Naxitamab: Side Effects, Uses & Monitoring
Facts extracted from current FDA product labeling for Naxitamab. Educational only — not medical advice.
Labeled uses
DANYELZA is indicated, in combination with granulocyte-macrophage colony-stimulating factor (GM-CSF), for the treatment of pediatric patients 1 year of age and older and adult patients with relapsed or refractory high-risk neuroblastoma in the bone or bone marrow who have demonstrated a partial response, minor response, or stable disease to prior therapy. This indication is approved under accelerated approval based on overall response rate and duration of response [see Clinical Studies (14) ] . Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s).
Medical disclaimer: Always consult a qualified healthcare professional about any medication.