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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 September 30, 2024
Incannex Healthcare Inc.
(Exact
name of registrant as specified in its charter)
Delaware |
|
001-41106 |
|
93-2403210 |
(State or other Jurisdiction
of Incorporation) |
|
(Commission File Number) |
|
(IRS Employer
Identification No.) |
Suite 105, 8 Century Circuit Norwest,
NSW 2153 Australia |
|
Not applicable |
(Address of Principal Executive Offices) |
|
(Zip Code) |
Registrant’s
Telephone Number, including Area Code: +61 409 840 786
(Former Name or Former
Address, if Changed Since Last Report): Not Applicable
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:
| ☐ | 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 Stock, $0.0001 par value per share |
|
IXHL |
|
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 8.01
On September 30, 2024, Incannex Healthcare
Inc. Reports Fiscal Full Year 2024 Financial Results and Business Updates. Further information is included in the press release attached
as Exhibit 99.1 hereto, which is incorporated by reference into this Item 8.01.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits
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.
|
Incannex Healthcare Inc. |
|
|
|
Date: September 30, 2024 |
/s/ Joel Latham |
|
Name: |
Joel Latham |
|
Title: |
Chief Executive Officer and President |
2
Exhibit 99.1
Incannex
Healthcare Inc. Reports Fiscal Full Year 2024 Financial Results and Business Updates
| ● | Announced
strategic financing with Arena Investors, providing access to up to $59.0 million USD in
gross proceeds to Incannex |
| ● | Announced
positive top-line results from our Phase 2 proof-of-concept clinical trial of PSX-001, known
as the PsiGAD1 study, in which synthetic psilocybin in combination with psychotherapy was
observed to significantly reduce anxiety scores and to be well tolerated in patients with
generalised anxiety disorder (GAD) |
| ● | Commenced
dosing in the RePOSA Phase 2/3 clinical trial of IHL-42X, an oral investigational treatment
for patients with obstructive sleep apnea |
| ● | Received
Investigational New Drug (IND) application clearance from the U.S. Food and Drug Administration
(FDA) to initiate PsiGAD2, a Phase 2 clinical trial of PSX-001 |
| ● | Successfully
completed redomiciliation to the United States and listing shares of Incannex common stock
on Nasdaq under the ticker “IXHL” in late 2023 |
NEW
YORK and MELBOURNE, Australia, September 30, 2024 (GLOBE NEWSWIRE) -- Incannex Healthcare Inc. (Nasdaq: IXHL), (Incannex), a clinical-stage
biopharmaceutical company developing innovative medicines for people with serious chronic diseases and significant unmet medical needs,
today reported fiscal full year financial results and provided business updates.
“The
past year has been transformative for Incannex as we successfully completed our transition to the Nasdaq as a company domiciled in the
United States, reported positive top-line data from our proof-of-concept clinical trial of PSX-001, known as PsiGAD1, and initiated dosing
in our Phase 2/3 IHL-42X RePOSA trial. These achievements demonstrate our commitment to advancing new oral cannabinoids and psychedelic
treatments. With our recent strategic financing and clinical trials underway for three programs, we are excited to share updates later
this year,” said Joel Latham, Incannex’s President and Chief Executive Officer. “We are grateful to all of the physicians,
investigators and patients involved in our U.S. and Australian clinical trials for their support of our investigational synthetic cannabinoid
and psilocybin-based therapeutic programs.”
Operational
Highlights
| ● | Announced
strategic financings with Arena Investors, which may provide up to $59.0 million USD in gross
proceeds to Incannex through a $50 million USD equity line of credit and the sale in future
closings of convertible debentures with an aggregate principal amount of up to $9.0 million
USD. Incannex intends to use the proceeds from this strategic financing to support the ongoing
clinical trials of its drug candidates, and for working capital and other general corporate
purposes. Drawdown of the capital will be determined according to the Incannex’s strategic
needs. |
| ● | Announced
the opening of Clarion Clinics, one of the first psychedelic-assisted psychotherapy clinics
in Australia, which will serve as a model for potential future sites. Incannex believes this
first clinic will provide real-world experience in treating mental health patients utilizing
psychedelic-assisted psychotherapy. Assuming regulatory approval of PSX-001, the Clarion
Clinics model has the potential to provide insight into the potential commercialization of
PSX-001. |
| ● | Completed
the redomiciliation of Incannex from Australia to the United States, effective November
28, 2023 and listing our common stock on the Nasdaq Global Market under the ticker “IXHL.”
