Viewing Study NCT02805218


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Study NCT ID: NCT02805218
Status: COMPLETED
Last Update Posted: 2016-06-20
First Post: 2016-06-13
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: PEG-rhG-CSF in Patients With Lymphoma Receiving Chemotherapy
Sponsor:
Organization:

Raw JSON

{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D008223', 'term': 'Lymphoma'}], 'ancestors': [{'id': 'D009370', 'term': 'Neoplasms by Histologic Type'}, {'id': 'D009369', 'term': 'Neoplasms'}, {'id': 'D008232', 'term': 'Lymphoproliferative Disorders'}, {'id': 'D008206', 'term': 'Lymphatic Diseases'}, {'id': 'D006425', 'term': 'Hemic and Lymphatic Diseases'}, {'id': 'D007160', 'term': 'Immunoproliferative Disorders'}, {'id': 'D007154', 'term': 'Immune System Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'C423652', 'term': 'pegylated granulocyte colony-stimulating factor'}, {'id': 'C455861', 'term': 'pegfilgrastim'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE4'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NA', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'PREVENTION', 'interventionModel': 'SINGLE_GROUP'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 410}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2013-09'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2016-06', 'completionDateStruct': {'date': '2016-02', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2016-06-16', 'studyFirstSubmitDate': '2016-06-13', 'studyFirstSubmitQcDate': '2016-06-15', 'lastUpdatePostDateStruct': {'date': '2016-06-20', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2016-06-17', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2016-02', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'The occurrence rate of adverse event', 'timeFrame': 'up to 30 days after the patient study completion'}, {'measure': 'The severity of adverse event', 'timeFrame': 'up to 30 days after the patient study completion'}], 'secondaryOutcomes': [{'measure': 'the occurrence rate of grade III/ IV neutropenia during chemotherapy cycles', 'timeFrame': 'through the study completion,an average of 5 months'}]}, 'conditionsModule': {'conditions': ['Lymphoma']}, 'descriptionModule': {'briefSummary': 'The purpose of this study is to estimate the safety and efficacy of PEG-rhG-CSF in patients with lymphoma receiving chemotherapy.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria:\n\n* Patients with age ≥ 18 years\n* diagnosis of lymphoma(Hodgkin's lymphoma and non-Hodgkin's lymphoma) patients\n* Karnofsky Performance Status Z70\n* life expectancy of at least 8 months\n* normal white blood cell count and platelet count\n* Written informed consent are acquired\n\nExclusion Criteria:\n\n* uncontrolled infection\n* pregnancy\n* Have accepted any other anti-tumor drug within 4 weeks before anticipated the study\n* Other situations that investigators consider as contra-indication for this study"}, 'identificationModule': {'nctId': 'NCT02805218', 'briefTitle': 'PEG-rhG-CSF in Patients With Lymphoma Receiving Chemotherapy', 'organization': {'class': 'INDUSTRY', 'fullName': 'CSPC Baike (Shandong) Biopharmaceutical Co., Ltd.'}, 'officialTitle': 'The Multi-center,Open-label,Single Arm Clinical Trial of Efficacy and Safety of PEG-rhG-CSF in Patients With Lymphoma Receiving Chemotherapy', 'orgStudyIdInfo': {'id': 'CSPC-PGC-IV-02-1'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'PEG-rhG-CSF', 'description': 'patients received a single dose of 100 ug/kg of PEG-rhG-CSF(pegfilgrastim), on the basis of actual body weight, as a single subcutaneous injection on day 3 after chemotherapy', 'interventionNames': ['Drug: PEG-rhG-CSF']}], 'interventions': [{'name': 'PEG-rhG-CSF', 'type': 'DRUG', 'otherNames': ['pegfilgrastim'], 'armGroupLabels': ['PEG-rhG-CSF']}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'CSPC Baike (Shandong) Biopharmaceutical Co., Ltd.', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}