: New Insights from the CMND-100 Psychedelic Clinical Trial” on Wednesday, June 10, 2026, from 4:00 PM to 5:00 PM IDT.

Interested participants are invited to register and secure their spot in this exclusive session.

The webinar will provide an in-depth review of the latest clinical data from the Company’s ongoing FDA-approved Phase I/IIa multi-center trial evaluating CMND-100, its proprietary non-hallucinogenic MEAI-based oral drug candidate, for the treatment of Alcohol Use Disorder (AUD).

The webinar will feature presentations and discussions by leading clinical investigators from the CMND-100 multi-center trial. Dr. Anahita Bassir Nia, MD, an addiction psychiatrist and Assistant Professor of Psychiatry at the Yale School of Medicine, will share insights from the Yale trial site. Her research focuses on developing novel treatments for addiction and stress-related disorders, with a particular emphasis on cannabinoids and psychedelics. She leads clinical trials examining the therapeutic potential of psychedelics and other novel compounds for alcohol use disorder, depression, and PTSD, while conducting mechanistic studies using advanced brain imaging to explore neuroplasticity, functional connectivity, and endocannabinoid system dysregulation in addiction and trauma-related conditions.

Joining her will be Dr. Jennifer Ellis, Ph.D., Assistant Professor and licensed clinical psychologist at Johns Hopkins Medicine, who serves as a principal investigator at the Johns Hopkins trial site. Dr. Ellis’s research centers on identifying new therapeutics for substance use disorders and optimizing treatment outcomes for individuals with co-occurring psychiatric conditions.

Dr. Adi Zuloff-Shani, Ph.D., Chief Executive Officer of Clearmind Medicine, who will moderate the session and provide an overview of the clinical development strategy and corporate updates, said: “The positive safety data and encouraging signals we have seen, together with the expertise of our distinguished clinical investigators, reinforce our belief in MEAI’s potential as a transformative, non-hallucinogenic treatment option for Alcohol Use Disorder.”

The event is open to the public and will include a live Q&A session. Registration is available via Eventbrite.

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 its belief in MEAI’s potential as a transformative, non-hallucinogenic treatment option for Alcohol Use Disorder.. 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.


FAQ

What is the Clearmind Medicine (CMND) “Inside MEAI” webinar about on June 10, 2026?

The webinar will review new clinical insights from Clearmind’s CMND-100 psychedelic trial for Alcohol Use Disorder. According to Clearmind, investigators will discuss Phase I/IIa data, neuroplasticity research, and the company’s broader clinical development strategy for its non-hallucinogenic MEAI-based oral candidate.

When is the Clearmind Medicine (CMND) CMND-100 clinical trial webinar and how long will it last?

Clearmind’s “Inside MEAI” webinar is scheduled for June 10, 2026, from 4:00 PM to 5:00 PM IDT. According to Clearmind, the one-hour session will cover latest CMND-100 clinical data, feature expert presentations, and end with a live investor-focused Q&A.

Who are the key speakers at Clearmind Medicine’s (CMND) Inside MEAI CMND-100 webinar?

The webinar will feature Dr. Anahita Bassir Nia from Yale and Dr. Jennifer Ellis from Johns Hopkins. According to Clearmind, CEO Dr. Adi Zuloff-Shani will moderate, highlight clinical development plans, and provide corporate updates around CMND-100 for Alcohol Use Disorder.

What will investors learn about the CMND-100 Alcohol Use Disorder trial at the Clearmind (CMND) webinar?

Investors will hear an in-depth review of CMND-100 Phase I/IIa clinical data for Alcohol Use Disorder. According to Clearmind, speakers will discuss safety findings, therapeutic signals, and how non-hallucinogenic MEAI-based therapy fits into the company’s broader addiction treatment pipeline.

How can investors register for Clearmind Medicine’s (CMND) Inside MEAI CMND-100 webinar?

Registration for the Inside MEAI webinar is open to the public via Eventbrite. According to Clearmind, interested investors can secure a free spot online and join live to hear clinical investigators, review new CMND-100 data, and participate in the Q&A session.