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Incannex Healthcare Ltd (IXHL) is a clinical-stage biopharmaceutical innovator developing novel cannabinoid and psychedelic-assisted therapies for chronic medical conditions. This dedicated news hub provides investors and healthcare professionals with essential updates on the company's research advancements and operational milestones.
Access authoritative information about IXHL's clinical trials, regulatory developments, and strategic partnerships. Our curated collection includes press releases on sleep apnea therapies, inflammatory disease treatments, and neurological disorder research – all critical to understanding the company's progress in psychedelic medicine and cannabinoid science.
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Incannex Healthcare (Nasdaq: IXHL) has reported positive Phase 2 trial results for IHL-42X in treating Obstructive Sleep Apnoea (OSA). The trial demonstrated significant clinical efficacy with AHI reductions of up to 83% in the high-dose group and 79% in the low-dose group.
Patient-reported outcomes were notably strong, with 57.6% of participants reporting improved OSA and 89.5% describing the improvements as meaningful. The drug showed statistically significant benefits in multiple endpoints including oxygen desaturation, sleep quality, and fatigue reduction. Importantly, IHL-42X maintained an excellent safety profile with no serious adverse events reported.
The company remains well-capitalized but noted concerns about share price volatility and potential short-selling affecting market valuation.
Incannex Healthcare (NASDAQ: IXHL) has addressed stockholder concerns regarding its At-The-Market (ATM) offering program, confirming it does not plan to fully utilize the facility in the near term. The company maintains a strong cash position of US$50 million and has used the ATM sparingly, with a recent sale of 9.2 million shares representing only 1.97% of daily trading volume.
CEO Joel Latham emphasized that the ATM serves as a strategic tool for efficient capital access. The company recently achieved significant success in its Phase 2 clinical trial for IHL-42X, reporting statistically significant improvements across key endpoints with a superior safety profile. Incannex is now preparing to advance IHL-42X into Phase 3 development.
Incannex Healthcare (NASDAQ:IXHL) has announced positive topline results from its RePOSA Phase 2 clinical trial for IHL-42X, a novel oral drug candidate for obstructive sleep apnea (OSA). The trial demonstrated significant improvements in key endpoints, with the drug reducing the Apnoea-Hypopnoea Index (AHI) by up to 83% in the high-dose group and 79% in the low-dose group.
The study, involving 121 adult participants, showed statistically significant improvements across multiple measures including oxygen desaturation, sleep quality, and patient-reported outcomes. Both dosage groups demonstrated strong efficacy, with 33.3% to 41.2% of patients achieving >30% AHI reduction. The drug exhibited an excellent safety profile with no serious adverse events reported.
Following these positive results, Incannex is preparing for an End-of-Phase 2 meeting with the FDA to discuss the path toward Phase 3 trials and potential commercialization.
[ "Significant AHI reduction of up to 83% from baseline in high-dose group", "33.3% to 41.2% of patients achieved >30% reduction in AHI across dose groups", "Statistically significant improvements in oxygen desaturation and patient-reported outcomes", "Excellent safety profile with no serious adverse events reported", "Strong potential as first oral pharmaceutical treatment for 900M+ global OSA patients" ]Incannex Healthcare (Nasdaq: IXHL) has appointed Dr. Charlene E. Gamaldo to its IHL-42X Obstructive Sleep Apnea (OSA) Clinical Advisory Board. Dr. Gamaldo, a Professor at Johns Hopkins School of Medicine, brings extensive expertise in neurology, psychiatry, and sleep medicine to support the company's OSA program.
The appointment comes ahead of IHL-42X Phase 2 data readout expected next week. Dr. Gamaldo's credentials include over 120 scholarly publications, joint appointments across multiple departments at Johns Hopkins, and numerous prestigious awards in sleep medicine, education, and leadership.
Incannex Healthcare (Nasdaq: IXHL) has appointed Dr. Douglas B. Kirsch to its IHL-42X Obstructive Sleep Apnea Clinical Advisory Board. Dr. Kirsch, currently Medical Director of Atrium Health Sleep Medicine and Clinical Professor at Wake Forest School of Medicine, brings significant expertise as a former President of the American Academy of Sleep Medicine (2018-2019).
Dr. Kirsch joins other recently appointed advisors to support the development of IHL-42X, an oral fixed-dose combination therapy for obstructive sleep apnea. The company expects to report Phase 2 topline data from its RePOSA study in July 2025, with Phase 3 initiation planned for later in the year.
Incannex Healthcare (NASDAQ: IXHL) has received FDA clearance to advance its IHL-42X RePOSA clinical trial to Phase 3 for treating obstructive sleep apnea (OSA). The trial will evaluate IHL-42X, which aims to become the first FDA-approved oral therapy for OSA, a condition affecting approximately one billion people globally.
The Phase 3 study will be conducted exclusively in the U.S., building on the Phase 2 infrastructure. The trial will involve approximately 30 sites (20 existing and 10 new) and will evaluate the drug's safety and efficacy over 12 months. The study includes a 3-month head-to-head comparison against dronabinol and acetazolamide to demonstrate the combination therapy's synergistic effect. The primary endpoint will measure changes in the Apnea-Hypopnea Index (AHI).