Publication

Pharmacokinetics and Safety of Elotuzumab Combined With Lenalidomide and Dexamethasone in Patients With Multiple Myeloma and Various Levels of Renal Impairment: Results of a Phase Ib Study

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Last modified
  • 05/14/2025
Type of Material
Authors
    Jesus Berdeja, Sarah Cannon Research InstituteSundar Jagannath, Mt Sinai HospitalJeffrey Zonder, Wayne State UniversityAshraf Badros, University of MarylandJonathan Kaufman, Emory UniversityRobert Manges, Investigative Clinical Research of IndianaManish Gupta, Bristol-Myers SquibbAmol Tendolkar, Bristol-Myers SquibbMark Lynch, Bristol-Myers SquibbEric Bleickardt, Bristol-Myers SquibbPrashni Paliwal, Bristol-Myers SquibbRavi Vij, Washington University
Language
  • English
Date
  • 2016-03-01
Publisher
  • Elsevier Inc.
Publication Version
Copyright Statement
  • © 2021 Elsevier Inc
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 16
Issue
  • 3
Start Page
  • 129
End Page
  • 138
Grant/Funding Information
  • The present analysis was supported by research funding from Bristol-Myers Squibb.
Abstract
  • Renal impairment is associated with a poor prognosis in patients with multiple myeloma (MM), and more treatment options are needed. The pharmacokinetics of elotuzumab, a humanized IgG1 monoclonal antibody, combined with lenalidomide and dexamethasone, is not significantly different between patients with MM with and without renal impairment, suggesting that elotuzumab might be administered without dose adjustment for renal function.
Author Notes
  • Address for correspondence: Jesus Berdeja, MD, Sarah Cannon Research Institute, 250 25th Avenue North, Suite 412, Nashville, TN 37203 jberdeja@tnonc.com.
Keywords
Research Categories
  • Health Sciences, Oncology

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