Ignite Creation Date:
2025-12-24 @ 3:33 PM
Ignite Modification Date:
2025-12-27 @ 6:49 AM
Study NCT ID:
NCT05623592
Status:
ACTIVE_NOT_RECRUITING
Last Update Posted:
2024-04-10
First Post:
2022-11-08
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Methotrexate as Remission Maintenance Therapy After Remission-Induction With Tocilizumab and Glucocorticoids in Giant Cell Arteritis
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D013700', 'term': 'Giant Cell Arteritis'}, {'id': 'D014657', 'term': 'Vasculitis'}, {'id': 'D012216', 'term': 'Rheumatic Diseases'}], 'ancestors': [{'id': 'D020293', 'term': 'Vasculitis, Central Nervous System'}, {'id': 'D020274', 'term': 'Autoimmune Diseases of the Nervous System'}, {'id': 'D009422', 'term': 'Nervous System Diseases'}, {'id': 'D002561', 'term': 'Cerebrovascular Disorders'}, {'id': 'D001927', 'term': 'Brain Diseases'}, {'id': 'D002493', 'term': 'Central Nervous System Diseases'}, {'id': 'D014652', 'term': 'Vascular Diseases'}, {'id': 'D002318', 'term': 'Cardiovascular Diseases'}, {'id': 'D001167', 'term': 'Arteritis'}, {'id': 'D017445', 'term': 'Skin Diseases, Vascular'}, {'id': 'D012871', 'term': 'Skin Diseases'}, {'id': 'D017437', 'term': 'Skin and Connective Tissue Diseases'}, {'id': 'D001327', 'term': 'Autoimmune Diseases'}, {'id': 'D007154', 'term': 'Immune System Diseases'}, {'id': 'D009140', 'term': 'Musculoskeletal Diseases'}, {'id': 'D003240', 'term': 'Connective Tissue Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D008727', 'term': 'Methotrexate'}, {'id': 'D012965', 'term': 'Sodium Chloride'}], 'ancestors': [{'id': 'D000630', 'term': 'Aminopterin'}, {'id': 'D011622', 'term': 'Pterins'}, {'id': 'D011621', 'term': 'Pteridines'}, {'id': 'D006574', 'term': 'Heterocyclic Compounds, 2-Ring'}, {'id': 'D000072471', 'term': 'Heterocyclic Compounds, Fused-Ring'}, {'id': 'D006571', 'term': 'Heterocyclic Compounds'}, {'id': 'D002712', 'term': 'Chlorides'}, {'id': 'D006851', 'term': 'Hydrochloric Acid'}, {'id': 'D017606', 'term': 'Chlorine Compounds'}, {'id': 'D007287', 'term': 'Inorganic Chemicals'}, {'id': 'D017670', 'term': 'Sodium Compounds'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE2'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 52}}, 'statusModule': {'overallStatus': 'ACTIVE_NOT_RECRUITING', 'startDateStruct': {'date': '2022-11-23', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2024-04', 'completionDateStruct': {'date': '2025-11', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2024-04-09', 'studyFirstSubmitDate': '2022-11-08', 'studyFirstSubmitQcDate': '2022-11-18', 'lastUpdatePostDateStruct': {'date': '2024-04-10', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2022-11-21', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2025-11', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Time to relapse during the 12 months treatment period', 'timeFrame': '12 months'}], 'secondaryOutcomes': [{'measure': 'Cumulative prednisone doses at months 6, 12 and 18', 'timeFrame': '18 months'}, {'measure': 'Number of relapses per patient during the 12 months treatment period', 'timeFrame': '12 months'}, {'measure': 'Time to first, second and third relapse after randomization', 'timeFrame': '18 months'}, {'measure': 'Percentage of patients with a relapse at month 6 and 18 after discontinuation of Tocilizumab', 'timeFrame': '18 months'}, {'measure': 'Health-related quality of life: Short Form-36', 'timeFrame': '18 months', 'description': 'The possible score ranges from 0 to 100 points, where 0 points represent the greatest possible health limitation, while 100 points represent no health limitation at all'}, {'measure': 'Self-reported fatigue : FACIT-Fatigue (Functional Assessment of Chronic Illness Therapy - Fatigue Scale)', 'timeFrame': '18 months', 'description': 'The possible score ranges from 0 to 52 points. The higher this value, the better the quality of life.'