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First‐in‐Human Phase I Study of MBC‐11 a Novel Bone‐Targeted Cytarabine‐Etidronate Conjugate in Patients with Cancer‐Induced Bone Disease

机译:MBC-11的首次人类第一阶段研究这是一种新型的针对骨癌患者的骨靶向阿糖胞苷-依替膦酸盐偶联物

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摘要

Lessons Learned. class="unordered" style="list-style-type:disc" id="onco12741-list-0001">
  • Results are consistent with MBC‐11 targeting and treating cancer‐induced bone lesions by concentrating cytarabine and etidronate at the site of disease.
  • MBC‐11 was well tolerated, with an maximum tolerated dose of 5 mg/kg per day and myelosuppression as the principal toxicity.
  • Treatment significantly reduced cancer cell activity in over half of bone lesions detected at baseline.
  • MBC‐11 pharmacokinetic and pharmacodynamic parameters are consistent with the novel drug design goals, and encouraging results warrant further clinical development.
  • 机译:得到教训。 class =“ unordered” style =“ list-style-type:disc” id =“ onco12741-list-0001”> <!-list-behavior = unordered prefix-word = mark-type = disc max-label- size = 0->
  • 结果与MBC-11靶向并通过在患病部位集中阿糖胞苷和依替膦酸盐治疗癌症诱发的骨病变一致。
  • MBC-11的耐受性良好,最大耐受剂量为每天5 mg / kg,以骨髓抑制为主要毒性。
  • 治疗显着降低了基线时检测到的一半以上骨病变中的癌细胞活性。
  • MBC-11的药代动力学和药效学参数与新药设计目标一致,令人鼓舞的结果值得进一步的临床开发。
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