Taiwan-based Formosa Pharmaceuticals Inc (TPE:6838) announced on Thursday that it has signed an exclusive licensing agreement with DÁVI Farmacêutica in Portugal.
The agreement covers exclusive rights to the commercialisation of clobetasol propionate ophthalmic suspension, 0.05% (APP13007), a marketed innovative medicine for the treatment of inflammation and pain following ocular surgery.
Approved by the US Food and Drug Administration (FDA) in March 2024, the product was launched in the United States in September 2024.
The DÁVI licensing agreement includes an upfront payment, commercialisation and sales milestones, and additional considerations throughout the term of the contract.
Erick Co, Formosa Pharmaceuticals' president and CEO, said: "This partnership with DÁVI Farmacêutica marks our first entry into a competitive EU market, opening the door for growth into other EU territories. DÁVI's experience and commitment to novel ophthalmic therapies is steadily apparent and Formosa Pharma appreciates their recognition of APP13007 as a worthy offering to patients recovering from ocular surgery."
Cereno Scientific's Phase IIb trial of CS1 in PAH approved by US FDA
ALR Technologies announces GluCurve Pet CGM relaunch in Canada
Mirum Pharmaceuticals to acquire Bluejay Therapeutics for HDV treatment
PureTech clears key FDA milestone for Phase 3 development of deupirfenidone
J & D Pharmaceuticals' investigational therapy for HCC receives US FDA Orphan Drug Designation
FDA lifts partial clinical hold on Vanda Pharmaceuticals' tradipitant for motion sickness
TransThera publishes clinical results from US-based Phase 2 trial of tinengotinib in CCA
Hope Medicine wins FDA Fast Track Designation for HMI-115 in endometriosis
MED-EL cochlear implant FDA approved for children 7 months and older