Ignite Creation Date:
2025-12-24 @ 3:45 PM
Ignite Modification Date:
2025-12-25 @ 7:39 PM
Study NCT ID:
NCT03565692
Status:
UNKNOWN
Last Update Posted:
2020-04-10
First Post:
2018-05-31
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Lum-Iva-biota: Exploring the Respiratory Mycobiota and Microbiota Profile in French CF Patients Taking Lumacaftor-Ivacaftor
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D003550', 'term': 'Cystic Fibrosis'}], 'ancestors': [{'id': 'D010182', 'term': 'Pancreatic Diseases'}, {'id': 'D004066', 'term': 'Digestive System Diseases'}, {'id': 'D008171', 'term': 'Lung Diseases'}, {'id': 'D012140', 'term': 'Respiratory Tract Diseases'}, {'id': 'D030342', 'term': 'Genetic Diseases, Inborn'}, {'id': 'D009358', 'term': 'Congenital, Hereditary, and Neonatal Diseases and Abnormalities'}, {'id': 'D007232', 'term': 'Infant, Newborn, Diseases'}]}}, 'protocolSection': {'designModule': {'bioSpec': {'retention': 'SAMPLES_WITHOUT_DNA', 'description': 'Human sputum and stool specimen'}, 'studyType': 'OBSERVATIONAL', 'designInfo': {'timePerspective': 'RETROSPECTIVE', 'observationalModel': 'COHORT'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 250}, 'patientRegistry': False}, 'statusModule': {'overallStatus': 'UNKNOWN', 'lastKnownStatus': 'RECRUITING', 'startDateStruct': {'date': '2018-07-01', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2020-04', 'completionDateStruct': {'date': '2023-02-28', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2020-04-09', 'studyFirstSubmitDate': '2018-05-31', 'studyFirstSubmitQcDate': '2018-06-11', 'lastUpdatePostDateStruct': {'date': '2020-04-10', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2018-06-21', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2023-02-28', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Change of specific bacterial and/or fungal pathogens', 'timeFrame': '18 months', 'description': 'Measure by conventional methods (history of microbial culture and GM assay) and particularly by metagenomic analysis of pulmonary pro- and eukaryotic microbiota.'}], 'secondaryOutcomes': [{'measure': 'Forced expiratory volume in 1 second (FEV1)', 'timeFrame': 'Day 1', 'description': 'Difference between the amount of air exhaled may be measured during the first second'}, {'measure': 'Forced expiratory volume (FEV1)', 'timeFrame': '6 Months', 'description': 'Difference between the amount of air exhaled may be measured during the first second'}, {'measure': 'Forced expiratory volume (FEV1)', 'timeFrame': '12 Months', 'description': 'Difference between the amount of air exhaled may be measured during the first second'}, {'measure': 'Change of specific bacterial and/or fungal pathogens', 'timeFrame': '12 months', 'description': 'Measure by conventional methods (history of microbial culture and GM assay) and particularly by metagenomic analysis of lung pro- and eukaryotic microbiota.'}, {'measure': 'Change of specific bacterial and/or fungal pathogens', 'timeFrame': '12 months', 'description': 'Measure by metagenomic analysis of gut pro- and eukaryotic microbiota.'}]}, 'oversightModule': {'oversightHasDmc': False, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['Microbiome', 'Microbiota', 'Mycobiota', 'Mycobiome', 'Deep-Sequencing', 'Cystic Fibrosis'], 'conditions': ['Cystic Fibrosis']}, 'referencesModule': {'references': [{'pmid': '36971560', 'type': 'DERIVED', 'citation': 'Enaud R, Lussac-Sorton F, Charpentier E, Velo-Suarez L, Guiraud J, Bui S, Fayon M, Schaeverbeke T, Nikolski M; LumIvaBiota Study Group; Burgel PR, Hery-Arnaud G, Delhaes L. Effects of Lumacaftor-Ivacaftor on Airway Microbiota-Mycobiota and Inflammation in Patients with Cystic Fibrosis Appear To Be Linked to Pseudomonas aeruginosa Chronic Colonization. Microbiol Spectr. 