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临床试验/NCT03317366
NCT03317366No Longer Available不适用

Expanded Access to Provide ARQ 092 for the Treatment of Overgrowth Diseases and/or Vascular Anomalies With Genetic Alterations of the PI3K/AKT Pathway

ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA)0 个研究点开始时间: 2017年10月23日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
No Longer Available
发起方

研究概览

简要总结

ARQ 092 is being investigated for patients with overgrowth diseases and/or vascular anomalies with genetic alterations of the PI3K/AKT pathway and may be available for patients who are ineligible for an ongoing ARQ 092 clinical trial or have other considerations that prevent access to ARQ 092 through an existing clinical trial.

研究设计

研究类型
Expanded Access

入排标准

年龄范围
2 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Severe overgrowth diseases and/or vascular anomalies with confirmed somatic genetic alterations of PIK3CA or AKT
  • Are unable to participate in an ongoing ARQ 092 clinical trial
  • Willing and able to provide written, signed informed consent. In the case of a minor, a parent or legal guardian must sign an informed consent form.
  • Medically suitable for treatment with ARQ 092
  • Not eligible for any other available therapy for the diagnosed overgrowth disease and/or vascular anomaly with confirmed somatic genetic alterations of PIK3CA or AKT

排除标准

  • Currently enrolled in an ongoing clinical study of ARQ 092 or other investigational drug
  • Currently being treated with any inhibitor of the PI3K/AKT/mTOR pathway

研究者

发起方
ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA)
申办方类型
Industry
责任方
Sponsor

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