Phase I Clinical Trial of JNJ-67571244 in Patients with Relapsed or Refractory Acute Myeloid Leukemia or Myelodysplastic Syndrome


A Study of JNJ-67571244 in Participants With Relapsed or Refractory Acute Myeloid Leukemia (AML) or Myelodysplastic Syndrome (MDS)

Janssen Research & Development Identifier: NCT03915379

Janssen Research & DevelopmentInvestigators at Janssen Research & Development have opened a Phase I clinical trial to determine the recommended dose(s) (RP2D), schedule, maximum tolerated dose, safety and tolerability, and preliminary clinical activity of JNJ-67571244 (a bispecific antibody targeting CD33 and CD3) in adult patients with relapsed or refractory acute myeloid leukemia or myelodysplastic syndromes who are ineligible for or have exhausted standard therapeutic options.

One center, the Sarah Cannon Research Institute in Nashville, Tennessee, is currently recruiting participants. Other centers planned for the study in the United States and Spain are not yet recruiting.

See additional details, including study location(s), eligibility criteria, contact information, and study results (when available) at

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