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Cybin’s Helus Pharma CEO to speak at Morgan Stanley

Cybin’s Helus Pharma brand will feature its CEO in a fireside chat at the Morgan Stanley Global Healthcare Conference on September 16, 2026.

(Neutral)
(Neutral)
Form Type
6-K

Rhea-AI Filing Summary

Cybin Inc. (Helus Pharma) reported that its commercial operating name, Helus Pharma, will participate in the Morgan Stanley 24th Annual Global Healthcare Conference in New York City. Chief Executive Officer Michael Halstead is scheduled for a fireside chat on September 16, 2026 at 8:30 a.m. EDT, with a live webcast and replay available through the company’s investor relations website.

The company describes itself as a clinical-stage pharmaceutical business focused on proprietary novel serotonergic agonists (NSAs) aimed at improving treatments for depression, anxiety and other mental health conditions. Its lead candidate HLP003 is in Phase 3 development for adjunctive treatment of major depressive disorder and has received FDA Breakthrough Therapy Designation, while HLP004 is in Phase 2 development for generalized anxiety disorder.

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Conference date September 16, 2026 Date of Helus Pharma CEO fireside chat at Morgan Stanley Global Healthcare Conference
Conference time 8:30 a.m. EDT Scheduled start time of the fireside chat webcast
HLP003 development stage Phase 3 Adjunctive treatment of major depressive disorder
HLP004 development stage Phase 2 Treatment of generalized anxiety disorder
Breakthrough Therapy Designation Granted to HLP003 U.S. Food and Drug Administration designation for HLP003 in major depressive disorder
novel serotonergic agonists medical
"developing novel serotonergic agonists (“NSAs”)"
Breakthrough Therapy Designation regulatory
"that has received Breakthrough Therapy Designation from the U.S. Food and Drug"
A breakthrough therapy designation is a regulatory fast-track given to a drug or treatment that shows early signs of providing a major improvement over existing options for a serious condition. Think of it as a VIP lane that can speed up development and more intensive guidance from regulators, which matters to investors because it can shorten time to market, reduce development risk and potentially increase a company’s value — though it does not guarantee approval.
major depressive disorder medical
"for the adjunctive treatment of major depressive disorder"
A clinical condition characterized by persistent, severe low mood, loss of interest in daily activities, and reduced ability to function at work or home, lasting weeks or longer. It matters to investors because it drives demand for treatments and mental health services, affects workforce productivity and absenteeism, influences health-care and insurance costs, and shapes risks and opportunities for companies developing drugs, therapies or workplace programs—like a long-lasting storm that lowers economic output.
generalized anxiety disorder medical
"in Phase 2 for generalized anxiety disorder"
Generalized anxiety disorder is a chronic mental health condition marked by persistent, excessive worry about everyday things that is hard to control and interferes with daily life. Think of it like a smoke alarm that stays on for weeks or months, making work, decision-making and productivity harder; for investors it matters because it drives demand for treatments, affects workforce performance and can influence regulatory scrutiny, clinical trial design and healthcare spending.
neuroplasticity medical
"activate serotonin pathways that are believed to promote neuroplasticity"
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.

FAQ

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

What did Cybin Inc. (HELP), operating as Helus Pharma, announce in this Form 6-K?

Helus Pharma announced that CEO Michael Halstead will participate in a fireside chat at the Morgan Stanley 24th Annual Global Healthcare Conference in New York City, with a live webcast and replay available via the company’s investor relations website.

When will Helus Pharma’s (HELP) fireside chat at the Morgan Stanley conference take place?

The fireside chat is scheduled for September 16, 2026 at 8:30 a.m. EDT. It will be webcast live, and a replay will be accessible on Helus Pharma’s Events & Presentations page on its investor relations website.

What is Helus Pharma’s lead drug candidate HLP003 and what stage is it in?

HLP003 is a proprietary novel serotonergic agonist being developed for adjunctive treatment of major depressive disorder. It is currently in Phase 3 clinical development and has received Breakthrough Therapy Designation from the U.S. Food and Drug Administration.

What is Helus Pharma’s HLP004 program mentioned by Cybin (HELP)?

HLP004 is another proprietary novel serotonergic agonist in Helus Pharma’s pipeline. It is in Phase 2 clinical development for the treatment of generalized anxiety disorder, complementing the company’s focus on mental health conditions such as depression and anxiety.

In which regions does Cybin’s Helus Pharma operate according to this filing?

Helus Pharma states that it operates in Canada, the United States, the United Kingdom and Ireland, reflecting a multi-jurisdictional clinical and corporate footprint for its development of novel serotonergic agonists for mental health conditions.

What therapeutic focus does Helus Pharma (HELP) highlight in this disclosure?

Helus Pharma focuses on proprietary novel serotonergic agonists (NSAs), synthetic molecules designed to activate serotonin pathways believed to promote neuroplasticity. Its goal is to address large unmet needs in depression, anxiety and other mental health conditions with durable improvements in mental health.

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

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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: 001-40673


Cybin Inc.
(Exact Name of Registrant as Specified in Charter)

100 King Street West, Suite 5600, Toronto, Ontario, M5X 1C9
(Address of principal executive offices)

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






SIGNATURE
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.
CYBIN INC.
(Registrant)
Date:September 10, 2026By:
/s/ Greg Cavers    
Name:Greg Cavers
Title:Chief Financial Officer





EXHIBIT INDEX

99.1
News Release dated September 10, 2026





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Helus Pharma to Participate at the Morgan Stanley 24th Annual Global Healthcare Conference in New York

CEO Michael Halstead to participate in a fireside chat on Wednesday, September 16, 2026 at 8:30 a.m. EDT.

