Ignite Creation Date:
2025-12-24 @ 5:22 PM
Ignite Modification Date:
2025-12-30 @ 3:55 PM
Study NCT ID:
NCT02579850
Status:
COMPLETED
Last Update Posted:
2021-10-29
First Post:
2015-05-12
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
2-arm Parallel Group Study of Fixed Combination of CHF 5993 vs Ultibro® in COPD Patients
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D029424', 'term': 'Pulmonary Disease, Chronic Obstructive'}], 'ancestors': [{'id': 'D008173', 'term': 'Lung Diseases, Obstructive'}, {'id': 'D008171', 'term': 'Lung Diseases'}, {'id': 'D012140', 'term': 'Respiratory Tract Diseases'}, {'id': 'D002908', 'term': 'Chronic Disease'}, {'id': 'D020969', 'term': 'Disease Attributes'}, {'id': 'D010335', 'term': 'Pathologic Processes'}, {'id': 'D013568', 'term': 'Pathological Conditions, Signs and Symptoms'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE3'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 1532}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2015-05-29', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2021-10', 'completionDateStruct': {'date': '2017-07-10', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2021-10-28', 'studyFirstSubmitDate': '2015-05-12', 'studyFirstSubmitQcDate': '2015-10-16', 'lastUpdatePostDateStruct': {'date': '2021-10-29', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2015-10-20', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2017-07-10', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Moderate and severe COPD exacerbation rate over 52 weeks of treatment', 'timeFrame': '1 year', 'description': 'Exacerbations will be evaluated at each study visit and collected using EXACT-PRO filled-in by patient every day throughout the study'}], 'secondaryOutcomes': [{'measure': 'Time to first moderate to severe COPD exacerbation', 'timeFrame': '1 year'}, {'measure': 'Rate of severe COPD exacerbation over 52 weeks of treatment', 'timeFrame': '1 year'}, {'measure': 'Rate of moderate COPD exacerbation over 52 weeks of treatment', 'timeFrame': '1 year'}, {'measure': 'Change from Baseline at each visit and over the entire treatment period in pre-dose morning FEV1', 'timeFrame': '1 year'}]}, 'oversightModule': {'oversightHasDmc': False}, 'conditionsModule': {'keywords': ['COPD', 'COPD Exacerbation', 'EXACT-PRO'], 'conditions': ['Chronic Obstructive Pulmonary Disease (COPD)']}, 'referencesModule': {'references': [{'pmid': '30587953', 'type': 'BACKGROUND', 'citation': 'Vanfleteren L, Fabbri LM, Papi A, Petruzzelli S, Celli B. Triple therapy (ICS/LABA/LAMA) in COPD: time for a reappraisal. Int J Chron Obstruct Pulmon Dis. 2018 Dec 12;13:3971-3981. doi: 10.2147/COPD.S185975. eCollection 2018.'}, {'pmid': '30880943', 'type': 'BACKGROUND', 'citation': 'Singh D, Fabbri LM, Vezzoli S, Petruzzelli S, Papi A. Extrafine triple therapy delays COPD clinically important deterioration vs ICS/LABA, LAMA, or LABA/LAMA. Int J Chron Obstruct Pulmon Dis. 2019 Feb 28;14:531-546. doi: 10.2147/COPD.S196383. eCollection 2019.'}, {'pmid': '30792343', 'type': 'BACKGROUND', 'citation': 'Singh D, Fabbri LM, Corradi M, Georges G, Guasconi A, Vezzoli S, Petruzzelli S, Papi A. Extrafine triple therapy in patients with symptomatic COPD and history of one moderate exacerbation. Eur Respir J. 2019 May 18;53(5):1900235. doi: 10.1183/13993003.00235-2019. Print 2019 May.'}, {'pmid': '31000665', 'type': 'BACKGROUND', 'citation': 'Papi A, Petruzzelli S, Vezzoli S, Georges G, Fabbri LM. Triple therapy for all patients with severe symptomatic COPD at risk of exacerbations. Eur Respir J. 2019 Apr 18;53(4):1900147. doi: 10.1183/13993003.00147-2019. Print 2019 Apr. No abstract available.'}, {'pmid': '29429593', 'type': 'RESULT', 'citation': 'Papi A, Vestbo J, Fabbri L, Corradi M, Prunier H, Cohuet G, Guasconi A, Montagna I, Vezzoli S, Petruzzelli S, Scuri M, Roche N, Singh D. Extrafine inhaled triple therapy versus dual bronchodilator therapy in chronic obstructive pulmonary disease (TRIBUTE): a double-blind, parallel group, randomised controlled trial. Lancet. 