- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT02242253
Free Combinations of Tiotropium Inhalation Powder Capsule + Salmeterol Metered Dose Inhaler, Tiotropium Inhalation Powder Capsule and Salmeterol Metered Dose Inhaler in Patients With Chronic Obstructive Pulmonary Disease (COPD)
A Randomised, Double-blind, Double-dummy, Crossover Efficacy and Safety Comparison of 6-week Treatment Periods of the Free Combinations of Tiotropium Inhalation Powder Capsule (18 μg) QD + Salmeterol Metered Dose Inhaler (2 Puffs of 25 μg) QD or BID, Tiotropium Inhalation Powder Capsule (18 μg) QD and Salmeterol Metered Dose Inhaler (2 Puffs of 25 μg) BID in Patients With (COPD)
Main Study: To evaluate and to compare the lung function response to the free combinations of tiotropium 18 μg (QD) + salmeterol 50 μg (QD or BID), salmeterol 50 μg BID and tiotropium 18 μg QD at the end of 6-week treatment periods in patients with COPD.
Sub-Study: Was performed in subset of patients participating in the Main Study to assess the effect of the four randomised treatments on dynamic hyperinflation.
Extension Study: To establish whether the FEV1 time profile following combination bronchodilator therapy of tiotropium plus salmeterol is affected by the pharmaceutical formulation of salmeterol, i.e. the MDI or the Diskus®.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 2
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- All patients must sign an informed consent consistent with International Conference on Harmonization Good Clinical Practice (ICH-GCP) guidelines prior to participation in the trial, which includes medication washout and restrictions
All patients must have a diagnosis of chronic obstructive pulmonary disease and must meet the following spirometric criteria:
Patients must have relatively stable, moderate to severe airway obstruction with an FEV1 ≤ 60% of predicted normal and FEV1 ≤ 70% of FVC (Visits 1 and 2)
- Male or female patients 40 years of age or older
- Patients must be current or ex-smokers with a smoking history of more than 10 pack-years (Patients who had never smoked cigarettes have to be excluded)
- Patients must be able to perform technically acceptable pulmonary function tests and must be able to maintain records (Patient Daily Diary Card) during the study period as required in the protocol
- Patients must be able to inhale medication in a competent manner from the HandiHaler® device and from a metered dose inhaler (MDI)
Exclusion Criteria:
- Patients with significant diseases other than COPD will be excluded. A significant disease is defined as a disease which in the opinion of the investigator may either put the patient at risk because of participation in the study or a disease which may influence the results of the study or the patient's ability to participate in the study
- Patients with clinically relevant abnormal baseline haematology, blood chemistry, or urinalysis, if the abnormality defines a significant disease as defined in exclusion criterion No. 1
- Patients with a recent history (i.e. six months or less) of myocardial infarction
- Patients with any unstable or life-threatening cardiac arrhythmia or patients who have been hospitalised for such an event within the past year
- Patients with a malignancy for which the patient has undergone resection, Radiation therapy or chemotherapy within the last five years. Patients with treated basal cell carcinoma are allowed
- Patients with known narrow-angle glaucoma
- Patients with a history of asthma, allergic rhinitis or who have a total blood eosinophil count ≥600 mm3
- Patients with a history of life-threatening pulmonary obstruction, or a history of cystic fibrosis or clinically evident bronchiectasis
- Patients with known active tuberculosis
- Patients with a history of and/or active significant alcohol or drug abuse. See exclusion criterion No. 1
- Patients who have undergone thoracotomy with pulmonary resection. Patients with a history of thoracotomy for other reasons should be evaluated as per exclusion criterion No. 1
- Patients who have completed a pulmonary rehabilitation program in the six weeks prior to the Screening Visit (Visit 1)
- Patients who regularly use daytime oxygen therapy
- Patients who have taken an investigational drug within one month or six half lives (whichever is greater) prior to Screening Visit (Visit 1)
- Patients who are being treated with oral beta-adrenergics
- Patients who are being treated with cromolyn sodium or nedocromil sodium
- Patients who are being treated with antihistamines (H1 receptor antagonists), antileukotrienes or leukotriene receptor antagonists for asthma or excluded allergic conditions. See exclusion criterion No. 7
- Patients using oral corticosteroid medication at unstable doses (i.e., less than six weeks on a stable dose) or at doses in excess of the equivalent of 10 mg of prednisone per day or 20 mg every other day
- Patients with known hypersensitivity to anticholinergic drugs, beta-adrenergics, lactose or any other components of the medication delivery systems
- Pregnant or nursing women or women of childbearing potential not using a medically approved means of contraception for the previous 3 months (i.e. oral contraceptives, intrauterine devices, diaphragm or subdermal implants eg: Norplant®)
