- CSR Summary Not Yet Available
- NCT01236391
- Primary Citation
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Trial Information
Generic NameIbrutinibProduct NameIMBRUVICA®Therapeutic AreaCancers and Other NeoplasmsEnrollment115% Female23.4%% WhiteN/A
Product ClassKinase InhibitorsSponsor Protocol NumberPCYC-1104-CAData PartnerJohnson & JohnsonCondition StudiedLymphoma, Mantle Cell/Small LymphocyticMean/Median Age (Years)67.1
Supporting Documentation
- Collected Datasets 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
- 2022-5123 : CYP3A4 Interactions and Adverse Drug Reactions in Ibrutinib Therapy: Revisting multiple clinical trials
- 2022-5066 : Predictors of exposure, therapeutic and adverse effects of ibrutinib used in the treatment of B-cell lymphomas
- 2019-3840 : Identifying clinical and electrocardiogram (ECG) findings predicting for tachyarrhythmia in patients on ibrutinib treatment