Condition: Obstructive Sleep Apnea (OSA) · Sponsor: Incannex Healthcare Ltd
The goal of this randomized, double-blind, multi-dose crossover clinical trial is to determine the safety and efficacy of IHL-42X in subjects with obstructive sleep apnea. The primary endpoint is: Change in AHI4 at the end of each treatment period compared to baseline (each treatment period is 28 days). The study will consist of three separate four-way crossover dose-comparison studies each comparing three dose strengths of IHL-42X to placebo. The double-blind four-way crossover will be conducted according to a Williams design. Each of the crossover studies will test different doses of dronabinol in combination with a distinct, set dose of acetazolamide. In total, nine different combinations of dronabinol and acetazolamide formulated as IHL-42X will be tested in the study. The optimal dose strength will be selected based on safety and efficacy over a 4-week treatment period.
This description comes directly from the study's public registry record.
Mark Bleackley · +61 2 9634 4508 · mark@incannex.com.au
Pia Kroner · +61 (2) 9634 4508 · pia@incannex.com.au
Always discuss trial participation with your own doctor first.
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+ 2 more locations — full list on the registry record.
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