Apnimed, Inc. (APMD)
Apnimed, Inc. operates as a clinical pharmaceutical company that develops and manufactures novel oral therapies that address the neurobiology of sleep-related breathing diseases in global markets. Its products include AD109, an oral therapy designed to treat obstructive sleep apnea (OSA) by targeting the underlying neuromuscular dysfunction. The company was incorporated in 2017 and is based in Cambridge, Massachusetts.
Sector: Pharmaceutical Preparations
Industry: Biotechnology
Apnimed, Inc.
Trials need funding. See this company's dilution risk and cash position.
- Phase 3Completed
Parallel Arm Trial of AD109 and Placebo With Patients With OSA (LunAIRo)
AD109, Placebo
OSA
NCT05811247Enrollment660StartAug 2023Primary CompletionMay 2025CompletionMay 2025 - Phase 3Completed
Parallel-Arm Study to Compare AD109 to Placebo With Patients With OSA (SynAIRgy Study)
AD109, Placebo
OSA
NCT05813275Enrollment646StartSep 2023Primary CompletionMar 2025CompletionMar 2025 - Phase 3Enrolling by invitation
Continuation Protocol for Obstructive Sleep Apnea (OSA)
Aroxybutynin and Atomoxetine
OSA
NCT06566820Enrollment1,280StartJul 2024Primary CompletionJun 2026est.CompletionJun 2026est. - Phase 2Completed
Trial of AD036 in Obstructive Sleep Apnea
AD036 Dose 1, AD036 Dose 2
Obstructive Sleep Apnea
NCT03845023Enrollment140StartMar 2019Primary CompletionOct 2019CompletionOct 2019 - Phase 2Completed
Crossover Trial of AD036 in Obstructive Sleep Apnea
AD036, Atomoxetine
Obstructive Sleep Apnea
NCT04445688Enrollment62StartJul 2020Primary CompletionDec 2020CompletionDec 2020 - Phase 2Completed
Crossover Trial of AD109 in Obstructive Sleep Apnea
AD109, Atomoxetine
Obstructive Sleep Apnea
NCT04580394Enrollment60StartOct 2020Primary CompletionMay 2021CompletionMay 2021 - Phase 2Completed
AD109 Dose Finding in Mild to Moderate OSA
AD109 dose1- A, AD109 dose2- B
Obstructive Sleep Apnea
NCT04631107Enrollment32StartDec 2020Primary CompletionMay 2021CompletionMay 2021 - Phase 2Completed
Crossover Trial of AD182 and AD504 in Obstructive Sleep Apnea
AD182, AD504
Obstructive Sleep Apnea
NCT04645524Enrollment15StartDec 2020Primary CompletionSep 2021CompletionSep 2021 - Phase 2Completed
Trial of AD113 and Atomoxetine in OSA Patients With Hypertension
AD113, Atomoxetine
Obstructive Sleep Apnea, Hypertension
NCT04905979Enrollment21StartJul 2021Primary CompletionJan 2023CompletionMay 2023 - Phase 2Completed
Parallel Arm Trial of AD109 and AD504 In Patients With OSA
AD109, AD504
OSA - Obstructive Sleep Apnea
NCT05071612Enrollment294StartNov 2021Primary CompletionJul 2022CompletionAug 2022 - Phase 2Completed
AD816 Crossover Study
Period A, Period B
OSA, Obstructive Sleep Apnea
NCT05793684Enrollment25StartApr 2023Primary CompletionNov 2023CompletionNov 2023 - Phase 2Completed
Study That Tests AD109 in Patients Taking GLP-1 Drugs
AD109
OSA
NCT06400615Enrollment40StartMay 2024Primary CompletionDec 2024CompletionDec 2024 - Phase 1/2Completed
Study for Efficacy and Dose Escalation of AD313 + Atomoxetine (SEED)
Dosing 1: Atomoxetine, AD313
Obstructive Sleep Apnea
NCT05101122Enrollment15StartOct 2021Primary CompletionApr 2022CompletionApr 2022
| Drug / Therapy | Link | ||
|---|---|---|---|
| Phase 3 | Completed | AD109, Placebo | NCT05811247 |
| Phase 3 | Completed | AD109, Placebo | NCT05813275 |
| Phase 3 | Enrolling by invitation | Aroxybutynin and Atomoxetine | NCT06566820 |
| Phase 2 | Completed | AD036 Dose 1, AD036 Dose 2 | NCT03845023 |
| Phase 2 | Completed | AD036, Atomoxetine | NCT04445688 |
| Phase 2 | Completed | AD109, Atomoxetine | NCT04580394 |
| Phase 2 | Completed | AD109 dose1- A, AD109 dose2- B | NCT04631107 |
| Phase 2 | Completed | AD182, AD504 | NCT04645524 |
| Phase 2 | Completed | AD113, Atomoxetine | NCT04905979 |
| Phase 2 | Completed | AD109, AD504 | NCT05071612 |
| Phase 2 | Completed | Period A, Period B | NCT05793684 |
| Phase 2 | Completed | AD109 | NCT06400615 |
| Phase 1/2 | Completed | Dosing 1: Atomoxetine, AD313 | NCT05101122 |