At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Phase II,Open Label,Multicenter Study to Evaluate the Efficacy,Safety,and Tolerability of LM-168 Combined With Other Anti-tumor Therapies in Participants With Advanced Solid Tumor Trials
In Brief
A Phase 2 clinical trial evaluating LM-168, Tislelizumab, and 1 other intervention for Advanced Solid Tumor. Not yet recruiting, targeting 108 participants across 1 site.
Detailed Summary
For Safety introduction phase,this study is to evaluate the safety and tolerability of LM-168 in combination with other anti-tumor treatment regimens in participants of advanced solid tumor trials, determine the maximum tolerated dose (MTD), and explore the recommended phase II dose (RP2D). For Dose expansion phase,this study is to evaluate the preliminary antitumor activity of LM-168 in combination with other antitumor treatment regimens in participants of advanced solid tumor trials, measured by objective response rate (ORR)
Study Details
Timeline
Arms & Interventions
Interventions
Q3W,Intravenous Drip
Q3W,Intravenous Drip
Q3W,Intravenous Drip