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CSR Summary Not Yet Available
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NCT02264574
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Primary Citation
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Trial Information
Generic NameIbrutinibProduct NameIMBRUVICA®Therapeutic AreaAntineoplastic and Immunomodulating AgentsProduct ClassAntineoplastic AgentsPharmacological SubgroupProtein Kinase InhibitorsChemical SubgroupBruton's Tyrosine Kinase (BTK) InhibitorsCondition StudiedLeukemia, Chronic Lymphocytic
Sponsor Protocol NumberPCYC-1130-CAEnrollment229Data PartnerJohnson & Johnson% FemaleN/AMean/Median Age (Years)71% WhiteN/A
Supporting Documentation
- Collected Datasets Available
- Data Definition Specification Available
- Protocol with Amendments Available
- Statistical Analysis Plan Available
- Clinical Study Report Available
Approved Data Requests Associated with this Trial
- 2024-0828 : Prognostic Impacts of Clinical and Molecular Characteristics of Patients with Hematologic Malignancy and Potential Mechanisms
- 2023-5534 : Quality tolerance limit and duplicated patient investigation in clinical trials
- 2023-5247 : Identifying Prognostic and Predictive Factors for Causal Exposure-Response Analysis of Ibrutinib in treatment of non-Hodgkin Lymphoma