drugset / Trial / NCT01449461

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Anti-Tumor Activity of the Oral Anaplastic Lymphoma Kinase (ALK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Brigatinib (AP26113)

NCT01449461

Phase 1/2 Completed 137 enrolled Ariad Pharmaceuticals
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is 2-fold: initially, in the dose escalation phase, the goal is to determine the safety profile of orally administered brigatinib, including: the maximum tolerated dose (MTD), dose limiting toxicities (DLTs), recommended phase 2 dose (RP2D), and pharmacokinetic (PK) profile. Then, once the RP2D is established, an expansion phase will assess the preliminary anti-tumor activity of brigatinib, both in non-small cell lung cancer (NSCLC) with ALK gene rearrangement (including participants with active brain metastases) or mutated EGFR, and in other cancers with abnormal targets against which brigatinib is active.

Timeline

Start
2011-09-20
Primary completion
2015-11-16
Completion
2020-02-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Brigatinib Small molecule 30 mg Oral
Subject Brigatinib Small molecule 60 mg Oral
Subject Brigatinib Small molecule 90 mg Oral
Subject Brigatinib Small molecule 120 mg Oral
Subject Brigatinib Small molecule 180 mg Oral
Subject Brigatinib Small molecule 240 mg Oral
Subject Brigatinib Small molecule 300 mg Oral