- Patients with previous participation (receipt of randomised treatment) in this study
- Patients who are currently participating in another study
- The randomisation of patients with any respiratory infection or COPD exacerbation in the six weeks prior to the Screening Visit (Visit 1) or during the baseline period should be postponed. Patients may be randomised six weeks following recovery from the infection or exacerbation
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione incrociata
- Mascheramento: Doppio
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Tiotropium+salmeterol QD
free combination of tiotropium and salmeterol
|
administered via HandiHaler®
administered via metered dose inhaler (MDI)
|
|
Comparatore attivo: Tiotropium+salmeterol BID
free combination of tiotropium and salmeterol
|
administered via HandiHaler®
administered via metered dose inhaler (MDI)
|
|
Comparatore attivo: Tiotropium QD
|
administered via HandiHaler®
|
|
Comparatore attivo: Salmeterol BID
|
administered via metered dose inhaler (MDI)
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
Area under the curve of forced expiratory volume in one second (FEV1 AUC0-24h)
Lasso di tempo: up to 12 hours after morning and evening dose
|
up to 12 hours after morning and evening dose
|
|
FEV1 AUC0-12h
Lasso di tempo: up to 12 hours after morning and evening dose
|
up to 12 hours after morning and evening dose
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Number of inhalations of rescue salbutamol therapy used per day
Lasso di tempo: weeks 4 to 6 of each treatment period
|
weeks 4 to 6 of each treatment period
|
|
|
FEV1 AUC12-24h
Lasso di tempo: after 6 weeks of each treatment
|
after 6 weeks of each treatment
|
|
|
AUC of forced vital capacity (FVC AUC0-12h)
Lasso di tempo: after 6 weeks of each treatment
|
after 6 weeks of each treatment
|
|
|
FVC AUC0-24h
Lasso di tempo: after 6 weeks of each treatment
|
after 6 weeks of each treatment
|
|
|
FVC AUC12-24h
Lasso di tempo: after 6 weeks of each treatment
|
after 6 weeks of each treatment
|
|
|
Peak FEV1
Lasso di tempo: after 6 weeks of each treatment
|
after 6 weeks of each treatment
|
|
|
Trough FEV1
Lasso di tempo: after 6 weeks of each treatment
|
Trough FEV1 was defined as the pre-dose FEV1 measured just prior to the last administration of the morning dose of randomised treatment.
|
after 6 weeks of each treatment
|
|
Peak FVC
Lasso di tempo: after 6 weeks of each treatment
|
after 6 weeks of each treatment
|
|
|
Trough FVC
Lasso di tempo: after 6 weeks of each treatment
|
Trough FVC was defined as the pre-dose FVC measured just prior to the last administration of the morning dose of randomised treatment
|
after 6 weeks of each treatment
|
|
Individual FEV measurements at each time point
Lasso di tempo: up to 6 weeks
|
up to 6 weeks
|
|
|
Individual FVC measurements at each time point
Lasso di tempo: up to 6 weeks
|
up to 6 weeks
|
|
|
Peak expiratory flow rate (PEFR) measured twice daily
Lasso di tempo: weeks 4 to 6 of each treatment period
|
weeks 4 to 6 of each treatment period
|
|
|
Change in focal score of the Mahler Transition Dyspnea Index (TDI)
Lasso di tempo: after 6 weeks of each treatment
|
The TDI focal score is the sum of the three components of the TDI: Functional Impairment, Magnitude of Task and Magnitude of Effort
|
after 6 weeks of each treatment
|
|
Number of patients with adverse events
Lasso di tempo: up to 33 weeks
|
up to 33 weeks
|
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
- Processi patologici
- Malattie delle vie respiratorie
- Disturbi respiratori
- Malattie polmonari, ostruttive
- Malattie polmonari
- Malattia polmonare, cronica ostruttiva
- Aspirazione respiratoria
- Effetti fisiologici delle droghe
- Agenti adrenergici
- Agenti neurotrasmettitori
- Meccanismi molecolari dell'azione farmacologica
- Parasimpaticolitici
- Agenti autonomi
- Agenti del sistema nervoso periferico
- Antagonisti colinergici
- Agenti colinergici
- Agonisti adrenergici
- Agenti broncodilatatori
- Agenti antiasmatici
- Agenti del sistema respiratorio
- Agonisti del recettore adrenergico beta-2
- Beta-agonisti adrenergici
- Salmeterolo Xinafoato
- Tiotropio bromuro
Altri numeri di identificazione dello studio
- 1184.7
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 .
Prove cliniche su Placebo HandiHaler®
-
Novartis PharmaceuticalsCompletatoMalattie polmonari croniche ostruttive (BPCO)Argentina
-
Boehringer IngelheimCompletato
-
GlaxoSmithKlineCompletatoMalattia polmonare, cronica ostruttivaRegno Unito, Olanda
-
Mylan Inc.Theravance BiopharmaCompletatoMalattia polmonare ostruttiva cronica, BPCO | Flusso inspiratorio di picco basso (PIFR)Stati Uniti
-
GlaxoSmithKlineCompletatoMalattia polmonare, cronica ostruttivaStati Uniti
-
Boehringer IngelheimTerminato
-
Boehringer IngelheimCompletatoMalattia polmonare, cronica ostruttivaCina
-
Pearl Therapeutics, Inc.CompletatoBroncopneumopatia cronica ostruttivaStati Uniti
-
Teva Branded Pharmaceutical Products R&D, Inc.Completato
-
GlaxoSmithKlineCompletatoMalattia polmonare, cronica ostruttivaStati Uniti