Incannex Receives IRB Approval for the RePOSA Phase 2/3 Clinical Trial Protocol to Assess IHL-42X Drug in Patients with Obstructive Sleep Apnea
IRB approval of the protocol is a key step in activation of clinical trial sites for the RePOSA study.
- IRB approval of the protocol is a key step in activation of clinical trial sites for the RePOSA study.
- The approval process involves review of the research protocol, informed consent procedures, recruitment materials, and participant risk versus benefit analysis.
- The study is designed to facilitate a seamless transition between Phase 2 and Phase 3, reducing downtime and accelerating development timelines.
- IRB approval of the protocol allows the U.S.-based sites to proceed with site-specific approval, which is a critical step in site activation.