drugset / Trial / NCT06650566

Study of LM-299 in Subjects Advanced Malignant Tumors

NCT06650566 ↗

Phase 1/2 Recruiting 108 enrolled LaNova Medicines Limited
Non-randomizedParallel-groupOpen-labelTreatment

Summary

For Phase I Dose Escalation Stage, to assess the safety and tolerability of LM-299 in patients with advanced solid tumors,determine the maximum tolerated dose (MTD) or optimal biological dose (OBD), and explorethe recommended dose for expansion (RDE) in patients with advanced solid tumours.. For Phase II Dose Expansion Stage, to assess the antitumor activity of LM-299 in patients with various advanced solid tumors.

Timeline

Start
2024-10-09
Primary completion
2026-12
Completion
2027-07

Drugs

EvaluationDrugModalityDoseRoute
Subject LM-299 Unknown — Intravenous

Indications