Hansa Biopharma announces first patient treated in the post-authorization efficacy study (PAES) of Idefirix® (imlifidase) in highly sensitized kidney transplant patients
· The PAES is an open-label Phase 3 study to further investigate the long-term graft survival in 50 highly sensitized patients who have undergone kidney transplantation after Idefirix® administration in the EU1 · The PAES is an obligation under the conditional marketing authorization for Idefirix® granted by the European Medicines Agency (EMA) in August 20202 · The study will provide further important insights to the Idefirix® desensitization treatment of highly sensitized kidney transplant patients Lund, Sweden, July 11, 2022. Hansa Biopharma AB, “Hansa” (Nasdaq Stockholm: HNSA),