drugset / Trial / NCT02513394

Summary

This is a prospective, two arm, international, multicenter, randomized, open-label Phase III study evaluating the addition of 2 years of palbociclib to standard adjuvant endocrine therapy for patients with HR+ / HER2- early breast cancer (EBC). The purpose of the PALLAS study is to determine whether the addition of palbociclib to adjuvant endocrine therapy will improve outcomes over endocrine therapy alone for HR+/HER2- early breast cancer. Assessment of a variety of correlative analysis, including evaluation of the effect of palbociclib in genomically defined tumor subgroups, is planned.

Timeline

Start
2015-08
Primary completion
2020-11
Completion
2028-12

Outcome

Missed primary endpoint

registry analysis (other test); Palbociclib Plus Endocrine Therapy (Arm A) vs Endocrine Therapy Alone (Arm B); p = 0.65; Hazard Ratio (HR) 0.96 NCT02513394 ↗

paper At this final analysis of the PALLAS trial, the addition of adjuvant palbociclib to standard endocrine therapy did not improve outcomes over endocrine therapy alone PMID 34874182 ↗

release “PALLAS determined that the trial is unlikely to show a statistically significant improvement in the primary endpoint” pfizer.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Palbociclib Small molecule 125 mg Oral

Indications