8-K
InMed Pharmaceuticals Inc. (INM)
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):September 23, 2025
INMED PHARMACEUTICALS INC.
(Exact Name of Company as Specified in Charter)
| British Columbia | 001-39685 | 98-1428279 |
|---|---|---|
| (State or Other Jurisdiction of Incorporation) | (Commission File Number) | (IRS Employer Identification No.) |
| InMed Pharmaceuticals Inc. Suite 1445 - 885 W. Georgia Street, Vancouver, B.C. Canada | V6C 3E8 | |
| --- | --- | |
| (Address of Principal Executive Offices) | (Zip Code) |
Company’s telephone number, including
area code: (604) 669-7207
Not applicable
(Former Name or Former Address, if Changed SinceLast 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(s) | Name of each exchange on which registered |
|---|---|---|
| Common Shares, no par value | INM | 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 7.01 Regulation FD Disclosure.
On September 23, 2025, the Company announced financial results for its fiscal year ending June 30, 2025 and provided a business update on its pharmaceutical drug development programs as well as the commercial segment for its wholly-owned subsidiary, BayMedica, LLC (“BayMedica”).
The information set forth in this Item 7.01, including Exhibits 99.1, is being furnished and shall not be deemed “filed” for 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. The information set forth in this Item 7.01, including Exhibit 99.1, shall not be deemed incorporated by reference into any other filing under the Securities Act of 1933, as amended, or the Exchange Act, except as shall be expressly set forth by specific reference in such a filing.
Item 9.01. Financial Statements and Exhibits.
(d) Exhibits:
The following exhibits shall be deemed to be furnished, and not filed:
| Exhibit No. | Description |
|---|---|
| 99.1 | News release, dated September 23, 2025 |
| 104 | Cover Page Interactive Data File (embedded within the Inline XBRL document and included as Exhibit 101) |
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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.
| INMED PHARMACEUTICALS INC. | ||
|---|---|---|
| Date: September 23, 2025 | By: | /s/ Eric A Adams |
| Eric A Adams | ||
| President & CEO |
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Exhibit 99.1
| NASDAQ: INM |
|---|
| 1445 – 885 West Georgia St. |
| Vancouver, BC, Canada V6C 3E8 |
| Tel: +1.604.669.7207 |
| Email: info@inmedpharma.com |
| www.inmedpharma.com |
InMed Pharmaceuticals Reports Full Year Fiscal2025 Financial Results and Provides Business Update
| ● | Advances INM-901 program, addressing multiple key biological pathwaysimplicated in Alzheimer’s disease pathology |
|---|
| ● | Further develops INM-089 demonstrating neuroprotection in the treatmentof dry Age-related Macular Degeneration |
|---|---|
| ● | Cash of $11.1M to support pharmaceutical developments into the fourthquarter of calendar year 2026 |
| --- | --- |
Vancouver, BC September 23, 2025 – InMed Pharmaceuticals Inc. (“InMed” or the “Company”) (Nasdaq: INM), a pharmaceutical company focused on developing a pipeline of proprietary small molecule drug candidates for diseases with high unmet medical needs, today announced financial results for its fiscal year ending June 30, 2025 and provided a business update on its pharmaceutical drug development programs as well as the commercial segment for its wholly-owned subsidiary, BayMedica, LLC (“BayMedica”).
The Company’s full financial statements and related MD&A for the fiscal year ended June 30, 2025, are available at www.inmedpharma.com and at www.sedar.com.
Eric A. Adams, InMed Chief Executive Officer, commented, “Throughout fiscal 2025, InMed continued to advance its pharmaceutical pipeline, in particular showcasing INM-901’s potential as a small-molecule drug candidate that addresses Alzheimer’s disease across several interrelated biological pathways rather than relying on a single mechanism. We are encouraged by the growing body of neuroinflammation data with INM-901. Across various studies, INM-901 has demonstrated statistically significant reductions in key neuroinflammation signals that are widely implicated in Alzheimer’s pathology and may operate independently of amyloid or tau. These results, alongside favorable behavioral outcomes in long-term preclinical studies, strengthen our conviction that a multi-pathway therapy like INM-901 can contribute meaningfully to disease modification.”
