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临床试验/NCT06068946
NCT06068946已完成2 期

A Phase 2 Randomized, Double-Blind, Placebo-Controlled, 13-week Study of VK2735 for Weight Management in Subjects Who Are Obese, or Overweight With at Least One Weight-related Comorbid Condition

Viking Therapeutics, Inc.20 个研究点 分布在 1 个国家目标入组 176 人开始时间: 2023年8月31日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
176
试验地点
20
主要终点
Percent (relative) change from baseline to Week 13 in body weight

研究概览

简要总结

This is a phase 2, 13-week randomized, double-blind, placebo-controlled, parallel arm study that will evaluate the safety, tolerability, weight loss efficacy, pharmacodynamic effects, and pharmacokinetics of VK2735 in adults who are obese (BMI ≥30 kg/m2) or who are overweight (BMI ≥27 kg/m2) with at least one weight-related co-morbid condition.

VK2735 or matched placebo will be administered once weekly.

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
Triple (Participant, Care Provider, Investigator)

入排标准

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

入选标准

  • Age ≥18 years of age at the time of signing the informed consent
  • Body mass index (BMI) ≥30 kg/m2 OR ≥27 kg/m2 with at least one weight-related co-morbid condition (treated or untreated), and BMI <50 kg/m2

排除标准

  • History of or current clinically significant medical or psychiatric disorder that, in the opinion of the Investigator, does not support study participation
  • Self-reported body weight change of 5% or more within 3 months of screening
  • Current or past diagnosis of diabetes mellitus (including type 1, type 2, gestational)
  • Current or past diagnosis of chronic pancreatitis
  • Calcitonin ≥20 ng/L measured by central laboratory at screening (individuals with elevated calcitonin at initial screening may be re-screened)
  • Any GLP-1 receptor agonist or GLP-1/GIP dual agonist within 6 months of Screening
  • Any prescription or over-the-counter medications intended for weight loss within 6 months of screening

研究组 & 干预措施

VK2735 (Placebo)

Placebo Comparator

Placebo

干预措施: Placebo (Biological)

VK2735 (Dose #1)

Experimental

VK2735 is a peptide GLP-1 and GIP dual agonist

干预措施: VK2735 (Biological)

VK2735 (Dose #2)

Experimental

VK2735 is a peptide GLP-1 and GIP dual agonist

干预措施: VK2735 (Biological)

VK2735 (Dose #3)

Experimental

VK2735 is a peptide GLP-1 and GIP dual agonist

干预措施: VK2735 (Biological)

VK2735 (Dose #4)

Experimental

VK2735 is a peptide GLP-1 and GIP dual agonist

干预措施: VK2735 (Biological)

结局指标

主要结局

Percent (relative) change from baseline to Week 13 in body weight

时间窗: 13 weeks

To measure the efficacy of VK2735 for weight loss in adult Subjects who are obese, or overweight with at least one weight-related comorbid condition

次要结局

  • Proportion of Subjects losing ≥5% and ≥10% of baseline weight at Week 13(13 weeks)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (20)

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