
ENHERTU® Variation Application Accepted in EU for Post-Neoadjuvant Use in Early HER2-Positive Breast Cancer
ENHERTU® Type II Variation Application Validated in the EU as Post-Neoadjuvant Treatment for Patients with HER2 Positive Early Breast Cancer The European Medicines Agency (EMA) has validated the Type II Variation marketing authorization application for ENHERTU® (trastuzumab deruxtecan) as a monotherapy for…












