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Incannex Healthcare Delivers Transformational 2025 Progress and Outlines Well-Funded Outlook for 2026 Company enters 2026 with over $70 million in cash, two positive Phase 2 programs, FDA Fast Track Designation and runwa

Key Takeaway: Incannex Healthcare has reported significant progress in 2025, noting two positive Phase 2 clinical readouts for its programs targeting obstructive sleep apnea and generalized anxiety disorder. The company has secured FDA Fast Track designation for its leading candidate, IHL-42X, and is well-funded entering 2026 with over $70 million in cash. This financial backing positions Incannex for continued execution and transition into later-stage development of its drug candidates. The firm also established a Clinical Advisory Board to enhance its strategic direction in advancing treatment solutions.

Market Sentiment Analysis

POSITIVE FACTORS

  • Incannex Healthcare achieved positive Phase 2 results for its drug programs.
  • The company has received FDA Fast Track designation, accelerating its development process.
  • Incannex enters 2026 with over $70 million in cash, ensuring financial stability.
  • The establishment of an advisory board with experts indicates commitment to advancing clinical programs.

Full Press Release Details

Incannex Healthcare Delivers Transformational
2025 Progress and Outlines Well-Funded Outlook for 2026
Company enters 2026 with over $70 million in
cash, two positive Phase 2 programs, FDA Fast Track Designation and runway well into 2027
MELBOURNE, Australia and NEW YORK, USA - January 14, 2026
- Incannex Healthcare Inc. (Nasdaq: IXHL), a clinical-stage biopharmaceutical company developing innovative combination therapies,
provides a 2025 corporate year-in-review and outlook for 2026, highlighting substantial clinical, regulatory and financial progress that
positions the Company for continued execution.
"The year 2025 was a defining one for Incannex," stated
Joel Latham, Incannex Healthcare Chief Executive Officer. "We delivered two independent, positive Phase 2 clinical readouts across
distinct CNS programs, achieved FDA Fast Track designation for our lead OSA candidate, and materially strengthened our balance sheet.
Importantly, we enter 2026 with more than $70 million in cash with runway extending well into 2027, allowing us to focus primarily on
execution. With clinical validation, regulatory momentum and financial flexibility now in place, we are in a very exciting position as
we advance our programs toward later-stage development and continue building long-term value for patients and shareholders."
2025 Corporate Highlights
Clinical and Regulatory Progress
IHL-42X (Obstructive Sleep Apnea)
During 2025, Incannex advanced IHL-42X, its oral combination therapy
for obstructive sleep apnea, through several critical milestones:
PSX-001 (Psi-GAD - Generalized Anxiety Disorder)
In parallel, Incannex reported positive Phase 2 clinical results for
PSX-001, its psilocybin-assisted therapy for generalized anxiety disorder:
Clinical Advisory Board Expansion
To support advancing programs toward later-stage development, Incannex
established a dedicated Obstructive Sleep Apnea Clinical Advisory Board comprised of leading experts in sleep medicine and respiratory
Financial Position and Capital Discipline
About Incannex Healthcare Inc.
Incannex is leading the way in developing
combination medicines that target the underlying biological pathways associated with chronic conditions, including obstructive sleep
apnea, rheumatoid arthritis and generalized anxiety disorder. The company is advancing three clinical-stage product candidates
based on evidence-based innovation and supported by streamlined operations. Incannex's lead clinical program, IHL-42X, is an oral
fixed-dose combination of dronabinol and acetazolamide designed to target underlying mechanisms and act synergistically in the
treatment of obstructive sleep apnea. In a Phase 2 development program, IHL-675A is an oral fixed-dose combination of cannabidiol
and hydroxychloroquine sulfate designed to act synergistically to alleviate inflammatory conditions, such as rheumatoid arthritis.
Approved for Phase 2 clinical development, PSX-001 is an oral synthetic psilocybin treatment for the treatment of generalized
anxiety disorder. Incannex's programs target disorders that have limited, inadequate, or no approved pharmaceutical treatment
options. For additional information on Incannex, please visit our website at www.incannex.com.
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. Forward-looking statements are statements other than historical facts and relate to future events, future circumstances and Incannex's
future performance. These statements are based on management's current assumptions, expectations, and beliefs. Examples of forward-looking
statements in this press release include statements about, among other things: Incannex's future intentions regarding its efforts to maintain
and/or regain compliance with applicable Nasdaq listing standards; business strategy, future operations; Incannex's ability to execute
on its objectives, prospects o plans; evaluations and judgments regarding Incannex's research and development efforts and potential future
commercialization, including any implications that the results of earlier clinical trials or interim or topline results will be representative
or consistent with later clinical trials or their respective interim or final results; the potential benefits and safety of Incannex's
drug candidates and the market opportunity for these candidates; and potential shareholder value. 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: that Incannex may fail to comply with Nasdaq listing standards within the applicable
extended grace period or following the applicable extended grace period; that Incannex may fail to comply with Nasdaq listing standards
other than the bid price rule; the closing price of the common stock may fall below $0.10 for ten consecutive trading days and be subject
to Nasdaq's low bid price rules and subject to delisting or denial of compliance periods; the continued availability of financing;
Incannex's ability to raise capital to fund continuing operations and to maintain or potentially further improve its capital structure;
Incannex's ability to maintain the listing of its shares of common stock on the Nasdaq Stock Market; 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 and to obtain necessary regulatory approvals for commercialization
of its product candidates; the effects of competition from other providers and products as currently existing or that may be developed
in the future; that the market for its drug candidates may not grow at the rates anticipated or at all or that estimates for these markets
may ultimately be incorrect; that Incannex may be unable to successfully execute upon any commercial discussions; Incannex's ability to
comply 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 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, 2025, filed with the SEC on September 29, 2025, 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. For additional information
on Incannex, please visit our website at www.incannex.com.
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Frequently Asked Questions

What financial position does Incannex hold for 2026?

Incannex enters 2026 with over $70 million in cash and funding well into 2027.

Which Phase 2 programs did Incannex complete in 2025?

Incannex delivered positive Phase 2 results for IHL-42X and PSX-001 in 2025.

What is IHL-42X used for?

IHL-42X is an oral therapy for treating obstructive sleep apnea.

What designation did Incannex achieve for its lead product?

Incannex received FDA Fast Track designation for its OSA candidate, IHL-42X.

What type of company is Incannex Healthcare?

Incannex Healthcare develops innovative combination therapies for chronic conditions.

Last updated: Jan 14, 2026