Partner Therapeutics is a private Massachusetts company that owns sargramostim (Leukine), the recombinant GM-CSF used after chemotherapy and transplant and, since 2020, in high-risk neuroblastoma with dinutuximab.
Partner Therapeutics, based in Lexington, Massachusetts, acquired sargramostim (Leukine) from Sanofi in 2018. Leukine, a recombinant granulocyte-macrophage colony-stimulating factor first approved in 1991, is used to speed neutrophil recovery after induction chemotherapy for acute myeloid leukaemia and after stem cell transplant, to mobilise stem cells, and, following an FDA supplemental approval in 2020, as part of dinutuximab immunotherapy for high-risk paediatric neuroblastoma. The company also studied it in acute radiation syndrome and respiratory illness. It appears on OnCo as an FDA oncology applicant and a sponsor of cancer trials on ClinicalTrials.gov.
The antibody that raised cure rates in high-risk childhood neuroblastoma by about 20 points when given after transplant with immune boosters and retinoid.
Sargramostim is a lab-made version of GM-CSF, the signal that tells bone marrow to make white cells; approved in 1991, it shortens the dangerous low-count period after leukaemia chemotherapy and stem cell transplants.
Shares Sargramostim, Dinutuximab (ch14.18) / dinutuximab beta, Neuroblastoma (paediatric).
Shares Sargramostim, Dinutuximab (ch14.18) / dinutuximab beta, Neuroblastoma (paediatric).
Shares Sargramostim, Dinutuximab (ch14.18) / dinutuximab beta, Neuroblastoma (paediatric).
Shares Dinutuximab (ch14.18) / dinutuximab beta, Neuroblastoma (paediatric).
Shares Sargramostim, Acute myeloid leukaemia.
Shares Dinutuximab (ch14.18) / dinutuximab beta, Neuroblastoma (paediatric).
Shares Dinutuximab (ch14.18) / dinutuximab beta, Neuroblastoma (paediatric).
Shares Dinutuximab (ch14.18) / dinutuximab beta, Neuroblastoma (paediatric).