2018 Mar 17;391(10125):1076-1084. doi: 10.1016/S0140-6736(18)30206-X. Epub 2018 Feb 9.'}], 'seeAlsoLinks': [{'url': 'https://www.clinicaltrialsregister.eu/ctr-search/trial/2014-001704-22/results', 'label': 'Study Record on EU Clinical Trials Register including results'}, {'url': 'https://www.chiesi.com/clinic/33_CSR_Synopsis_CCD-05993AA1-08.pdf', 'label': 'CSR Synopsis available in the CHIESI Clinical Study Register'}]}, 'descriptionModule': {'briefSummary': 'The aim of the present study is to evaluate the superiority of the fixed triple therapy with BDP/FF/GB at a daily dose of 400/24/50 mcg respectively with that of Ultibro® Breezhaler® (DPI), fixed combination of indacaterol 85 mcg and of glycopyrronium 43 mcg in COPD patients.', 'detailedDescription': "Outpatients attending the hospital clinics/study centres will be recruited. Patients with severe and very severe COPD airflow obstruction according to GOLD 2014 criteria. A total of approximately 2192 patients will need to be screened in order to obtain 1534 (767 per arm) randomized and evaluable patients. Approximately 200 sites will be involved worldwide.\n\nEach patient will perform a total of 8 clinic visits (V0 to V7) during the study.\n\nThe Primary objective is to demonstrate the superiority of CHF 5993 pMDI over Ultibro® in terms of moderate and severe COPD exacerbation rate over 52 weeks of treatment.\n\nThe Secondary objectives are:\n\n1. To evaluate the effect of CHF 5993 pMDI on other lung function parameters, patient's health status and clinical outcome measures;\n2. To assess the safety and the tolerability of the study treatments.\n\nA 2-week open-label run-in period under Ultibro® followed by a 52-week randomised treatment period.\n\nThe trial design will be optimised to measure exacerbation rates by using the Exacerbations of Chronic Pulmonary Disease Tool (EXACT), developed means of collecting patient-reported outcome (PRO) data, which helps to capture the frequency of exacerbations."}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '40 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion :\n\n1. Male and female ≥ 40 years\n2. Severe or very severe COPD diagnosed for at least 12 months\n3. Current smokers or ex-smokers who quit smoking at least 6 months prior to screening visit, with a smoking history of at least 10 pack years\n4. Post-bronchodilator FEV1 \\< 50% of the predicted normal value and a post-bronchodilator FEV1/FVC ratio \\< 0.7\n5. Documented history of at least one exacerbation in the 12 months\n6. Patient under double therapy for at least 2 months prior to screening. Double therapy will be defined by treatment with any of the following:\n\n Orally inhaled corticosteroid (ICS) and (long-acting beta2-agonist) LABA ICS and long-acting muscarinic antagonist (LAMA) Orally LABA and LAMA Monotherapy with LAMA for at least 2 months prior to screening\n7. Symptomatic patient at screening with a CAT score ≥ 10.\n8. Cooperative attitude and ability to use correctly the inhalers, the spacer AeroChamber Plus (only to patients who are using a spacer), the electronic devices with COPD questionnaire.\n\nExclusion :\n\n1. Pregnant or lactating women and all women physiologically capable of becoming pregnant UNLESS are willing to use one or more of the reliable methods of contraception\n2. Patient with a current clinical diagnosis of asthma with a physician-judged need for inhaled or oral corticosteroid therapy\n3. Patient requiring use of the following medications:\n\n Course of systemic steroids \\> 3 days for COPD exacerbation in the 4 weeks prior to screening Course of antibiotics for COPD exacerbation \\> 7 days in the 4 weeks prior to screening Phosphodiesterase-4 inhibitor in the 4 weeks prior to screening Use of antibiotics for a lower respiratory tract infection in the 4 weeks prior to screening\n4. COPD exacerbation requiring prescription of systemic corticosteroids and/or antibiotics or hospitalization during the run-in period\n5. Patient treated with non-cardioselective β-blockers in the month preceding the screening or during the run-in period.