Quantitation of the next-generation imipridone ONC206 in human plasma by a simple and sensitive UPLC-MS/MS assay for

Jennifer C Goodell1, Sara M Zimmerman1, Cody J Peer1

  • 1Clinical Pharmacology Program, Office of the Clinical Director, National Cancer Institute, Bethesda, MD, USA.

Insights

A new ultra-high-performance liquid chromatography-tandem mass spectrometry (uHPLC-MS/MS) method accurately quantifies ONC206 in human plasma. This validated assay is crucial for understanding the pharmacokinetics of ONC206 in its first-in-human clinical trial.

Area of Science:

  • Pharmacology
  • Analytical Chemistry
  • Clinical Pharmacology

Background:

  • ONC206, an imipridone derivative, is undergoing a first-in-human oral clinical trial.
  • Pharmacokinetic analysis is essential for characterizing ONC206's drug profile.
  • No established bioanalytical method exists for ONC206 quantification.

Purpose of the Study:

  • Develop and validate a sensitive and simple bioanalytical method for ONC206.
  • Quantify ONC206 in human plasma for clinical pharmacokinetic studies.
  • Establish the reliability and applicability of the developed assay.

Main Methods:

  • Ultra-high-performance liquid chromatography-tandem mass spectrometry (uHPLC-MS/MS) was employed.
  • Protein precipitation was used for sample preparation.
  • A Phenomenex Kinetex C18 column and [2H]7-ONC206 as internal standard were utilized.

Main Results:

  • The assay demonstrated high accuracy (< ±9% deviation) and precision (<11% CV).
  • A wide calibration range (1-500 ng/mL) with excellent linearity (r² > 0.99732) was achieved.
  • ONC206 showed stability in human plasma under various conditions.

Conclusions:

  • A fully validated uHPLC-MS/MS method enables sensitive and specific ONC206 quantification in human plasma.
  • The method is suitable for pharmacokinetic analysis in clinical trials.
  • This bioanalytical tool supports the ongoing clinical development of ONC206.

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