A Post-authorization Safety Study to Evaluate the Incidence of and Risk Factors for Severe and Fatal Infusion-related Reactions in Participants Treated with Daratumumab (Intravenous or Subcutaneous) (HALO)

22/11/2022
26/11/2025
EU PAS number:
EUPAS49827
Study
Ongoing
Documents
Study protocol
Study results
Study report
Other information