NEW YORK & TORONTO – September 10, 2026 – Helus Pharma (Nasdaq: HELP) (Cboe CA: HELP) (the “Company” or “Helus Pharma”), a clinical-stage pharmaceutical company committed to helping minds heal by developing novel serotonergic agonists (“NSAs”), today announced that Michael Halstead, Helus Pharma’s Chief Executive Officer, will participate in a fireside chat at the Morgan Stanley 24th Annual Global Healthcare Conference in New York City.

The fireside chat will be webcast live on Wednesday, September 16, 2026 at 8:30 a.m. EDT.

To register for the webcast, click here. A replay will be available on the Events & Presentations page of Helus Pharma’s investor relations website.

About Helus Pharma

Helus Pharma, the commercial operating name of Cybin Inc., is a clinical stage pharmaceutical company committed to helping minds heal by developing proprietary NSAs, synthetic molecules designed to activate serotonin pathways that are believed to promote neuroplasticity. The Company’s proprietary NSAs are intended to address the large unmet need for people who suffer from depression, anxiety, and other mental health conditions.

With class leading data, Helus Pharma aims to improve the treatment landscape through the introduction of NSAs that aim to provide durable improvements in mental health. Helus Pharma is currently developing HLP003, a proprietary NSA, in Phase 3 clinical development for the adjunctive treatment of major depressive disorder that has received Breakthrough Therapy Designation from the U.S. Food and Drug Administration and HLP004, also a proprietary NSA in Phase 2 for generalized anxiety disorder. Additionally, Helus Pharma has an extensive research portfolio of investigational NSAs.

The Company operates in Canada, the United States, the United Kingdom, and Ireland. For Company updates and to learn more about Helus Pharma, visit www.helus.com or follow the








team on X, LinkedIn, YouTube and Instagram. Helus Pharma™ is a trademark of Helus Pharma Corp.

Cautionary Notes and Forward-Looking Statements

Certain statements in this news release relating to the Company are forward-looking statements or forward-looking information within the meaning of applicable securities laws (collectively, “forward-looking statements”) and are prospective in nature. Forward-looking statements are 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 “may”, “should”, “could”, “potential”, “possible”, “intend”, “estimate”, “plan”, “anticipate”, “expect”, “believe” or “continue”, or the negative thereof or similar variations. Forward-looking statements in this news release include statements regarding the Company’s anticipated participation in the Morgan Stanley Healthcare Conference; and plans to engineer proprietary drug discovery platforms, innovative drug delivery systems, novel formulation approaches and treatment regimens for mental health conditions.

These forward-looking statements are based on reasonable assumptions and estimates of management of the Company at the time such statements were made. Actual future results may differ materially as forward-looking statements involve known and unknown risks, uncertainties, and other factors which may cause the actual results, performance, or achievements of the Company to materially differ from any future results, performance, or achievements expressed or implied by such forward-looking statements. Such factors, among other things, include: fluctuations in general macroeconomic conditions; fluctuations in securities markets; expectations regarding the size of the NSA market; the ability of the Company to successfully achieve its business objectives; plans for growth; political, social and environmental uncertainties; employee relations; the presence of laws and regulations that may impose restrictions in the markets where the Company operates; implications of disease outbreaks on the Company's operations; and the risk factors set out in each of the Company's management's discussion and analysis for the three months ended June 30, 2026, and the Company’s annual information form for the year ended March 31, 2026, which are available under the Company's profile on SEDAR+ at www.sedarplus.ca/ and with the U.S. Securities and Exchange Commission on EDGAR at www.sec.gov/edgar. Although the forward-looking statements contained in this news release are based upon what management of the Company believes, or believed at the time, to be reasonable assumptions, the Company cannot assure shareholders that actual results will be consistent with such forward-looking statements, as there may be other factors that cause results not to be as anticipated, estimated or intended. Readers should not place undue reliance on the forward-looking statements contained in this news release. The Company assumes no obligation to update the forward-looking statements of beliefs, opinions, projections, or other factors, should they change, except as required by law.









The Company makes no medical, treatment or health benefit claims about the Company’s proposed products. The US Food and Drug Administration, Health Canada or other similar regulatory authorities have not evaluated claims regarding NSAs or HLP003, HLP004 and other programs of the Company. The efficacy of such products has not been confirmed by approved research. There is no assurance that the use of NSAs, HLP003, HLP004 or other programs of the Company can diagnose, treat, cure or prevent any disease or condition. Rigorous scientific research and clinical trials are needed. If Helus Pharma cannot obtain the approvals or research necessary to commercialize its business, it may have a material adverse effect on the Company’s performance and operations.

Neither Cboe Canada, nor the Nasdaq Global Market stock exchange, have approved or disapproved the contents of this news release and are not responsible for the adequacy and accuracy of the contents herein.


Investor Contact:
Matthew Beck
astr partners
Managing Partner
(917) 415-1750
Matthew.beck@astrpartners.com

Gabriel Fahel
Chief Legal Officer
Helus Pharma
1-866-292-4601
irteam@helus.com – or – media@helus.com


Media Contact:
Victoria Verdeja
RXMD
Public Relations Director
(212) 537-9495
vverdeja@rxmedyn.com







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