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Clearmind Medicine CEO Dr. Adi Zuloff-Shani named Delegate to Federal Policy Summit on Psychedelic Medicine in Washington, D.C.

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Clearmind Medicine (Nasdaq: CMND) announced that CEO Dr. Adi Zuloff-Shani was named a delegate to the Psychedelic Medicine Coalition’s annual federal policy summit held May 14, 2026 at the National Press Club in Washington, D.C.

The summit gathered U.S. federal officials, legislators, researchers, clinicians and biopharma leaders to discuss psychedelic medicine policy. Clearmind is advancing a non-hallucinogenic psychedelic candidate in Phase IIa clinical trials at Johns Hopkins, Yale, and other leading sites.

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News Market Reaction – CMND

-1.63%
1 alert
-1.63% Session close to close
$792,814 Market Cap
5.92K Volume

In the May 15 session, CMND declined 1.63%, reflecting a mild negative market reaction.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement highlights Clearmind’s CEO participating as a delegate at a federal policy summit ...
Analysis

This announcement highlights Clearmind’s CEO participating as a delegate at a federal policy summit on psychedelic medicine, reinforcing the company’s role in shaping U.S. dialogue around non-hallucinogenic therapies. It complements ongoing Phase IIa clinical work at leading sites like Johns Hopkins and Yale. In evaluating the news, investors may track progress of these trials, future regulatory interactions, and any changes in financing structures linked to the existing Form F-3 registration for note-related share resales.

Key Figures

Trial phase: Phase IIa Summit date: May 14, 2026
2 metrics
Trial phase Phase IIa Non-hallucinogenic psychedelic candidate clinical trials at Johns Hopkins and Yale
Summit date May 14, 2026 Federal policy summit at National Press Club in Washington, D.C.

Historical Context

5 past events · Latest: May 12 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 12 Clinical milestone Positive +3.8% Reported 20 participants treated in FDA-approved Phase I/IIa CMND-100 AUD trial.
May 11 Clinical update Positive -5.6% Announced “Inside MEAI” webinar to review latest Phase I/IIa CMND-100 data.
May 05 IP expansion Positive -9.6% Filed European patent for non-hallucinogenic PTSD compounds under global Yissum license.
Apr 27 Regulatory evaluation Positive -10.1% Began evaluating CMND-100 for potential FDA Breakthrough Therapy Designation in AUD.
Apr 20 Policy support Positive -28.1% Welcomed U.S. Executive Order prioritizing FDA review of certain psychedelic therapies.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent history shows frequent divergence: largely positive clinical and policy updates have often been followed by negative price reactions, with only one of the last five news events aligning positively with the subsequent move.

Recent Company History

Over the past month, Clearmind reported several clinical and policy milestones. On Apr 15, a DSMB review supported advancing CMND-100 to a 160 mg dose, followed by additional convertible note financing and governance changes on Apr 20–30. Subsequent filings covered a European PTSD patent and a 20-participant milestone in the Phase I/IIa AUD trial at sites including Yale and Johns Hopkins. Despite broadly constructive news, shares often moved lower afterward, highlighting a pattern of weak price follow-through.

Key Terms

psychedelic medicine, neuroplastogen-derived therapeutics, phase iia
3 terms
psychedelic medicine medical
"Federal Officials, Researchers, Clinicians and Biopharma Leadership Convened by Psychedelic Medicine Coalition at the National Press Club"
Psychedelic medicine is the therapeutic use of mind‑altering compounds, given in supervised clinical settings alongside psychological support, to help reset or rewire patterns of thinking and emotion in conditions like depression, PTSD, and addiction — think of it as a guided ‘reboot’ for a stuck brain. It matters to investors because clinical trial results, regulatory approvals, and changing laws can rapidly create or shrink new markets, affect valuations, and shift risk for companies developing these treatments.
neuroplastogen-derived therapeutics medical
"novel, non-hallucinogenic, second-generation, neuroplastogen-derived therapeutics to solve major under-treated health problems"
Neuroplastogen-derived therapeutics are drugs or biological treatments developed from compounds that promote neuroplasticity — the brain’s ability to rewire and form new connections after injury or in response to learning. For investors, they matter because these therapies target underlying brain repair mechanisms rather than only masking symptoms, offering the potential for durable benefits in conditions like depression, stroke recovery, or neurodegeneration; if effective, they can create large, high-value markets similar to replacing a faulty bridge with a stronger one.
phase iia medical
"Clearmind Medicine is currently advancing its non-hallucinogenic psychedelic candidate, with Phase IIa clinical trials underway at Johns Hopkins, Yale"
Phase IIa is an early mid-stage clinical study that tests whether a new drug or treatment shows the intended biological effect in patients and helps identify the best dose. Think of it as a focused test-drive to see if a medicine does what it’s supposed to and what dose is tolerable before larger trials. Investors watch Phase IIa results because positive findings reduce technical risk and can materially increase the program’s value, while negative results raise the likelihood of costly delays or failure.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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Federal Officials, Researchers, Clinicians and Biopharma Leadership Convened by Psychedelic Medicine Coalition at the National Press Club

Vancouver, Canada, May 15, 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 that Clearmind Medicine’s CEO, Dr. Adi Zuloff-Shani, was named a delegate to this year’s annual invite-only federal policy summit that convened on May 14 at the National Press Club in Washington, D.C. 

