Références Scientifiques

Consultez la littérature scientifique qui soutient nos cibles moléculaires et notre approche létale synthétique.

juin 2024

Phase I study of the PKMYT1 inhibitor lunresertib (lunre) in combination with FOLFIRI in advanced gastrointestinal (GI) cancers (MINOTAUR study)

juin 2024

Characterizing intra-tumoral heterogeneity of CCNE1 amplification in ovarian cancer using digital pathology

mai 2024

Identification and Biosynthesis of an N-Glucuronide Metabolite of Camonsertib

mai 2024

ATR inhibitor, camonsertib, dose optimization in patients with biomarker-selected advanced solid tumors (TRESR study)

avril 2024

Loss of the DNA Repair Gene RNase H2 Identifies a Unique Subset of DDR-Deficient Leiomyosarcomas

avril 2024

Post-therapy emergence of an NBN reversion mutation in a patient with pancreatic acinar cell carcinoma

janvier 2024

Detection and characterization of DDR reversion alterations in baseline tissue and plasma samples from patients enrolled in the TRESR and ATTACC Phase I clinical trials

octobre 2023

KRAS alterations combined with TP53 mutations as novel synthetic lethal genomic lesions for PKMYT1 inhibition

Notre pipeline comprend plusieurs programmes de développement.