drugset / Trial / NCT02646852

A Phase I Study of PLX038 in Patients With Advanced Solid Tumors

NCT02646852

Phase 1 Completed 40 enrolled ProLynx LLC
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This is a Phase I, open-label, two-arm, dose escalation study of PLX038 intravenous infusion administered to patients with refractory or relapsed solid tumors. This study will explore two different dosing schedules: Arm 1, once every 3 week (q3w), and Arm 2, once weekly for 2 consecutive weeks of a 4-week cycle.

Timeline

Start
2016-03
Primary completion
2023-02
Completion
2023-07

Drugs

EvaluationDrugModalityDoseRoute
Subject DFP-13318 Other / unclassified Intravenous

Indications