Ignite Creation Date:
2025-12-25 @ 2:51 AM
Ignite Modification Date:
2026-03-02 @ 4:01 PM
Study NCT ID:
NCT01391533
Status:
COMPLETED
Last Update Posted:
2016-04-13
First Post:
2011-07-06
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Study of SAR125844 Single Agent Administered as Slow Intravenous Infusion in Adult Patients With Advanced Malignant Solid Tumors
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'interventionBrowseModule': {'meshes': [{'id': 'C000602444', 'term': 'SAR125844'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE1'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NON_RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'interventionModel': 'SINGLE_GROUP'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 72}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2011-07'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2016-04', 'completionDateStruct': {'date': '2016-04', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2016-04-12', 'studyFirstSubmitDate': '2011-07-06', 'studyFirstSubmitQcDate': '2011-07-08', 'lastUpdatePostDateStruct': {'date': '2016-04-13', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2011-07-12', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2016-04', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Dose Escalation To determine the maximum tolerated dose (MTD) of SAR125844', 'timeFrame': 'At day 28 of Cycle 1 of each treated patient, DLT is assessed'}, {'measure': 'Expansion Cohorts To evaluate the preliminary anti-tumoral effect of SAR125844', 'timeFrame': 'Anticancer activity is assessed at Day 28 and then every 8 weeks thereafter up to an expected maximum of 2 years'}], 'secondaryOutcomes': [{'measure': 'Number of patients with treatment emergent events', 'timeFrame': 'Up to 2 years'}, {'measure': 'Assessment of PK parameter Cmax', 'timeFrame': 'Up to 2 years'}, {'measure': 'Assessment of PK parameter AUCs', 'timeFrame': 'Up to 2 years'}, {'measure': 'Assessment of PK parameter CL', 'timeFrame': 'Up to 2 years'}, {'measure': 'Assessment of PD parameter ShedMET', 'timeFrame': 'Up to 2 years'}, {'measure': 'Assessment of PD parameter HGF', 'timeFrame': 'Up to 2 years'}]}, 'conditionsModule': {'conditions': ['Malignant Solid Tumors']}, 'referencesModule': {'references': [{'pmid': '29145039', 'type': 'DERIVED', 'citation': 'Angevin E, Spitaleri G, Rodon J, Dotti K, Isambert N, Salvagni S, Moreno V, Assadourian S, Gomez C, Harnois M, Hollebecque A, Azaro A, Hervieu A, Rihawi K, De Marinis F. A first-in-human phase I study of SAR125844, a selective MET tyrosine kinase inhibitor, in patients with advanced solid tumours with MET amplification. Eur J Cancer. 2017 Dec;87:131-139. doi: 10.1016/j.ejca.2017.10.016. Epub 2017 Nov 14.'}]}, 'descriptionModule': {'briefSummary': 'Primary Objectives:\n\nTo determine the maximum tolerated dose (MTD) of SAR125844. To confirm safety profile of SAR125844 when administered as single agent at the MTD.\n\nTo evaluate the preliminary anti-tumoral effect of SAR125844 in patients with MET-gene amplified solid tumors (including sub-group of MET-amplified non-small cell lung cancer \\[NSCLC\\] patients) and in patients with Phospho-MET positive tumors without MET-gene amplification.\n\nSecondary Objectives:\n\nTo characterize the global safety profile including cumulative toxicities. To evaluate the pharmacokinetic profile of SAR125844 in the proposed dosing schedule(s).\n\nTo assess preliminary antitumor activity in patients with measurable/evaluable disease, according to RECIST 1.1 criteria.\n\nTo explore the pharmacodynamic effects (PD) of SAR125844. To explore MET gene amplification status in Circulating Tumoral Cells (CTCs) and on tumor biopsies collected during the study, in the escalation part only.\n\nTo evaluate other pharmacodynamic biomarkers and help selection of patients who could benefit from SAR125844.\n\nTo explore MET-gene amplification status in circulating DNA.', 'detailedDescription': 'The duration of the study for one patient in the dose escalation phase of the study will include a screening period of up to 3 weeks and a 4-week treatment cycle(s). The patients may continue treatment until disease progression, unacceptable toxicity, or willingness to stop, followed by a minimum of 30-day follow-up. The study will also include 2 expansion cohorts. If a patient treated in dose escalation part or in an expansion cohorts, continues to benefit from the treatment at the time of Clinical Study Report, the patient can continue study treatment for a maximum of 1 year and will continue to undergo all assessments as per the study flowchart. Such patients will be followed at least until 30 days after the last IMP administration.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion criteria:\n\nIn the dose escalation part: patients with high MET tumor expression, evaluable or measurable solid tumors for which no standard therapy is available.\n\nIn the expansion cohorts: in the first cohort, patients with diagnosed MET gene amplified including NSCLC patients and measurable tumors for which no standard therapy is available will be eligible. In the second cohort, patients with advanced P-MET positive measurable solid tumor without MET- gene amplification for which no standard therapy is available will be eligible.