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临床试验/NCT07587710
NCT07587710尚未招募1 期

A Study Investigating the Pharmacokinetic Properties, Safety and Tolerability of NNC0487-0111 in Participants With Various Degrees of Hepatic Impairment and Participants With Normal Hepatic Function

Novo Nordisk A/S2 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2026年5月13日最近更新:
适应症

试验速览

阶段
1 期
状态
尚未招募
入组人数
35
试验地点
2

研究概览

简要总结

The study is testing a new study medicine to treat people with overweight/obesity and type 2 diabetes. The aim of this study is to see if it is safe and to find out how it works in people with reduced liver function and people with normal liver function.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female (sex at birth).
  • Age 18-80 years (both inclusive) at the time of signing informed consent.
  • Participants with stable hepatic impairment classified as Child-Pugh grade A, B or C as assessed by the investigator. Stable hepatic impairment is defined as no clinically significant change in disease status, as judged by the investigator.

排除标准

  • Known or suspected hypersensitivity to study intervention(s) or related products.
  • Female who is pregnant, breast-feeding or intends to become pregnant or is of child-bearing potential and not using a highly effective contraceptive method.

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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