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Helus Pharma™ Announces Closing of US$50 Million Underwritten Offering

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Helus Pharma (Nasdaq: HELP, Cboe CA: HELP) closed a US$50 million underwritten offering of 10,309,280 common shares at US$4.85 per share. Underwriters received a US$3 million cash commission.

Net proceeds are intended to fund HLP003 (Phase 3 for major depressive disorder), HLP004 for generalized anxiety disorder, HLP005, and for working capital and general corporate purposes. Phase 3 APPROACH data for HLP003 are expected in Q4 2026.

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Positive

  • Underwritten equity financing raises US$50 million gross proceeds
  • Offering price set at US$4.85 per common share
  • Proceeds allocated to advance HLP003 Phase 3 for major depressive disorder
  • Funding directed to HLP004 for generalized anxiety disorder and HLP005 programs
  • Additional capital available for working capital and corporate purposes

Negative

  • Issuance of 10,309,280 new shares implies shareholder dilution
  • Underwriters received a US$3 million cash commission, reducing net proceeds

News Market Reaction – HELP

+18.27% 5.4x vol
53 alerts
+18.27% Session close to close
+24.3% Peak in 26 hr 22 min
$330.14M Market Cap
5.4x Rel. Volume

In the Jun 25 session, HELP gained 18.27%, reflecting a significant positive market reaction. Argus tracked a peak move of +24.3% during that session. Our momentum scanner triggered 53 alerts that day, indicating high trading interest and price volatility. Trading volume was exceptionally heavy at 5.4x the daily average, suggesting very strong buying interest.

Data tracked by StockTitan Argus on the day of publication.

Market Context

The stock surged +18.3% in the session following this news. A strong positive reaction aligns with p...
Analysis

The stock surged +18.3% in the session following this news. A strong positive reaction aligns with prior financing news, suggesting investors previously welcomed added capital to fund HLP003, HLP004 and HLP005. Dilution from new shares and relatively low short positioning remain key risks to sustaining gains.

Key Figures

Shares offered: 10,309,280 common shares Offering price: US$4.85 per share Gross proceeds: US$50 million +5 more
8 metrics
Shares offered 10,309,280 common shares Underwritten offering size
Offering price US$4.85 per share Equity financing terms
Gross proceeds US$50 million Total before expenses from offering
Underwriter commission US$3 million Cash commission paid to underwriters
Phase 3 data timing Q4 2026 Expected APPROACH Phase 3 data for HLP003
Base shelf date September 17, 2025 Short form base shelf prospectus date
Shelf amendment date December 19, 2025 Amendment to base shelf prospectus
Form F-10 file no. 333-292294 Registration statement reference

Previous Offering Reports

1 past event · Latest: Jun 24 (Negative)
Same Type Pattern 1 events
Date Event Sentiment 24h Move Catalyst
Jun 24 Equity offering Negative +5.0% Underwritten US$50M equity offering to fund HLP003, HLP004 and HLP005.

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

Pattern Detected

Limited history: the only prior offering headline was followed by a positive price reaction, contrary to typical dilution concerns.

Key Terms

underwritten offering, prospectus supplement, short form base shelf prospectus, registration statement on form f-10, +1 more
5 terms
underwritten offering financial
"it has closed its previously announced underwritten offering of 10,309,280 common shares"
An underwritten offering is when a bank or group of banks agrees to buy all of a company's new shares or bonds and then resell them to outside investors, guaranteeing the company will raise a specific amount of money. It matters to investors because it adds certainty that the funding will close while increasing the number of shares or debt in the market, which can lower the price per share and change each existing owner's ownership percentage—think of a wholesaler buying an entire shipment from a maker before it reaches stores.
prospectus supplement regulatory
"pursuant to a prospectus supplement (the “Prospectus Supplement”) to the Company’s short form base shelf prospectus"
A prospectus supplement is an additional document provided alongside a company's main offering details, offering updated or extra information about a specific financial product being sold. It helps investors understand the latest terms, risks, and details of the investment, similar to how an update or revision clarifies or expands on original instructions, ensuring they have current and complete information before making a decision.
short form base shelf prospectus regulatory
"to the Company’s short form base shelf prospectus dated September 17, 2025, as amended on December 19, 2025"
A short form base shelf prospectus is a pre-approved, reusable document that lets a company register a pool of securities (like stocks or bonds) it can sell over time without repeating a full disclosure process each time. Think of it as a menu the company files once so it can quickly offer items from that menu later; investors care because it speeds up capital raises, can dilute existing holdings, and signals the company’s ability to access funding when needed.
registration statement on form f-10 regulatory
"as part of a registration statement on Form F-10 (File No. 333-292294) which was filed with the SEC"
A registration statement on Form F-10 is a standardized filing used to register and offer securities to investors in Canada, combining the required prospectus disclosure with ongoing public reporting information from eligible issuers. It matters to investors because it provides a single, organized source of verified financial and business details they need to judge the risks and value of an offering—similar to a product label that lists ingredients and warnings before purchase—and signals the company can legally sell shares in that market.
multijurisdictional disclosure system regulatory
"in accordance with the Multijurisdictional Disclosure System established between Canada and the United States"
A multijurisdictional disclosure system is a regulatory framework that lets a company file one set of official documents and have them accepted by regulators in multiple countries, rather than preparing separate filings for each place. For investors, it means faster, more consistent access to a company’s financial reports and material news across borders, reducing delays and making it easier to compare information the way a single, shared form simplifies multiple applications.

