STOCK TITAN

Clearmind highlights 3 U.S. psychedelic patent bids

The publications add to a company-reported portfolio of 19 patent families, including 32 granted patents.

(Neutral)
(Neutral)
Form Type
6-K

Rhea-AI Filing Summary

Clearmind Medicine Inc. (CMND) announced the U.S. publication of three patent applications covering combinations of LSD, ketamine and ibogaine with N-acylethanolamines, such as palmitoylethanolamide (PEA). The applications describe potential uses across conditions including depression, PTSD, pain and substance use disorders.

The publications expand intellectual property developed through Clearmind’s ongoing collaboration with NeuroThera Labs Inc., whose PEA technology is integrated into Clearmind’s psychedelic-derived therapeutic programs. Clearmind’s current intellectual property portfolio consists of 19 patent families, including 32 granted patents; it had previously announced a U.S. application covering MDMA and N-acylethanolamines.

Clearmind said it believes the combination approach may support therapeutic benefits at lower doses while preserving efficacy and may improve tolerability. It cautioned that it cannot assure a pending application will result in a patent or that any patent issued will be advantageous to the company.

Positive

  • None.

Negative

  • None.

Filing Explained

This Form 6-K makes its September 23 press release part of the company’s listed Form F-3 and Form S-8 registration statements from submission, so the new effect here is incorporation of disclosure into those filings.

Published patent applications 3 applications U.S. publications covering combinations with N-acylethanolamines.
Patent families 19 families Clearmind’s current intellectual property portfolio.
Granted patents 32 patents Included in Clearmind’s current intellectual property portfolio.
N-acylethanolamines technical
"combinations of LSD, ketamine and ibogaine with N-acylethanolamines"
N-acylethanolamines are a family of naturally occurring fatty molecules that act as small chemical messengers inside the body, helping cells communicate about inflammation, appetite, pain and other processes. Investors care because these molecules can be targets or biomarkers for drugs, diagnostics and wellness products — like a visible readout on a dashboard that indicates whether a treatment is working or a condition is present — which affects clinical development, regulatory approval and market potential.
palmitoylethanolamide medical
"such as palmitoylethanolamide (PEA)"
Palmitoylethanolamide (PEA) is a naturally occurring fatty molecule produced in the body and sold as a supplement or experimental therapy for reducing pain and inflammation; think of it as a built‑in calming signal that helps quiet irritated tissues. Investors watch PEA because its potential medical benefits, regulatory path (supplement vs. drug), and clinical evidence drive market demand, pricing and the risk/reward of companies developing or selling PEA-based products — similar to how a promising ingredient can change the fortunes of a consumer brand.
neuroplastogen medical
"non-hallucinogenic, second generation, neuroplastogen-derived therapeutics"
A neuroplastogen is a drug or compound designed to boost the brain’s ability to rewire and form new connections, enhancing recovery or adaptation after injury, stress, or disease. For investors, these molecules matter because they target underlying brain repair processes rather than just masking symptoms, offering the potential for durable benefits in conditions like depression, neurodegeneration, or cognitive decline—akin to giving a tired garden fresh tools to regrow and reshape itself.
substance use disorders medical
"pain and substance use disorders"
A substance use disorder is a medical condition in which a person’s use of drugs or alcohol becomes compulsive, persists despite harmful consequences, and interferes with daily life; it changes brain pathways that control judgment and self-control, similar to a damaged navigation system that keeps sending someone the wrong directions. Investors should care because prevalence, treatment demand, approval of therapies, regulatory scrutiny, litigation, and related healthcare costs can materially affect the revenue, expenses, and risk profile of companies in health care, pharmaceuticals, insurers, and employers.

FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

What did CMND announce about its U.S. patent applications?

CMND announced the U.S. publication of three patent applications covering combinations of LSD, ketamine and ibogaine with N-acylethanolamines, such as PEA.

Which compounds are covered by the CMND applications?

The applications cover combinations of LSD, ketamine and ibogaine with N-acylethanolamines, including palmitoylethanolamide (PEA).

What potential uses do the CMND applications describe?

The applications describe potential therapeutic uses for mental health disorders, including depression and PTSD, as well as pain and substance use disorders.

How is NeuroThera Labs involved with CMND?

The publications expand intellectual property generated through Clearmind’s ongoing collaboration with NeuroThera Labs Inc. NeuroThera’s PEA technology is integrated into Clearmind’s psychedelic-derived therapeutic programs.

How many patent families and granted patents does CMND report?

Clearmind says its current intellectual property portfolio consists of 19 patent families, including 32 granted patents.

Have the three CMND applications become granted patents?

CMND announced publication of three patent applications. The company said it cannot assure that a pending application will result in a patent or, if issued, that it will issue in a form advantageous to the company.

