drugset / Trial / NCT07387081

Phase II Study of LM-24C5

NCT07387081

Phase 2 Recruiting 130 enrolled LaNova Medicines Limited
Non-randomizedSequentialOpen-labelTreatment

Summary

This study is to evaluate the efficacy and safety of the LM-24C5 in combination with other therapies in subjects with CEACAM5-positive advanced solid tumor

Timeline

Start
2025-12-15
Primary completion
2028-05-21
Completion
2028-10-25

Drugs

EvaluationDrugModalityDoseRoute
Subject LM-24C5 Unknown Intravenous
Background Bevacizumab Monoclonal antibody Intravenous
Background Docetaxel Small molecule Intravenous
Background Penpulimab Monoclonal antibody Intravenous
Background Tipiracil Small molecule Oral
Background Trifluridine Small molecule Oral

Indications

No indication recorded.