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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the
Securities Exchange Act of 1934
Date of Report (Date of earliest event reported): June
10, 2026
Edesa Biotech, Inc.
(Exact name of registrant as specified in its charter)
| British Columbia, Canada |
|
001-37619 |
|
N/A |
(State or other jurisdiction
of incorporation) |
|
(Commission File Number) |
|
(IRS Employer
Identification No.) |
| 100 Spy Court, Markham, Ontario, Canada |
|
L3R 5H6 |
| (Address of principal executive offices) |
|
(Zip Code) |
(289) 800-9600
Registrant’s telephone number, including area code
| N/A |
| (Former name or former address, if changed since last report) |
Check the appropriate box below if the Form 8-K filing is intended to simultaneously
satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):
| ☐ |
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
| ☐ |
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
| ☐ |
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
| ☐ |
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Securities registered pursuant to Section 12(b) of the Act:
| Title of each class |
|
Trading Symbol |
|
Name of exchange on which registered |
| Common Shares |
|
EDSA |
|
The Nasdaq Stock Market LLC |
Indicate by check mark whether the registrant is an emerging growth company
as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934
(§240.12b-2 of this chapter). Emerging growth company ☐
If an emerging growth company, indicate by check mark if the registrant has
elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant
to Section 13(a) of the Exchange Act. ☐
Item 1.01. Entry into a Material Definitive Agreement.
On June 10, 2026, Edesa Biotech,
Inc. (the “Company”) entered into a Securities Purchase Agreement (the “Purchase Agreement”) for a private
placement (the “Private Placement”) with certain investors (each, a “Purchaser” and collectively, the “Purchasers”).
The closing of the Private Placement (the “Closing”) is expected to occur on June 15, 2026, subject to the satisfaction of
customary closing conditions.
Pursuant to the Purchase Agreement,
the Purchasers have agreed to purchase, for an aggregate purchase price of approximately $3.5 million, an aggregate of 729,241 common
shares (“Shares”), without par value, at a purchase price of $4.69 per Share for Purchasers other than the Company’s
Chief Executive Officer, and $5.21 per Share for the Company’s Chief Executive Officer. The Company intends to use the net proceeds
from the Private Placement to fund the continued advancement of the Company’s vitiligo program, the Company’s drug candidate,
paridiprubart, and for working capital and general corporate purposes.
Also on June 10, 2026, the
Company entered into a Registration Rights Agreement (the “Registration Rights Agreement”) with the Purchasers. Pursuant
to the Registration Rights Agreement, the Company has agreed to prepare and file, as promptly as reasonably practicable and in any event
no later than 45 days after the Closing, one or more registration statements with the Securities and Exchange Commission (the “SEC”)
to register for resale the Shares, and to cause the applicable registration statements to become effective within the time periods set
forth in the Registration Rights Agreement. The Company has granted the Purchasers customary indemnification rights in connection with
the Registration Rights Agreement. The Purchasers have also granted the Company customary indemnification rights in connection with the
Registration Rights Agreement.
The Purchase Agreement contains
customary representations, warranties and covenants that were made solely for the benefit of the parties to the Purchase Agreement. Such
representations, warranties and covenants (i) are intended as a way of allocating risk between the parties to the Purchase Agreement
and not as statements of fact, and (ii) may apply standards of materiality in a way that is different from what may be viewed as
material by shareholders of, or other investors in, the Company.
The foregoing is only a summary
of the terms of the Purchase Agreement and the Registration Rights Agreement, does not purport to be complete and is qualified in its
entirety by reference to the full text of (i) the form of the Purchase Agreement, a copy of which is attached as Exhibit 10.1
to this Current Report on Form 8-K and (ii) the form of the Registration Rights Agreement, a copy of which is attached as Exhibit
10.2 to this Current Report on Form 8-K, and are incorporated herein by reference.
Item 3.02. Unregistered Sales of Equity Securities.