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

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NEW YORK and TORONTO, June 25, 2026 (GLOBE NEWSWIRE) -- 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”), is pleased to announce that it has closed its previously announced underwritten offering of 10,309,280 common shares in the capital of the Company (the “Common Shares”) at an offering price of US$4.85 per Common Share for aggregate gross proceeds of US$50 million (the “Offering”).

Cantor and Barclays acted as joint bookrunning managers for the Offering. Bloom Burton Securities Inc. and Lucid Capital Markets acted as lead managers for the Offering.

The Company intends to use the net proceeds from the Offering to progress the Company’s HLP003 for major depressive disorder with Phase 3 APPROACH data expected in the fourth quarter of 2026, HLP004 for generalized anxiety disorder, and HLP005 programs, and for working capital and general corporate purposes.

The Company offered the Common Shares only in the United States and in certain other jurisdictions outside of Canada, pursuant to a prospectus supplement (the “Prospectus Supplement”) to the Company’s short form base shelf prospectus dated September 17, 2025, as amended on December 19, 2025 (the “Base Shelf Prospectus”). The Prospectus Supplement was filed with the securities commissions in all of the provinces and territories of Canada and with the United States Securities and Exchange Commission (the “SEC”), as part of a registration statement on Form F-10 (File No. 333-292294) which was filed with the SEC, under the United States Securities Act of 1933, as amended, on December 19, 2025, in accordance with the Multijurisdictional Disclosure System established between Canada and the United States. The Base Shelf Prospectus, the Prospectus Supplement and the documents incorporated by reference therein, including any marketing materials, are available on the Company’s SEDAR+ profile at www.sedarplus.ca and the Company’s EDGAR profile at www.sec.gov/edgar. An electronic or paper copy of the Base Shelf Prospectus and the Prospectus Supplement may be obtained, without charge, by contacting Cantor Fitzgerald & Co., Attention: Capital Markets, 110 East 59th Street, 6th Floor, New York, New York 10022, or by email at prospectus@cantor.com, or Barclays Capital Inc., c/o Broadridge Financial Solutions, 1155 Long Island Avenue, Edgewood, NY 11717, via telephone at (888) 603-5847, or via e-mail at Barclaysprospectus@broadridge.com.

In consideration for their services, the Company paid to the underwriters a cash commission of US$3 million.

This news release does not constitute an offer to sell or the solicitation of an offer to buy securities, nor will there be any sale of the securities, in any jurisdiction in which such offer, solicitation or sale would be unlawful.

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 – novel serotonergic agonists: 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 a portfolio of investigational NSAs.

The Company operates in Canada, the United States, the United Kingdom, and Ireland. 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 intended use of proceeds, and the Company’s ability to address the need for treatment options for people who suffer from depression, anxiety and other 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 and nine month periods ended December 31, 2025, and the Company’s annual information form for the year ended March 31, 2025, which are available under the Company’s profile on SEDAR+ at www.sedarplus.ca and the Company’s EDGAR profile 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 U.S. 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

George Tziras
Chief Business Officer
Helus Pharma
1-866-292-4601
irteam@cybin.com – or – media@cybin.com

Media Contact:
Johnny Tokarczyk
RXMD
Public Relations Director
jtokarczyk@rxmedyn.com
(914) 772-7562


FAQ

What did Helus Pharma (HELP) announce on June 25, 2026 about its stock offering?

Helus Pharma announced the closing of a US$50 million underwritten offering of common shares. According to Helus Pharma, 10,309,280 shares were sold at US$4.85 each, with Cantor and Barclays acting as joint bookrunning managers for the transaction.

How many shares did Helus Pharma (HELP) issue and at what price in the 2026 offering?

Helus Pharma issued 10,309,280 common shares at an offering price of US$4.85 per share. According to Helus Pharma, this underwritten transaction generated aggregate gross proceeds of US$50 million before underwriting commissions and expenses payable by the company.

How will Helus Pharma use the US$50 million raised in its HELP share offering?

Helus Pharma plans to use net proceeds to advance key clinical programs and corporate needs. According to Helus Pharma, funds will support HLP003 for major depressive disorder, HLP004 for generalized anxiety disorder, HLP005 programs, plus working capital and general corporate purposes.

What are the clinical milestones tied to Helus Pharma’s (HELP) HLP003 program?

Phase 3 APPROACH data for HLP003 in major depressive disorder are expected in Q4 2026. According to Helus Pharma, part of the offering proceeds will be used to progress this Phase 3 program toward that anticipated data readout timeline.

Who managed Helus Pharma’s June 2026 underwritten offering for HELP shares?

Cantor and Barclays served as joint bookrunning managers for the offering. According to Helus Pharma, Bloom Burton Securities and Lucid Capital Markets acted as lead managers, and underwriters collectively received a US$3 million cash commission for their services.

Where can investors find the Helus Pharma (HELP) prospectus for the US$50 million offering?

Investors can access the base shelf prospectus and prospectus supplement on SEDAR+ and EDGAR. According to Helus Pharma, documents are available via its SEDAR+ profile and SEC EDGAR profile, with free copies obtainable from Cantor Fitzgerald or Barclays on request.