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AstraZeneca (AZN) Announces Voydeya Approval in EU as add-on to ravulizumab or eculizumab

AstraZeneca (AZN) Announces Voydeya Approval in EU as add-on to ravulizumab or eculizumab
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United States , Marc Dunoyer , Hubert Schrezenmeier , Committee For Medicinal Products Human , University Of Ulm , Drug Administration , European Medicines Agency , European Union , European Commission , Institute Of Transfusion Medicine , Medicinal Products , Human Use , Lancet Haematology , Medical Director , Transfusion Medicine , Chief Executive Officer , Functional Assessment , Chronic Illness Therapy , Breakthrough Therapy , Orphan Drug Designation ,

AstraZeneca's Voydeya receives CHMP recommendation for rare blood disease PNH

AstraZeneca's Voydeya receives CHMP recommendation for rare blood disease PNH
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Hubert Schrezenmeier , Marc Dunoyer , Institute Of Transfusion Medicine , Committee For Medicinal Products Human Use , University Of Ulm , European Medicines Agency , Medicinal Products , Human Use , Transfusion Medicine ,

Attending Physician (m/f/d) job with University of Mainz

Attending Physician (m/f/d) job in Mainz, Rheinland-Pfalz (DE) with University of Mainz. Apply Today. ....

Johannes Gutenberg Universit , Transfusion Centre , Institute Of Transfusion Medicine , Transfusion Medicine ,

Rallybio Corporation (RLYB) Announces Preliminary Multiple Dose Data from the Completed Phase 1 Safety and Pharmacokinetics Study for RLYB212

Rallybio Corporation (RLYB) Announces Preliminary Multiple Dose Data from the Completed Phase 1 Safety and Pharmacokinetics Study for RLYB212
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Fraunhofer Institute For Translational Medicine , Clinical Research Department , Rallybio Corporation Nasdaq , Institute Of Transfusion Medicine , Package Complete , Including Maternal Fetal Toxicology , Key Activity , Support Phase , Expected To Commence , Fraunhofer Institute , Translational Medicine , German Red Cross , Clinical Research , Transfusion Medicine , Deutsches Rotes Kreuz , Blood Transfusion Service Baden W ,

Rallybio Announces Preliminary Multiple Dose Data from the Completed Phase 1 Safety and Pharmacokinetics Study for RLYB212, an Anti-HPA-1a Monoclonal Antibody for the Prevention of Fetal and Neonatal Alloimmune Thrombocytopenia

Preliminary Data Support RLYB212 Once Monthly Subcutaneous Dosing in Phase 2 Study

RLYB212 Toxicology Package Complete, Including Maternal-Fetal Toxicology; Key Activity to Support Phase 2. ....

New Haven , United States , Alloimmune Thrombocytopenia , Institute Of Transfusion Medicine , Fraunhofer Institute For Translational Medicine , Rallybio Corporation Nasdaq , Clinical Research Department , Exchange Commission , Rallybio Corporation , Fraunhofer Institute , Translational Medicine , German Red Cross , Clinical Research , Transfusion Medicine , Deutsches Rotes Kreuz , Blood Transfusion Service Baden W , Neonatal Alloimmune Thrombocytopenia , Technology Incubation Program , Quarterly Report ,