The disclosure regarding the securities
to be sold and issued under the Purchase Agreement as set forth under Item 1.01 of this report is incorporated by reference under this
Item 3.02.
The securities described above
under Item 1.01 have not been registered under the Securities Act of 1933, as amended (the “Securities Act”). Based in part
upon the representations of the Purchasers in the Purchase Agreement, the Company relied on the exemption afforded by Section 4(a)(2)
under the Securities Act and Rule 506(b) promulgated thereunder.
Neither this Current Report on
Form 8-K nor any exhibit attached hereto is an offer to sell or the solicitation of an offer to buy any securities of the Company.
Item 7.01. Regulation FD Disclosure.
On June 11, 2026, the Company
issued a press release announcing the Private Placement. A copy of the press release is furnished as Exhibit 99.1 to this Current Report
on Form 8-K.
The information contained in Item
7.01 of this Current Report on Form 8-K and in Exhibit 99.1 attached hereto will not be treated as “filed” for the purposes
of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities
of that section. This information will not be incorporated by reference into any filing under the Securities Act or into another filing
under the Exchange Act, unless that filing expressly incorporates this information by reference.
Item 9.01. Financial Statements and Exhibits.
(d) Exhibits
| Exhibit No. |
|
Description |
| 10.1* |
|
Form of Purchase Agreement, dated June 10, 2026, by and among the Company and the Purchasers. |
| 10.2 |
|
Form of Registration Rights Agreement, dated June 10, 2026, by and among the Company and the Purchasers. |
| 99.1 |
|
Press Release, dated June 11, 2026, announcing the Private Placement. |
| 104 |
|
Cover Page Interactive Data File (embedded within the Inline XBRL document) |
| * |
Schedules and exhibits have been omitted pursuant to Item 601(a)(5) of Regulation S-K. A copy of any omitted schedule and/or exhibit will be furnished to the SEC upon request. |
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 hereunto duly authorized.
| Dated: June 11, 2026 |
EDESA BIOTECH, INC. |
| |
|
|
| |
By: |
/s/ Peter J. Weiler |
| |
Name: |
Peter J. Weiler |
| |
Title: |
Chief Financial Officer |
EXHIBIT 99.1
Edesa Biotech Announces $3.5 Million Private Placement of Common
Shares Led by CEO and Healthcare-Focused Investors
TORONTO, June 11, 2026 (GLOBE NEWSWIRE) -- Edesa Biotech, Inc. (Nasdaq: EDSA) (the “Company” or “Edesa”),
a clinical-stage biopharmaceutical company focused on developing host-directed therapeutics for immuno-inflammatory diseases, today announced
that it has entered into a securities purchase agreement for a private investment in public equity (“PIPE”) financing that
is expected to result in gross proceeds of approximately $3.5 million to the Company, before deducting offering expenses payable by Edesa.
The common shares were placed without an agent, underwriter, broker or dealer. Investors in the PIPE include Edesa’s Chief Executive
Officer and healthcare-focused investors. The PIPE is expected to close on or about June 15, 2026, subject to the satisfaction of customary
closing conditions.
In the PIPE, the Company is selling an aggregate of 729,241 common shares, at a purchase price of $4.69 per common
share for investors and $5.21 per common share for Edesa’s Chief Executive Officer.
Edesa currently expects to use the net proceeds from the PIPE to fund the continued advancement of the Company’s
vitiligo program, the Company’s drug candidate, paridiprubart, and for working capital and general corporate purposes.
The securities described above were offered in a private placement under Section 4(a)(2) of the Securities Act of 1933,
as amended (the "Act"), and Regulation D promulgated thereunder and have not been and will not be registered under the Act, and may not
be offered or sold in the United States absent registration or an applicable exemption from registration requirements. The securities
described above may be offered to "accredited investors" within the meaning of the Canadian National Instrument 45-106 - Prospectus
Exemptions. Securities issued in Canada may be subject to applicable Canadian hold periods imposed under applicable securities legislation.
