Ignite Creation Date:
2025-12-25 @ 5:03 AM
Ignite Modification Date:
2026-02-20 @ 3:33 PM
Study NCT ID:
NCT01775618
Status:
COMPLETED
Last Update Posted:
2020-08-21
First Post:
2013-01-23
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Safety and Efficacy of BAY94-9027 in Previously Treated Male Children With Haemophilia A
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24', 'removedCountries': ['Germany', 'Hungary', 'Slovenia']}, 'conditionBrowseModule': {'meshes': [{'id': 'D006467', 'term': 'Hemophilia A'}], 'ancestors': [{'id': 'D025861', 'term': 'Blood Coagulation Disorders, Inherited'}, {'id': 'D001778', 'term': 'Blood Coagulation Disorders'}, {'id': 'D006402', 'term': 'Hematologic Diseases'}, {'id': 'D006425', 'term': 'Hemic and Lymphatic Diseases'}, {'id': 'D020147', 'term': 'Coagulation Protein Disorders'}, {'id': 'D006474', 'term': 'Hemorrhagic Disorders'}, {'id': 'D030342', 'term': 'Genetic Diseases, Inborn'}, {'id': 'D009358', 'term': 'Congenital, Hereditary, and Neonatal Diseases and Abnormalities'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D005169', 'term': 'Factor VIII'}], 'ancestors': [{'id': 'D001779', 'term': 'Blood Coagulation Factors'}, {'id': 'D001798', 'term': 'Blood Proteins'}, {'id': 'D011506', 'term': 'Proteins'}, {'id': 'D000602', 'term': 'Amino Acids, Peptides, and Proteins'}, {'id': 'D011498', 'term': 'Protein Precursors'}, {'id': 'D001685', 'term': 'Biological Factors'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE3'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NON_RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'SINGLE_GROUP'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 73}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2013-05-29', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2020-08', 'completionDateStruct': {'date': '2020-02-19', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2020-08-19', 'studyFirstSubmitDate': '2013-01-23', 'studyFirstSubmitQcDate': '2013-01-23', 'lastUpdatePostDateStruct': {'date': '2020-08-21', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2013-01-25', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2015-03-19', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Annualized number of all bleeds', 'timeFrame': 'At least 50 exposure days (ED) over 6 months, on average 245 days'}, {'measure': 'Pharmacokinetics profile of BAY94-9027 based on blood concentration over the defined time period', 'timeFrame': 'Pre-dose to 72 hours post-dose', 'description': 'Pharmacokinetics profile includes maximum concentration (Cmax), half-life (t1/2), area under the concentration versus time curve (AUC), mean residence time (MRT), volume of distribution at steady state (Vss), and clearance (CL)'}, {'measure': 'Response of acute bleeding events to treatment based on a 4-point scale (poor, moderate, good, or excellent)', 'timeFrame': 'At least 50 exposure days (ED) over 6 months, on average 245 days'}, {'measure': 'Characterization of a potential immune response', 'timeFrame': '12 weeks'}, {'measure': 'Inhibitor development in the extension study', 'timeFrame': 'At least 50 additional EDs to achieve at least 100 cumulative EDs, on average 5 years'}], 'secondaryOutcomes': [{'measure': 'Inhibitor development in the main study', 'timeFrame': 'After 10 to 15 and 50 exposure days (ED) over 6 months, on average 245 days'}, {'measure': 'Assessment of incremental recovery in main study', 'timeFrame': 'At least 50 exposure days (ED) over 6 months, on average 245 days'}, {'measure': 'Number of participants with adverse events as a measure of safety and tolerability', 'timeFrame': 'From the start of study treatment up to 7 days after the last dose (Main study: on average 245+7 days; Part 2: 12 weeks+7 days; Extension study: on average 5 years+7 days)'}]}, 'oversightModule': {'oversightHasDmc': True, 'isFdaRegulatedDrug': True, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['Hemophilia A', 'Factor VIII', 'Prophylaxis', 'Pediatric'], 'conditions': ['Hemophilia A']}, 'referencesModule': {'references': [{'pmid': '33724632', 'type': 'DERIVED', 'citation': 'Mancuso ME, Biss T, Fischer K, Maas Enriquez M, Steele M, Wang M, Tseneklidou-Stoeter D, Ahuja S, Kenet G. PROTECT VIII kids extension study: Long-term safety and efficacy of BAY 94-9027 (damoctocog alfa pegol) in children with severe haemophilia A. Haemophilia. 2021 May;27(3):434-444. doi: 10.1111/hae.14294. Epub 2021 Mar 16.'}], 'seeAlsoLinks': [{'url': 'https://www.clinicaltrialsregister.eu/', 'label': 'Click here to find information about studies related to Bayer Healthcare products conducted in Europe.'}, {'url': 'https://clinicaltrials.bayer.com/', 'label': 'Click here to find results for studies related to Bayer products.'