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Clinical Trial Summary

The use of venetoclax-based therapies for pediatric patients with relapsed or refractory malignancies is increasingly common outside of the clinical trial setting. For patients who cannot swallow tablets, it is common to crush the tablets and dissolve them in liquid to create a solution. However, no PK data exists in adults or children using crushed tablets dissolved in liquid in this manner, and as a result, the venetoclax exposure with this solution is unknown. Primary Objectives • To determine the pharmacokinetics of venetoclax when commercially available tablets are crushed and dissolved into a solution Secondary Objectives - To determine the pharmacokinetics of venetoclax solution in patients receiving concomitant strong and moderate CYP3A inhibitors - To determine potential pharmacokinetic differences based on route of venetoclax solution administration (ie. PO vs NG tube vs G-tube) - To determine the concentration of venetoclax in cerebral spinal fluid when administered as an oral solution


Clinical Trial Description

Peripheral blood will be drawn at multiple time points to evaluate venetoclax pharmacokinetics in patients who are receiving venetoclax solution made from crushed tablets as part of their oncology treatment. ;


Study Design


Related Conditions & MeSH terms

  • Acute Lymphocytic Leukemia
  • Acute Myelogenous Leukemia
  • ALL
  • AML
  • B Cell Lymphoma
  • Burkitt Lymphoma
  • Chronic Myelogenous Leukemia
  • CML
  • Diffuse Large B Cell Lymphoma
  • Follicular Lymphoma
  • Hematologic Malignancy
  • Hematologic Neoplasms
  • Hodgkin Lymphoma
  • Leukemia
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive
  • Leukemia, Myeloid
  • Leukemia, Myeloid, Acute
  • Lymphoma
  • Lymphoma, B-Cell
  • Lymphoma, Large B-Cell, Diffuse
  • Lymphoma, T-Cell
  • Lymphoma, T-Cell, Peripheral
  • Myeloproliferative Disorders
  • Myeloproliferative Neoplasm
  • Neoplasms
  • Non Hodgkin Lymphoma
  • Peripheral T Cell Lymphoma
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma
  • T-cell Lymphoma

NCT number NCT06131801
Study type Observational
Source Children's Hospital Medical Center, Cincinnati
Contact Site Public Contact
Phone (513) 636-2799
Email cancer@cchmc.org
Status Recruiting
Phase
Start date November 15, 2023
Completion date December 1, 2027

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