Ignite Creation Date:
2025-12-25 @ 1:23 AM
Ignite Modification Date:
2026-03-06 @ 7:47 AM
Study NCT ID:
NCT03211793
Status:
RECRUITING
Last Update Posted:
2025-09-10
First Post:
2017-04-27
Is Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Mesenchymal Stromal Cells as Treatment for Digital Ulcers in Systemic Sclerosis
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D012595', 'term': 'Scleroderma, Systemic'}, {'id': 'C000721267', 'term': 'digital ulcers'}, {'id': 'D045743', 'term': 'Scleroderma, Diffuse'}, {'id': 'D014652', 'term': 'Vascular Diseases'}], 'ancestors': [{'id': 'D003240', 'term': 'Connective Tissue Diseases'}, {'id': 'D017437', 'term': 'Skin and Connective Tissue Diseases'}, {'id': 'D012871', 'term': 'Skin Diseases'}, {'id': 'D002318', 'term': 'Cardiovascular Diseases'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE1', 'PHASE2'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 20}}, 'statusModule': {'overallStatus': 'RECRUITING', 'startDateStruct': {'date': '2021-10-06', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-09', 'completionDateStruct': {'date': '2026-11-01', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2025-09-03', 'studyFirstSubmitDate': '2017-04-27', 'studyFirstSubmitQcDate': '2017-07-05', 'lastUpdatePostDateStruct': {'date': '2025-09-10', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2017-07-07', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2026-11-01', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Toxicity of the treatment', 'timeFrame': '12 weeks after MSC administration', 'description': 'Toxicity of the treatment is defined as 1. Local toxicity, including signs of local inflammation (swelling, warmth, impairment of function), worsening of ulcers or new ulcers or hematomas after MSC administration 2. Other adverse events, graded according to the Common Terminology Criteria for Adverse Events version 4.0, expressed as maximum grade toxicity per organ system.'}], 'secondaryOutcomes': [{'measure': 'Serious adverse events', 'timeFrame': '48 hours, 2, 4, 8, 12, 24 weeks and 52 weeks after MSC administration', 'description': 'Any treatment-related serious adverse events (SAE) defined as events leading to hospitalization, death, or persistent or significant disability. To establish the presence or absence of a causal relationship, the World Health Organisation guidelines for pharmacovigilance will be followed.'}, {'measure': 'Change in perceived pain based on the Numerical Rating Scale', 'timeFrame': '48 hours, 2, 4, 8, 12, 24 weeks and 52 weeks after MSC administration', 'description': 'Change in pain as assessed using the Numerical Rating Scale,'}, {'measure': 'Change in perceived pain based on the digital ulcer visual analogue scale (part of the S-HAQ)', 'timeFrame': '48 hours, 2, 4, 8, 12, 24 weeks and 52 weeks after MSC administration', 'description': 'Change in pain as assessed using the digital ulcer visual analogue scale (part of the S-HAQ).'}, {'measure': 'Change in perceived pain based on the pain VAS ( part of the S-HAQ)', 'timeFrame': '48 hours, 2, 4, 8, 12, 24 weeks and 52 weeks after MSC administration', 'description': 'Change in pain as assessed using the pain VAS (S-HAQ), use of analgesics.'}, {'measure': 'Change in perceived pain based on the use of analgesics.', 'timeFrame': '48 hours, 2, 4, 8, 12, 24 weeks and 52 weeks after MSC administration', 'description': 'Change in pain as assessed by analyzing the use of analgesics.'}, {'measure': 'Quality of life - SF-36', 'timeFrame': '12, 24 and 52 weeks after MSC administration', 'description': 'SF-36 questionnaire.'}, {'measure': 'Quality of life - Euroqol', 'timeFrame': '12, 24 and 52 weeks after MSC administration', 'description': 'EuroQol questionnaire'}, {'measure': 'Disability', 'timeFrame': '12, 24 and 52 weeks after MSC administration', 'description': 'Assessed with the HAQ-DI questionnaire.'}, {'measure': 'Hand function', 'timeFrame': '12, 24 and 52 weeks after MSC administration', 'description': 'Cochin Hand Function Score'}, {'measure': 'Number (and change in number) of digital ulcers', 'timeFrame': '48 hours, 2, 4, 8, 12, 24 weeks and 52 weeks after MSC administration'}, {'measure': 'Healing of digital ulcers', 'timeFrame': '48 hours, 2, 4, 8, 12, 24 weeks and 52 weeks after MSC administration', 'description': 'Healing of ulcers is defined as complete epithelialization, regardless of residual pain. This will be established using sequential pictures in addition to the clinical examination.'