drugset / Trial / NCT05254743

A Study of Pirtobrutinib (LOXO-305) Versus Ibrutinib in Participants With Chronic Lymphocytic Leukemia (CLL)/Small Lymphocytic Lymphoma (SLL)

NCT05254743 ↗

Phase 3 Recruiting 737 enrolled Loxo Oncology, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of Part 1 of this study is to compare the efficacy and safety of pirtobruitinib (LOXO-305) to ibrutinib in participants with CLL/SLL; participants may or may not have already had treatment for their cancer. The purpose of Part 2 of this study evaluates pirtobrutinib monotherapy in treatment-naïve participants with CLL/SLL with 17p deletions. Participation could last up to six years for Part 1. Participation could last up to 2 years for Part 2.

Timeline

Start
2022-07-22
Primary completion
2027-10
Completion
2028-01

Outcome

Met primary endpoint

paper The study met its primary end points, demonstrating statistically significant noninferiority (NI) of IRC-ORR for pirtobrutinib versus ibrutinib PMID 41353787 ↗

paper two-sided P < .0001 PMID 41353787 ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ibrutinib Small molecule — Oral
Subject Pirtobrutinib Small molecule — Oral