drugset / Trial / NCT06187402

A Study of LM-24C5 For Advanced Solid Tumors

NCT06187402

Phase 1/2 Recruiting 49 enrolled LaNova Medicines Limited
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To assess the safety and tolerability, obtain the recommended phase 2 dose (RP2D)/optimal biologic dose (OBD) and/or Maximum Tolerated Dose (MTD) for LM-24C5 in subjects with advanced solid tumors.

Timeline

Start
2023-12-20
Primary completion
2026-06-30
Completion
2026-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject LM-24C5 Unknown Intravenous

Indications