• OBI Pharma announced FDA clearance of its IND application for OBI-902, a novel TROP2-targeting antibody-drug conjugate utilizing their proprietary GlycOBI® technology platform, with patient enrollment for Phase 1/2 trials expected in the second half of 2025.
• Preclinical data presented at AACR 2025 demonstrated OBI-902's superior antitumor activity, favorable pharmacokinetics, and enhanced stability compared to benchmark TROP2 ADCs across various animal models, positioning it as a potential best-in-class therapy.
• The GlycOBI® platform represents a breakthrough in ADC development with its site-specific glycan technology enabling versatile drug-antibody ratios up to 16 and dual payload conjugations, while the complementary ThiOBI® platform offers improved stability through irreversible cysteine conjugation.