Mr. Adams continued, “Looking ahead, we remain focused on advancing IND-enabling studies and generating additional data that underscore INM-901’s differentiated approach. Notably, the emphasis on neuroinflammation and multi-pathway approaches appears well aligned with the themes emerging from the recent Alzheimer’s Association International Conference (“AAIC”), where leading researchers highlighted the need to move beyond amyloid and tau pathologies alone. We believe this convergence further validates our strategy and positions InMed to contribute meaningfully to the next generation of Alzheimer’s treatments.”
“Additionally, InMed has significantly strengthened its balance sheet, positioning the Company to advance its pharmaceutical development programs and deliver on key milestones into the fourth quarter of calendar year 2026.”
Business Update
Pharmaceutical DevelopmentPrograms
INM-901: Targetingseveral biological pathways associated with Alzheimer’s disease (“AD”)
InMed’s proprietary small molecule drug candidate INM-901 continues to advance as a potential treatment for Alzheimer’s disease through its multiple mechanisms of action that target several biological pathways associated with disease progression. Throughout fiscal 2025, the Company announced several key findings for INM-901:
Neuroinflammation
| ● | Reported statistically significant reductions<br>in neuroinflammation in a long-term (7-month dosing) preclinical study, including decreases in multiple plasma and brain markers of inflammation<br>recognized as contributors to AD progression. |
|---|---|
| ● | Presented ex vivo study results showing<br>significant reductions in neuroinflammation, including key pro-inflammatory markers, independent of amyloid beta or tau pathology. |
| --- | --- |
Cognition & BehavioralOutcomes
| ● | Demonstrated improvements in cognitive function,memory, and locomotor activity, with statistical significance achieved in certain behavioral assessments in a well-established 5xFAD<br>AD mouse model, using a longer treatment duration and subjects with more advanced disease to validate and expand upon previous findings.<br>These findings were presented at AAIC 2025, the world’s leading forum for Alzheimer’s disease and dementia research. |
|---|
Drug Delivery
| ● | Confirmed INM-901 can be administered orally<br>while achieving therapeutic brain levels comparable to intraperitoneal injection in a in vivo model, offering important advantages<br>over routes of administration used by currently approved products. |
|---|
Scientific Advisoryand Intellectual Property
| ● | Strengthened the Company’s scientific advisory<br>board with the appointment of Dr. Barry Greenberg, Director of the Alzheimer’s Disease Translational Center and Associate Professor<br>of Neurology at Johns Hopkins University School of Medicine. |
|---|---|
| ● | Expanded the Company’s<br>intellectual property with the filing of an additional international patent application under the Patent Cooperation Treaty (“PCT”),<br>covering pharmaceutical composition and method of use for INM-901 in the treatment of neurodegenerative diseases, including Alzheimer’s<br>disease. |
| --- | --- |
In fiscal 2026, InMed plans to develop its Alzheimer’s program, advancing Chemistry, Manufacturing, and Controls (“CMC”) activities and preparing for a pre-IND meeting and GLP-enabling studies to support an IND submission.
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INM-089: Neuroprotectionin the treatment of dry age-related macular degeneration (“AMD”)
INM-089 is a proprietary small molecule drug candidate being studied in the treatment of dry AMD. The Company continues to advance preclinical studies demonstrating significant functional and pathological improvements in a dry AMD disease study model In addition, the Company announced the selection of an intravitreal (“IVT”) formulation for INM-089, which has been successfully delivered to the targeted area of the eye in preclinical studies at doses up to 10 times the calculated safety margin relative to the intended therapeutic dose.
BayMedica commercialsubsidiary
BayMedica, a leading supplier of non-intoxicating rare cannabinoids to the health and wellness sector, has experienced sustained revenue growth during the fiscal year 2025, reaching $4.9M, representing an 8% increase over the previous year. BayMedica continues to hold a strong competitive position in its commercial portfolio of non-intoxicating rare cannabinoids.
Financial commentary:
For the year ended June 30, 2025, the Company recorded a net loss of $8.2M, compared with a net loss of $7.7M for the previous year.
