Incannex Complete Successful Pre-IND Meeting with the FDA for CannQuit-O for treatment of opioid use disorder
07 Mai 2024 - 1:30PM
Incannex Healthcare Inc. (Nasdaq: IXHL), (Incannex or the
Company), a leading cannabinoid and psychedelic medicine
biotechnology company, is pleased to announce the successful
completion of a pre-IND (Investigational New Drug) meeting with the
U.S. Food and Drug Administration (FDA) regarding the development
of CannQuit-O for treatment of Opioid Use Disorder (OUD).
The pre-IND teleconference included
representatives from various divisions of the FDA providing input
on the CannQuit-O development program. The Agency had reviewed the
CannQuit-O meeting package and provided recommendations on the
proposed clinical development strategy, including patient
populations, the selection and timing of efficacy endpoints and
safety monitoring. These recommendations were discussed during the
pre-IND teleconference where the company had the opportunity to
seek further clarification on the agency’s initial response.
The productive discussion with the FDA is an
important milestone for the development of CannQuit-O and provides
Incannex with clarity on the data required to open an IND with the
FDA for this product and provides valuable guidance for successful
clinical development in the OUD indication.
Incannex Chief Scientific Officer Dr Mark
Bleackley said: “Opioid use disorder is a significant issue
impacting millions of patients and their families. Developing new
therapies, such as CannQuit-O, is critical for helping control the
disease and improve quality of life for those who are suffering
from the disease and those around them. Feedback from the FDA on
the proposed development strategy for CannQuit-O will be taken on
board so that the outcomes of research activities meet agency
expectations and ensure that the appropriate steps are being taken
towards drug registration.”
About CannQuit-O
CannQuit-O is a chewable tablet with unique
characteristics provided by novel combination of
registered/FDA-approved polymers allowing for rapid and sustained
release of its active ingredients, including an opioid agonist,
antagonist and cannabidiol (CBD). The working hypothesis is that
the bioavailability profile of the drugs can be significantly
improved when formulated as water-soluble, chewable tablet.
Incannex owns patents on chewable formulations cannabinoids and
opioid agonists and/or antagonists and it is hypothesised that this
combination of active pharmaceutical ingredients and delivery
system will provide benefits for sufferers of OUD, of which there
are estimated 26.8 million people worldwide1. In the USA the opioid
epidemic has been declared a public health emergency, affecting
millions with the misuse of prescription opioids and illicit
substances. According to the National Institute of Health (NIH), by
far the largest components of the overall economic burden, however,
are the value of reduced quality of life from opioid use disorder
($390.0 billion) and life lost to opioid overdose ($480.7 billion).
These two cost components account for over 85% of the total
economic burden2.
The Global OUD market size was valued at USD 2.8
Billion in 2022 and is estimated to grow at CAGR of 10.7% from
2022-2032, reaching USD 7.8 Billion in 2032. Asia Pacific is
expected to grow the fastest during the forecasted period3.
This announcement has been approved for release to
NASDAQ by the Incannex Board of Directors.
About Incannex Healthcare Inc.
Incannex is a clinical stage pharmaceutical
development company that is developing unique medicinal cannabis
pharmaceutical products and psychedelic medicine therapies for the
treatment of obstructive sleep apnoea (OSA), traumatic brain injury
(TBI) and concussion, lung inflammation (ARDS, COPD, asthma,
bronchitis), rheumatoid arthritis, inflammatory bowel disease,
anxiety disorders, addiction disorders, and pain, among other
indications.
U.S. FDA approval and registration, subject to
ongoing clinical success, is being pursued for each drug and
therapy under development. Each indication under investigation
currently has no, or limited, existing registered pharmacotherapy
(drug) treatments available to the public and represent major
global economic opportunities to Incannex and its shareholders.
Incannex has a strong patent filing strategy in
place as it develops its products and therapies in conjunction with
its medical and scientific advisory board and partners. The Company
holds 19 granted patents and 30 pending patent applications.
Incannex is listed on the NASDAQ as IXHL
Website:
www.incannex.com.au Investors:
investors@incannex.com.au
Forward-looking statementsThis
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. These forward-looking
statements are made as of the date they were first issued and were
based on current expectations and estimates, as well as the beliefs
and assumptions of management. The forward-looking statements
included in this press release represent Incannex's views as of the
date of this press release. Incannex anticipates that subsequent
events and developments may cause its views to change. Incannex
undertakes no intention or obligation to update or revise any
forward-looking statements, whether as of a result of new
information, future events or otherwise. These forward-looking
statements should not be relied upon as representing Incannex's
views as of any date after the date of this press release.
Contact Information:
Incannex Healthcare Inc.Mr Joel
LathamChief Executive Officer, President and
Directoradmin@incannex.com.au
Investor Relations Contact – United States
Laine YonkerEdison Group+1 (610) 716
2868lyonker@edisongroup.com
________________1
https://www.nature.com/articles/s41572-019-0137-52
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC80914803
https://www.sphericalinsights.com/reports/opioid-use-disorder-oud-market
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