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非在研适应症- |
最高研发阶段临床1/2期 |
首次获批国家/地区- |
首次获批日期- |
A Phase 1/2, Dose-Escalation and Cohort-Expansion Study to Evaluate the Safety, Tolerability, Immunogenicity, Pharmacokinetics, and Efficacy of LAT010 in Patients with Advanced Solid Tumors (LIGHTSPEED-1)
This is an open-label, multicenter, Phase 1/2, first-in-human (FIH), dose-escalation and cohort-expansion study of LAT010 to evaluate the safety, tolerability, immunogenicity, PK, PD, and antitumor activity in patients with advanced solid tumors. The study consists of 2 parts: Phase 1 dose-escalation and Phase 2 cohort expansion.
100 项与 Latticon Antibody Therapeutics, Inc 相关的临床结果
0 项与 Latticon Antibody Therapeutics, Inc 相关的专利(医药)
100 项与 Latticon Antibody Therapeutics, Inc 相关的药物交易
100 项与 Latticon Antibody Therapeutics, Inc 相关的转化医学