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Last update 23 Jan 2025
GPRC5D x Tubulin
Last update 23 Jan 2025
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Target |
Mechanism |
Active Org. |
Originator Org. |
Active Indication |
Inactive Indication |
Drug Highest Phase |
First Approval Ctry. / Loc. |
First Approval Date |
CTR20223084
LM-305在复发或难治性多发性骨髓瘤及其它浆细胞疾病患者中的安全性、耐受性、药代动力学特征以及初步疗效的开放标签、剂量递增和剂量扩展的I/II期临床研究
[Translation] An open-label, dose-escalation and dose-expansion Phase I/II clinical study to evaluate the safety, tolerability, pharmacokinetic characteristics and preliminary efficacy of LM-305 in patients with relapsed or refractory multiple myeloma and other plasma cell diseases
NCT05647512
A Phase I/II, Open-Label, Multiple Centre Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Immunogenicity and Preliminary Efficacy of LM-305 in Patients With Relapsed or Refractory Multiple Myeloma (RRMM) and Other Plasma Cell Diseases
100 Clinical Results associated with GPRC5D x Tubulin
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100 Translational Medicine associated with GPRC5D x Tubulin
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