drugset / Trial / NCT03505554

A Study of Oral Lorlatinib in Patients With Relapsed ALK Positive Lymphoma

NCT03505554

Phase 2 Completed 9 enrolled University of Milano Bicocca Pfizer · collab
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to define the objective response rates (ORR) of Lorlatinib in subjects with ALK+ lymphomas resistant or refractory to ALK inhibitors.

Timeline

Start
2019-09-28
Primary completion
2025-12-31
Completion
2025-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Lorlatinib Small molecule 100 mg Oral