drugset / Trial / NCT05053659

Loncastuximab Tesirine and Venetoclax for Relapsed/ Refractory Non-Hodgkin Lymphoma

NCT05053659

Phase 1 Active not recruiting 23 enrolled Paolo Caimi, MD
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the correct dose and safety of combining two new cancer drugs, loncastuximab tesirine and venetoclax, as a treatment for relapsed or refractory B cell lymphoma.These drugs are used to treat some lymphomas, but have not yet been tested in combination for the treatment of lymphoma. The main goal of this study is to determine the safety of the combination.

Timeline

Start
2022-06-20
Primary completion
2026-11
Completion
2026-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Loncastuximab Tesirine Other / unclassified 50 ug/kg Intravenous
Subject Loncastuximab Tesirine Other / unclassified 150 ug/kg Intravenous
Subject Venetoclax Small molecule 400 mg Oral
Subject Venetoclax Small molecule 600 mg Oral
Subject Venetoclax Small molecule 800 mg Oral

Indications