Found 32 matching trials
A Continuation Clinical Trial of Oral Vorinostat (MK-0683) in Advanced Cancers (MK-0683-007) PHASE2 This study will evaluate the safety and tolerability of continuing vorinost...
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Randomised Study of Azacitidine Versus Azacitidine With Vorinostat in Patients With AML or High Risk MDS PHASE2 This is a multicentre, open-label, randomised phase II trial comparing azac...
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Barts and the London NHS Trust
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Vorinostat (MK-0683) Phase I Study in Cutaneous T-Cell Lymphoma (CTCL) Patients (MK-0683-089 EXT1) PHASE1 Part I evaluates the safety, tolerability and pharmacokinetics (PK) of vori...
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Phase I Trial of Vorinostat (MK-0683, SAHA) in Combination With Decitabine in Patients With AML or MDS (MK-0683-055 EXT1) PHASE1 This study is to evaluate the safety and tolerability of vorinostat in comb...
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A Phase I/II Clinical Trial of Vorinostat in Combination With Erlotinib for Patients With Relapsed/Refractory Non-Small-Cell Lung Cancer (0683-025) PHASE1 The reason for this study will be to find the safest maximum tolerated dose...
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Phase I Study of MK-0683 in Combination With Bortezomib in Participants With Multiple Myeloma (MK-0683-098) PHASE1 The primary purpose of this clinical study is to determine the recommended ...
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Study to Evaluate Effects of Vorinostat and HXTC on Persistent HIV-1 Infection in HIV-Infected Subjects Started on Antiretroviral Therapy (ART) PHASE1 This is a phase I, single-site, study to evaluate the effects of VOR and HI...
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University of North Carolina at Chapel Hill
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Suberoylanilide Hydroxamic Acid in Advanced Solid Tumors PHASE1 The purpose of this investigational study is to determine the safety and to...
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Study of Vorinostat (MK-0683) With Follicular Lymphoma (FL), Other Indolent B-cell Non-Hodgkin's Lymphoma (B-NHL), or Mantle Cell Lymphoma (MCL) Participants (MK-0683-103) PHASE2 The purpose of this study is to evaluate the safety, tolerability, and effi...
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Phase IIa Vorinostat (MK0683, Suberoylanilide Hydroxamic Acid (SAHA)) Study in Lower Risk Myelodysplastic Syndromes (0683-064) PHASE2 This study is to evaluate the efficacy, safety and tolerability of vorinost...
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