drugset / Trial / NCT07803783

A Study to Compare the Efficacy and Safety of YL201 With Standard Chemotherapy in Patients With Metastatic Pancreatic Cancer After Failure of Gemcitabine-Based Systemic Chemotherapy

NCT07803783 ↗

Phase 3 Not yet recruiting 320 enrolled MediLink Therapeutics (Suzhou) Co., Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and efficacy of an investigational B7-H3 antibody drug-conjugate administered as monotherapy, compared with standard of care (SOC) chemotherapy in metastatic pancreatic cancer patients who have failed prior Gemcitabine-based systemic therapy.

Timeline

Start
2026-10
Primary completion
2029-01
Completion
2029-05

Drugs

EvaluationDrugModalityDoseRoute
Comparator IRINOTECAN Small molecule — Intravenous
Comparator Leucovorin Small molecule — Intravenous
Subject YL201 Other / unclassified 2 mg/kg Intravenous
Comparator fluorouracil Small molecule — Intravenous