Ignite Creation Date:
2025-12-24 @ 4:04 PM
Ignite Modification Date:
2025-12-25 @ 7:29 PM
Study NCT ID:
NCT00410566
Status:
TERMINATED
Last Update Posted:
2015-03-19
First Post:
2006-12-11
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Safety Study of rhASM Enzyme Replacement Therapy in Adults With Acid Sphingomyelinase Deficiency (Niemann-Pick Disease)
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D009542', 'term': 'Niemann-Pick Diseases'}, {'id': 'D016464', 'term': 'Lysosomal Storage Diseases'}], 'ancestors': [{'id': 'D013106', 'term': 'Sphingolipidoses'}, {'id': 'D020140', 'term': 'Lysosomal Storage Diseases, Nervous System'}, {'id': 'D020739', 'term': 'Brain Diseases, Metabolic, Inborn'}, {'id': 'D001928', 'term': 'Brain Diseases, Metabolic'}, {'id': 'D001927', 'term': 'Brain Diseases'}, {'id': 'D002493', 'term': 'Central Nervous System Diseases'}, {'id': 'D009422', 'term': 'Nervous System Diseases'}, {'id': 'D015616', 'term': 'Histiocytosis, Non-Langerhans-Cell'}, {'id': 'D015614', 'term': 'Histiocytosis'}, {'id': 'D008206', 'term': 'Lymphatic Diseases'}, {'id': 'D006425', 'term': 'Hemic and Lymphatic Diseases'}, {'id': 'D008661', 'term': 'Metabolism, Inborn Errors'}, {'id': 'D030342', 'term': 'Genetic Diseases, Inborn'}, {'id': 'D009358', 'term': 'Congenital, Hereditary, and Neonatal Diseases and Abnormalities'}, {'id': 'D008064', 'term': 'Lipidoses'}, {'id': 'D008052', 'term': 'Lipid Metabolism, Inborn Errors'}, {'id': 'D008659', 'term': 'Metabolic Diseases'}, {'id': 'D009750', 'term': 'Nutritional and Metabolic Diseases'}, {'id': 'D052439', 'term': 'Lipid Metabolism Disorders'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE1'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NON_RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 11}}, 'statusModule': {'whyStopped': 'Terminated by sponsor - Single dose safety objective achieved.', 'overallStatus': 'TERMINATED', 'startDateStruct': {'date': '2006-12'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2015-03', 'completionDateStruct': {'date': '2009-04', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2015-03-17', 'studyFirstSubmitDate': '2006-12-11', 'studyFirstSubmitQcDate': '2006-12-11', 'lastUpdatePostDateStruct': {'date': '2015-03-19', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2006-12-13', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2009-03', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Safety assessments via physical exam,AE reporting,telemetry heartrate monitoring,ECG,ECHO,clinical lab evaluations,liver and adrenal function tests,cytokine testing,adrenal hormone levels,lipid profile,chest Xrays,liver biopsies,MRI of internal', 'timeFrame': 'Pre-, During-, and Post-infusion (up to 72 hrs); 14 day and 28 day follow-up visit'}, {'measure': 'Immune Response Measure', 'timeFrame': 'Pre-infusion and final visit (Day 28)'}], 'secondaryOutcomes': [{'measure': 'PK measurements', 'timeFrame': 'Pre- and Post-infusion up to 72 hrs.'}]}, 'oversightModule': {'oversightHasDmc': True}, 'conditionsModule': {'keywords': ['Acid sphingomyelinase deficiency', 'Niemann-Pick disease', 'Lysosomal storage disorder', 'Enzyme replacement therapy', 'Treatment'], 'conditions': ['Acid Sphingomyelinase Deficiency', 'Niemann-Pick Disease']}, 'descriptionModule': {'briefSummary': 'The purpose of this study is to determine the safe range of single doses of rhASM administered to adults with ASM deficiency.', 'detailedDescription': 'ASM deficiency (ASMD), also known as Niemann-Pick A and B disease, is a rare genetic disorder in which reduced activity of the lysosomal enzyme, ASM, leads to the accumulation of sphingomyelin primarily in macrophages throughout the body. This deficiency results in characteristic features such as hepatosplenomegaly, thrombocytopenia, interstitial lung disease, growth retardation, coronary artery disease, fatigue, and in severe cases, neurodegeneration with death in early childhood. There is no specific treatment for this disease. This Phase 1 safety study will seek to enroll a minimum of 12 and a maximum of 30 eligible adults patients with ASMD with each patient participating for approximately 7 weeks.