RecruitingPhase 1Phase 2NCT06650566

Study of LM-299 in Subjects Advanced Malignant Tumors

A Phase I/II, Open-label, Dose Escalation and Dose Expansion Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of LM-299 Injection as Monotherapy or in Combination With Other Anti-tumor Therapies in Patients With Advanced Solid Tumors


Sponsor

LaNova Medicines Limited

Enrollment

108 participants

Start Date

Oct 9, 2024

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called LM-299 for people with malignant tumors. The study is currently recruiting participants at 6 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGLM-299

Q2W/Q3W,Intravenous Drip


Locations(6)

One Clinical Research

Perth, Western Australia, Australia

the first affiliated hospital of Xinxiang medical University

Xinxiang, Henan, China

Liaocheng people's hospital

Liaocheng, Shandong, China

Zibo municipal hospital

Zibo, Shandong, China

Shanghai Dongfang Hospital (Tongji University Affiliated Dongfang Hospital)

Shanghai, Shanghai Municipality, China

Shanghai GoBroad Cancer Hospital China Pharmaceutical University

Shanghai, Shanghai Municipality, China

View Full Details on ClinicalTrials.gov

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NCT06650566


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