Measuring Atomoxetine and Aroxybutynin In Patients With OSA
Phase 2 Randomized Double-Blind Placebo-Controlled Parallel-Arm Dose Finding Study to Compare Fixed Dose Combinations of Atomoxetine/Aroxybutynin (AD109) to Atomoxetine Alone or Placebo in Obstructive Sleep Apnea
| Patrocinadores |
Patrocinador Principal: Apnimed |
|---|---|
| Fonte | Apnimed |
| Sumário breve | MARIPOSA is a randomized, double blind, placebo-controlled, parallel-arm 1-month study of AD109 in participants with OSA. Enrolled participants will be randomized to one of 5 parallel treatment arms. |
| Descrição detalhada | MARIPOSA is a randomized, double blind, placebo-controlled, parallel-arm 1-month study in participants with OSA. A screening visit and polysomnograms (PSGs) will be conducted to establish that each participant meets study enrollment criteria. The screening PSGs will serve as the baseline for the PSGs conducted during the 3rd and 4th weeks of drug treatment. Enrolled participants will be randomized to one of 5 parallel treatment arms. The first week of dosing will be with a lower dose run-in of AD109 (or corresponding single-drug component or placebo), followed by the full dose taken in weeks 2-4. One combination tablet is taken each night immediately before lights out. A total of approximately 260 participants will be enrolled. |
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| Estado geral | Not yet recruiting | ||||||||
| Data de início | 2021-09-30 | ||||||||
| Data de conclusão | 2022-04-01 | ||||||||
| Data de Conclusão Primária | 2022-04-01 | ||||||||
| Estágio | Phase 2 | ||||||||
| tipo de estudo | Interventional | ||||||||
| Resultado primário |
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| Resultado Secundário |
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| Inscrição | 260 |
| Doença | |
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| Intervenção |
Tipo de intervenção: Drug Nome da Intervenção: AD109 (atomoxetine/aroxybutynin) Descrição: Matching (blinded) formulated AD109 oral tablet administered before sleep Tipo de intervenção: Drug Nome da Intervenção: Atomoxetine Hydrochloride Descrição: Matching (blinded) formulated atomoxetine oral tablet administered before sleep Etiqueta do Grupo de Armas: Atomoxetine Tipo de intervenção: Drug Nome da Intervenção: Placebo Descrição: Matching (blinded) formulated placebo oral tablet administered before sleep Etiqueta do Grupo de Armas: Placebo |
| Elegibilidade |
Critério:
Inclusion Criteria: - Between 18 to 65 years of age for men and 75 for women, inclusive - AHI between 10 to 45 with <25% events central or mixed apneas - BMI between 18.5 and 38 kg/m2 Exclusion Criteria: - Current clinically significant sleep disorder other than OSA - Clinically significant craniofacial malformation or grade ≥3 tonsillar hypertrophy. - Clinically significant cardiac disease (e.g., rhythm disturbances, coronary artery disease or cardiac failure) or hypertension requiring more than 2 drugs for control (combination drugs count as 1 drug). - Clinically significant neurological disorder, including epilepsy/convulsions. - History of clinically significant urinary retention, gastric retention or other severe decreased gastrointestinal motility condition - Severe or frequent gastroesophageal reflux or constipation - Participants with a history of using devices for OSA treatment, including CPAP, oral or nasal devices, or positional devices, may enroll as long as the devices have not been used for at least 2 weeks prior to first PSG and are not used during participation in the study Gênero: All Idade minima: 18 Years Idade Máxima: 75 Years Voluntários Saudáveis: No |
| Contato Geral | As informações de contato são exibidas apenas quando o estudo está recrutando indivíduos. |
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| Data de Verificação |
2021-06-01 |
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| Parte Responsável |
Tipo: Sponsor |
| Tem Acesso Expandido | No |
| Navegar condição | |
| Número de armas | 5 |
| Grupo de Armas |
Rótulo: AD109 Dose 1 Tipo: Experimental Descrição: AD109 Dose 1 Rótulo: AD109 Dose 2 Tipo: Experimental Descrição: AD109 Dose 2 Rótulo: AD109 Dose 3 Tipo: Experimental Descrição: AD109 Dose 3 Rótulo: Atomoxetine Tipo: Active Comparator Descrição: Atomoxetine Rótulo: Placebo Tipo: Placebo Comparator Descrição: Placebo |
| Acrônimo | MARIPOSA |
| Dados do Paciente | No |
| Informações de design de estudo |
Alocação: Randomized Modelo de Intervenção: Parallel Assignment Objetivo Primário: Treatment Mascaramento: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) |
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