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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 October
24, 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 October 24, 2024, Incannex Healthcare Inc.
announces appointment of Dr. Lou Barbato as Chief Medical Officer. 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.
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: October 24, 2024 |
/s/ Joel Latham |
|
Name: |
Joel Latham |
|
Title: |
Chief Executive Officer and President |
2
Exhibit 99.1
|
Date: October 24, 2024
Public Announcement (NASDAQ: IXHL) |
Incannex Announces Appointment of Dr. Lou Barbato
as Chief Medical Officer
NEW YORK and MELBOURNE, Australia, October 24, 2024 (GLOBE NEWSWIRE)
-- Incannex Healthcare Inc. (Nasdaq: IXHL), (Incannex), a clinical-stage biopharmaceutical company developing innovative medicines for
people with chronic diseases and significant unmet medical needs, today announced the appointment of Lou Barbato, M.D., as Chief Medical
Officer (CMO) effective immediately. Dr. Barbato’s drug development experience includes senior clinical development and operational
roles at Jazz Pharmaceuticals, AbbVie, Biogen, Novartis, and Solvay. He joins Incannex as the company continues to advance its lead clinical-stage
programs in obstructive sleep apnea, generalized anxiety disorder, and rheumatoid arthritis.
“We are delighted to welcome Dr. Barbato to Incannex as our Chief
Medical Officer. With an established track record in directing drug development through late-stage clinical trials and multiple product
launches, Lou is a valuable addition to the Incannex team,” said Joel Latham, Incannex’s President and Chief Executive Officer.
“Lou’s deep expertise in leading clinical development across CNS and neurodegenerative disorders, coupled with experience
in the synthetic cannabinoid therapeutics will be instrumental in driving the success of our global development programs.”
With more than 25 years of experience in clinical development, regulatory
strategy, and global medical affairs, Dr. Barbato brings significant drug development expertise in psychiatric and neurological disorders,
having contributed to the successful approval and launches of multiple therapeutics, including Marplan® (treatment-resistant depression),
Luvox® CR (anxiety, OCD), Marinol® (synthetic cannabinoid appetite stimulant, chemotherapy-induced nausea and vomiting) and Gilenya®
(multiple sclerosis). Dr. Barbato joins Incannex from Jazz Pharmaceuticals, where he served as Global Medical Lead for several clinical-stage
therapeutic programs addressing neurological disorders. At Jazz, he led cross-functional teams, with responsibility for global medical
strategies working with the FDA, EMA, and PMDA. Prior to joining Jazz, Dr. Barbato served as Global Senior Medical Director at AbbVie,
and, prior to AbbVie, held leadership roles at Biogen Idec, Novartis, Stiefel Laboratories (GSK), Forest Research Institute, and Solvay
Pharmaceuticals, where he contributed to successful U.S. and global product registration and approval of multiple psychiatric, neurologic,
and oncologic therapeutics. Dr. Barbato served as a Clinical Assistant Professor of Psychiatry and Behavioral Science at Emory University
School of Medicine and has authored or co-authored more than 65 papers and presentations. Dr. Barbato earned his M.D. from St. George’s
University School of Medicine and B.S. in Biology at St. Peter’s University.
“This is an exciting time to join Incannex with three clinical-stage
therapeutics that have all demonstrated clinical proof-of-concept. We believe Incannex’s science-driven development programs hold
great therapeutic potential for chronic conditions with unmet patient needs, including obstructive sleep apnea, generalized anxiety disorder,
and rheumatoid arthritis,” said Dr. Barbato. “I look forward to leading our global clinical strategy for IHL-42X, PSX-001
and IHL-675A, and the opportunity to advance these important new therapeutics to patients and clinicians.”
Incannex Healthcare Inc.
Level 39, Rialto South Tower, 525 Collins
Street, Melbourne VIC 3000
Email: admin@incannex.com.au
|
Date: October 24, 2024
Public Announcement (NASDAQ: IXHL) |
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 an Australian Phase 2 clinical trial, IHL-42X was observed to reduce the apnea hypopnea
index (AHI) and be well-tolerated in OSA patients. A global Phase 2/3 clinical trial investigating the safety and efficacy of IHL-42X
is underway with the Phase 2 portion conducted in the United States. The expanded Phase 3 portion will include sites in the United Kingdom
and European Union. A top-line readout from the U.S. Phase 2 portion of the Phase 2/3 trial is anticipated in the first half of 2025.
In addition, top-line results from an ongoing pharmacokinetic and safety study in Australia are expected in late 2024.
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 Generalized Anxiety Disorder (GAD). In the Australian
Phase 2 “PsiGAD1” clinical trial, PSX-001 was observed to reduce anxiety scores and be well-tolerated in GAD patients. Forty-four
percent of the subjects in the psilocybin group exhibited a clinically meaningful improvement of at least 50% in anxiety score from baseline;
a ‘response rate' more than four times higher than that of the placebo group. Incannex anticipates reporting full data results from
the PsiGAD1 trial in the first half of 2025. The “PsiGAD2” Phase 2 trial is expected to recruit 94 patients with GAD, including
those currently treated with selective serotonin reuptake inhibitors (SSRIs), who meet the study inclusion and exclusion criteria in the
United States and United Kingdom.
About IHL-675A
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 clinical 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. IHL-675A is in an Australian
Phase 2 trial investigating the safety and efficacy in rheumatoid arthritis (RA) patients, enrolling 128 subjects with pain and reduced
function regardless of current treatment regimen.
About Incannex Healthcare Inc.
Incannex is a clinical-stage biopharmaceutical company focused on developing
innovative medicines for patients living with 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, an oral synthetic psilocybin treatment in combination with psychotherapy,
for the treatment of generalized anxiety disorder, in a Phase 2 trial conducted in the United States and United Kingdom, and IHL-675A,
an oral fixed dose combination of cannabidiol and hydroxychloroquine sulfate, acting synergistically to alleviate inflammation, in an
Australian Phase 2 trial. Incannex’s programs target disorders that have limited, inadequate, or no approved pharmaceutical treatment
options.
Incannex Healthcare Inc.
Level 39, Rialto South Tower, 525 Collins
Street, Melbourne VIC 3000
Email: admin@incannex.com.au
|
Date: October 24, 2024
Public Announcement (NASDAQ: IXHL) |
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
skills and experience of the newly appointed officer of Incannex and expectations with respect to his future contributions to the Company
and statements, 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.
Level 39, Rialto South Tower, 525 Collins
Street, Melbourne VIC 3000
Email: admin@incannex.com.au
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