drugset / Trial / NCT06359002

Safety, Pharmacokinetics, and Preliminary Efficacy of BYON4413 in Acute Myeloid Leukemia and Myelodysplastic Neoplasms.

NCT06359002 ↗

Phase 1 Active not recruiting 16 enrolled Byondis B.V.
NaSequentialOpen-labelTreatment

Summary

This is the first-in-human trial with BYON4413 to evaluate safety, PK, immunogenicity, and anti-leukemia activity of BYON4413 in patients with AML or MDS.

Timeline

Start
2024-06-25
Primary completion
2025-09-30
Completion
2026-02

Drugs

EvaluationDrugModalityDoseRoute
Subject BYON4413 Unknown — Intravenous