drugset / Trial / NCT02365662

A Study Evaluating Safety and Pharmacokinetics of ABBV-221 in Subjects With Advanced Solid Tumor Types Likely to Exhibit Elevated Levels of Epidermal Growth Factor Receptor

NCT02365662 ↗

Phase 1 Terminated 46 enrolled AbbVie
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label, Phase I, dose escalation study to determine the recommended Phase 2 dose, maximum tolerated dose, and evaluate the safety and pharmacokinetic profile of ABBV-221 in participants with advanced solid tumors likely to exhibit elevated levels of Epidermal Growth Factor Receptor (EGFR).

Timeline

Start
2015-01-09
Primary completion
2018-03-15
Completion
2018-03-15

Outcome

Outcome not reported

Stopped: “Safety”

Drugs

EvaluationDrugModalityDoseRoute
Subject LOSATUXIZUMAB VEDOTIN Unknown — Intravenous