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- Ensayo clínico NCT02986321
A 24-wk Dose Ranging Study to Evaluate the Efficacy and Safety of 4 Doses of a New PDE4 Inhibitor in Patients With COPD (PIONEER)
A 24-week, Multicenter, Randomized, Double-blind, Double-dummy, Placebo and Active Controlled, Parallel Group, Dose Ranging Study to Evaluate the Efficacy and Safety of 4 Doses of CHF6001 DPI in Patients With COPD on a Background Therapy
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
This is a phase II, randomized, double-blind, double-dummy, placebo and active controlled multinational, multicenter, dose ranging, 6-arm parallel-group study to identify the optimal dose of CHF6001, PDE4 inhibitor under development, with respect to lung functions and symptoms.
After a 2-wk run-in period under formoterol (Oxis Turbohaler®) and rescue salbutamol prn, patients will be randomized to one of the 6 treatment groups. After the randomization, patients will be assessed after 3, 6, 12, 18 and 24 weeks of treatment at clinic/hospital. A follow-up visit will be performed 12 days after the last visit.
During the study, patients will report daily symptoms with the EXACT-PRO/E-RS questionnaire, rescue/background medication use and compliance with the study medications. AEs, SAEs and COPD exacerbations will be monitored throughout the study. At randomization and subsequent visits, patients will undergo physical and vital signs examinations, spirometry measurement, 12-lead ECG. Symptoms and Health status will be assessed through validated questionnaires. Routine lab analysis and blood biomarkers will be done.
Tipo de estudio
Inscripción (Actual)
Fase
- Fase 2
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- COPD patients
- Non- childbearing potential or woman permanently sterilized or on one or more highly effective contraception
- Current/ex smokers (history > 10 pack years)
- Post bronchodilatator FEV1 >=30% and <=70% predicted normal value and FEV1/FVC ratio <0.7
- Documented history of at least 1 moderate or severe exacerbation in the 12 months prior to study entry
- Symptomatic patients (MMRC score ≥2 and a CAT score ≥10)
- Patients on daily maintenance therapy with an ICS/LABA .
Exclusion Criteria:
- Diagnosis of asthma or other respiratory disorders
- Maintenance bronchodilators therapy only (eg LABA alone)
- Maintenance triple therapy.
- Occurrence of a moderate or severe COPD exacerbation within 6 weeks prior to study entry or during the run-in period.
- Patients requiring long term oxygen therapy.
- Concomitant or recent pulmonary rehabilitation programme
- Known respiratory disorders other than COPD
- Lung cancer or a history of lung cancer, active or history of cancer with less than 5 years disease free survival time
- Hypersensitivity to β2-agonist, corticosteroids, PDE4 inhibitors or any of the excipients
- Depression, generalised anxiety disorder, suicidal ideation
- Any clinically significant cardiovascular disease (IM, CHF III/IV; AF not controlled by therapy, etc) within 1 year of study entry
- Any relevant clinically significant cardiovascular condition, clinically abnormal significant 12-lead ECG (QTcF>450 ms for male and >470 for female) or clinically significant laboratory abnormalities
- Serum potassium value ≤3.5 mEq/L or >5.5mEq/L and/or a fasting serum glucose value ≥140 mg/dL.
- History or symptoms of significant neurological disease
- Unstable concurrent disease: eg uncontrolled Thyroid disease or other endocrine diseases, gastrointestinal uncontrolled disease, uncontrolled immune diseases
- Renal impairment.
- Patients with abnormal alanine aminotransferase and/ or aspartate aminotransferase and/or bilirubin
- Current or chronic history of liver disease, or known hepatic or biliary abnormalities and patients receiving treatment with any drug known to have a well defined potential for hepatotoxicity before Study entry
- Severely obese (BMI ≥35 kg/m2) or have experienced excessive weight loss recently
- History of alcohol abuse and/or substance/drug abuse within 12 months prior to screening visit.
- Any recent participation to a clinical Study with other investigational drug
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Cuadruplicar
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: CHF6001 DOSE1
DOSE1
|
Dose response: Test one of 4 different doses of CHF6001
Otros nombres:
|
|
Experimental: CHF6001 DOSE2
DOSE2
|
Dose response: Test one of 4 different doses of CHF6001
Otros nombres:
|
|
Experimental: CHF6001 DOSE3
DOSE3
|
Dose response: Test one of 4 different doses of CHF6001
Otros nombres:
|
|
Experimental: CHF6001 DOSE4
DOSE4
|
Dose response: Test one of 4 different doses of CHF6001
Otros nombres:
|
|
Comparador de placebos: Matched placebo
placebo control
|
controles con placebo
|
|
Comparador activo: Budesonide
Budesonide DPI 800µg
|
active control
Otros nombres:
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Change from baseline in predose morning FEV1 at 12 weeks
Periodo de tiempo: week 12
|
overall effect of CHF6001 on change from baseline in predose morning FEV1
|
week 12
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Change from baseline in predose morning FEV1 at other timepoints
Periodo de tiempo: weeks 3, 6, 18, 24
|
Change from Baseline
|
weeks 3, 6, 18, 24
|
|
Change from baseline in pre-dose morning IC
Periodo de tiempo: weeks 3, 6, 12, 18, 24
|
Change from Baseline for other lung function parameters
|
weeks 3, 6, 12, 18, 24
|
|
Change from baseline in pre-dose morning FVC
Periodo de tiempo: weeks 3, 6, 12, 18, 24
|
Change from Baseline for other lung function parameters
|
weeks 3, 6, 12, 18, 24
|
|
Change from baseline in TDI focal score
Periodo de tiempo: weeks 3, 6, 12, 18, 24
|
Change of TDI score
|
weeks 3, 6, 12, 18, 24
|
|
Change from baseline in SGRQ score
Periodo de tiempo: weeks 3, 6, 12, 18, 24
|
Change of SGRQ score
|
weeks 3, 6, 12, 18, 24
|
|
Change from baseline in E-RS score
Periodo de tiempo: weeks 3, 6, 12, 18, 24
|
Change of E-RSI score
|
weeks 3, 6, 12, 18, 24
|
|
COPD exacerbation rate over 24 weeks of treatment
Periodo de tiempo: 24 weeks
|
exacerbation rate
|
24 weeks
|
|
Time to first COPD exacerbation
Periodo de tiempo: 24 weeks
|
Time to first COPD exacerbation
|
24 weeks
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Dave Singh, Medicines Evaluation Unit, Manchester, UK
Publicaciones y enlaces útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Enfermedades de las vías respiratorias
- Enfermedades pulmonares
- Enfermedades Pulmonares Obstructivas
- Enfermedad Pulmonar Obstructiva Crónica
- Efectos fisiológicos de las drogas
- Agentes Autonómicos
- Agentes del sistema nervioso periférico
- Agentes antiinflamatorios
- Glucocorticoides
- Hormonas
- Hormonas, sustitutos hormonales y antagonistas hormonales
- Agentes broncodilatadores
- Agentes antiasmáticos
- Agentes del sistema respiratorio
- Budesonida
Otros números de identificación del estudio
- CCD-06001AA1-01
- 2015-005548-32 (Número EudraCT)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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