2023 Mar 27;11(2):e0225122. doi: 10.1128/spectrum.02251-22. Online ahead of print.'}]}, 'descriptionModule': {'briefSummary': 'n2015, VERTEX company - producing already KALYDECO (IVACAFTOR, VX-770) potentiator molecule that is recommended for the treatment of CF patients aged ≥ 6 y, with CFTR mutation altering the channel regulation (class III mutations) as G551D, G1244E, G1349D, G178R, G551S, S1251N, S1255P, S549Nou S549R) -was allowed by the Federal Drug Administration (FDA) and European Medicines Agency (EMEA) for producing and using ivacaftor combination (such as lumacaftor/ ivacaftor initially, and more recently tezacaftor/ivacaftor, tezacaftor/ivacaftor/VX-659, tezacaftor/ivacaftor/VX-445 and tezacaftor/ivacaftor/VX-152) in clinical trials for patient with cystic fibrosis, according to age and mutation eligibility criteria.\n\nSince 2016, the French patients homozygous for the p.Phe508del mutation and older than 12 years are able to be treated with the association LUMACAFTOR-IVACAFTOR and this French authorization is being extended for 6-11 years old children (while the European Commission has already granted an extension of the Marketing Authorization for lumacaftor/ivacaftor to include 6-11 years old children with cystic fibrosis since January 2018). Patients treated by lumacaftor/ivacaftor (or other ivacaftor new combinations) are closely monitored according to criteria established by the working group "New Therapeutic Approaches" of the French Society Cystic fibrosis.\n\nThis study is a phase IV observational trial for a period of 1 year. In this context, the team aims at initiating a comprehensive monitoring of the lung and gut mycobiota and microbiota evolution under LUMACAFTOR-IVACAFTOR (or other ivacaftor combinations) treatment. This project is directly linked to the monitoring of cystic fibrosis patients who begin treatment with LUMACAFTOR-IVACAFTOR (or other ivacaftor combinations) in France. The pro- and eukaryotic microbiota analysis is based on the secondary use of sputum and stool samples associated with several clinical data of CF patients under ivacaftor combinations and follow-up during the 1st year of therapy. According to the French law, Lum-Iva-Biota project is a non-interventional study. It aims at demonstrating that changes in the hydration of secretions at the pulmonary and intestinal levels related to LUMACAFTOR-IVACAFTOR therapy (or other new generation of ivacaftor combinations) promote a change in the lung and gut mycobiota and microbiota profiles which may achieve the characteristics of the "healthy type" (in terms of composition, richness and diversity).', 'detailedDescription': 'Cystic Fibrosis (CF) is related to structural and/or functional defects of chloride channel CFTR (Cystic Fibrosis Transport Regulator). These anomalies are associated with different classes of genetic mutations (class I to VI). The most common mutation is p.Phe508del class II (40% of homozygous and 70% heterozygous patients), it is responsible for the phenylalanine deletion at position 508 with improper intracellular processing of CFTR with less than normal amounts of CFTR protein at the apical cell membrane.\n\nOver the last 20 years the CF patient outcome has been mainly improved using symptomatic treatments. More recently, new therapeutic strategies targeting directly CFTR defects have been developed. Initially potentiators which correct functional defects of CFTR (class Mutations 3 and 4) were studied. Then, correctors that target CFTR production were also developed. These molecules demonstrated substantial effect.