Opinion/decision on a Paediatric investigation plan (PIP): Ibrexafungerp citrate, decision type: , therapeutic area: , PIP number: P/0370/2022

Opinion/decision on a Paediatric investigation plan (PIP): Ibrexafungerp citrate, decision type: , therapeutic area: , PIP number: P/0370/2022

Opinion/decision on a Paediatric investigation plan (PIP): Aspaveli,Pegcetacoplan, decision type: , therapeutic area: , PIP number: P/0403/2022

Opinion/decision on a Paediatric investigation plan (PIP): Aspaveli,Pegcetacoplan, decision type: , therapeutic area: , PIP number: P/0403/2022

Human medicines European public assessment report (EPAR): Hepcludex, bulevirtide, Hepatitis D, Chronic, Date of authorisation: 31/07/2020, Revision: 11, Status: Authorised

Human medicines European public assessment report (EPAR): Hepcludex, bulevirtide, Hepatitis D, Chronic, Date of authorisation: 31/07/2020, Revision: 11, Status: Authorised

Opinion/decision on a Paediatric investigation plan (PIP): Monovalent, recombinant, replication-incompetent human adenovirus serotype 26-vectored vaccine encoding the pre-fusion conformation-stabilised F protein derived from the RSV A2 strain, decision t

Opinion/decision on a Paediatric investigation plan (PIP): Monovalent, recombinant, replication-incompetent human adenovirus serotype 26-vectored vaccine encoding the pre-fusion conformation-stabilised F protein derived from the RSV A2 strain, decision type: , therapeutic area: , PIP number: P/0442/2022

Human medicines European public assessment report (EPAR): Imatinib Teva, imatinib, Leukemia, Myelogenous, Chronic, BCR-ABL Positive;Precursor Cell Lymphoblastic Leukemia-Lymphoma;Myelodysplastic-Myeloproliferative Diseases;Hypereosinophilic Syndrome;Derm

Human medicines European public assessment report (EPAR): Imatinib Teva, imatinib, Leukemia, Myelogenous, Chronic, BCR-ABL Positive;Precursor Cell Lymphoblastic Leukemia-Lymphoma;Myelodysplastic-Myeloproliferative Diseases;Hypereosinophilic Syndrome;Dermatofibrosarcoma, Date of authorisation: 07/01/2013, Revision: 19, Status: Authorised

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