Incannex Healthcare Commences DReAMzz Clinical Study for IHL-42X in OSA
The crossover dose optimization study aims to refine the dosing profile of the oral therapy and strengthen the design of the planned phase III development program.
The crossover dose optimization study aims to refine the dosing profile of the oral therapy and strengthen the design of the planned phase III development program.
Incannex shares key developments, including the ongoing clinical trials for its lead product, IHL-42X, in development for the treatment of sleep apnea.
No oral pharmacologic treatment to maintain open airways for people with obstructive sleep apnea has been approved by the FDA—yet.
Incannex received approval from the US Food and Drug Administration for an Investigational New Drug opening pivotal IHL-42X phase 2/3 clinical trial in the United States as planned.
Read MoreThe IND application details the clinical trial protocol for the IND opening clinical trial, which is a multi-site phase 2/3 trial investigating IHL-42X, a cannabinoid combination product, for the treatment of OSA.
Read MoreThe phase 2/3 clinical trial will assess the safety and efficacy of IHL-42X, a cannabinoid combination product, in people with OSA who are intolerant, non-compliant, or naïve to CPAP.
Read MoreThe clinical trial will assess the pharmacokinetics and tolerability of the two active pharmaceutical ingredients in IHL-42X: dronabinol (THC) and acetazolamide.
Read MoreIHL-42X, a cannabinoid combination product, is being developed as a pharmacological option for obstructive sleep apnea.
Read MoreDronabinol, synthetic THC, shows promise for the treatment of sleep apnea, and new advances from pharmaceutical companies suggest how it can be optimized.
Read MoreThe acquisition of APIRx will significantly strengthen Incannex’s position with regard to cannabinoid and psychedelic treatment development.
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