|
|
|
|
|
|
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 1/2a Open-Label, Dose-Escalation/Dose-Expansion Safety, Tolerability and Pharmacokinetic Study of IMX-110 in Patients With Advanced Solid Tumors
Phase 1 is an open-label, multi-center dose escalation/dose expansion study designed to assess the safety, tolerability and pharmacokinetics (PK) for the recommended phase 2 dose (RP2D) of IMX-110. The RP2D will be evaluated in a further dose expansion Phase 2a study submitted.
100 项与 Immix Biopharma Australia Pty Ltd 相关的临床结果
0 项与 Immix Biopharma Australia Pty Ltd 相关的专利(医药)
100 项与 Immix Biopharma Australia Pty Ltd 相关的药物交易
100 项与 Immix Biopharma Australia Pty Ltd 相关的转化医学