drugset / Trial / NCT03386513

Study of IMGN632 in Patients With Untreated BPDCN and Relapsed/Refractory BPDCN

NCT03386513

Phase 1/2 Active not recruiting 179 enrolled AbbVie
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label, multi-center, Phase 1/2 study to determine the MTD and assess the safety, tolerability, PK, immunogenicity, and anti-leukemia activity of IMGN632 when administered as monotherapy to patients with CD123+ disease.

Timeline

Start
2018-01-02
Primary completion
2023-09-06
Completion
2026-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Pivekimab Sunirine Unknown 0.015 mg/kg Intravenous
Subject Pivekimab Sunirine Unknown 0.045 mg/kg Intravenous
Subject Pivekimab Sunirine Unknown 0.09 mg/kg Intravenous
Subject Pivekimab Sunirine Unknown 0.18 mg/kg Intravenous
Subject Pivekimab Sunirine Unknown 0.3 mg/kg Intravenous
Subject Pivekimab Sunirine Unknown 0.45 mg/kg Intravenous