drugset / Trial / NCT04737122

Study of LM-061 in Subjects in Advanced Tumors

NCT04737122

Phase 1 Terminated 18 enrolled LaNova Medicines Limited
Non-randomizedSequentialOpen-labelTreatment

Summary

This is a phase I, open-label, dose escalation study to evaluate the safety, tolerability, PK, and preliminary efficacy of LM-061 in subjects with advanced tumors.

Timeline

Start
2021-05-06
Primary completion
2022-07-19
Completion
2022-12-01

Drugs

EvaluationDrugModalityDoseRoute
Subject LM-061 Unknown Oral
Subject Toripalimab Monoclonal antibody 240 mg Intravenous

Indications