}, {'measure': 'Ulcer size', 'timeFrame': '48 hours, 2, 4, 8, 12, 24 weeks and 52 weeks after MSC administration', 'description': 'Using sequential pictures, ulcer area and circumference will be measured.'}, {'measure': 'Time to healing of digital ulcers', 'timeFrame': '48 hours, 2, 4, 8, 12, 24 weeks and 52 weeks after MSC administration'}, {'measure': 'Need to alter medication regime', 'timeFrame': '48 hours, 2, 4, 8, 12, 24 weeks and 52 weeks after MSC administration', 'description': "The need to alter the medication regime as determined by the patient's attending rheumatologist."}, {'measure': 'Modified Rodnan Skin Score', 'timeFrame': '12, 24 and 52 weeks after MSC administration'}, {'measure': "Severity of Raynaud's symptoms", 'timeFrame': '12 , 24 and 52 weeks after MSC administration', 'description': 'Raynaud Condition Score'}, {'measure': 'Changes in capillary morphology and architecture', 'timeFrame': '2, 12, 24 weeks and 52 weeks after MSC administration', 'description': 'as visualized with video-assisted nailfold capillaroscopy by a trained investigator. The images will be scored by a certified rheumatologist and a trained investigator.'}, {'measure': 'Changes in laboratory parameters', 'timeFrame': '48 hours, 2, 4, 8, 12 weeks after MSC administration', 'description': 'A range of haematological and chemical parameters will be measured for safety assessment. Additionally, serum, plasma and peripheral blood mononuclear cells will be collected and stored for analysis at a later time point. Samples will be analysed and used to assess markers for endothelial activation and injury, proangiogenic factors, inflammation and oxidative stress. The presence of HLA-antibodies will be determined as well.'}, {'measure': 'Changes in circulating cell populations', 'timeFrame': '48 hours, 2, 4, 8, 12 weeks after MSC administration', 'description': 'Circulating cell populations will be studied by immunofluorescence labelling and analysis using fluorescence assisted cell sorting (FACS Canto machine).'}]}, 'oversightModule': {'isUsExport': False, 'oversightHasDmc': True, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['systemic sclerosis', 'scleroderma', 'digital ulcer', 'vasculopathy', 'mesenchymal stromal cell', 'mesenchymal stem cell'], 'conditions': ['Systemic Sclerosis', 'Digital Ulcer']}, 'referencesModule': {'references': [{'pmid': '30127049', 'type': 'DERIVED', 'citation': 'van Rhijn-Brouwer FCC, Gremmels H, Fledderus JO, Schuurman AH, Bonte-Mineur F, Vonk MC, Voskuyl AE, de Vries-Bouwstra JK, Coert JH, Radstake TRDJ, van Laar JM, Verhaar MC; MANUS Study Group. A randomised placebo-controlled double-blind trial to assess the safety of intramuscular administration of allogeneic mesenchymal stromal cells for digital ulcers in systemic sclerosis: the MANUS Trial protocol. BMJ Open. 2018 Aug 20;8(8):e020479. doi: 10.1136/bmjopen-2017-020479.'}]}, 'descriptionModule': {'briefSummary': 'The MANUS Trial aims to examine the safety, feasibility and potential efficacy of intramuscularly injected allogeneic mesenchymal stromal cells as treatment for digital ulcers of systemic sclerosis.', 'detailedDescription': 'The MANUS Trial is a randomized double-blind, placebo-controlled clinical trial. Patients with systemic sclerosis (SSc) and digital ischemia with intractable ischemic digital ulcers refractory to conventional treatments are eligible to participate.\n\n20 participants will be randomised (1:1) to undergo intramuscular injection (8 sites) of allogeneic bone marrow derived mesenchymal stromal cells (BM-MSC) (45-50\\*10\\^6) or placebo in the most affected limb.\n\nMain study parameters/endpoints: The primary outcome is the toxicity of the treatment at 12 weeks after MSC administration, defined as\n\n1. Local toxicity, including signs of local inflammation (swelling, warmth, impairment of function), worsening of ulcers or new ulcers or hematomas after MSC administration\n2. Other adverse events, graded according to the Common Terminology Criteria for Adverse Events version 4.0, expressed as maximum grade toxicity per organ system.