\n\nIn 2015, the American company VERTEX - producing already KALYDECO (IVACAFTOR, VX-770) potentiator molecule that is recommended for the treatment of CF patients aged ≥ 6 y, with mutation altering the channel regulation (class III mutations) as G551D, G1244E, G1349D, G178R, G551S, S1251N, S1255P, S549Nou S549R) - was allowed by the Federal Drug Administration (FDA) and European Medicines Agency (EMA) for producing and using LUMACAFTOR-IVACAFTOR in clinical trials to manage CF patients over 12 years and having two p.Phe508del mutations. ORKAMBI represents the combination of two molecules (LUMACAFTOR + IVACAFTOR) respectively correctors and potentiator of CFTR.\n\nThis EMA authorization follows the results of two international studies (TRAFFIC and TRANSPORT) based on more than 1,000 CF patients showing that patients under LUMACAFTOR-IVACAFTOR compared to the group taking placebo have:\n\n1. A moderate improvement in lung function (FEV1) at 24 weeks of 4.3 to 6.7%,\n2. A significant reduction in lung exacerbations (bronchitis) up - 39%,\n3. An increase in body mass index (BMI). These results confirm that LUMACAFTOR-IVACAFTOR may represent the first medicine to treat the whole underlying cause of CF in people ages 12 and older who have two copies of the p.Phe508del mutation. They complete the decrease or disappearance of pulmonary colonization with Pseudomonas aeruginosa (including mucoid phenotype isolates) observed under IVACAFTOR alone (KALYDECO treatment), even if the impact on fungal flora (or mycobiota) has not been described up to date.\n\nIn 2016, the French patients homozygous for the p.Phe508del mutation and older than 12 years were treated with this molecule association. Since January 2018, the European Commission has granted an extension of the Marketing Authorization for lumacaftor/ivacaftor to include 6 to 11 years old children with cystic fibrosis, and this authorization\'s extension is in process in France.\n\nSince 2018 in France, VERTEX company has been allowed for producing and using new generations of ivacaftor combinations (tezacaftor/ivacaftor, tezacaftor/ivacaftor/VX-659, tezacaftor/ivacaftor/VX-445 and tezacaftor/ivacaftor/VX-152) in clinical trials for patient with cystic fibrosis, according to age (from 6 years old) and mutation eligibility criteria.\n\nPatients treated by lumacaftor/ivacaftor or other ivacaftor combinations are closely monitored according to criteria established by the working group "New Therapeutic Approaches" of the French Society Cystic fibrosis. This study was a phase IV observational trial for a period of 1 year. In this context, the team aims at initiating a comprehensive monitoring of the lung and gut mycobiota and microbiota evolution under ivacaftor combinations (lumacaftor/ivacaftor or other ivacaftor combination).\n\nThis project is directly linked to the monitoring of homozygous p.Phe508del patients who begin treatment with ivacaftor combination in France (in agreement with the working group "New Therapeutic Approaches" of the French Society Cystic Fibrosis for lumacaftor/ivacaftor therapy, and the working group "Fungal Risks in CF").\n\nAs LUMACAFTOR-IVACAFTOR (or other ivacaftor combinations) impacts chloride secretion through CFTR at the apical site epithelial cells, with an expected improvement in secretion hydration and mucociliary clearance, it should modify the whole pulmonary microbial flora, including fungal microbiota (mycobiota) of CF lungs; this newly modified flora being expected achieving the characteristics of the "healthy type" in terms of flora composition, richness and diversity. We can expect same processes at the gut levels.