- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT02172326
Pharmacokinetic Study in Elderly Patients With Chronic Obstructive Bronchitis (COPD)
The Pharmacokinetics, Safety and Tolerability of Tiotropium in Elderly COPD Patients (Open Label, Monocenter Study).
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription
Phase
- Phase 3
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
All patients were required to have a diagnosis of COPD and to meet the following spirometric criteria:
- Relatively stable, moderate to severe airway obstruction with an FEV1 ≤ 65% of predicted normal and FEV1/FVC ≤ 70%
Patients were required to have normal renal clearance. Renal clearance will be evaluated by the determination of creatinine clearance. To qualify for this trial, the patient's measured creatinine clearance was required to be within 20% of the calculated creatinine clearance, as given by the following equations:
- Males: Calculated Creatinine Clearance (ml/min) = [140 - Age (yrs)] x weight(kg) / 72 x serum creatinine (mg/dL)
- Females: Calculated Creatinine Clearance (ml/min) = [140 - Age (yrs)] x weight (kg) / 85 x serum creatinine (mg/dL)
- Both male or female patients were eligible. Twelve patients ≥ 70 years old and twelve patients ≤ 50 years
- Patients were required to have a smoking history of more than ten pack-years, where a pack-year was defined as the equivalent of smoking one pack of cigarettes per day for a year
- Patients must be able to perform all specified procedures and maintain records during the study period as required in the protocol
- Patients were required to be able to inhale medication from the HandiHaler®
- Patients were required to sign an Informed Consent Form prior to participation in the trial, including any necessary prior to pre-study washout of their usual pulmonary medications
Exclusion Criteria:
- Patients with significant diseases other than COPD were excluded from participation in the trial. A significant disease was defined as a disease which in the opinion of the investigator may either have put the patient at risk because of participation in the trial or a disease which may have influenced the results of the trial or the patient's ability to participate in the trial;
- Patients with clinically significant abnormal baseline haematology, blood chemistry or urinalysis, if the abnormality defined a disease listed as an exclusion criterion;
- Patients with alanine transaminase (ALT/SGOT) > 80 IU/L or aspartate transaminase (AST/SGPT) > 80 IU/L, or bilirubin > 2.0 mg/dL or creatinine > 2.0 mg/dL were excluded from participation in the trial, regardless of the patient's clinical condition. Repeat laboratory evaluations were not conducted in these patients;
- Patients with a recent history (i.e., one year or less) of myocardial infarction (MI);
- Patients with a recent history (i.e., three years or less) of heart failure or patients with any cardiac arrhythmia requiring drug therapy;
- Patients with regular use of daytime oxygen therapy;
- Patients with known active tuberculosis;
- Patients with a history of cancer within the last five years. However, patients with treated basal cell carcinoma are allowed to participate;
- Patients with a history of life-threatening pulmonary obstruction, or a history of cystic fibrosis or bronchiectasis;
- Patients who had undergone thoracotomy with pulmonary resection. Patients with a history of a thoracotomy for other reasons were evaluated as per exclusion criterion # 1;
- Patients who had developed an upper respiratory tract infection in six weeks prior to the Screening Visit (Visit 1) or during the baseline period;
- Patients with known hypersensitivity to anticholinergic drugs, lactose or any other components of the inhalation capsule delivery system;
- Patients with known symptomatic prostatic hypertrophy or bladder neck obstruction;
- Patients with known narrow-angle glaucoma;
- Patients treated with cromolyn sodium or nedocromil sodium;
- Patients treated with antihistamines (H1 receptor antagonists);
- Patients using oral corticosteroid medication at unstable doses (i.e. less than six weeks on a stable dose) or at a dose in excess of the equivalent of 10 mg of prednisone per day (or 20 mg every other day);
- Pregnant or nursing women or women of childbearing potential not using a medically approved means of contraception (i.e. oral contraceptives, intrauterine devices, diaphragm or Norplant®);
- Patients with a history of asthma, allergic rhinitis or atopy or patients with a total blood eosinophil count ≥ 600/mm3. A repeat eosinophil count was not conducted in these patients;
- Patients with history and/or active alcohol or drug abuse.
