drugset / Trial / NCT03260491

U3-1402 in Metastatic or Unresectable Non-Small Cell Lung Cancer

NCT03260491

Phase 1 Active not recruiting 312 enrolled Daiichi Sankyo Merck Sharp & Dohme LLC · collab
Non-randomizedSequentialOpen-labelTreatment

Summary

This study was designed to evaluate safety and antitumor activity of HER3-DXd in two parts: Dose Escalation and Dose Expansion. In Dose Escalation, HER3-DXd was evaluated in participants with metastatic or unresectable NSCLC with epidermal growth factor receptor (EGFR) activating mutation after disease progression during/after EGFR tyrosine kinase inhibitor (TKI) therapy. In Dose Expansion, HER3-DXd will be evaluated in participants with metastatic or unresectable NSCLC with EGFR activating mutation or squamous or non-squamous NSCLC (ie, without EGFR-activating mutations) with disease progression during/after systemic treatment for locally advanced or metastatic disease. In addition, HER3-DXd will be evaluated in participants with locally advanced or metastatic NSCLC whose tumors harbor a KRAS-G12C mutation after progression on the most recent line of therapy (Cohort 5).

Timeline

Start
2017-10-30
Primary completion
2026-03-31
Completion
2026-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Patritumab deruxtecan Monoclonal antibody 3.2 mg/kg Intravenous
Subject Patritumab deruxtecan Monoclonal antibody 4.8 mg/kg Intravenous
Subject Patritumab deruxtecan Monoclonal antibody 5.6 mg/kg Intravenous
Subject Patritumab deruxtecan Monoclonal antibody 6.4 mg/kg Intravenous