The Psychedelic Medicine Coalition’s Federal Policy Summit brought together members of the U.S. Senate and House and key Federal figures to build consensus with global psychedelic biopharma CEOs, noted researchers, eminent clinicians, and professors from some of America’s distinguished academic institutions, including Johns Hopkins, Harvard and Yale Universities. 

“It was an honor to participate in this important policy summit convening alongside leading researchers, clinicians and policymakers,” said Dr. Adi Zuloff-Shani, CEO of Clearmind Medicine. “We look forward to contributing to constructive dialogue that advances responsible development of psychedelic-derived therapies for patients in need.”

Known for her collaborative leadership style, Dr. Zuloff-Shani’s thinking on the importance of achieving harmonization between regulators, legislators, and the biopharma community was recently featured in Psychology Today.   

Clearmind Medicine is currently advancing its non-hallucinogenic psychedelic candidate, with Phase IIa clinical trials underway at Johns Hopkins, Yale, and additional leading sites.

Participants included:

  • Congressman Lou Correa (D-CA), Co-Chair Congressional Psychedelics Caucus
  • Congressman Jack Bergman (R-MI), Co-Chair Congressional Psychedelics Caucus
  • Senator Tim Sheehy (R-MT), lead sponsor of the Novel Therapeutics Preparedness Act, advancing veteran access to emerging therapies
  • Matthew Zorn, JD, Deputy General Counsel, HHS
  • Professor John Krystal, MD, of Yale School of Medicine where he chairs the Department of Psychiatry, serves as Chief of Psychiatry for the Yale-New Haven Health System, co-leads the Yale Center for Clinical Investigation (CTSA), co-directs the NIAAA Center for the Translational Neuroscience of Alcohol, and leads the Clinical Neuroscience Division of the National Center for PTSD (VA)
  • Nora Volkow, MD, Director of  National Institute on Drug Abuse, NIDA, at the National Institutes of Health NIH

“This invite-only convening goes beyond the four walls of a symposium and instead serves a practical purpose as a bipartisan working group”, said Melissa Lavasani, founder and CEO of the nonprofit Psychedelic Medicine Coalition. She added, “As federal support accelerates, this Federal Summit is how we build that critical bridge between policy, practice, and patient care."

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 contributing to constructive dialogue that advances responsible development of psychedelic-derived therapies for patients in need. 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 did Clearmind Medicine (NASDAQ: CMND) announce about its CEO and the 2026 federal policy summit?

Clearmind Medicine announced that CEO Dr. Adi Zuloff-Shani was named a delegate to the 2026 Federal Policy Summit on psychedelic medicine. According to Clearmind Medicine, the invite-only event convened May 14, 2026, at the National Press Club in Washington, D.C.

What is the Psychedelic Medicine Coalition Federal Policy Summit attended by Clearmind Medicine’s CEO?

The Psychedelic Medicine Coalition Federal Policy Summit is an invite-only bipartisan working meeting on psychedelic medicine policy. According to Clearmind Medicine, it brought together U.S. senators, representatives, key federal figures, researchers, clinicians and psychedelic biopharma CEOs at the National Press Club in Washington, D.C.

Why is Dr. Adi Zuloff-Shani’s participation in the psychedelic policy summit important for Clearmind Medicine (CMND) investors?

Dr. Adi Zuloff-Shani’s participation highlights Clearmind Medicine’s involvement in federal-level discussions on psychedelic-derived therapies. According to Clearmind Medicine, this role supports dialogue on regulatory harmonization, which may be relevant to how future policies shape development pathways for its non-hallucinogenic psychedelic candidates.

What clinical trials is Clearmind Medicine (CMND) advancing alongside its participation in the Washington, D.C. summit?

Clearmind Medicine is advancing a non-hallucinogenic psychedelic candidate in Phase IIa clinical trials. According to Clearmind Medicine, the trials are underway at Johns Hopkins, Yale, and additional leading clinical sites, focusing on psychedelic-derived therapeutics aimed at major under-treated health problems.

Who were some key participants at the 2026 psychedelic federal policy summit attended by Clearmind Medicine’s CEO?

Key participants included members of the U.S. Senate and House and senior federal officials. According to Clearmind Medicine, attendees featured Congressman Lou Correa, Congressman Jack Bergman, Senator Tim Sheehy, HHS Deputy General Counsel Matthew Zorn, and leading researchers such as Dr. John Krystal and Dr. Nora Volkow.