- ICH GCP
- Registre américain des essais cliniques
- Essai clinique 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
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
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.
Type d'étude
Inscription (Réel)
Phase
- Phase 2
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
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 d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Quadruple
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: CHF6001 DOSE1
DOSE1
|
Dose response: Test one of 4 different doses of CHF6001
Autres noms:
|
|
Expérimental: CHF6001 DOSE2
DOSE2
|
Dose response: Test one of 4 different doses of CHF6001
Autres noms:
|
|
Expérimental: CHF6001 DOSE3
DOSE3
|
Dose response: Test one of 4 different doses of CHF6001
Autres noms:
|
|
Expérimental: CHF6001 DOSE4
DOSE4
|
Dose response: Test one of 4 different doses of CHF6001
Autres noms:
|
|
Comparateur placebo: Matched placebo
placebo control
|
contrôle placebo
|
|
Comparateur actif: Budesonide
Budesonide DPI 800µg
|
active control
Autres noms:
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change from baseline in predose morning FEV1 at 12 weeks
Délai: week 12
|
overall effect of CHF6001 on change from baseline in predose morning FEV1
|
week 12
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change from baseline in predose morning FEV1 at other timepoints
Délai: weeks 3, 6, 18, 24
|
Change from Baseline
|
weeks 3, 6, 18, 24
|
|
Change from baseline in pre-dose morning IC
Délai: 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
Délai: 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
Délai: weeks 3, 6, 12, 18, 24
|
Change of TDI score
|
weeks 3, 6, 12, 18, 24
|
|
Change from baseline in SGRQ score
Délai: weeks 3, 6, 12, 18, 24
|
Change of SGRQ score
|
weeks 3, 6, 12, 18, 24
|
|
Change from baseline in E-RS score
Délai: 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
Délai: 24 weeks
|
exacerbation rate
|
24 weeks
|
|
Time to first COPD exacerbation
Délai: 24 weeks
|
Time to first COPD exacerbation
|
24 weeks
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Dave Singh, Medicines Evaluation Unit, Manchester, UK
Publications et liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Maladies des voies respiratoires
- Maladies pulmonaires
- Maladies pulmonaires obstructives
- Maladie pulmonaire obstructive chronique
- Effets physiologiques des médicaments
- Agents autonomes
- Agents du système nerveux périphérique
- Agents anti-inflammatoires
- Glucocorticoïdes
- Les hormones
- Hormones, substituts hormonaux et antagonistes hormonaux
- Agents bronchodilatateurs
- Agents anti-asthmatiques
- Agents du système respiratoire
- Budésonide
Autres numéros d'identification d'étude
- CCD-06001AA1-01
- 2015-005548-32 (Numéro EudraCT)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
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