Research and development expenses were $2.9M for year ended June 30, 2025, compared with $3.2M for the year ended June 30, 2024. However, the Company expects research and development expenses to increase significantly in future periods as it continues to advance its pharmaceutical pipeline.
The Company incurred general and administrative expenses of $6.6M for the year ended June 30, 2025, compared to $5.8M in the previous year. The increase was primarily from a combination of changes including higher legal expenses, and consulting fees, offset by a decrease in office and administrative fees.
The Company realized sales of $4.9M in our BayMedica segment for the year ended June 30, 2025, representing an increase of $0.34M, or 8%, as compared to the year ended June 30, 2024.
As of June 30, 2025, we had cash, cash equivalents and short-term investments of $11.1M. The Company expects its cash will be sufficient to fund its planned operating expenses and capital expenditures into the fourth quarter of calendar year 2026, depending on the level and timing of realizing BayMedica revenues as well as the level and timing of the Company’s operating expenses.
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Table 1. Consolidated Balance Sheet
Expressed in U.S. Dollars
| June 30, | |||
|---|---|---|---|
| 2024 | |||
| ASSETS | |||
| Current | |||
| Cash and cash equivalents | |||
| Short-term investments | |||
| Accounts receivable (less provision for credit losses of 2,424 and nil as of June 30, 2025 and 2024, respectively) | |||
| Inventories, net | |||
| Prepaids and other current assets | |||
| Total current assets | |||
| Non-Current | |||
| Property, equipment and ROU assets, net | |||
| Intangible assets, net | |||
| Other assets | |||
| Total Assets | |||
| LIABILITIES AND SHAREHOLDERS’ EQUITY | |||
| Current | |||
| Accounts payable and accrued liabilities | |||
| Current portion of lease obligations | |||
| Total current liabilities | |||
| Non-current | |||
| Lease obligations, net of current portion | |||
| Total Liabilities | |||
| Commitments and Contingencies (Note 12) | |||
| Shareholders’ Equity | |||
| Common shares, no par value, unlimited authorized shares: 2,002,186 and 445,908 as of June 30, 2025 and 2024, respectively, issued and outstanding | |||
| Additional paid-in capital | |||
| Accumulated deficit | ) | ) | |
| Accumulated other comprehensive income | |||
| Total Shareholders’ Equity | |||
| Total Liabilities and Shareholders’ Equity |
All values are in US Dollars.
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Table 2. Consolidated Statements of Operations
Expressed in U.S. Dollars
| For the Year Ended | ||||
|---|---|---|---|---|
| June 30, | ||||
| 2025 | 2024 | |||
| Sales | ||||
| Cost of sales | ||||
| Gross profit | ||||
| Operating Expenses | ||||
| Research and development | ||||
| General and administrative | ||||
| Amortization and depreciation | ||||
| Foreign exchange loss | ||||
| Total operating expenses | ||||
| Other Income (Expense) | ||||
| Interest and other income | ||||
| Finance expense | ) | |||
| Loss before income tax expense | ) | ) | ||
| Income tax expense | ) | |||
| Net loss for the year | ) | ) | ||
| Net loss per share for the year | ||||
| Basic and diluted | ) | ) | ||
| Weighted average outstanding common shares | ||||
| Basic and diluted |
All values are in US Dollars.
