Apnimed Reports Positive Topline Results From Second Phase 3 Trial of AD109, Reinforcing Potential of First Oral Pill for Obstructive Sleep Apnea
UNITED STATES, JUL 23 – AD109 reduced apnea severity by nearly 47% at 26 weeks in a 660-participant trial, supporting Apnimed's planned FDA new drug application in early 2026.
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Apnimed Reports Positive Topline Results from Second Phase 3 Trial of AD109, Reinforcing Potential of First Oral Pill for Obstructive Sleep Apnea
LunAIRo, Apnimed's second Phase 3 trial of AD109, met its primary endpoint, demonstrating a reduction in the Apnea-Hypopnea Index (AHI) from baseline at 26...
Apnimed Reports Positive Topline Results from Second Phase 3 Trial of AD109, Reinforcing Potential of First Oral Pill for Obstructive Sleep Apnea - PressReach
Apnimed, Inc., a pharmaceutical company advancing an industry-leading pipeline of first-in-class oral therapies that address the root causes of obstructive sleep apnea (OSA) and
Apnimed announces results from second study of sleep apnea drug
On July 23, Apnimed announced positive topline results from LunAIRo, the second phase 3 clinical trial of AD109 (aroxybutynin 2.5mg, atomoxetine 75mg) in adults with obstructive sleep apnea. Apnimed previously announced results from its SynAIRgy trial of AD109 in May. LunAIRo study results Apnimed reports that the 12-month LunAIRo study demonstrated clinically meaningful and statistically significant reductions in airway obstruction at 26 weeks.…
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