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InMed Pharmaceuticals Inc.

For the period ended Sep 30, 2026. Filed Nov 3, 2026.

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About this filing

A company's report for each of its first three quarters. The financial statements are not audited. It shows how the business has moved since the last annual report, and what management says changed.

Sep 30, 2026 · Filed Nov 3, 2026

INM$15.56+17.8%Stored close · as of Nov 6, 2026
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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

FORM 10-Q

☒ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the quarterly period ended September 30, 2026

or

☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the transition period from __________ to __________

Commission File Number:001-39685

INMED PHARMACEUTICALS INC.

(Exact name of registrant as specified in its charter)

British Columbia, Canada98-1428279
(State or other jurisdiction of incorporation or organization)(I.R.S. Employer Identification No.)
c/o Norton Rose Fulbright Canada LLP Suite 1800 – 510 West Georgia Street Vancouver, B.C. CanadaV6B 0M3
(Address of Principal Executive Offices)(Zip Code)

(604) 669-7207

(Registrant’s telephone number, including area code)

Securities registered pursuant to Section 12(b) of the Act:

Title of each classTrading Symbol(s)Name of each exchange on which registered
Common Shares, no par valueINMThe Nasdaq Stock Market LLC

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes ☒ No ☐

Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files). Yes ☒ No ☐

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange Act.

Large accelerated filer☐Accelerated filer☐
Non-accelerated filer☒Smaller reporting company☒
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. ☐

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Act): Yes ☐ No☒

On October 30, 2026, there were 5,493,735 shares of the registrant’s common shares, no par value (the “Common Shares”), outstanding.

INDEX

Page
PART I – FINANCIAL INFORMATION1
ITEM 1. CONDENSED CONSOLIDATED FINANCIAL STATEMENTS1
ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS19
ITEM 3. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK29
ITEM 4. CONTROLS AND PROCEDURES29
PART II – OTHER INFORMATION30
ITEM 1. LEGAL PROCEEDINGS30
ITEM 1A. RISK FACTORS31
ITEM 2. UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS31
ITEM 3. DEFAULTS UPON SENIOR SECURITIES31
ITEM 4. MINE SAFETY DISCLOSURE32
ITEM 5. OTHER INFORMATION32
ITEM 6. EXHIBITS32
SIGNATURES33

i

CAUTIONARY STATEMENT REGARDING FORWARD-LOOKING STATEMENTS

This Quarterly Report on Form 10-Q (this “Quarterly Report”) contains “forward-looking statements” within the meaning of the United States Private Securities Litigation Reform Act of 1995 and “forward-looking information” within the meaning of applicable Canadian securities law, which include but are not limited to statements with respect to the Company’s anticipated results and progress of the Company’s operations, research and development in future periods, plans related to its business strategy, the proposed Merger (as defined below) and other matters that may occur in the future. These statements relate to analyses and other information that are based on forecasts of future results, estimates of amounts not yet determinable and assumptions of management. We may, in some cases, use words such as “anticipate”, “believe”, “could”, “estimate”, “expect”, “intend”, “may”, “plan”, “predict”, “project”, “will”, “would”, and similar expressions that convey uncertainty of future events or outcomes to identify these forward-looking statements. Any statements contained herein that are not statements of historical facts may be deemed to be forward-looking statements. Some of the important risks and uncertainties that could materially affect forward-looking statements are described further under Item 1A. “Risk Factors” in our Annual Report on Form 10-K for the year ended June 30, 2026, which was originally filed with the SEC on September 9, 2026 (the “2026 Annual Report”), under “Risk Factors” in our proxy statement/prospectus and management information circular dated October 1, 2026 (the “Proxy Statement”) relating to, among other things, the Company’s proposed merger transaction (the “Merger”) with Mentari (as defined herein), Item 1A. “Risk Factors” in this Quarterly Report and Item 2. “Management’s Discussion and Analysis of Financial Condition and Results of Operations” in this Quarterly Report, and include, but are not limited to, the following:

●Our ability to stem operating losses;
●Our ability to successfully identify and consummate strategic and/or transformative corporate opportunities and transactions and to obtain the additional financing that we need to fund our operations;
●The risk that the conditions to the closing of the proposed Merger are not satisfied, including the failure to obtain the shareholder approvals required to complete the Merger, and our ability to meet expectations regarding the timing and completion of the Merger, including Mentari’s pre-closing financing;
●The completion of the potential reverse stock split and proposed redomestication of the Company from British Columbia to Nevada;
●Our ability to correctly estimate our operating expenses and expenses associated with the Merger, and the impact of any delay in the closing of the Merger on our net cash and the exchange ratio in relation to the Merger;
●The risk that the Merger Agreement (as defined herein) may be terminated in circumstances that require us to pay a termination fee;
●The effect of the announcement or pendency of the Merger on our business, and the outcome of any legal proceedings that may be instituted against us or our directors or officers related to the Merger;
●The possibility that holders of contingent value rights may never receive any proceeds, and that our shareholders will not receive any dividend of cash prior to the closing of the Merger;
●The possibility that, if the Merger is not completed, our board of directors may decide to pursue a dissolution and liquidation of the Company;
●The material adverse impact of the winding down of the BayMedica commercial business segment due to recent legislation in the United States impacting its inventory of rare, non-intoxicating cannabinoids;
●The timing, costs and outcome of the assignment for the benefit of creditors process in respect of BayMedica, as described herein;
●Our ability to effectively research, develop, manufacture and commercialize pharmaceutical drug candidates that will treat diseases with high unmet medical needs;
●The continued optimization of key, proprietary manufacturing approaches and technologies;
●Our ability to commercialize and, where required, register products in the pharmaceutical R&D programs (“Product Candidates”) in the United States and other jurisdictions;
●Our success in initiating discussions with potential partners for licensing various aspects of our Product Candidates;
●Our ability to successfully access existing manufacturing capacity via leases with third-parties or to transfer our manufacturing processes to contract manufacturing organizations;
●Our belief that manufacturing approaches that we are developing are robust and effective and will result in commercially viable yields of cannabinoids and will be a significant improvement upon existing manufacturing platforms;

ii

●Our ability to successfully scale up our IntegraSyn approach to cannabinoid manufacturing. We have created genetically engineered microbes that produce proprietary enzymes, which are then used to optimize subsequent biotransformation reactions or other cost-effective manufacturing approaches so that it may be a potential manufacturing method in the future which could reduce the need to source active pharmaceutical ingredients (“APIs”) from third-party API manufacturers;
●The success of the key next steps in our manufacturing approaches, including continuing efforts to diversify the number of products produced, scaling-up the processes to larger vessels and identifying external vendors to assist in the commercial scale-up of the process;
●Our ability to successfully make determinations as to which research and development programs to continue based on several strategic factors;
●Our ability to continue to outsource the majority of our research and development activities through scientific collaboration agreements and arrangements with various scientific collaborators, academic institutions and their personnel;
●The success of work to be conducted under the research and development collaboration between us and various contract development and manufacturing organizations (“CDMOs”);
●Our ability to develop our therapies through early human testing;
●Our ability to evaluate the financial returns on various commercialization approaches for our Product Candidates, such as a ‘go-it-alone’ commercialization effort, out-licensing to third parties, or co-promotion agreements with strategic collaborators;
●Our ability to find a partnership early in the development process for our various programs;
●Our ability to explore our manufacturing technologies as processes which may confer certain benefits, including cost, yield, speed, or all the above, when pursuing specific types of molecules, and filing a provisional patent application for same;
●Plans regarding our next steps, options, and targeted benefits of our manufacturing technologies;
●Our Products being bio-identical to the naturally occurring molecules, and offering superior ease, control and quality of manufacturing when compared to alternative methods;
●U.S. Food and Drug Administration (“FDA”) regulatory acceptance of Product Candidates for potential use in the pharmaceutical industry;
●Our ability to successfully file, prosecute and defend patent applications;
●The potential for any of our patent applications to provide intellectual property protection for us;
●The termination or renegotiation of our supplier, technology and other material contracts, including the invoking of force majeure or termination clauses, and actual or threatened claims of our failure to comply with any obligations set forth under such contracts;
●The adequacy of, or gaps in, insurance coverage upon the occurrence of a catastrophic or other material adverse event, as well as our ability to (i) expand our insurance coverage to include the commercial sale of Products and Product Candidates and (ii) secure insurance coverage for shipping and storage of Product Candidates, and clinical trial insurance;
●Developing patentable New Chemical Entities (“NCE”) which, if issued, will confer market exclusivity to us for the potential development into pharmaceutical Product Candidates, license, partner or sell to interested external parties;
●Our ability to initiate discussions and conclude strategic partnerships to assist with development of certain programs;
●Our ability to position ourselves to achieve value-driving, near term milestones for our Product Candidates with limited investment;
●Our ability to effectively execute our business strategy;