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['CHILD', 'ADULT', 'OLDER_ADULT'], 'minimumAge': '2 Years', 'samplingMethod': 'NON_PROBABILITY_SAMPLE', 'studyPopulation': 'French patients with cystic fibrosis who start a treatment with an ivacaftor combination (lumacaftor/ivacaftor or new other combination) according to the age and mutations criteria in effect in France and monitored according to criteria established by the working group "New Therapeutic Approaches" of the French Society Cystic fibrosis.', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* CF Patient\'s ability to expectorate at inclusion time\n* CF patient treated with an ivacaftor combination (lumacaftor/ivacaftor or new generation combination) for a period of at least 1 year and managed by the National working group "New therapeutic approaches" under the National CF Observatory and who haven\'t expressed a non-opposition to the secondary use of their sputum and stool samples in the context on Lum-Iva-biota project.\n\nExclusion Criteria:\n\n* CF patient who stop ivacaftor combination treatment.\n* CF patient who doesn\'t want to participate anymore to Lum-Iva-Biota'}, 'identificationModule': {'nctId': 'NCT03565692', 'acronym': 'Lum-Iva-Biota', 'briefTitle': 'Lum-Iva-biota: Exploring the Respiratory Mycobiota and Microbiota Profile in French CF Patients Taking Lumacaftor-Ivacaftor', 'organization': {'class': 'OTHER', 'fullName': 'University Hospital, Bordeaux'}, 'officialTitle': 'Lum-Iva-biota: Exploring the Respiratory Mycobiota and Microbiota Profile in French CF Patients Taking Lumacaftor-Ivacaftor', 'orgStudyIdInfo': {'id': 'CHUBX 2016/22'}}, 'armsInterventionsModule': {'armGroups': [{'label': 'Patients treated by LUMACAFTOR-IVACAFTOR', 'description': 'Patients treated by LUMACAFTOR-IVACAFTOR (or other ivacaftor combinations) Patients over 6 years who are currently able to benefit from LUMACAFTOR-IVACAFTOR (or other ivacaftor combinations) according the mutation eligibility criteria and for whom conventional microbiological analysis of sputum samples and stool will be collected during their follow-up after the treatment onset.', 'interventionNames': ['Biological: the lung mycobiota and microbiota profile', 'Biological: the gut mycobiota and microbiota profile']}], 'interventions': [{'name': 'the lung mycobiota and microbiota profile', 'type': 'BIOLOGICAL', 'description': 'All sputum samples will follow regarding mycological and metagenomic analyses as summarized :\n\n* Pre-analytical treatment combining pre-treatment with mucolytic agent and sonication action\n* Separation of the pellet and supernatant, stored at -20 ° C until testing\n* Galactomannan (GM) Assay on each sputum supernatant to correlate with Aspergillus colonization history\n* Targeted metagenomics of bacterial communities (based on 16S amplification) and of fungal community (based on ITS2 amplification)\n* Bioinformatic analysis of metagenomics raw data, correlation with bioclinical data of each patient, statistical analysis, and characterization of phenomena of co-evolution/co-exclusion according to evolutionary ecology concepts.\n* Pseudomonas aeruginosa load measured by qPCR', 'armGroupLabels': ['Patients treated by LUMACAFTOR-IVACAFTOR']}, {'name': 'the gut mycobiota and microbiota profile', 'type': 'BIOLOGICAL', 'description': 'All stool samples will follow regarding mycological and metagenomic analyses as summarized : - Separation of the pellet and supernatant, stored at -20 ° C until testing - Targeted metagenomics of bacterial communities (based on 16S amplification) and of fungal community (based on ITS2 amplification) - Bioinformatic analysis of metagenomics raw data, correlation with bioclinical data of each patient, statistical analysis, and characterization of phenomena of co-evolution/co-exclusion according to evolutionary ecology concepts. - Measurement of inflammation.', 'armGroupLabels': ['Patients treated by LUMACAFTOR-IVACAFTOR']}]}, 'contactsLocationsModule': {'locations': [{'zip': '33000', 