\n\nExclusion criteria:\n\nPatient less than 18 years old. ECOG performance status \\>2. Any serious active disease or co-morbid condition, which, in the opinion of the Investigator, may interfere with the safety or the compliance with the study.\n\nPoor bone marrow reserve as defined by absolute neutrophil count \\<1.5 x 10\\^9/L or platelets \\<100 x 10\\^9/L.\n\nPoor organ function as defined by one of the following:\n\n* Total bilirubin \\>1.5 x ULN\n* AST, ALT, alkaline phosphatase \\>2.5 x ULN or \\>5 x ULN in case of documented liver metastasis. Alkaline phosphatase up to 5 x ULN in case of osteolytic bone metastasis without liver metastases is allowed\n* Serum creatinine \\>1.5 x ULN or\n* Serum creatinine between 1.0 and 1.5 x ULN associated with calculated creatinine clearance \\<60 mL/min\n* Proteinuria \\>500 mg/24H Pregnant or breast-feeding women. No use of effective birth control methods, when applicable. No measurable or evaluable tumor lesion in the Dose Escalation part, and no measurable lesions in the expansion cohorts.\n\nBrain metastasis (other than totally resected or previously pre-irradiated and no progressive/relapsing) or lepto-meningeal carcinomatosis.\n\nNo resolution of any specific toxicities (excluding alopecia) related to any prior anti-cancer therapy to grade ≤1 according to the NCI CTCAE v.4.03.\n\nWash out period of less than 3 weeks from previous antitumor therapy or any investigational treatment (and less than 6 weeks in case of prior nitroso-urea and or mitomycin C treatment).\n\nAny surgery with major risk of bleeding performed less than 10 days prior to study treatment administration.\n\nAny other severe underlying medical conditions, which could impair the ability to participate in the study or the interpretation of its results.\n\nPatients treated with potent CYP3A inhibitor unless it can be discontinued at least 2 weeks prior to study treatment or 5 elimination half-life, whichever is the longest.\n\nPatients treated with potent and moderate CYP3A inducers unless it can be discontinued at least 2 weeks prior to study treatment or 5 elimination half-life, whichever is the longest. Patients treated with weak CYP3A inducers such as dexamethasone are eligible.\n\nKnown hypersensitivity or any adverse event related to the study drug excipient.\n\nPrior treatment with any compound in the same class. Mean QTc interval prolongation.\n\nThe above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial."}, 'identificationModule': {'nctId': 'NCT01391533', 'acronym': 'SARMET', 'briefTitle': 'Study of SAR125844 Single Agent Administered as Slow Intravenous Infusion in Adult Patients With Advanced Malignant Solid Tumors', 'organization': {'class': 'INDUSTRY', 'fullName': 'Sanofi'}, 'officialTitle': 'Dose Escalation, Safety, Pharmacokinetic and Pharmacodynamic, First in Man Study, of SAR125844 Single Agent Administered as Slow Intravenous Infusion in Adult Patients With Advanced Malignant Solid Tumors', 'orgStudyIdInfo': {'id': 'TED11449'}, 'secondaryIdInfos': [{'id': '2010-021398-36', 'type': 'EUDRACT_NUMBER'}, {'id': 'U1111-1117-9878', 'type': 'OTHER', 'domain': 'UTN'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Dose Escalation', 'description': 'Dose escalation phase: The starting dose of SAR125844 will be 50 mg/m\\^2 up to 960 mg/m\\^2', 'interventionNames': ['Drug: SAR125844']}], 'interventions': [{'name': 'SAR125844', 'type': 'DRUG', 'description': 'Pharmaceutical form:solution\n\nRoute of administration: intravenous', 'armGroupLabels': ['Dose Escalation']}]}, 'contactsLocationsModule': {'locations': [{'zip': '02114', 'city': 'Boston', 'state': 'Massachusetts', 'country': 'United States', 'facility': 'Investigational Site Number 840001', 'geoPoint': {'lat': 42.35843, 'lon': -71.05977}}, {'zip': '21079', 'city': 'Dijon', 'country': 'France', 'facility': 'Investigational Site Number 250002', 'geoPoint': {'lat': 47.31344, 'lon': 5.01391}}, {'zip': '94805', 'city': 'Villejuif', 'country': 'France', 'facility': 'Investigational Site Number 250001', 'geoPoint': {'lat': 48.7939, 'lon': 2.35992}}, {'zip': '40138', 'city': 'Bologna', 'country': 'Italy', 'facility': 'Investigational Site Number 380004', 'geoPoint': {'lat': 44.49381, 'lon': 11.33875}}, {'zip': '20133', 'city': 'Milan', 'country': 'Italy', 'facility': 'Investigational Site Number 380002', 'geoPoint': {'lat': 42.78235, 'lon': 12.59836}}, {'zip': '20141', 'city': 'Milan', 'country': 'Italy', 'facility': 'Investigational Site Number 380001', 'geoPoint': {'lat': 42.78235, 'lon': 12.59836}}, {'zip': '08035', 'city': 'Barcelona', 'country': 'Spain', 'facility': 'Investigational Site Number 724001', 'geoPoint': {'lat': 41.38879, 'lon': 2.15899}}, {'zip': '28040', 'city': 'Madrid', 'country': 'Spain', 'facility': 'Investigational Site Number 724003', 'geoPoint': {'lat': 40.4165, 'lon': -3.70256}}], 'overallOfficials': [{'name': 'Clinical Sciences & Operations', 'role': 'STUDY_DIRECTOR', 'affiliation': 'Sanofi'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Sanofi', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}