Drs Alison Schram and Elena Garralda share expert insights on the PYNNACLE Phase 2 initial analysis at AACR–NCI–EORTC 2025.
The PYNNACLE phase 2 study evaluates rezatapopt, a first-in-class p53 reactivator, as a treatment for TP53 Y220C–mutant advanced solid tumours.
In this video, the experts discuss:
• TP53 Y220C mutation and the rationale for mutant p53 reactivation
• Study overview and practice implications, spotlighting ovarian cancer
• Testing strategies for early and accurate patient identification
*Rezatapopt is an investigational agent which is not approved by a regulatory agency
Visit the COR2ED website to learn more and download the accompanying slides and poster for more information here: https://cor2ed.com/n-connect/programmes/update-from-aacr-nci-eortc-2025/
Clinical takeaways:
• Reactivating p53 Y220C protein is a promising therapeutic strategy for patients with solid tumours specifically ovarian cancer, with TP53 Y220C mutations, where effective targeted therapies and biomarkers are limited.
• Rezatapopt is a first-in-class investigational p53 reactivator that selectively binds to the mutated p53 Y220C protein, stabilising its structure to restore wild-type tumour suppressor activity.
• Rezatapopt demonstrates rapid, durable and broad antitumour activity in TP53 Y220C–mutant solid tumours, with a particularly strong signal in ovarian cancer, and a generally manageable safety profile.
• Looking ahead, it will be important to prioritise early and accurate identification through up-front comprehensive genomic profiling using NGS with TP53 gene coverage. Tissue is preferred; when tissue is limited, selected ctDNA assays capable of excluding CHIP may be used.
This programme has been sponsored by PMV Pharma
Published October 2025
The PYNNACLE phase 2 study evaluates rezatapopt, a first-in-class p53 reactivator, as a treatment for TP53 Y220C–mutant advanced solid tumours.
In this video, the experts discuss:
• TP53 Y220C mutation and the rationale for mutant p53 reactivation
• Study overview and practice implications, spotlighting ovarian cancer
• Testing strategies for early and accurate patient identification
*Rezatapopt is an investigational agent which is not approved by a regulatory agency
Visit the COR2ED website to learn more and download the accompanying slides and poster for more information here: https://cor2ed.com/n-connect/programmes/update-from-aacr-nci-eortc-2025/
Clinical takeaways:
• Reactivating p53 Y220C protein is a promising therapeutic strategy for patients with solid tumours specifically ovarian cancer, with TP53 Y220C mutations, where effective targeted therapies and biomarkers are limited.
• Rezatapopt is a first-in-class investigational p53 reactivator that selectively binds to the mutated p53 Y220C protein, stabilising its structure to restore wild-type tumour suppressor activity.
• Rezatapopt demonstrates rapid, durable and broad antitumour activity in TP53 Y220C–mutant solid tumours, with a particularly strong signal in ovarian cancer, and a generally manageable safety profile.
• Looking ahead, it will be important to prioritise early and accurate identification through up-front comprehensive genomic profiling using NGS with TP53 gene coverage. Tissue is preferred; when tissue is limited, selected ctDNA assays capable of excluding CHIP may be used.
This programme has been sponsored by PMV Pharma
Published October 2025
- Categoria
- Oncology
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