drugset / Trial / NCT06162351

A Study to Evaluate the Efficacy and Toxicities of PLX038, in Patients With Locally Advanced or Metastatic Triple-negative Breast Cancer

NCT06162351

Phase 2 Terminated 14 enrolled Institut Curie ProLynx LLC · collab
NaSingle-groupOpen-labelTreatment

Summary

Single arm phase II study for with primary objective to evaluate the efficacy of PLX038 on response rate for patients with pretreated, metastatic or locally advanced triple negative breast cancer.

Timeline

Start
2024-04-17
Primary completion
2025-05-15
Completion
2025-05-15

Drugs

EvaluationDrugModalityDoseRoute
Subject DFP-13318 Other / unclassified 1730 mg/m2 Intravenous

Indications