drugset / Trial / NCT03419403

UNITE Study: Understanding New Interventions With GBM ThErapy

NCT03419403 ↗

Phase 3 Terminated 40 enrolled AbbVie
RandomizedParallel-groupOpen-labelTreatment

Summary

The objective of this study was to evaluate the effect of several ophthalmologic prophylactic treatment strategies for the management of ocular side effects (OSEs) in participants with epidermal growth factor receptor (EGFR)-amplified glioblastoma (GBM) who were being treated with depatuxizumab mafodotin (ABT-414).

Timeline

Start
2018-07-30
Primary completion
2019-09-05
Completion
2020-03-03

Outcome

Outcome not reported

Stopped: “The study was terminated because clinical development of depatuxizumab mafodotin in glioblastoma was stopped due to lack of survival benefit.”

Drugs

EvaluationDrugModalityDoseRoute
Background Depatuxizumab mafodotin Other / unclassified 1.25 mg/kg Intravenous
Background Temozolomide Small molecule — —

Indications