drugset / Trial / NCT05829226

A Phase 1 Study With LYT-200 in Patients With Relapsed/Refractory Acute Myeloid Leukemia (AML), or With Relapsed/Refractory, High-risk Myelodysplastic Syndrome (MDS)

NCT05829226

Phase 1 Completed 101 enrolled PureTech
Non-randomizedSequentialOpen-labelTreatment

Summary

A Phase 1 Open-label, Multi-center Study of the Safety, Pharmacokinetics (PK), and Anti-tumor Activity of LYT- 200 in Patients with Relapsed/Refractory Acute Myeloid Leukemia (AML), or with Relapsed/refractory, High-risk Myelodysplastic Syndrome (MDS)

Timeline

Start
2022-12-12
Primary completion
2025-12-31
Completion
2025-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject LYT-200 Monoclonal antibody Intravenous
Background Azacitidine Other / unclassified 75 mg/m2 Subcutaneous
Background Decitabine Small molecule 20 mg/m2 Intravenous
Background Venetoclax Small molecule 400 mg Oral