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.
Abstract:
ONC206 is an imipridone derivative that is being developed clinically as a single agent given orally in a first-in-human trial (NCT04541082). This ongoing clinical trial requires pharmacokinetic analysis of ONC206 to fully characterize its pharmacologic profile. There is currently no published bioanalytical method for ONC206 quantitation. To understand the clinical pharmacokinetics of ONC206, a sensitive yet simple uHPLC-MS/MS method for quantitation of ONC206 in human plasma was developed. Protein-precipitation allowed rapid and sensitive bioanalytical measurement of ONC206 in human plasma. A Phenomenex Kinetex C18 (50 ×2.1 mm, 1.3 µm, 100 Å) analytical column achieved symmetrical and sharp chromatography peaks of ONC206 and the internal standard, [2H]7-ONC206, which were detected using multiple reaction monitoring. The assay calibration range was 1-500 ng/mL and was best fit by a linear regression model (r2 > 0.99732 ± 0.0010). The method proved accurate (< ± 9% deviation), precise (<11%CV), selective and specific with no interference and low inter-lot matrix variability. ONC206 demonstrated excellent short-term, long-term, and multiple freeze-thaw cycle stability in solution and human plasma. This fully validated method was used to quantitate ONC206 plasma concentrations from patients enrolled in the aforementioned clinical trial at the NCI to demonstrate its clinical applicability.
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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