CTRI/2010/091/000169已完成3 期
A Phase III, Multicenter, Open Label, Randomized, Single Treatment study to evaluate the efficacy and safety of alpha,beta - arteether injection 150 mg/mL in patient of P. falciparum malaria.
incoln Pharmaceuticals 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
- 3 期
- 状态
- 已完成
- 发起方
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
- •1.Written informed consent from the patient.
- •2.Male and Female patients with aged 18 years above inclusive.
- •3. Diagnosis of Patients with P. falciparum malaria by the presence of ring forms of P. falciparum in thick and thin peripheral blood smears (parasitemia > 5%).
排除标准
- •1. Patients with any condition which in the opinion of the investigator makes the patient unsuitable for inclusion.
- •2. Patient is a female who is pregnant or willing to get pregnant, not ready to use contraceptive measures during the trial period or breast feeding.
- •3. Known hypersensitivity to alpha,beta-arteether.
- •4. Patient with renal failure and other systemic disorder.
- •5. Patient who is consuming/ has received drugs, which have interaction with alpha,beta-arteether, during last 14 days.
- •6. Participation in any other clinical trial during last 30 days.
研究者
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