}, {'measure': 'Patient Global Assessment of disease activity (PGA)', 'timeFrame': '18 months', 'description': 'The possible score ranges from 0 to 100 points, where 0 points represent the lowest disease activity and 100 the highest.'}, {'measure': 'Patient Assessment of pain', 'timeFrame': '18 months', 'description': 'The possible score ranges from 0 to 100 points, where 0 points represent the least pain intensity and 100 the most pain intensity'}, {'measure': 'Investigator reported Evaluator Global Assessment of disease activity (EGA)', 'timeFrame': '18 months', 'description': 'The possible score ranges from 0 to 100 points, where 0 points represent the lowest disease activity and 100 the highest.'}, {'measure': 'Occurrence of symptoms and signs related to Giant cell arteritis', 'timeFrame': '18 months'}, {'measure': 'Number of vasculitic vessels and change of intima-media-values of temporal and axillary arteries', 'timeFrame': '18 months'}, {'measure': 'Prevalence of aortitis at baseline and month 12 and 18 in MRI', 'timeFrame': '18 months'}, {'measure': 'Proportion of subjects with increased Erythrocyte Sedimentation Rate (>20mm/h) and C-Reactive Protein levels (> 10mg/L)', 'timeFrame': '18 months'}, {'measure': 'Occurrence of adverse events and serious adverse events', 'timeFrame': '12 months'}]}, 'oversightModule': {'oversightHasDmc': True, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['Giant cell arteritis', 'Methotrexate', 'Tocilizumab', 'Glucocorticoids', 'Remission maintenance', 'Vasculitis', 'Rheumatic disease', 'Ultrasound'], 'conditions': ['Giant Cell Arteritis']}, 'referencesModule': {'references': [{'pmid': '38225579', 'type': 'DERIVED', 'citation': 'Kreis L, Dejaco C, Schmidt WA, Nemeth R, Venhoff N, Schafer VS. The Meteoritics Trial: efficacy of methotrexate after remission-induction with tocilizumab and glucocorticoids in giant cell arteritis-study protocol for a randomized, double-blind, placebo-controlled, parallel-group phase II study. Trials. 2024 Jan 15;25(1):56. doi: 10.1186/s13063-024-07905-4.'}]}, 'descriptionModule': {'briefSummary': 'The standard treatment for Giant Cell arteritis (GCA) is Glucocorticoids(GC), even if GC-related adverse events are commonly occuring. Therefore, other practises for reducing relapses and cumulative GC-doses are needed. Currently, the Interleukin-6-inhibitor tocilizumab is used in combination with GC to achieve higher remission rates and lower cumulative GC-doses. The use of tocilizumab also has some disadvantages. One is the increased susceptibility to infections. On top of that, a long-term follow-up of the phase II study by Villiger et al. showed a 55% relapse-rate after discontinuation of intravenous tocilizumab after a median of five months.\n\nStudies have also shown that methotrexate(MTX) in combination with GC was able to prevent relapses and reduce cumulative GC doses.\n\nThe aim of the study is to evaluate whether MTX is superior to placebo to prevent relapses in subjects with GCA after Remission-Induction Therapy with Glucocorticoids and Tocilizumab. Our hypothesis is that Methotrexate can maintain remission, once stable remission has been induced by GC and Tocilizumab and will prevent the occurrence of relapses.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Subjects male or female, aged ≥18 years\n* Written informed consent of the capable subject for voluntary participation in the study.\n* Diagnosis of GCA as confirmed by the investigator fulfilment (also in retrospect) of the proposed extended 1990 classification criteria for GCA .\n* Previous treatment with glucocorticoids and tocilizumab for new or relapsing GCA\n* GCA patients who have been treated with tocilizumab and in whom discontinuation of tocilizumab therapy has been decided by the treating rheumatologist, within standard treatment at the department of rheumatology are eligible.\n* total tocilizumab therapy should have been at least 6 months before inclusion.