drugset / Trial / NCT01808573

A Study of Neratinib Plus Capecitabine Versus Lapatinib Plus Capecitabine in Patients With HER2+ Metastatic Breast Cancer Who Have Received Two or More Prior HER2 Directed Regimens in the Metastatic Setting

NCT01808573 ↗

Phase 3 Completed 621 enrolled Puma Biotechnology, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a randomized, multi-center, multinational, open-label, active-controlled, parallel design study of the combination of neratinib plus capecitabine versus the combination of lapatinib plus capecitabine in HER2+ MBC patients who have received two or more prior HER2 directed regimens in the metastatic setting.

Timeline

Start
2013-03-29
Primary completion
2018-09-28
Completion
2019-12-09

Outcome

Sources disagree · no verdict is set; each source's reading is shown below

paper Centrally reviewed PFS was improved with N+C (hazard ratio [HR], 0.76; 95% CI, 0.63 to 0.93; stratified log-rank P = .0059). reads as mixed primary results PMID 32678716 ↗

paper The OS HR was 0.88 (95% CI, 0.72 to 1.07; P = .2098). reads as mixed primary results PMID 32678716 ↗

release “The NALA study met its primary endpoint, with the neratinib arm having significantly improved PFS vs. the lapatinib arm” reads as met primary endpoint pumabiotechnology.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule 750 mg/m2 Oral
Subject Capecitabine Small molecule 1000 mg/m2 Oral
Comparator Lapatinib Small molecule 1250 mg Oral
Subject Neratinib Small molecule 240 mg Oral