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'maximumAge': '65 Years', 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Signed, informed consent by the patient or legal guardian prior to performing any study-related procedures;\n* Have ≤ 0.2 nmol/hr/mg protein ASM activity in peripheral leukocytes, as measured by the reference laboratory;\n* Have a diffusing capacity (DLco) \\> 30% of the predicted normal value;\n* Have a spleen volume ≥ 2x normal\n* Female patients of childbearing potential must have a serum pregnancy test negative for β-hCG and agree to use a reliable birth control method for the duration of the study.\n\nExclusion Criteria:\n\n* Is pregnant or lactating;\n* Has received an investigational drug within 30 days prior to study enrollment;\n* Has a medical condition, including serious intercurrent illness, active hepatitis B or C or human immunodeficiency virus (HIV) infection, cirrhosis, \\> stage 3 liver fibrosis, INR \\>1.5, platelet count \\< 60.0x10\\^3/µL, significant cardiac disease (e.g. pulmonary artery pressure \\> 40 mm Hg, moderate or severe valvular dysfunction, or \\< 40% left ventricular ejection fraction by echocardiography (ECHO)), or any other extenuating circumstances that may significantly interfere with study compliance including all prescribed evaluations and follow-up activities;\n* Has had a major organ transplant (e.g. bone marrow or liver);\n* Has had a total splenectomy;\n* Has an alanine aminotransferase (ALT) or aspartate aminotransferase (AST) value \\>250 IU/L or a total bilirubin \\>3.6 mg/dL;\n* Is unwilling or unable to avoid the use of alcohol, medications that may decrease rhASM activity, medications or herbal supplements that may cause or prolong bleeding, and the use of medications or herbal supplements with potential hepatoxicity within 14 days prior to and 28 days afte the rhASM infusion.'}, 'identificationModule': {'nctId': 'NCT00410566', 'briefTitle': 'Safety Study of rhASM Enzyme Replacement Therapy in Adults With Acid Sphingomyelinase Deficiency (Niemann-Pick Disease)', 'organization': {'class': 'INDUSTRY', 'fullName': 'Sanofi'}, 'officialTitle': 'A Phase I, Single-Center, Single Dose, Dose Escalation Study of Recombinant Human Acid Sphingomyelinase (rhASM) in Adults With Acid Sphingomyelinase Deficiency (ASMD)', 'orgStudyIdInfo': {'id': 'SPHINGO00605'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': '1', 'interventionNames': ['Drug: rhASM']}, {'type': 'EXPERIMENTAL', 'label': '2', 'interventionNames': ['Drug: rhASM']}, {'type': 'EXPERIMENTAL', 'label': '3', 'interventionNames': ['Drug: rhASM']}, {'type': 'EXPERIMENTAL', 'label': '4', 'interventionNames': ['Drug: rhASM']}, {'type': 'EXPERIMENTAL', 'label': '5', 'interventionNames': ['Drug: rhASM']}], 'interventions': [{'name': 'rhASM', 'type': 'DRUG', 'description': 'Single dose of 0.03mg/kg body weight IV', 'armGroupLabels': ['1']}, {'name': 'rhASM', 'type': 'DRUG', 'description': 'Single dose of 0.1mg/kg body weight IV', 'armGroupLabels': ['2']}, {'name': 'rhASM', 'type': 'DRUG', 'description': 'Single dose of 0.3mg/kg body weight IV', 'armGroupLabels': ['3']}, {'name': 'rhASM', 'type': 'DRUG', 'description': 'Single dose of 0.6mg/kg body weight IV', 'armGroupLabels': ['4']}, {'name': 'rhASM', 'type': 'DRUG', 'description': 'Single dose of 1.0mg/kg body weight IV', 'armGroupLabels': ['5']}]}, 'contactsLocationsModule': {'locations': [{'zip': '10029', 'city': 'New York', 'state': 'New York', 'country': 'United States', 'geoPoint': {'lat': 40.71427, 'lon': -74.00597}}], 'overallOfficials': [{'name': 'Medical Monitor', 'role': 'STUDY_DIRECTOR', 'affiliation': 'Genzyme, a Sanofi Company'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Genzyme, a Sanofi Company', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}