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

See more from StockTitan in Google Search and AI answers. Adds StockTitan as a preferred source · opens Google
Add on Google
Learn about SEC filing dates

 

  

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

Form 6-K

 

Report of Foreign Private Issuer

Pursuant to Rule 13a-16 or 15d-16

under the Securities Exchange Act of 1934

 

For the month of: September 2026

 

Commission file number: 001-41557

 

CLEARMIND MEDICINE INC.

(Translation of registrant’s name into English)

 

101 – 1220 West 6th Avenue

Vancouver, British Columbia

(Address of principal executive offices)

 

Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F.

 

Form 20-F       Form 40-F 

 

 

 

 

 

CONTENTS

 

Attached hereto and incorporated herein is the Registrant’s press release issued on September 23, 2026, titled “Clearmind Enhances U.S. IP Presence with Publication of Three Patent Applications Covering LSD, Ketamine and Ibogaine Combinations.”

 

The two paragraphs of the press release attached to this Form 6-K as Exhibit 99.1 are incorporated by reference into the Registrant’s Registration Statements on Form F-3 (File Nos. 333-275991333-270859333-273293333-290404333-293521 and 333-295455) and Form S-8 (File No. 333-283695), filed with the Securities and Exchange Commission, to be a part thereof from the date on which this report is submitted, to the extent not superseded by documents or reports subsequently filed or furnished. 

 

 1 

 

 

EXHIBIT INDEX

 

Exhibit No.    
99.1   Press release titled: “Clearmind Enhances U.S. IP Presence with Publication of Three Patent Applications Covering LSD, Ketamine and Ibogaine Combinations”

 

 2 

 

 

SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

 

  Clearmind Medicine, Inc.
  (Registrant)
     
Date: September 23, 2026 By: /s/ Adi Zuloff-Shani
  Name:  Adi Zuloff-Shani
  Title: Chief Executive Officer

 

 3 

Exhibit 99.1

 

 

Clearmind Enhances U.S. IP Presence with Publication of Three Patent Applications Covering LSD, Ketamine and Ibogaine Combinations

 

The covered applications address potential therapeutic uses across a range of indications, including mental health disorders, such as depression and PTSD as well as substance use disorders

 

Vancouver, Canada, Sept. 23, 2026 (GLOBE NEWSWIRE) -- Clearmind Medicine Inc. (Nasdaq: CMND) (the “Company”), a clinical-stage biopharmaceutical company advancing non-hallucinogenic psychedelic-derived neuroplastogen for scalable treatment of neuropsychiatric, metabolic, and addiction disorders including Alcohol Use Disorder (“AUD”), today announced the publication in the United States of three patent applications covering novel proprietary combinations of lysergic acid diethylamide (“LSD”), ketamine and ibogaine with N-acylethanolamines, such as palmitoylethanolamide (“PEA”). The covered applications address potential therapeutic uses across a range of indications, including mental health disorders, such as depression, post-traumatic stress disorder (“PTSD”), pain and substance use disorders.

 

The publications expand the intellectual property generated through Clearmind’s ongoing collaboration with NeuroThera Labs Inc. (TSXV: NTLX), under which NeuroThera’s PEA technology is integrated into Clearmind’s psychedelic-derived therapeutic programs. The collaboration has resulted in a growing portfolio of patent applications covering combinations of PEA with psychedelic and psychoactive compounds. Clearmind previously announced U.S. publication of a patent application covering the combination of MDMA and N-acylethanolamines for potential treatment of PTSD, anxiety and eating disorders.

 

“The publication of these patents come at a significant time as clinical and regulatory interest in LSD, ketamine and ibogaine continues to receive growing recognition and support for their therapeutic potential. Clearmind believes its combination approach may offer the potential for an effective and safer treatment paradigm, aiming to achieve therapeutic benefits at lower doses while preserving efficacy. By reducing the dose required to achieve the intended pharmacological effect, this approach may support improved tolerability while maintaining therapeutic potential.,” said Adi Zuloff-Shani, Ph.D., Chief Executive Officer of Clearmind.

 

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 32 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 potential therapeutic applications of the combinations covered by the published patent applications; the potential benefits, advantages and characteristics of such combinations, including the possibility of achieving therapeutic benefits at lower doses and supporting tolerability; the Company’s intellectual property strategy and patent portfolio; the expected benefits of its collaboration with NeuroThera Labs Inc.; and the development, advancement and commercial potential of the Company’s product candidates and technologies. The Company cannot assure that any patent will issue as a result of a pending patent application or, if issued, whether it will issue in a form that will be advantageous to the Company. 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. 

 

   

Filing Exhibits & Attachments

1 document

Keep reading