\n6. Patient treated with long-acting antihistamines unless taken at stable regimen at least 2 months prior to screening and to be maintained constant during the study or if taken as needed\n7. Patient requiring long term (at least 12 hours daily) oxygen therapy for chronic hypoxemia\n8. Known respiratory disorders other than COPD which may impact the efficacy of the study drug\n9. Patient who have clinically significant cardiovascular condition\n10. Patient with atrial fibrillation (AF): Paroxysmal atrial fibrillation, Persistent, Long standing or Permanent\n11. Abnormal and clinically significant 12-lead ECG that results in active medical problem which may impact the safety of the patient\n12. Patient whose ECG shows QTcF \\>450 ms for males or QTcF \\>470 ms for females at screening visit are not eligible (not applicable for patient with pacemaker)\n13. Medical diagnosis of narrow-angle glaucoma, clinically relevant prostatic hypertrophy or bladder neck obstruction would prevent use of anticholinergic agents\n14. History of hypersensitivity to M3 Antagonists, β2-agonist, corticosteroids or any of the excipients contained in any of the formulations used in the trial which may raise contra-indications or impact the efficacy of the study drug\n15. Clinically significant laboratory abnormalities indicating a significant or unstable concomitant disease which may impact the efficacy or the safety of the study drug\n16. Patients with hypokalaemia (serum potassium \\<3.5 mEq/L or 3.5 mmol/L) or uncontrolled hyperkalaemia\n17. Unstable concurrent disease which may impact the results of the study\n18. Patients with any history of malignancy likely to result in significant disability or likely to require significant medical or surgical intervention within the next six months (after V1) or with malignancy for which they are currently undergoing radiation therapy or chemotherapy\n19. History of alcohol abuse or substance/drug abuse within 12 months prior to screening visit\n20. Participation in another clinical trial if investigational drug was received less than 8 weeks prior to screening visit'}, 'identificationModule': {'nctId': 'NCT02579850', 'acronym': 'TRIBUTE', 'briefTitle': '2-arm Parallel Group Study of Fixed Combination of CHF 5993 vs Ultibro® in COPD Patients', 'organization': {'class': 'INDUSTRY', 'fullName': 'Chiesi Farmaceutici S.p.A.'}, 'officialTitle': '52-week, Double Blind, Randomized, 2 Active Parallel Arms Study of Fixed Combination CHF 5993 Administered vs Ultibro® in COPD Patients', 'orgStudyIdInfo': {'id': 'CCD-05993AA1-08'}, 'secondaryIdInfos': [{'id': '2014-001704-22', 'type': 'EUDRACT_NUMBER'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'CHF 5993 + Ultibro matched placebo', 'description': "Fixed triple therapy with BDP/FF/GB 100/6/12.5 mcg (CHF 5993) administered 2 puffs twice daily via pMDI + Fixed combination of indacaterol and of glycopyrronium (Ultibro® Breezhaler®) matched placebo administered once daily via DPI for 52-week treatment.\n\nPatient used to take pMDI medication using a spacer will be provided with a new spacer for the study.\n\n7 study visits including : central spirometry tests, Local laboratory, COPD assessment test (visit 1 only), Local laboratory Assessments Saint George's Respiratory Questionnaire EXACT-pro questionnaire", 'interventionNames': ['Drug: CHF 5993 + Ultibro matched placebo', 'Procedure: Central spirometry', 'Other: COPD assessment test', 'Procedure: Local laboratory Assessments', "Other: Saint George's Respiratory Questionnaire", 'Other: EXACT-pro questionnaire']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'Ultibro + CHF 5993 matched placebo', 'description': "Fixed combination of indacaterol 85 mcg and of glycopyrronium 43 mcg (Ultibro® Breezhaler®) administered once daily via DPI + Fixed triple therapy with BDP/FF/GB (CHF 5993) matched placebo administered 2 puffs twice daily via pMDI for 52-week treatment.