drugset / Trial / NCT03000257

A Study of Budigalimab (ABBV-181) in Participants With Advanced Solid Tumors

NCT03000257

Phase 1 Completed 182 enrolled AbbVie
Non-randomizedSequentialOpen-labelTreatment

Summary

This is an open-label, Phase I, dose-escalation study to determine the recommended Phase 2 dose (RPTD), maximum tolerated dose (MTD), and evaluate the safety and pharmacokinetic (PK) profile of budigalimab. This study will also evaluate the safety and tolerability of budigalimab in combination with Rovalpituzumab Tesirine and budigalimab in combination with venetoclax. The study will consist of 3 parts: budigalimab monotherapy dose escalation and expansion, budigalimab in combination with Rovalpituzumab Tesirine and budigalimab in combination with venetoclax.

Timeline

Start
2016-12-14
Primary completion
2022-03-29
Completion
2022-03-29

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Budigalimab Monoclonal antibody 1 mg/kg Intravenous
Subject Budigalimab Monoclonal antibody 3 mg/kg Intravenous
Subject Budigalimab Monoclonal antibody 10 mg/kg Intravenous
Subject Budigalimab Monoclonal antibody 250 mg Intravenous
Subject Budigalimab Monoclonal antibody 500 mg Intravenous
Subject Rovalpituzumab tesirine Other / unclassified 0.3 mg/kg Intravenous
Subject Venetoclax Small molecule Oral

Indications