Identification of Degradation Products of the New Anticancer Drug Substance ONC201 by Liquid Chromatography–High-Resolution Multistage Mass Spectrometry

Author:

Annereau Maxime12ORCID,Vignes Marina12,Bouchema Tahar Sif Eddine1,Denis Lucas2,Solgadi Audrey3ORCID,Vieillard Victoire4,Paul Muriel45,Rieutord André2ORCID,Grill Jacques67,Secretan Philippe-Henri1ORCID,Do Bernard14

Affiliation:

1. Matériaux et Santé, Université Paris-Saclay, 91400 Orsay, France

2. Clinical Pharmacy Department, Gustave Roussy Cancer Campus, 114 rue Edouard Vaillant, 94800 Villejuif, France

3. CNRS, Ingénierie et Plateformes au Service de l’Innovation Thérapeutique, Université Paris-Saclay, Inserm, 91400 Orsay, France

4. Department of Pharmacy, Henri Mondor Hospital, AP-HP, 94000 Créteil, France

5. EpidermE, Université Paris Est Creteil, 94010 Creteil, France

6. Molecular Predictors and New Targets in Oncology, INSERM, Gustave Roussy, Université Paris-Saclay, 94800 Villejuif, France

7. Département de Cancérologie de l’Enfant et de l’Adolescent, Gustave Roussy, Université Paris-Saclay, 94800 Villejuif, France

Abstract

ONC201 (dordaviprone) is a new drug substance used in a compassionate manner to treat patients with glioblastoma. Given the clinical context and the particularly promising preclinical results, we have been asked by the medical authorities to make a first treatment available throughout France as a hospital preparation to allow access to treatment and to conduct clinical trials. However, to control the quality and safety conditions inherent in this academic manufacturing process, while there is virtually no data available to date to understand the stability of ONC201, we had to determine the stability profile of ONC201, i.e., its sensitivity to different stressors and the types of impurities that could form during its degradation. We found that ONC201 was sensitive to oxidation in the presence of hydrogen peroxide or under light irradiation. Both conditions resulted in the formation of 20 degradation products detected and identified by liquid chromatography–high-resolution mass spectrometry. Their structural elucidation required an in-depth study of the fragmentation pattern of protonated ONC201, described for the first time. The product ions of the degradation products were compared to those of ONC201 protonated ion to assign the most plausible structures for all the detected degradation products. Of these degradation products, those that were rapidly produced, of high intensity and/or identified as potentially having a different toxicity profile to ONC201 by in silico studies, were selected to be monitored during batch release testing and stability studies.

Publisher

MDPI AG

Subject

Physical and Theoretical Chemistry,Analytical Chemistry

Reference35 articles.

1. (2023, March 01). Clinicaltrials.gov. Chimerix Oral ONC201 in Recurrent Glioblastoma, H3 K27M-Mutant Glioma, and Diffuse Midline Glioma, Available online: https://clinicaltrials.gov/ct2/show/NCT02525692.

2. (2023, March 01). Clinicaltrials.gov. Chimerix ONC201 for the Treatment of Newly Diagnosed H3 K27M-Mutant Diffuse Glioma Following Completion of Radiotherapy: A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study, Available online: https://clinicaltrials.gov/ct2/show/NCT05580562.

3. (2023, March 01). Clinicaltrials.gov. Winer, I. Phase II Study of ONC201 Plus Weekly Paclitaxel in Patients with Platinum-Resistant Refractory or Recurrent Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer, Available online: https://clinicaltrials.gov/ct2/show/NCT04055649.

4. (2023, March 01). Clinicaltrials.gov. National Cancer Institute (NCI) Phase 1 Trial of ONC201 for Chemoprevention of Colorectal Cancer, Available online: https://clinicaltrials.gov/ct2/show/NCT05630794.

5. Mechanisms of imipridones in targeting mitochondrial metabolism in cancer cells;Bonner;Neuro. Oncol.,2021

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