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临床试验/NL-OMON51840
NL-OMON51840撤回不适用

An Investigation of the Mass Balance, Pharmacokinetics, Excretion and Metabolism of [14C]-Nanatinostat in Patients with Advanced Solid Tumors: A Phase 1, Open-Label Study - CS0383-210288 VT3996-101

Viracta Therapeutics, Inc.0 个研究点目标入组 6 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
撤回
入组人数
6

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • 1. Men or women that are at least 18 years of age at the time of informed
  • 2. Has histologically confirmed metastatic or advanced solid tumors refractory
  • to standard therapy, and for whom no standard curative therapy exists.
  • 3. Eastern Cooperative Oncology Group (ECOG) performance status: 0-2.
  • 4. Adequate laboratory parameters (in absence of transfusion support within
  • three weeks or growth factor within two weeks of Screening), including:
  • Absolute neutrophil count (ANC) >=1500/mm3 = 1.5 × 109/L.
  • Platelets count >=90,000/mm3 = 90 × 109/L.
  • Hemoglobin >=9.0 g/dL.
  • Aspartate aminotransferase (AST), alanine aminotransferase (ALT) <=2.5 × upper
  • limit of normal (ULN), or < 5x ULN in the presence of liver metastases.
  • Total bilirubin <=1.5 × ULN unless considered due to Gilbert*s syndrome, in
  • which case, <=3.0 × ULN.
  • Estimated glomerular filtration rate (eGFR) >=60 mL/min by CKD-EPI equation.
  • Serum potassium, magnesium, and corrected calcium outside normal limits for
  • institution that are assessed as clinically significant by the Investigator
  • should be treated to correct abnormalities with confirmation on repeat lab
  • 5. Life expectancy >3 months, as determined by the treating physician.

排除标准

  • 1. Known history of central nervous system and/or leptomeningeal disease.
  • 2. Prior treatment with [14C]-nanatinostat or history of allergic reactions
  • attributed to compounds
  • of similar chemical or biologic composition to [14C]-nanatinostat.
  • 3. Inability to take or tolerate oral medication.
  • 4. Any gastrointestinal, liver, or kidney condition that may affect drug
  • absorption and metabolism.
  • 5.Is currently participating in or has participated in an interventional study
  • of an investigational agent or has used an investigational device within 4
  • weeks or 5 half-lives prior to dosing, whichever is longer.

研究者

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