Ignite Creation Date:
2025-12-25 @ 2:15 AM
Ignite Modification Date:
2025-12-31 @ 11:48 AM
Study NCT ID:
NCT01063660
Status:
COMPLETED
Last Update Posted:
2010-02-05
First Post:
2010-02-03
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Treosulfan Based Conditioning Acute Myeloid Leukaemia (AML)
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D015470', 'term': 'Leukemia, Myeloid, Acute'}], 'ancestors': [{'id': 'D007951', 'term': 'Leukemia, Myeloid'}, {'id': 'D007938', 'term': 'Leukemia'}, {'id': 'D009370', 'term': 'Neoplasms by Histologic Type'}, {'id': 'D009369', 'term': 'Neoplasms'}, {'id': 'D006402', 'term': 'Hematologic Diseases'}, {'id': 'D006425', 'term': 'Hemic and Lymphatic Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'C018404', 'term': 'treosulfan'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE2'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NA', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'SUPPORTIVE_CARE', 'interventionModel': 'SINGLE_GROUP'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 75}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2004-03'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2010-02', 'completionDateStruct': {'date': '2007-07', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2010-02-04', 'studyFirstSubmitDate': '2010-02-03', 'studyFirstSubmitQcDate': '2010-02-04', 'lastUpdatePostDateStruct': {'date': '2010-02-05', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2010-02-05', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Efficacy - Evaluation of engraftment. Safety - Evaluation of the incidence of the following CTC grade 3 and 4 adverse events between day -6 and day +28 - hyperbilirubinemia and mucositis / stomatitis - veno-occlusive disease - seizures', 'timeFrame': '3.5 years'}], 'secondaryOutcomes': [{'measure': 'Efficacy - Evaluation of disease free survival (DFS) - Evaluation of overall survival (OS) - Evaluation of relapse incidence (RI) - Donor chimerism on day +28, +56 and +100. Safety - Evaluation of NRM on days +28 and +100', 'timeFrame': '3.5 years'}]}, 'oversightModule': {'oversightHasDmc': False}, 'conditionsModule': {'keywords': ['Treosulfan', 'Fludarabine', 'ATG', 'AML'], 'conditions': ['Acute Myeloid Leukaemia']}, 'referencesModule': {'references': [{'pmid': '22158386', 'type': 'DERIVED', 'citation': 'Casper J, Holowiecki J, Trenschel R, Wandt H, Schaefer-Eckart K, Ruutu T, Volin L, Einsele H, Stuhler G, Uharek L, Blau I, Bornhaeuser M, Zander AR, Larsson K, Markiewicz M, Giebel S, Kruzel T, Mylius HA, Baumgart J, Pichlmeier U, Freund M, Beelen DW. Allogeneic hematopoietic SCT in patients with AML following treosulfan/fludarabine conditioning. Bone Marrow Transplant. 2012 Sep;47(9):1171-7. doi: 10.1038/bmt.2011.242. Epub 2011 Dec 12.'}]}, 'descriptionModule': {'briefSummary': 'This is a multicenter, multinational, non-randomized, non-controlled open-label phase II trial to evaluate the safety and efficacy of treosulfan in a combination regimen with fludarabine as conditioning therapy prior to allogeneic stem cell transplantation (SCT) in patients with AML.\n\nThe aim is to demonstrate a clinical benefit compared with historical data on intravenous busulfan (BusulfexTM, BusilvexTM), the only drug so far registered in the indication conditioning before allogeneic stem cell transplantation.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT'], 'maximumAge': '60 Years', 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Patients with acute myeloid leukaemia (AML) according to WHO classification (\\> 20% myeloblasts in peripheral blood or bone marrow at initial diagnosis) with \\< 5% myeloblast in the bone marrow, indicated for allogeneic transplantation\n* Availability of an HLA-identical sibling donor (MRD) or HLA-identical unrelated donor (MUD) HLA-identity defined by the following markers: A, B, DRB1, DQB1.\n* Target graft size (unmanipulated)\n* bone marrow: 2 - 10 x 106 CD34+ cells/kg BW recipient or \\> 2 x 108 nucleated cells/kg BW recipient or\n* peripheral blood: 4 - 10 x 106 CD34+ cells/kg BW recipient\n* Age \\> 18 and \\< 60 years\n* Karnofsky Index \\> 80 %\n* Adequate contraception in female patients of child-bearing potential\n* Written informed consent\n\nExclusion Criteria:\n\n* Therapy related secondary AML\n* AML with t(8;21)(q22;q22) in CR1\n* Acute promyelocytic leukaemia with t(15;17)(q22;q12) in CR1\n* Secondary malignancies\n* Previous allogeneic transplantation\n* Severe concomitant illnesses / medical conditions (e.g. impaired respiratory and/or cardiac function)\n* Known and manifested malignant involvement of the CNS\n* Active infectious disease\n* HIV- positivity or active hepatitis infection\n* Impaired liver function (Bilirubin \\> upper normal limit; Transaminases \\> 3.0 x upper normal limit)\n* Impaired renal function (Creatinine-clearance \\< 60 ml/min; Serum Creatinine \\> 1.5 x upper normal limit).\n* Pleural effusion or ascites \\> 1.0 L\n* Pregnancy or lactation\n* Known hypersensitivity to treosulfan and/or fludarabine\n* Participation in another experimental drug trial within 4 weeks before day -6\n* Non-co-operative behaviour or non-compliance\n* Psychiatric diseases or conditions that might impair the ability to give informed consent'}, 'identificationModule': {'nctId': 'NCT01063660', 'briefTitle': 'Treosulfan Based Conditioning Acute Myeloid Leukaemia (AML)', 'organization': {'class': 'INDUSTRY', 'fullName': 'medac GmbH'}, 'officialTitle': 'Clinical Phase II Trial to Evaluate the Safety and Efficacy of Treosulfan Based Conditioning Prior to Allogeneic Haematopoietic Stem Cell Transplantation in Patients With Acute Myeloid Leukaemia', 'orgStudyIdInfo': {'id': 'MC-FludT.7/AML'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Treosulfan', 'description': 'Patients with acute myeloid leukaemia (AML) according to WHO classification (\\> 20% myeloblasts in peripheral blood or bone marrow at initial diagnosis) with \\< 5% myeloblasts in the bone marrow, indicated for allogeneic transplantation', 'interventionNames': ['Drug: Treosulfan']}], 'interventions': [{'name': 'Treosulfan', 'type': 'DRUG', 'otherNames': ['Ovastat'], 'description': '14 g/m²/d day -6 to -4', 'armGroupLabels': ['Treosulfan']}]}, 'contactsLocationsModule': {'locations': [{'zip': '18057', 'city': 'Rostock', 'country': 'Germany', 'facility': 'University of Rostock', 'geoPoint': {'lat': 54.0887, 'lon': 12.14049}}], 'overallOfficials': [{'name': 'Mathias Freund, MD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'University of Rostock'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'medac GmbH', 'class': 'INDUSTRY'}, 'responsibleParty': {'oldNameTitle': 'Prof. Dr. Mathias Freund', 'oldOrganization': 'University of Rostock'}}}}