EMA Validates Bristol Myers Squibb's Applications for Opdivo + Yervoy and Opdivo + Chemotherapy as First-Line Treatments for Unresectable Advanced, Recurrent or Metastatic Esophageal Squamous Cell Carcinoma
Applications based on positive results from the Phase 3 CheckMate -648 trial, in which both Opdivo -based combinations demonstrated a significant survival benefit over chemotherapy alone Bristol Myers Squibb today announced that the European Medicines Agency has validated its Type II Variation Marketing Authorization Applications for both Opdivo in combination with Yervoy and Opdivo in combination with ...