Frontier Medicines Corporation, a clinical-stage precision medicines company, announced on Wednesday that it has entered into an exclusive licensing agreement with South Korean chemical company LG Chem Ltd (KRX:051910) for FMC-220, granting LG Chem worldwide rights outside Greater China while Frontier retains full ownership in Greater China.
FMC-220 is Frontier's first-in-class covalent p53 Y220C activator targeting solid tumours with TP53 loss-of-function mutations.
Under the agreement, LG Chem will lead regulatory filings, clinical development, manufacturing, and commercialisation in its territories, while Frontier retains an option to participate in co-development for enhanced financial returns. Frontier will receive an upfront payment and is eligible for development, regulatory, commercial, and sales milestone payments, along with royalties on net product sales.
Preclinical data presented at the American Association for Cancer Research Annual Meeting 2025 demonstrated FMC-220's potency, selective target engagement, and durable anti-tumour activity at low doses across multiple tumour models. The therapy targets the TP53 Y220C mutation, present in approximately 1-3% of cancers, including lung, breast, ovarian, and colorectal tumours.
FMC-220 was developed using Frontier's platform integrating chemoproteomics and artificial intelligence and represents the company's second first-in-class programme following FMC-376, a dual ON/OFF KRASG12C inhibitor currently in clinical development.
Mary's Medicinals to participate in CMS trial programme with cannabinoid-based wellness products
Lilly's Foundayo (orforglipron) weight loss pill gains US FDA approval
Thermo Fisher Scientific unveils CHOvantage GS Kit to speed biologics development
Frontier Medicines licenses FMC-220 oncology programme to LG Chem in global deal
Natera study shows Signatera MRD may help select breast cancer patients for non-surgical management
ALK secures EU approval for EURneffy 1 mg as needle-free adrenaline option for children
Delonix Bioworks launches Phase 1 trial of next-generation MenB OMV vaccine DX-104
Hengrui Pharma and Braveheart Bio report positive Phase 2 results for HRS/BHB-1893 in oHCM
Innovent and Ollin Biosciences report IBI324 study data in wAMD and DME
Boston Scientific receives FDA clearance for Asurys fluid management system
GSK's bepirovirsen accepted for review in China as potential Hepatitis B functional cure
4DMedical secures EU approval for CT:VQ as EUR83m funding fuels European expansion
Aurinia Pharmaceuticals agrees to acquire Kezar Life Sciences
GXO appointed to manage NHS England bowel cancer home testing kits