drugset / Trial / NCT02573324

A Study of ABT-414 in Participants With Newly Diagnosed Glioblastoma (GBM) With Epidermal Growth Factor Receptor (EGFR) Amplification

NCT02573324 ↗

Phase 3 Completed 691 enrolled AbbVie Radiation Therapy Oncology Group · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

This study seeks to determine whether the addition of ABT-414 to concomitant radiotherapy and temozolomide (TMZ) followed by combination of ABT-414 with adjuvant TMZ prolongs overall survival (OS) among participants with newly diagnosed glioblastoma (GBM) with epidermal growth factor receptor (EGFR) amplification. In addition, there is a Phase 1, open-label, multicenter sub-study to assess the pharmacokinetics, safety and tolerability of ABT-414 in participants with newly diagnosed EGFR-amplified GBM who have mild or moderate hepatic impairment.

Timeline

Start
2015-01-04
Primary completion
2022-04-04
Completion
2022-04-04

Outcome

Missed primary endpoint

registry analysis (superiority test); Placebo, Radiation and TMZ vs Depatuxizumab Mafodotin, Radiation and TMZ; p = 0.633 NCT02573324 ↗

release “the Phase 3 INTELLANCE-1 study did not meet its primary endpoint of overall survival at the interim analysis” abbvie.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Depatuxizumab mafodotin Other / unclassified — Intravenous
Background Temozolomide Small molecule — —

Indications