\n\nSecondary outcome measures are: number of serious adverse events, pain and disability parameters; healing, time to healing and reduction of new ischemic digital ulcers; modified Rodnan skin score; Scleroderma Health Assessment Questionnaire (S-HAQ) including visual analogue scales (VAS) for scleroderma-specific symptoms; Quality-of-life (SF-36, EuroQol (EQ-5D); Cochin hand function score. We will also evaluate changes in capillary morphology and architecture using capillaroscopy; biochemical parameters; markers for endothelial activation and injury, inflammation, oxidative stress, circulating cells including endothelial cells, hematopoietic and endothelial progenitor cells, cytokines and growth factors, immunological responses. Follow-up visits will be scheduled at 48 hours and 2, 4, 8, 12, 24 and 52 weeks post-treatment.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria:\n\n* Established diagnosis of SSc according to the 2013 ACR/EULAR criteria\n* At least one active digital ulcer (painful area, \\>2 mm in diameter with visible depth and loss of dermis) refractory to intravenous prostacyclins\n\n * 'Refractory to prostacyclins' is defined as\n * Worsening of ulcer(s) within 1 month after prostacyclins iv\n * No improvement of ulcer(s) after 2 months after prostacyclins iv, as judged by the referring physician\n * Recurrence of exactly the same ulcer(s) (same location) within 3 months after prostacyclins iv\n* Written informed consent\n\nExclusion Criteria:\n\n* Ulcer with underlying calcinosis (ruled out by X-ray prior to screening/inclusion)\n* History of neoplasm or malignancy in the past 10 years\n* Pregnancy or unwillingness to use adequate contraception during study\n* Serious known concomitant disease with life expectancy \\<1 year\n* Uncontrolled hypertension\n* Uncontrolled acute or chronic infection with systemic symptoms (e.g. fever)\n* Follow-up impossible"}, 'identificationModule': {'nctId': 'NCT03211793', 'acronym': 'MANUS', 'briefTitle': 'Mesenchymal Stromal Cells as Treatment for Digital Ulcers in Systemic Sclerosis', 'organization': {'class': 'OTHER', 'fullName': 'UMC Utrecht'}, 'officialTitle': 'Mesenchymal Stromal Cells for Angiogenesis and Neovascularisation in Digital Ulcers of Systemic Sclerosis: the MANUS Trial', 'orgStudyIdInfo': {'id': 'MANUS'}, 'secondaryIdInfos': [{'id': '2015-000168-32', 'type': 'EUDRACT_NUMBER'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'MSC injections', 'description': 'Intramuscular injection of mesenchymal stromal cells (50 million allogeneic MSCs in 0.9% NaCl and 10% human serum albumin).', 'interventionNames': ['Drug: Mesenchymal stromal cells']}, {'type': 'PLACEBO_COMPARATOR', 'label': 'Placebo injections', 'description': 'Intramuscular injection of placebo (NaCl 0.9% + 10% human serum albumin)', 'interventionNames': ['Other: Placebo']}], 'interventions': [{'name': 'Mesenchymal stromal cells', 'type': 'DRUG', 'description': '8 intramuscular injections at designated sites in the hand/forearm muscles of the most affected side. Blinded syringes will be used. Injections will be administered by an experienced clinician (plastic surgeon or hand surgeon).', 'armGroupLabels': ['MSC injections']}, {'name': 'Placebo', 'type': 'OTHER', 'description': '8 intramuscular injections at designated sites in the hand/forearm muscles of the most affected side. Blinded syringes will be used. Injections will be administered by an experienced clinician (plastic surgeon or hand surgeon).', 'armGroupLabels': ['Placebo injections']}]}, 'contactsLocationsModule': {'locations': [{'zip': '3584 CX', 'city': 'Utrecht', 'status': 'RECRUITING', 'country': 'Netherlands', 'contacts': [{'name': 'Marianne Verhaar, MD, PhD', 'role': 'PRINCIPAL_INVESTIGATOR'}, {'name': 'Jaap van Laar, MD, PhD', 'role': 'SUB_INVESTIGATOR'}, {'name': 'Femke van Rhijn, MD', 'role': 'SUB_INVESTIGATOR'}], 'facility': 'Universitair Medisch Centrum Utrecht', 'geoPoint': {'lat': 52.09083, 'lon': 5.12222}}], 'centralContacts': [{'name': 'Femke van Rhijn, MD', 'role': 'CONTACT', 'email': 'f.c.c.brouwer-3@umcutrecht.nl', 'phone': '0031887557329'}], 'overallOfficials': [{'name': 'Marianne Verhaar, MD, PhD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'UMC Utrecht'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'UNDECIDED'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'UMC Utrecht', 'class': 'OTHER'}, 'collaborators': [{'name': 'ZonMw: The Netherlands Organisation for Health Research and Development', 'class': 'OTHER'}], 'responsibleParty': {'type': 'PRINCIPAL_INVESTIGATOR', 'investigatorTitle': 'prof. dr.', 'investigatorFullName': 'prof dr. M. C. Verhaar', 'investigatorAffiliation': 'UMC Utrecht'}}}}