\n\nPatient used to take pMDI medication using a spacer will be provided with a new spacer for the study.\n\n7 study visits including : central spirometry tests, Local laboratory, COPD assessment test (visit 1 only), Local laboratory Assessments, Saint George's Respiratory Questionnaire, EXACT-pro questionnaire", 'interventionNames': ['Drug: Ultibro + CHF 5993 matched placebo', 'Procedure: Central spirometry', 'Other: COPD assessment test', 'Procedure: Local laboratory Assessments', "Other: Saint George's Respiratory Questionnaire", 'Other: EXACT-pro questionnaire']}], 'interventions': [{'name': 'CHF 5993 + Ultibro matched placebo', 'type': 'DRUG', 'otherNames': ['CHF 5993'], 'description': 'Active medication treatment CHF 5993 and Ultibro matched placebo administered twice a day', 'armGroupLabels': ['CHF 5993 + Ultibro matched placebo']}, {'name': 'Ultibro + CHF 5993 matched placebo', 'type': 'DRUG', 'otherNames': ['Ultibro Breezhaler'], 'description': 'Active medication treatment Ultibro and CHF 5993 matched placebo administered twice a day', 'armGroupLabels': ['Ultibro + CHF 5993 matched placebo']}, {'name': 'Central spirometry', 'type': 'PROCEDURE', 'description': 'Central spirometry to assess forced expiratory volume at one second and forced vital capacity', 'armGroupLabels': ['CHF 5993 + Ultibro matched placebo', 'Ultibro + CHF 5993 matched placebo']}, {'name': 'COPD assessment test', 'type': 'OTHER', 'description': 'COPD assessment test (CAT) at visit 1', 'armGroupLabels': ['CHF 5993 + Ultibro matched placebo', 'Ultibro + CHF 5993 matched placebo']}, {'name': 'Local laboratory Assessments', 'type': 'PROCEDURE', 'description': 'ECG + Standard Haematology and Biochemistry', 'armGroupLabels': ['CHF 5993 + Ultibro matched placebo', 'Ultibro + CHF 5993 matched placebo']}, {'name': "Saint George's Respiratory Questionnaire", 'type': 'OTHER', 'description': "Saint George's Respiratory Questionnaire", 'armGroupLabels': ['CHF 5993 + Ultibro matched placebo', 'Ultibro + CHF 5993 matched placebo']}, {'name': 'EXACT-pro questionnaire', 'type': 'OTHER', 'description': 'daily from randomization (Visit 2) to end of study (Visit 7)', 'armGroupLabels': ['CHF 5993 + Ultibro matched placebo', 'Ultibro + CHF 5993 matched placebo']}]}, 'contactsLocationsModule': {'locations': [{'zip': '43123', 'city': 'Parma', 'country': 'Italy', 'facility': 'Chiesi Farmaceutici S.p.A.', 'geoPoint': {'lat': 44.79935, 'lon': 10.32618}}], 'overallOfficials': [{'name': 'Mario Scuri, MD', 'role': 'STUDY_CHAIR', 'affiliation': 'Chiesi Farmaceutici S.p.A.'}, {'name': 'Nicolas Roche, Pr', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'Hopitaux Universitaires Paris Centre - Groupe Hospitalier Cochin'}]}, 'ipdSharingStatementModule': {'url': 'https://www.chiesi.com/en/chiesi-clinical-trial-data-request-portal/', 'ipdSharing': 'YES', 'description': 'Chiesi commits to sharing with qualified scientific and medical Researchers, conducting legitimate research, Patient-level Data, Study-level Data, the Clinical Protocol and the full CSR, providing access to clinical trial information consistently with the principle of safeguarding commercially confidential information and patient privacy. Any shared Patient-level Data is anonymized to protect personally identifiable information.\n\nChiesi access criteria and complete process for clinical data sharing is available on the Chiesi Group website.', 'accessCriteria': 'Chiesi access criteria and complete process for clinical data sharing is available on the Chiesi Group website.'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Chiesi Farmaceutici S.p.A.', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}