Sacituzumab Tirumotecan in Combination With Furmonertinib as Second-line Treatment for EGFR-mutant Advanced or Metastatic NSCLC After Failure of First-line Third-generation EGFR-TKI Therapy

PHASE2Not yet recruitingINTERVENTIONAL
Enrollment

45

Participants

Timeline

Start Date

November 1, 2025

Primary Completion Date

July 1, 2026

Study Completion Date

May 30, 2027

Conditions
NSCLC (Non-small Cell Lung Cancer)
Interventions
DRUG

Sacituzumab Tirumotecan

fixed dosage 4mg/kg iv, D1, D15, each 4 weeks one cycle. Drug reduction will be implemented according to the research plan.

DRUG

Furmonertinib

160mg QD or 80mg QD, each 4 weeks one cycle, according to the safety run-in phase, until confirmed by the investigator as imaging disease progression, intolerable toxicity, subject's request to terrminate treatment, or other treatment termination criteria specified in the protocol. Drug reduction will be implemented according to the research plan.

All Listed Sponsors
lead

Fudan University

OTHER