With no material changes to its operations, Incannex believes this will provide access to
a broader set of investors, streamline financial reporting comparably with industry peers,
and provide greater flexibility in accessing capital. |
Clinical
Highlights
| ● | Commenced
dosing in the RePOSA Phase 2/3 clinical trial of IHL-42X, an oral fixed dose combination
of dronabinol and acetazolamide for the treatment of patients with obstructive sleep apnea
(OSA). RePOSA, a randomized, double-blind trial, is designed to assess the safety and efficacy
of IHL-42X in patients with OSA who are intolerant, non-compliant, or naïve to positive
airway pressure. The Phase 2 portion of this clinical trial is being conducted in the United
States, and the expanded Phase 3 portion will include sites in the United Kingdom and European
Union. Incannex plans to recruit 560 subjects, with an estimated 355 participants in the
active study arms, and anticipates reporting top-line data from the Phase 2 portion of this
clinical trial in the first half of 2025. |
| ● | Completed
dosing of 115 subjects in a bioavailability/bioequivalence (BA/BE) clinical trial conducted
in Australia assessing the pharmacokinetics and tolerability of IHL-42X, our drug product
for the treatment of obstructive sleep apnea. Data analysis is underway, with no serious
adverse events reported to date. Incannex expects to release top-line results from this BA/BE
clinical trial in 2024. |
| ● | Announced
positive results from its proof-of-concept Australian Phase 2 clinical trial, PsiGAD1, of
PSX-001. In the PsiGAD2 trial the combination of an oral synthetic psilocybin with psychotherapy
was observed to significantly reduced anxiety scores and was well tolerated in patients with
generalized anxiety disorder (GAD). The reduction in
HAM-A from baseline, the trial’s primary endpoint, in the psilocybin group was 12.8
points from baseline, representing a 9.2-point improvement over psychotherapy with placebo
(p<0.0001). |
| ● | Received
IND clearance from the FDA to initiate PsiGAD2, a Phase 2b clinical trial of PSX-001 evaluating
change in the HAM-A anxiety score, and other measures of efficacy and safety at sites in
the U.S. and UK. The trial is expected to include approximately
94 patients, including those currently treated with selective serotonin reuptake inhibitors
(SSRIs), who meet the study inclusion and exclusion criteria. |
| ● | Initiated
dosing in an Australian Phase 2 clinical trial of IHL-675A
for patients with rheumatoid arthritis (RA). IHL-675A is an oral fixed dose combination of
cannabidiol and hydroxychloroquine sulfate designed to target two different pathways, acting
synergistically to alleviate inflammation. The trial is planned to include approximately
128 subjects. Incannex anticipates reporting top-line data in the second half of 2025. |
Financial
Results
| ● | General
and Administration (G&A) expenses for the twelve months ended June 30, 2024 were $17.2
million USD, as compared to $8.0 million USD for the twelve months ended June 30, 2023, due
to associated completed the redomicilation to the United States, listing of common stock
on Nasdaq, and expanded U.S. operations. |
| ● | Research
and development (R&D) expenses were for $12.9 million USD for the twelve months ended
June 30, 2024 compared to $6.3 million USD for the twelve months ended June 30, 2023, due
to increased clinical research activities. |
| ● | Net
loss for the twelve-month period ended June 30, 2024 was $18.5 million USD, as compared to
$48.8 million USD for the twelve months ended June 30, 2023. |
| ● | Cash
and cash equivalents were $5.9 million USD as of June 30, 2024, compared to $22.1 million
USD as of June 30, 2023. |
About
IHL-42X
IHL-42X
is Incannex’s oral fixed dose combination of dronabinol and acetazolamide designed to act synergistically, targeting two different
physiological pathways associated with the intermittent hypoxia (IH) and hypercapnia
that characterize OSA. In a proof-of-concept Australian Phase 2 clinical trial, IHL-42X was observed to reduce the apnea hypopnea index
and be well tolerated in OSA patients. An ongoing pivotal Phase 2/3 clinical trial investigating the safety and efficacy of IHL-42X is
underway with the Phase 2 portion conducted in the U.S., the expanded Phase 3 portion will also include the UK and EU. Top-line results
from an ongoing pharmacokinetic and safety study in Australia are expected in late 2024. The top-line readout from the U.S. Phase 2 portion
of the pivotal Phase 2/3 trial is anticipated in the first half of 2025.
