FDA Grants Orphan Drug Designation to IH Drug Contender
A phase 3 trial is underway to evaluate the drug’s efficacy and safety in adults with IH, with enrollment expected to complete by the end of 2025.
Read MoreA phase 3 trial is underway to evaluate the drug’s efficacy and safety in adults with IH, with enrollment expected to complete by the end of 2025.
Read MoreAn Interview with Vyto Kab, CEO, Persante Health Care
Read MoreThe enhanced platform integrates FDA-cleared tools like BodySleep, ventilatory burden, hypoxic burden, and OSA endotyping to support personalized care.
Read MoreThe SRS has selected four sleep and circadian scientists as recipients of the 2025 Sleep Research Society awards, which recognize excellence in sleep and circadian research.
Read MoreThis on-demand webinar helps attendees examine differences between peripheral arterial tone-based devices and summarizes steps for verifying or editing automated results.
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