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PureTech Receives Orphan Drug Designation for LYT-200 in Acute Myeloid Leukemia

LYT-200 is being advanced in hematological malignancies such as acute myeloid leukemia and high-risk myelodysplastic syndrome , and locally advanced/metastatic solid tumors, including head and neck.

PureTech Health celebrates drug designation for LYT-200 from US FDA

PureTech Health PLC on Wednesday touted the efficacy of its acute myeloid leukaemia therapy, after securing a regulatory designation from the US Food & Drug Administration. According to the Boston,.

FDA Grants Orphan Drug Designation to LYT-200 in AML

Tibsovo Approved for IDH1-Mutated Relapsed/Refractory Myelodysplastic Syndromes

The FDA has approved Tibsovo (ivosidenib) for the treatment of adults with relapsed or refractory MDS with a susceptible IDH1 mutation.

FDA Approves Tibsovo for Patients with R/R Myelodysplastic Syndromes

The Food and Drug Administration approved Tibsovo for patients with relapsed or refractory myelodysplastic syndromes with a susceptible isocitrate dehydrogenase-1 mutation.

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