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临床试验/2023-505576-29-00
2023-505576-29-00已完成2 期

A Phase 1/2a, First in Human, Open-Label, Multicenter, Dose Escalation Study with Expansion Cohorts to Evaluate the Safety, Tolerability, and Preliminary Activity of LB101 in Subjects with Advanced Solid Tumors

Centessa Pharmaceuticals UK Limited1 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2023年11月20日最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
6
试验地点
1

研究概览

简要总结

暂无简介。

入排标准

年龄范围
18 years 至 65+ years(18-64 Years, 65+ Years)
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究者

发起方
Centessa Pharmaceuticals UK Limited
申办方类型
Pharmaceutical company
责任方
Principal Investigator
主要研究者

SVP, Clinical Development, Innovative Medicines

Scientific

Centessa Pharmaceuticals UK Limited

研究点 (1)

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