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Brief Title: A Phase 1, Open Label Study of Intravenous GSK3745417 to Evaluate Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Determine RP2D & Schedule in Participants With Relapsed or Refractory Myeloid Malignancies Including AML and HR MDS
Official Title: A Phase 1, Open Label Study of Intravenous GSK3745417 to Evaluate Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Determine RP2D and Schedule in Participants With Relapsed or Refractory Myeloid Malignancies Including Acute Myeloid Leukemia (AML) and High-risk Myelodysplastic Syndrome (HR-MDS)
Study ID: NCT05424380
Brief Summary: This is a Phase 1, open label, two-part study to determine recommended phase 2 dose (RP2D) and schedule of GSK3745417 administration in participants with relapsed/refractory AML or HR-MDS.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
GSK Investigational Site, Toronto, Ontario, Canada
GSK Investigational Site, Halle, Sachsen-Anhalt, Germany
GSK Investigational Site, Dresden, Sachsen, Germany
GSK Investigational Site, Leipzig, Sachsen, Germany
GSK Investigational Site, Meldola, , Italy
GSK Investigational Site, Perugia, , Italy
GSK Investigational Site, Roma, , Italy
GSK Investigational Site, Rotterdam, , Netherlands
GSK Investigational Site, Madrid, , Spain
GSK Investigational Site, Madrid, , Spain
GSK Investigational Site, Valencia, , Spain