\n* Patients should be in stable remission (defined as the absence of signs or symptoms of GCA and normal C-Reactive Protein (\\<1mg/dl), off glucocorticoids for at least 1 months at screening.\n* Willing and able to inject methotrexate or placebo subcutaneously at randomization\n* Male and female subjects agreeing to conduct efficient contraception (unless they have no childbearing potential)\n\nExclusion Criteria:\n\n* Severe renal (glomerular filtration rate \\<30/min) failure\n* Conditions other than GCA requiring continuous or intermittent treatment with oral or parenteral Glucocorticoids unless the last exposure to Glucocorticoids was \\>1 months before screening\n* Other inflammatory rheumatic diseases (e.g. rheumatoid arthritis)\n* Current treatment with any other conventional, biologic or targeted synthetic DMARD except tocilizumab\n* Elevation of transaminases above three times the norm\n* Simultaneous participation in another clinical trial, or participation in a clinical trial taking an investigational product, up to 30 days prior to participation in this clinical trial.\n* Pregnant or breast feeding women\n* Contraindications for therapy with Methotrexate, as indicated in the summary of product characteristics'}, 'identificationModule': {'nctId': 'NCT05623592', 'acronym': 'MTXinGCA', 'briefTitle': 'Methotrexate as Remission Maintenance Therapy After Remission-Induction With Tocilizumab and Glucocorticoids in Giant Cell Arteritis', 'organization': {'class': 'OTHER', 'fullName': 'University of Bonn'}, 'officialTitle': 'A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy of Methotrexate as Remission Maintenance Therapy After Remission-Induction Therapy With Tocilizumab and Glucocorticoids in Subjects With Giant Cell Arteritis', 'orgStudyIdInfo': {'id': 'MED3-201802'}, 'secondaryIdInfos': [{'id': 'EU-CT No: 2022-501058-12-00', 'type': 'OTHER', 'domain': 'EU Clinical Trials Register'}, {'id': 'DRKS-ID: DRKS00030571', 'type': 'OTHER', 'domain': 'German Clinical Trials Register'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Methotrexate', 'description': 'The patient will be treated for 12 months weekly with methotrexate. Methotrexate will be provided at a dose of 17.5mg as a pre-filled syringe for self-injection. A dose reduction to 15 mg/week in case of intolerance, elevated liver enzymes \\>3x upper limit of normal or to 10 mg/week if glomerular filtration rate \\<50/min will be possible. If glomerular filtration rate \\<30/min, termination of treatment.', 'interventionNames': ['Drug: Methotrexate']}, {'type': 'PLACEBO_COMPARATOR', 'label': 'Placebo', 'description': 'Patients receive sodium chloride as a placebo subcutaneously. It will be administered in the form of a pre-filled syringe for self-injection once a week for 12 months.', 'interventionNames': ['Drug: Sodium chloride']}], 'interventions': [{'name': 'Methotrexate', 'type': 'DRUG', 'description': '17,5/15/10 mg Methotrexate subcutaneously', 'armGroupLabels': ['Methotrexate']}, {'name': 'Sodium chloride', 'type': 'DRUG', 'description': 'Sodium chloride subcutaneously', 'armGroupLabels': ['Placebo']}]}, 'contactsLocationsModule': {'locations': [{'city': 'Bonn', 'country': 'Germany', 'facility': 'Medical Clinic and Polyclinic III Internal medicine Oncology, Hematology University Hospital Bonn, Rheumatology and Clinical Immunology', 'geoPoint': {'lat': 50.73438, 'lon': 7.09549}}], 'overallOfficials': [{'name': 'Valentin S. Schäfer, Dr. med.', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'University Hospital of Bonn'}]}, 'ipdSharingStatementModule': {'timeFrame': 'We plan to share data, if an adequate proposal is submitted', 'ipdSharing': 'YES'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'University of Bonn', 'class': 'OTHER'}, 'responsibleParty': {'type': 'PRINCIPAL_INVESTIGATOR', 'investigatorTitle': 'PD Dr. med. MuDr.', 'investigatorFullName': 'Valentin Schäfer', 'investigatorAffiliation': 'University Hospital, Bonn'}}}}