Edesa has agreed to file a registration statement with the U.S. Securities and Exchange Commission (“SEC”) registering the
resale of the common shares within 45 days of the closing.
This press release shall not constitute an offer to sell or the solicitation of an offer to buy any securities described
herein, nor shall there be any sale of these securities in any state or jurisdiction in which such offer, solicitation or sale would be
unlawful prior to the registration or qualification under the securities laws of any such state or jurisdiction. The Company plans to
file a Current Report on Form 8-K with the SEC with additional details of the PIPE. In addition, in Canada, a material change report with
respect to the PIPE is expected to be filed less than 21 days before the expected closing date of the PIPE, which is reasonable and necessary
in the circumstances for the Company to take advantage of available financing opportunities.
About Edesa Biotech, Inc.
Edesa Biotech, Inc. (Nasdaq: EDSA) is a clinical-stage biopharmaceutical company developing innovative ways to treat
inflammatory and immune-related diseases. Its clinical pipeline is focused on two therapeutic areas: Medical Dermatology and Respiratory.
In Medical Dermatology, Edesa is developing EB06, an anti-CXCL10 monoclonal antibody candidate, as a therapy for vitiligo, a common autoimmune
disorder that causes skin to lose its color in patches. Its medical dermatology assets also include EB01 (1.0% daniluromer cream), a Phase
3-ready asset developed for use as a potential therapy for moderate-to-severe chronic Allergic Contact Dermatitis (ACD), a common occupational
skin condition. The company’s most advanced Respiratory drug candidate is paridiprubart, which is being developed as a potential
treatment for Acute Respiratory Distress Syndrome, a life-threatening form of respiratory failure. The paridiprubart program has been
the recipient of two funding awards from the Government of Canada to support the further development of this asset, and is currently being
evaluated in a U.S. government-funded platform study. Edesa is also pursuing additional uses for paridiprubart.
Edesa Forward-Looking Statements
This press release may contain forward-looking statements within the meaning of Section 27A of the Securities Act
of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. Forward-looking statements may be identified
by the use of words such as "anticipate," "believe," "plan," "estimate," "expect," "intend," "may," "will," "would," "could," "should,"
"might," "potential," or "continue" and variations or similar expressions, including statements related to Edesa’s ability to complete
the PIPE financing, the anticipated proceeds to be received in the PIPE financing, the expected timing of the closing of the PIPE financing
and the expected use of the proceeds from the PIPE financing. Readers should not unduly rely on these forward-looking statements, which
are not a guarantee of future performance. There can be no assurance that forward-looking statements will prove to be accurate, as all
such forward-looking statements involve known and unknown risks, uncertainties and other factors which may cause actual results or future
events to differ materially from the forward-looking statements. Such risks include: market and other conditions, those relating to the
anticipated use of proceeds, the ability of Edesa to obtain regulatory approval for or successfully commercialize any of its product candidates,
the risk that access to sufficient capital to fund Edesa's operations may not be available or may be available on terms that are not commercially
favorable to Edesa, the risk that Edesa's product candidates may not be effective against the diseases tested in its clinical trials,
the risk that Edesa fails to comply with the terms of license agreements with third parties and as a result loses the right to use key
intellectual property in its business, Edesa's ability to protect its intellectual property, the timing and success of submission, acceptance
and approval of regulatory filings, and the impacts of public health crises. Many of these factors that will determine actual results
are beyond the Company's ability to control or predict. For a discussion of further risks and uncertainties related to Edesa's business,
please refer to Edesa's reports filed with the U.S. Securities and Exchange Commission and the British Columbia Securities Commission.
All forward-looking statements are made as of the date hereof and are subject to change. Except as required by law, Edesa assumes no obligation
to update such statements.
Contact:
Gary Koppenjan
Edesa Biotech, Inc.
investors@edesabiotech.com