About
PSX-001
PSX-001
is Incannex’s oral synthetic psilocybin drug candidate, administered in combination with psychotherapy, for patients diagnosed
with moderate-to-severe GAD. In the Australian Phase 2 proof-of-concept PsiGad1 clinical trial, PSX-001 was observed to reduce anxiety
scores and was well tolerated in GAD patients. In this trial, 44% of subjects in the psilocybin group were observed to show a clinically
meaningful improvement of at least 50% subjects in anxiety score from baseline; a ‘response rate’ more than four times higher
than that of the placebo group. The FDA has cleared Incannex’s IND application for PsiGAD2 to conduct a U.S. Phase 2b clinical
trial, which is expected to include approximately 94 patients with GAD, including those currently
treated with selective serotonin reuptake inhibitors (SSRIs), who meet the study inclusion and exclusion criteria. Incannex anticipates
reporting full data results from PsiGAD1 trial in the first half of 2025.
About
IHL-675A
IHL-675A
is an oral drug candidate currently in an ongoing Australian Phase 2 trial for the treatment of inflammatory conditions, with an initial
focus on RA. IHL-675A is an oral fixed dose combination of cannabidiol and hydroxychloroquine sulfate designed to target two different
pathways, acting synergistically to alleviate inflammation. IHL-675A was observed to be well-tolerated and bioavailable in an Australian
Phase 1 trial. IHL-675A was also observed to reduce inflammatory markers and disease scores across multiple animal inflammatory disease
models and in vitro assays in preclinical evaluation. A Phase 2 trial investigating the safety and efficacy of IHL-675A in RA patients
is ongoing, enrolling 128 subjects with pain and reduced function regardless of current treatment regimen. Top-line data from this Phase
2 trial is anticipated in the second half of 2025.
About
Incannex Healthcare Inc.
Incannex
is a clinical-stage biopharmaceutical company focused on developing innovative medicines for patients living with serious chronic diseases
and significant unmet needs. The company is advancing oral synthetic cannabinoid and psilocybin drug candidates targeting sleep apnea,
anxiety, and inflammatory diseases. Incannex’s lead programs include IHL-42X, an oral fixed dose combination of dronabinol and
acetazolamide, designed to act synergistically in the treatment of OSA, in a global Phase 2/3 study for the treatment of obstructive
sleep apnea, PSX-001 in a Phase 2 trial conducted in the U.S. and UK to assess the combination of an oral synthetic psilocybin treatment
with psychotherapy for patients with generalized anxiety disorder, and IHL-675A, an oral fixed dose combination of cannabidiol and hydroxychloroquine
sulfate, acting synergistically to alleviate inflammation, in an Australian Phase 2 trial. Each of these programs target indications
that have limited, inadequate, or no approved pharmaceutical treatment options.
Forward
Looking Statements
This
press release contains “forward-looking statements” within the meaning of the “safe harbor” provisions of the U.S.
Private Securities Litigation Reform Act of 1995. Examples of forward-looking statements in this press release include statements about,
among other things: Incannex’s business strategy, future operations; Incannex’s ability to execute on its objectives, prospects,
or plans, the benefits of the redomiciliation and the Nasdaq common stock listing, future closings of the strategic financings with Arena,
which are subject to conditions and may not occur, evaluations and judgments regarding Incannex’s research and development efforts,
including any implications that the results of earlier clinical trials will be representative or consistent with later clinical trials
or final results; the expected timing of enrollment for these trials and the availability of data or results of these trials, and the
potential benefits, safety or of Incannex’s drug candidates. Forward-looking statements are statements other than historical facts
and relate to future events or circumstances or Incannex’s future performance, and they are based on management’s current
assumptions, expectations, and beliefs concerning future developments and their potential effect on Incannex’s business. These
forward-looking statements are subject to a number of risks and uncertainties, which may cause the forward-looking events and circumstances
described in this press release to not occur, and actual results to differ materially and adversely from those described in or implied
by the forward-looking statements. These risks and uncertainties include, among others: the continued availability of financing; Incannex’s
ability to raise capital to fund continuing operations and to complete capital raising transactions; the impact of any infringement actions
or other litigation brought against Incannex; the success of Incannex’s development efforts, including Incannex’s ability
to progress its drug candidates through clinical trials on the timelines expected; competition from other providers and products; that
the market for its drug candidates may not grow at the rates anticipated or at all; Incannex’s compliance with the various evolving
and complex laws and regulations applicable to its business and its industry; and Incannex’s ability to protect its proprietary
technology and intellectual property; and other factors relating to Incannex’s industry, its operations and results of operations.
The forward-looking statements made in this press release speak only as of the date of this press release, and Incannex assumes no obligation
to update publicly any such forward-looking statements to reflect actual results or to changes in expectations, except as otherwise required
by law. Incannex’s reports filed with the U.S. Securities and Exchange Commission (SEC) including its annual report on Form
10-K for the fiscal year ended June 30, 2024, filed with the SEC on September 30, 2024, and the other reports it
files from time to time, including subsequently filed annual, quarterly and current reports, are made available on Incannex’s website
upon their filing with the SEC. These reports contain more information about Incannex, its business and the risks affecting its
business, as well as its results of operations for the periods covered by the financial results included in this press release.
