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临床试验/NCT02041221
NCT02041221已完成1 期

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of SPARC1316

Sun Pharma Advanced Research Company Limited1 个研究点 分布在 1 个国家目标入组 64 人开始时间: 2014年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
64
试验地点
1
主要终点
Number of Subjects With Adverse Events

研究概览

简要总结

Sun Pharma Advanced Research company Limited has developed a dry powder inhaler of compound SPARC1316 for oral inhalation. This clinical study is a Phase I/IIa study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of single and multiple ascending doses of S0597 administered by oral inhalation to healthy volunteers and asthma patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects willing to provide informed consent
  • Male or female subjects aged 18 to 65 years inclusive
  • Body mass index (BMI) between 18.0 and 30.0 kg/m2 inclusive
  • Non-smokers or ex-smokers

排除标准

  • Subjects with a supine systolic blood pressure ≥160 mmHg and/or a supine diastolic blood pressure ≥100 mmHg
  • Subjects who have a significant infection or known inflammatory process on screening or admission.
  • Subjects who are unlikely to co-operate with the requirements of the study.
  • Positive serology for infectious disease (hepatitisB or C , HIV) at screening

研究组 & 干预措施

SPARC1316 Dose 1

Experimental

Subjects will be administered with SPARC1316 dose 1

干预措施: SPARC1316 Dose 1 (Drug)

Placebo

Placebo Comparator

The subjects will receive placebo.

干预措施: Placebo (Drug)

SPARC1316 Dose 2

Experimental

Subjects will be administered with SPARC1316 dose 2

干预措施: SPARC1316 Dose 2 (Drug)

SPARC1316 Dose 3

Experimental

Subjects will be administered with SPARC1316 dose 3

干预措施: SPARC1316 Dose 3 (Drug)

SPARC1316 Dose 4

Experimental

Subjects will be administered with SPARC1316 dose 4

干预措施: SPARC1316 Dose 4 (Drug)

SPARC1316 Dose 5

Experimental

Subjects will be administered with SPARC1316 dose 5

干预措施: SPARC1316 Dose 5 (Drug)

结局指标

主要结局

Number of Subjects With Adverse Events

时间窗: Two (2) Weeks

The no of adverse events will be assessed to evaluate the safety and tolerability of compound SO597 in healthy male subjects and asthma patients

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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