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Table 3. Consolidated Statements of Cash Flows
Expressed in U.S. Dollars
| June 30,<br> 2025 | June 30, <br>2024 | |||
|---|---|---|---|---|
| Cash provided by (used in): | ||||
| Operating Activities | ||||
| Net loss | ) | ) | ||
| Items not requiring cash: | ||||
| Amortization and depreciation | ||||
| Share-based compensation | ||||
| Amortization of right-of-use assets | ||||
| Interest income received on short-term investments | ) | ) | ||
| Unrealized foreign exchange loss | ||||
| Inventory write-down | ||||
| Credit losses | ||||
| Changes in operating assets and liabilities: | ||||
| Inventories | ||||
| Prepaids and other currents assets | ||||
| Other non-current assets | ||||
| Accounts receivable | ) | ) | ||
| Accounts payable and accrued liabilities | ) | |||
| Deferred rent | ) | |||
| Lease Obligations | ) | ) | ||
| Total cash used in operating activities | ) | ) | ||
| Investing Activities | ||||
| Purchase of property and equipment | ) | |||
| Sale of short-term investments | ||||
| Purchase of short-term investments | ) | ) | ||
| Total cash (used in) provided by investing activities | ) | |||
| Financing Activities | ||||
| Proceeds from the exercise of pre-funded warrants | ||||
| Proceeds from the private placement net of issuance costs | ||||
| Proceeds from the sale of pre-funded warrants | ||||
| Share issuance costs | ) | ) | ||
| Total cash provided by financing activities | ||||
| Increase (decrease) in cash and cash equivalents during the year | ) | |||
| Cash and cash equivalents beginning of the year | ||||
| Cash and cash equivalents end of the year | ||||
| SUPPLEMENTARY CASH FLOW INFORMATION: | ||||
| Cash Paid During the Year for: | ||||
| Income taxes | ||||
| Interest | ||||
| SUPPLEMENTARY DISCLOSURE OF NON-CASH INVESTING AND FINANCING ACTIVITIES: | ||||
| Preferred investment options to its placement agent | ||||
| Fair value of warrant modification recorded as equity issuance costs | ||||
| Recognition of Right-of-use asset and corresponding operating lease |
All values are in US Dollars.
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About InMed
InMed Pharmaceuticals is a pharmaceutical company focused on developing a pipeline of proprietary small molecule drug candidates targeting the CB1/CB2 receptors. InMed’s pipeline consists of three drug development programs in the treatment of Alzheimer’s, ocular and dermatological indications. Together with our subsidiary BayMedica, we are a global leader in the manufacturing, development and commercialization of products based on rare cannabinoids and their proprietary, small molecule drug analogs. For more information, visit www.inmedpharma.com.
Investor Contact:
Colin Clancy
Vice President, Investor Relations
and Corporate Communications
T: +1.604.416.0999
E: cclancy@inmedpharma.com
Cautionary Note Regarding Forward-Looking Information:
This news release contains “forward-looking information” and “forward-looking statements” (collectively, “forward-looking information”) within the meaning of applicable securities laws. Forward-looking information is based on management’s current expectations and beliefs and is subject to a number of risks and uncertainties that could cause actual results to differ materially from those described in the forward-looking statements. Forward-looking information in this news release includes statements about: statements regarding InMed’s belief in the potential of INM-901 as a multi-mechanism small molecule drug candidate for Alzheimer’s disease; expectations relating to the reduction of neuroinflammation and improvements in cognition and behavior observed in preclinical studies; the ability of INM-901 to provide disease-modifying benefits independent of amyloid or tau pathologies; the advancement of chemistry, manufacturing, and controls (CMC) activities, the planning of GLP-enabling studies, and the preparation of an IND submission; the ability to achieve therapeutic brain levels through oral administration; expectations relating to intellectual property protection; the further development, potential efficacy, and marketability of INM-089 for dry age-related macular degeneration, including its neuroprotective properties and intravitreal (IVT) delivery profile; the further development and potential commercial uses of INM-755; optimism regarding alignment of the Company’s strategy with emerging industry trends and findings presented at the Alzheimer’s Association International Conference (AAIC); expectations regarding the sufficiency of the Company’s strengthened balance sheet to fund operations, advance pharmaceutical development programs, and achieve milestones into the fourth quarter of calendar year 2026; and, other business initiatives, strategies, and prospects of the Company.
Additionally, there are known and unknown risk factors which could cause InMed’s actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking information contained herein. A complete discussion of the risks and uncertainties facing InMed’s stand-alone business is disclosed in InMed’s Annual Report on Form 10-K and other filings with the Securities and Exchange Commission on www.sec.gov.
All forward-looking information herein is qualified in its entirety by this cautionary statement, and InMed disclaims any obligation to revise or update any such forward-looking information or to publicly announce the result of any revisions to any of the forward-looking information contained herein to reflect future results, events or developments, except as required by law.
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