}]}, 'descriptionModule': {'briefSummary': "Hemophilia A is an inherited blood disorder in which one protein, Factor VIII, needed to form blood clots is missing or not present in sufficient levels. Hemophilia A causes the clotting process to be slowed and the person experiences bleeds causing serious problems that could lead to disability. The current standard treatment for severe hemophilia A is infusion of FVIII to stop bleeding, or regular scheduled treatment to prevent bleeds from occuring. Due to the short half-life of FVIII, prophylaxis may require treatment as often as every other day.\n\nIn this trial safety and efficacy of a long-acting recombinant Factor VIII molecule is being evaluated in 50 male subjects, \\< 12 years of age, with severe Hemophilia A. These subjects will receive open label treatment with long-acting rFVIII for approximately 6 months (or longer until 50 exposure days) on a regular schedule at least once every 7-days. Doses and dose intervals may be adapted to the subject's clinical need. A second group of patients will receive open label treatment with the same drug for 12 weeks on a regular schedule of 2x/week. Patients will attend the treatment center for routine blood samples and will be required to keep an electronic diary.\n\nSubjects will be offered participation in an optional extension study to collect observations for at least an additional 50 exposure days."}, 'eligibilityModule': {'sex': 'MALE', 'stdAges': ['CHILD'], 'maximumAge': '12 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Males \\< 12 years of age\n* Subjects with severe hemophilia A\n* Previously treated with FVIII for \\> 50 exposure days\n\nExclusion Criteria:\n\n* Subjects with current evidence of or history of inhibitors to FVIII\n* Any other inherited or acquired bleeding disorder\n* Platelet counts \\< 100,000/mm\\^3\n* Creatinine \\> 2x the upper limit of normal\n* Aspartate aminotransferase (AST) / Alanine aminotransferase (ALT) \\> 5x the upper limit of normal'}, 'identificationModule': {'nctId': 'NCT01775618', 'briefTitle': 'Safety and Efficacy of BAY94-9027 in Previously Treated Male Children With Haemophilia A', 'organization': {'class': 'INDUSTRY', 'fullName': 'Bayer'}, 'officialTitle': 'A Multi-center, Phase III, Non-controlled, Open-label Trial to Evaluate the Pharmacokinetics, Safety, and Efficacy of BAY94-9027 for Prophylaxis and Treatment of Bleeding in Previously Treated Children (Age <12 Years) With Severe Hemophilia A', 'orgStudyIdInfo': {'id': '15912'}, 'secondaryIdInfos': [{'id': '2012-004434-42', 'type': 'EUDRACT_NUMBER'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Main study', 'description': 'Participants were treated and prophylaxis administered with BAY94-9027 at a dose of 25-60 international units/kilogram (IU/kg) twice per week or 45-60 IU/kg every 5 days or 60 IU/kg every 7 days as an intravenous (IV) infusion as per clinical needs of each subject up to at least 50 exposure days (EDs) and a minimum of at least 6 months.', 'interventionNames': ['Biological: BAY94-9027']}, {'type': 'EXPERIMENTAL', 'label': 'Part 2 (Expansion group)', 'description': 'Participants were administered with BAY94-9027 at a dose of 25-60 IU/kg twice per week for prophylaxis for 12 weeks.', 'interventionNames': ['Biological: BAY94-9027']}, {'type': 'EXPERIMENTAL', 'label': 'Extension study', 'description': 'Participants were treated and prophylaxis administered with BAY94-9027 at a dose of 25- 60 IU/kg twice per week or 45-60 IU/kg every 5 days or 60 IU/kg every 7 days as an IV infusion as per clinical needs of each subject for at least 50 EDs or until marketing authorization of the drug.', 'interventionNames': ['Biological: BAY94-9027']}], 'interventions': [{'name': 'BAY94-9027', 'type': 'BIOLOGICAL', 'description': 'Study drug dosing was adjusted to the clinical needs of each subject in the range of 25-60 IU/kg/administration, intravenous infusion, at least 50 EDs and a minimum of at least 6 months', 'armGroupLabels': ['Main study']}, {'name': 'BAY94-9027', 'type': 'BIOLOGICAL', 'description': 'Twice per week prophylaxis: 25-60 IU/kg, intravenous infusion, for 12 weeks', 'armGroupLabels': ['Part 2 (Expansion group)']}, {'name': 'BAY94-9027', 'type': 'BIOLOGICAL', 'description': 'Study drug dosing was adjusted to the clinical needs of each subject in the range of 25-60 IU/kg/administration, intravenous infusion, at least 50 additional EDs to achieve at least 100 cumulative EDs, or until marketing authorization of the drug', 'armGroupLabels': ['Extension study']}]}, 'contactsLocationsModule': {'locations': [{'zip': '95817', 'city': 'Sacramento', 'state': 'California', 'country': 'United States', 'geoPoint': {'lat': 38.58157, 'lon': -121.4944}}, {'zip': '32504', 'city': 'Pensacola', 'state': 'Florida', 'country': 'United States', 'geoPoint': {'lat': 30.42131, 'lon': -87.21691}}, {'zip': '45229', 'city': 'Cincinnati', 'state': 'Ohio', 'country': 'United States', 'geoPoint': {'lat': 39.12711, 'lon': -84.51439}}, {'zip': '44106-6007', 'city': 'Cleveland', 'state': 'Ohio', 'country': 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'STUDY_DIRECTOR', 'affiliation': 'Bayer'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Bayer', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}