EV20/Omomyc: A novel dual MYC/HER3 targeting immunoconjugate.
Sandra BibbòEmily CaponeGiulio LovatoSara PonzianiAlessia LamolinaraManuela IezziRossano LattanzioKatia MazzoccoMartina MoriniFrancesco GiansantiVincenzo De LaurenziJonathan WhitfieldStefano IacobelliRodolfo IppolitiMarie-Eve BeaulieuLaura SoucekArturo SalaGianluca SalaPublished in: Journal of controlled release : official journal of the Controlled Release Society (2024)
MYC is one of the most important therapeutic targets in human cancer. Many attempts have been made to develop small molecules that could be used to curb its activity in patients, but most failed to identify a suitable direct inhibitor. After years of preclinical characterization, a tissue-penetrating peptide MYC inhibitor, called Omomyc, has been recently successfully used in a Phase I dose escalation study in late-stage, all-comers solid tumour patients. The study showed drug safety and positive signs of clinical activity, prompting the beginning of a new Phase Ib combination study currently ongoing in metastatic pancreatic adenocarcinoma patients. In this manuscript, we have explored the possibility to improve Omomyc targeting to specific cancer subtypes by linking it to a therapeutic antibody. The new immunoconjugate, called EV20/Omomyc, was developed by linking a humanised anti-HER3 antibody, named EV20, to Omomyc using a bifunctional linker. EV20/Omomyc shows antigen-dependent penetrating activity and therapeutic efficacy in a metastatic model of neuroblastoma. This study suggests that directing Omomyc into specific cell types using antibodies recognising tumour antigens could improve its therapeutic activity in specific indications, like in the paediatric setting.
Keyphrases
- end stage renal disease
- ejection fraction
- newly diagnosed
- small cell lung cancer
- chronic kidney disease
- squamous cell carcinoma
- clinical trial
- randomized controlled trial
- emergency department
- peritoneal dialysis
- prognostic factors
- stem cells
- immune response
- endothelial cells
- single cell
- papillary thyroid
- drug delivery
- patient reported outcomes
- induced pluripotent stem cells