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临床试验/NCT04503733
NCT04503733Unknown1 期

A Randomized, Double-blind, Placebo-Controlled, Dose Escalation Study to Assess Safety, Efficacy and Pharmacokinetics of GMA301 in Subjects With Pulmonary Arterial Hypertension

Gmax Biopharm LLC.7 个研究点 分布在 2 个国家目标入组 48 人开始时间: 2020年10月22日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
入组人数
48
试验地点
7
主要终点
The incidence of Treatment-emergent Adverse Events (TEAE) in subjects assigned to GMA301 compared with those assigned to placebo.

研究概览

简要总结

A Randomized, Placebo-Controlled, Double-blind, Dose Escalation Study to Assess Safety, Efficacy and Pharmacokinetics of GMA301 Injection in Subjects with Pulmonary Arterial Hypertension

详细描述

Drug: Q4W GMA301 IV injections (300 mg) Drug: Q4W GMA301 IV injections (600 mg) Drug: Q4W GMA301 IV injections (1000 mg) Drug: Q4W GMA301 IV injections (1800 mg) Other: Q4W placebo IV injections

研究设计

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

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Q4W GMA301 IV injections (600 mg)

Experimental

Drug: Q4W GMA301 IV injections (600 mg) Each cohort will contain 12 subjects, 9 of whom will be administered active GMA301 and 3 of whom will be administrated placebo.

Other: Q4W placebo IV injections Placebo is indistinguishable from GMA301

干预措施: Q4W placebo IV injections (Other)

Q4W GMA301 IV injections (300 mg)

Experimental

Drug: Q4W GMA301 IV injections (300 mg) Each cohort will contain 12 subjects, 9 of whom will be administered active GMA301 and 3 of whom will be administrated placebo.

Other: Q4W placebo IV injections Placebo is indistinguishable from GMA301

干预措施: Q4W GMA301 IV injections (300 mg) (Drug)

Q4W GMA301 IV injections (300 mg)

Experimental

Drug: Q4W GMA301 IV injections (300 mg) Each cohort will contain 12 subjects, 9 of whom will be administered active GMA301 and 3 of whom will be administrated placebo.

Other: Q4W placebo IV injections Placebo is indistinguishable from GMA301

干预措施: Q4W placebo IV injections (Other)

Q4W GMA301 IV injections (600 mg)

Experimental

Drug: Q4W GMA301 IV injections (600 mg) Each cohort will contain 12 subjects, 9 of whom will be administered active GMA301 and 3 of whom will be administrated placebo.

Other: Q4W placebo IV injections Placebo is indistinguishable from GMA301

干预措施: Q4W GMA301 IV injections (600 mg) (Drug)

Q4W GMA301 IV injections (1000 mg)

Experimental

Drug: Q4W GMA301 IV injections (1000 mg) Each cohort will contain 12 subjects, 9 of whom will be administered active GMA301 and 3 of whom will be administrated placebo.

Other: Q4W placebo IV injections Placebo is indistinguishable from GMA301

干预措施: Q4W GMA301 IV injections (1000 mg) (Drug)

Q4W GMA301 IV injections (1000 mg)

Experimental

Drug: Q4W GMA301 IV injections (1000 mg) Each cohort will contain 12 subjects, 9 of whom will be administered active GMA301 and 3 of whom will be administrated placebo.

Other: Q4W placebo IV injections Placebo is indistinguishable from GMA301

干预措施: Q4W placebo IV injections (Other)

Q4W GMA301 IV injections (1800 mg)

Experimental

Drug: Q4W GMA301 IV injections (1800 mg) Each cohort will contain 12 subjects, 9 of whom will be administered active GMA301 and 3 of whom will be administrated placebo.

Other: Q4W placebo IV injections Placebo is indistinguishable from GMA301

干预措施: Q4W GMA301 IV injections (1800 mg) (Drug)

Q4W GMA301 IV injections (1800 mg)

Experimental

Drug: Q4W GMA301 IV injections (1800 mg) Each cohort will contain 12 subjects, 9 of whom will be administered active GMA301 and 3 of whom will be administrated placebo.

Other: Q4W placebo IV injections Placebo is indistinguishable from GMA301

干预措施: Q4W placebo IV injections (Other)

结局指标

主要结局

The incidence of Treatment-emergent Adverse Events (TEAE) in subjects assigned to GMA301 compared with those assigned to placebo.

时间窗: Through study completion (up to 22 weeks)

次要结局

  • Pharmacokinetics (Area under the serum concentration- time curve from time zero to the last measurable concentration)(Through study completion (up to 22 weeks))
  • Comparison of GMA301 treatment effect at Week 12 versus baseline regarding the pulmonary vascular resistance (PVR) based on right heart catheterization (RHC)(Baseline to Week 12)
  • Comparing 6MWT distance(Baseline to Week 12)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (7)

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