跳至主要内容
临床试验/NCT07652658
NCT07652658招募中2 期

A Phase IIb Study to Evaluate the Efficacy, Safety, and Tolerability of AZD8965 in Participants With Idiopathic Pulmonary Fibrosis (IPF) (ARGiNAUT)

AstraZeneca190 个研究点 分布在 4 个国家目标入组 359 人开始时间: 2026年6月11日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
招募中
发起方
AstraZeneca
入组人数
359
试验地点
190

研究概览

简要总结

This Phase IIb study aims to evaluate the efficacy, safety, and tolerability of 3 doses of AZD8965 treatment compared to placebo in participants with IPF, including those on antifibrotic therapy (nintedanib, pirfenidone, nerandomilast), either alone or in combination, or in those not on antifibrotic therapy.

详细描述

This is a Phase IIb, randomized, placebo-controlled, double-blind, parallel-group 24-week study to assess the efficacy, safety and tolerability of three doses of AZD8965 versus placebo administered to participants with IPF. The enrolled participants will include those on stable dose(s) of one or two approved antifibrotic therapies and those who are not taking any antifibrotic therapy. Approximately 360 participants will be randomized across approximately 200 sites globally.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Age ≥ 40 years
  • IPF diagnosis
  • Participants with IPF receiving locally approved antifibrotic therapies at a stable dose, or participants with IPF not receiving local standard of care
  • FVC ≥ 45% predicted of normal
  • DLCO corrected for hemoglobin ≥ 25% predicted of normal

排除标准

  • ILD other than IPF
  • The extent of emphysema is greater than the extent of fibrotic changes on chest HRCT scan
  • Acute exacerbation of IPF
  • Lower respiratory tract infection requiring treatment
  • Acute coronary syndrome/acute myocardial infarction, unstable angina ± coronary intervention with Percutaneous Coronary Intervention, or Coronary Artery Bypass Grafting
  • Heart failure
  • History of organ transplantation or is likely to receive lung transplantation

研究组 & 干预措施

Placebo for AZD8965

Placebo Comparator

Placebo for AZD8965

干预措施: Placebo for AZD8965 (Other)

AZD8965 low dose

Experimental

AZD8965 low dose

干预措施: AZD8965 low dose (Drug)

AZD8965 medium dose

Experimental

AZD8965 medium dose

干预措施: AZD8965 medium dose (Drug)

AZD8965 high dose

Experimental

AZD8965 high dose

干预措施: AZD8965 high dose (Drug)

研究者

发起方
AstraZeneca
申办方类型
Industry
责任方
Sponsor

研究点 (190)

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