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临床试验/CTRI/2018/04/013086
CTRI/2018/04/013086进行中(未招募)未知

A prospective, open label, pilot, study to evaluate efficacy, safety and bio- availability of oral Arsenic compound prepared by Ayurvedic method (Somal- NTAX-44) in patients with solid tumours.

Rasayani Biologics Pvt Ltd0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
进行中(未招募)

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

入选标准

  • Male or female patient with solid tumours aged 20 to 70 of solid tumours
  • All those patients who have not responded to conventional anticancer therapies.
  • Cancer Patients who are not willing to take chemotherapy
  • Cancer patients who are eligible to receive treatment of Somal.
  • Cancer Patients who has expected survival of more than 3 months

排除标准

  • 1.Patients taking Chemotherapy.
  • 2.Patients taking conventional products containing Arsenic.
  • 3.Patient with deranged hepatic or renal profile at baseline.
  • 4.Patients with Pre-existing cardiac illness.
  • 5.Patients who has ECOG performance is >= 2.

研究者

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A study of Ayurvedic Arsenic compound (Somal) in... | 临床试验