The US Food and Drug Administration (FDA) has granted ATIR101™, Kiadis Pharma’s lead investigational product for blood cancers, the Regenerative Medicine Advanced Therapy (RMAT) designation.
Kiadis Pharma is focused on two therapeutic indications: leukemia and thalassemia. Its products address the key risks and limitations of hematopoietic stem cell transplantation, including opportunistic infections, Graft-versus-Host-Disease, cancer relapse and limited donor availability.
ATIR consists of donor lymphocytes specifically manufactured for individual patients where those T-cells from the haploidentical stem cell donor that can attack the patient are eliminated but the other donor immune cells are retained.
ATIR solves the problem of not finding a matched donor in time.
Kiadis Pharma is a clinical stage biopharmaceutical company focused on research, development and future commercialisation of cell-based immunotherapy products for the treatment of blood cancers and inherited blood disorders.
29, June, 2018,
Maarssen, The Netherlands
After the successful 2017 edition, Holland […]
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