iii

●The sufficiency of our internal controls, including any exposure arising from the failure to (i) establish and maintain effective internal control over financial reporting in accordance with applicable regulatory requirements, and (ii) fully remediate any material weakness identified with respect to such internal controls;
●Epidemics, pandemics, global health crises, or other public health events and concerns, and the effectiveness of associated vaccinations and treatments;
●Consolidation of our competitors and suppliers;
●Effects of new products and new technology on the market, including with respect to automation and the use of artificial intelligence;
●The impact of geopolitical, global, regional or local economic and financial market risks and challenges, applicability of foreign laws, including foreign labor and employment laws, foreign tax and customs regimes, and foreign currency exchange rate risk;
●Political disturbances, geopolitical instability and tensions, or terrorist attacks, and associated changes in global trade policies and economic sanctions, including, but not limited to, in connection with (i) global trade tensions; (ii) the Russo-Ukrainian war and (iii) any impact, effect, damage, destruction and/or bodily harm directly or indirectly relating to the ongoing hostilities in the Middle East;
●The outcome of any legal proceedings, disputes, claims and administrative proceedings that arise in the ordinary course of our business activities, including our ongoing matter with a third party licensor; and
●Our failure to satisfy any applicable listing standards, including compliance with the minimum shareholders’ equity requirement under Nasdaq Listing Rule 5550(b)(1) and the minimum bid price rule, the acceptance by the Nasdaq of our plan to regain compliance with such minimum shareholders’ equity requirement, and the actual or threatened delisting of our securities by Nasdaq.

This list is not exhaustive of the factors, events, conditions and circumstances that may affect the forward-looking statements contained in this Quarterly Report. Although we have attempted to identify important factors that could cause actual results to differ materially from those described in forward-looking statements, there may be other factors that cause results not to be as anticipated, estimated or intended. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove incorrect, actual results may vary materially from those anticipated, believed, estimated, or expected. Moreover, new risks regularly emerge, and it is not possible for our management to predict or articulate all risks we face, nor can we assess the impact of all risks on our business or the extent to which any risk, or combination of risks, may cause actual results to differ from those contained in any forward-looking statements, which differences could be material. There can be no assurance that the Merger will be completed or, if it is completed, that it will be completed within the anticipated time period or that the expected benefits of the Merger will be realized. We caution readers not to place undue reliance on any such forward-looking statements, which speak only as of the date made and are based only on the information available to us at that time. Except as required by law, we disclaim any obligation to subsequently revise any forward-looking statements to reflect events or circumstances after the date of such statements or to reflect the occurrence of anticipated or unanticipated events. We qualify all of our forward-looking statements by these cautionary statements.

iv

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