'city': 'Bordeaux', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Mickael FAYON, MD,PhD', 'role': 'CONTACT', 'email': 'mickael.fayon@chu-bordeaux.fr'}, {'name': 'Mickael FAYON, MD,PhD', 'role': 'PRINCIPAL_INVESTIGATOR'}, {'name': 'Patrick BERGER, MD,PhD', 'role': 'SUB_INVESTIGATOR'}, {'name': 'Raphael ENAUD, MD', 'role': 'SUB_INVESTIGATOR'}], 'facility': 'CHU de Bordeaux - CRCM', 'geoPoint': {'lat': 44.84124, 'lon': -0.58046}}, {'zip': '38000', 'city': 'Grenoble', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Catherine Llerena, MD', 'role': 'CONTACT', 'email': 'CLlerena@chu-grenoble.fr'}, {'name': 'Catherine Llerena, MD', 'role': 'PRINCIPAL_INVESTIGATOR'}, {'name': 'Boubou Camara, MD', 'role': 'SUB_INVESTIGATOR'}], 'facility': 'Centre Hospitalier Universitaire Grenoble Alpes', 'geoPoint': {'lat': 45.17869, 'lon': 5.71479}}, {'zip': '69000', 'city': 'Lille', 'status': 'NOT_YET_RECRUITING', 'country': 'France', 'contacts': [{'name': 'Nathalie Wizla, MD', 'role': 'CONTACT', 'email': 'nathalie.wizla@chru-lille.fr'}, {'name': 'Nathalie Wizla, MD', 'role': 'PRINCIPAL_INVESTIGATOR'}, {'name': 'Anne Prévotat, MD', 'role': 'SUB_INVESTIGATOR'}], 'facility': 'CHRU de Lille', 'geoPoint': {'lat': 50.63391, 'lon': 3.05512}}, {'zip': '69000', 'city': 'Lyon', 'status': 'NOT_YET_RECRUITING', 'country': 'France', 'contacts': [{'name': 'Philippe Reix, MD', 'role': 'CONTACT', 'email': 'philippe.reix@chu-lyon.fr'}, {'name': 'Philippe Reix, MD', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'Hospices Civils de Lyon', 'geoPoint': {'lat': 45.74906, 'lon': 4.84789}}, {'zip': '13000', 'city': 'Marseille', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Jean Christophe Dubus, MD,PhD', 'role': 'CONTACT', 'email': 'JeanChristophe.DUBUS@ap-hm.fr'}, {'name': 'Jean Christophe Dubus, MD,PhD', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'Assistance publique Hôpitaux Marseille', 'geoPoint': {'lat': 43.29695, 'lon': 5.38107}}, {'zip': '75000', 'city': 'Paris', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Harriet Corvol, MD,PhD', 'role': 'CONTACT', 'email': 'harriet.corvol@aphp.fr'}, {'name': 'Harriet Corvol, MD,PhD', 'role': 'PRINCIPAL_INVESTIGATOR'}, {'name': 'Pierre-Regis BURGEL, MD', 'role': 'SUB_INVESTIGATOR'}, {'name': 'Isabelle Sermet-Gaudelus, MD,PhD', 'role': 'SUB_INVESTIGATOR'}, {'name': 'Michèle Gérardin Gérardin, MD', 'role': 'SUB_INVESTIGATOR'}], 'facility': 'Assistance Publique Hôpitaux de paris', 'geoPoint': {'lat': 48.85341, 'lon': 2.3488}}, {'zip': '92150', 'city': 'Suresnes', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Dominique Grenet, MD', 'role': 'CONTACT', 'email': 'd.grenet@hopital-foch.org'}, {'name': 'Dominique Grenet, MD', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'Hôpital FOCH', 'geoPoint': {'lat': 48.87143, 'lon': 2.22929}}, {'zip': '31000', 'city': 'Toulouse', 'status': 'RECRUITING', 'country': 'France', 'contacts': [{'name': 'Marlène Murris-Espin, MD', 'role': 'CONTACT', 'email': 'murris.m@chu-toulouse.fr'}, {'name': 'Murris-Espin', 'role': 'CONTACT'}, {'name': 'Marlène Murris-Espin, MD', 'role': 'PRINCIPAL_INVESTIGATOR'}], 'facility': 'CHU de Toulouse', 'geoPoint': {'lat': 43.60426, 'lon': 1.44367}}], 'centralContacts': [{'name': 'Laurence DELHAES, MD, PhD', 'role': 'CONTACT', 'email': 'laurence.delhaes@chu-bordeaux.fr', 'phone': '+335 56 79 56 67'}], 'overallOfficials': [{'name': 'Laurence DELHAES, MD,PhD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'University Hospital, Bordeaux'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'University Hospital, Bordeaux', 'class': 'OTHER'}, 'collaborators': [{'name': 'Societe Francaise de la Mucoviscidose', 'class': 'OTHER'}], 'responsibleParty': {'type': 'SPONSOR'}}}}