Expansion and Partnership Initiatives
Y-mAbs received a patent extension for DANYELZA, expiring in 2034, and entered into an exclusive license agreement with Noble Pharma for DANYELZA development and commercialization in Japan, with an upfront payment of $2 million and potential milestones of up to $31 million.
Clinical Progress in SADA Programs
Phase I trials for GD2-SADA and CD38-SADA are progressing well, with no dose-limiting toxicities reported. The GD2-SADA trial expanded to include adult neuroblastoma patients, demonstrating proof of concept.
Increased Physician Adoption
DANYELZA saw a 5% increase in demand and added 3 new U.S. accounts in the third quarter, indicating growing physician adoption and patient access.
Ex-U.S. Market Expansion
DANYELZA sales were recorded in Turkey for the first time, and sales continued in Brazil and Mexico, indicating progress in ex-U.S. market penetration.