Contact
Information
Jennifer
Drew-Bear
Edison Group for Incannex
Jdrew-bear@edisongroup.com
INCANNEX
HEALTHCARE INC.
Consolidated
Balance Sheets
(in
thousands, except share and per share amounts)
(expressed
in U.S. Dollars, unless otherwise stated)
| |
June 30, 2024 | | |
June 30, 2023 | |
Assets | |
| | |
| |
Current assets: | |
| | |
| |
Cash and cash equivalents | |
$ | 5,858 | | |
$ | 22,120 | |
Prepaid expenses and other assets | |
| 507 | | |
| 877 | |
R&D tax incentive receivable | |
| 9,837 | | |
| - | |
Total current assets | |
| 16,202 | | |
| 22,997 | |
Property, plant and equipment, net | |
| 472 | | |
| 294 | |
Operating lease right-of-use assets | |
| 373 | | |
| 492 | |
Total assets | |
$ | 17,047 | | |
$ | 23,783 | |
Liabilities and stockholders’ equity | |
| | | |
| | |
Current liabilities: | |
| | | |
| | |
Trade and other payables | |
$ | 612 | | |
$ | 1748 | |
Accrued expenses and other current liabilities | |
| 4,845 | | |
| 689 | |
Operating lease liabilities, current | |
| 163 | | |
| 113 | |
Total current liabilities | |
| 5,620 | | |
| 2,550 | |
Operating lease liabilities, non-current | |
| 210 | | |
| 408 | |
Total liabilities | |
| 5,830 | | |
| 2,958 | |
Commitments and contingencies | |
| | | |
| | |
Stockholders’ equity: | |
| | | |
| | |
Common stock, $0.0001 par value – 100,000,000 shares authorized; 15,873,113 and 15,873,113 shares issued and outstanding at June 30, 2024 and 2023, respectively | |
| 2 | | |
| 2 | |
Preferred stock, $0.0001 par value per share, 10,000,000 shares authorized; no shares issued or outstanding at June 30, 2024 and 2023, respectively | |
| - | | |
| - | |
Additional paid-in capital | |
| 125,218 | | |
| 116,290 | |
Accumulated deficit | |
| (110,671 | ) | |
| (92,212 | ) |
Foreign currency translation reserve | |
| (3,332 | ) | |
| (3,255 | ) |
Total shareholders’ equity | |
| 11,217 | | |
| 20,825 | |
Total liabilities and stockholders’ equity | |
$ | 17,047 | | |
$ | 23,783 | |
INCANNEX
HEALTHCARE INC.
Consolidated
Statements of Operations and Comprehensive Loss
(in
thousands, except share and per share amounts)
(expressed
in U.S. Dollars, unless otherwise stated)
| |
June 30, 2024 | | |
June 30, 2023 | |
Revenue from customers | |
| 12 | | |
| - | |
Operating expenses: | |
| | | |
| | |
Research and development | |
| (12,879 | ) | |
| (6,309 | ) |
Acquisition of in-process research and development | |
| - | | |
| (35,347 | ) |
General and administrative | |
| (17,174 | ) | |
| (8,012 | ) |
Total operating expenses | |
| (30,053 | ) | |
| (49,668 | ) |
Loss from operations | |
| (30,041 | ) | |
| (49,668 | ) |
Other income, net: | |
| | | |
| | |
R&D tax incentive | |
| 11,434 | | |
| 683 | |
Foreign exchange expense | |
| (28 | ) | |
| (67 | ) |
Interest income | |
| 206 | | |
| 241 | |
Total other income, net | |
| 11,612 | | |
| 857 | |
Loss before income tax expense | |
| (18,429 | ) | |
| (48,811 | ) |
Income tax expense | |
| (30 | ) | |
| - | |
Net loss | |
$ | (18,459 | ) | |
$ | (48,811 | ) |
Other comprehensive loss: | |
| | | |
| | |
Currency translation adjustment, net of tax | |
| (77 | ) | |
| (2,292 | ) |
Total comprehensive loss | |
$ | (18,536 | ) | |
$ | (51,103 | ) |
Net loss per share: Basic and diluted | |
$ | (1.15 | ) | |
| (3.32 | ) |
Weighted average number of shares outstanding, basic and diluted | |
| 16,164,338 | | |
| 15,384,704 | |
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