- Patients who had taken an investigational drug within one month or six half lives (whichever was greater) prior to Screening Visit (Visit 1).
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Gélules pour inhalation de tiotropium
|
Powder inhalation via HandiHaler®
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
Total area under the plasma drug concentration-time curve (AUC 0-4 h)
Délai: pre-dose and 5, 20 min., 1, 2,and 4 hours after dosing on days 1, 7 and 14
|
pre-dose and 5, 20 min., 1, 2,and 4 hours after dosing on days 1, 7 and 14
|
|
Urinary excretion of tiotropium (Ae(0-4 hours))
Délai: screening and on days 1, 7, 14, 15, 16, 20, 24, 28, 31, 35, 38
|
screening and on days 1, 7, 14, 15, 16, 20, 24, 28, 31, 35, 38
|
|
Renal clearance of tiotropium (CLren)
Délai: screening and on days 1, 7, 14, 15, 16, 20, 24, 28, 31, 35, 38
|
screening and on days 1, 7, 14, 15, 16, 20, 24, 28, 31, 35, 38
|
|
Terminal elimination half-life after the last dose
Délai: pre dose and 5, 20 min., 1, 2,and 4 hours after dosing on days 1, 7 and 14
|
pre dose and 5, 20 min., 1, 2,and 4 hours after dosing on days 1, 7 and 14
|
Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
|
Plasma concentration of drug 5 min after inhalation (C5min)
Délai: pre dose and 5, 20 min., 1, 2,and 4 hours after dosing on days 1, 7 and 14
|
pre dose and 5, 20 min., 1, 2,and 4 hours after dosing on days 1, 7 and 14
|
|
tmax (time of occurrence for maximum drug concentration)
Délai: pre dose and 5, 20 min., 1, 2,and 4 hours after dosing on days 1, 7 and 14
|
pre dose and 5, 20 min., 1, 2,and 4 hours after dosing on days 1, 7 and 14
|
|
Change from baseline in FEV1 (Forced expiratory volume in one second)
Délai: Baseline, Days 1, 7 and 14
|
Baseline, Days 1, 7 and 14
|
|
Change from baseline in FVC (Forced vital capacity)
Délai: Baseline, Days 1, 7 and 14
|
Baseline, Days 1, 7 and 14
|
|
FEV1/FVC
Délai: Baseline, Days 1, 7 and 14
|
Baseline, Days 1, 7 and 14
|
|
Symptom evaluation
Délai: 2 weeks
|
2 weeks
|
|
Use of salbutamol
Délai: 2 weeks
|
2 weeks
|
|
Occurrence of Adverse Events
Délai: up to day 39
|
up to day 39
|
|
Occurrence of Adverse Events
Délai: up to day 38
|
up to day 38
|
|
Changes form baseline in vital signs (pulse rate and blood pressure)
Délai: up to day 38
|
up to day 38
|
|
Changes from baseline in laboratory tests (haematology, clinical chemistry and urinalysis)
Délai: baseline, day 38
|
baseline, day 38
|
|
Changes from baseline in physical examination
Délai: baseline, day 38
|
baseline, day 38
|
|
Changes from baseline in ECG (Electrocardiogram)
Délai: baseline, day 1, 7, 14 and 38
|
baseline, day 1, 7, 14 and 38
|
Collaborateurs et enquêteurs
Parrainer
Publications et liens utiles
Liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement primaire (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 (Estimation)
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 neurotransmetteurs
- Mécanismes moléculaires de l'action pharmacologique
- Parasympatholytiques
- Agents autonomes
- Agents du système nerveux périphérique
- Antagonistes cholinergiques
- Agents cholinergiques
- Agents bronchodilatateurs
- Agents anti-asthmatiques
- Agents du système respiratoire
- Bromure de tiotropium
Autres numéros d'identification d'étude
- 205.133
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .