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- Sperimentazione clinica 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).
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Tipo di studio
Iscrizione
Fase
- Fase 3
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Bambino
- Adulto
- Adulto più anziano
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
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).
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Capsule per inalazione di tiotropio
|
Powder inhalation via HandiHaler®
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
Total area under the plasma drug concentration-time curve (AUC 0-4 h)
Lasso di tempo: 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))
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
|
Misure di risultato secondarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
Plasma concentration of drug 5 min after inhalation (C5min)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: Baseline, Days 1, 7 and 14
|
Baseline, Days 1, 7 and 14
|
|
Change from baseline in FVC (Forced vital capacity)
Lasso di tempo: Baseline, Days 1, 7 and 14
|
Baseline, Days 1, 7 and 14
|
|
FEV1/FVC
Lasso di tempo: Baseline, Days 1, 7 and 14
|
Baseline, Days 1, 7 and 14
|
|
Symptom evaluation
Lasso di tempo: 2 weeks
|
2 weeks
|
|
Use of salbutamol
Lasso di tempo: 2 weeks
|
2 weeks
|
|
Occurrence of Adverse Events
Lasso di tempo: up to day 39
|
up to day 39
|
|
Occurrence of Adverse Events
Lasso di tempo: up to day 38
|
up to day 38
|
|
Changes form baseline in vital signs (pulse rate and blood pressure)
Lasso di tempo: up to day 38
|
up to day 38
|
|
Changes from baseline in laboratory tests (haematology, clinical chemistry and urinalysis)
Lasso di tempo: baseline, day 38
|
baseline, day 38
|
|
Changes from baseline in physical examination
Lasso di tempo: baseline, day 38
|
baseline, day 38
|
|
Changes from baseline in ECG (Electrocardiogram)
Lasso di tempo: baseline, day 1, 7, 14 and 38
|
baseline, day 1, 7, 14 and 38
|
Collaboratori e investigatori
Sponsor
Pubblicazioni e link utili
Collegamenti utili
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Malattie delle vie respiratorie
- Malattie polmonari
- Malattie polmonari, ostruttive
- Malattia polmonare, cronica ostruttiva
- Effetti fisiologici delle droghe
- Agenti neurotrasmettitori
- Meccanismi molecolari dell'azione farmacologica
- Parasimpaticolitici
- Agenti autonomi
- Agenti del sistema nervoso periferico
- Antagonisti colinergici
- Agenti colinergici
- Agenti broncodilatatori
- Agenti antiasmatici
- Agenti del sistema respiratorio
- Tiotropio bromuro
Altri numeri di identificazione dello studio
- 205.133
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .