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Tiprelestat Versus Placebo When Added to Standard of Care for the Treatment of Pulmonary Arterial Hypertension (PAH) (ATHENA)

2026年5月15日 更新者:Roham T. Zamanian、Stanford University

A Phase II, Randomized, Double-Blind, Safety and Efficacy Study of Tiprelestat Versus Placebo When Added to Standard of Care for the Treatment of Pulmonary Arterial Hypertension (PAH)

The primary objective of this study is to compare the efficacy, safety, and tolerability of tiprelestat plus Standard of Care (SOC) compared with placebo plus SOC in patients with World Health Organization (WHO) functional class II-IV pulmonary arterial hypertension (PAH).

研究概览

研究类型

介入性

注册 (估计的)

90

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Arizona
      • Tucson、Arizona、美国、85719
        • The University of Arizona / Banner University Medical Center
    • California
      • San Francisco、California、美国、94143
        • University of California, San Francisco
      • Stanford、California、美国、94305
        • Stanford University
    • Colorado
      • Aurora、Colorado、美国、80045
        • University of Colorado (UCD) Anschutz
    • Massachusetts
      • Boston、Massachusetts、美国、02138
        • Harvard University / Brigham and Women's Hospital
    • North Carolina
      • Durham、North Carolina、美国、27710
        • Duke University
    • Pennsylvania
      • Philadelphia、Pennsylvania、美国、19104
        • University of Pennsylvania
    • Rhode Island
      • Providence、Rhode Island、美国、02904
        • Brown University/Rhode Island Hospital
    • Texas
      • Dallas、Texas、美国、75390
        • University of Texas Southwestern
    • Washington
      • Seattle、Washington、美国、98195
        • University of Washington

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Adults age 18 to 75 years.
  2. Willingness to give written informed consent prior to any study-related procedures being performed and to be able to adhere to the study restrictions and examination schedule.
  3. Diagnosis of WHO Group I PAH.
  4. WHO functional class II - IV despite optimized treatment SOC, with 1 or more modalities including phosphodiesterase 5 (PDE5) inhibitor, soluble guanylate cyclase stimulator (sGCS), endothelin receptor antagonist (ERA), and/or a prostacyclin analogue or receptor agonist (SC/inhaled/PO) (see #5), as well as Sotatercept (see #6).
  5. On stable doses of PDE5 inhibitor, ERA, sGCS, or prostacyclin analogue/receptor agonist for at least 90 days prior to screening; for infusion prostacyclins, dose adjustment within 10% of baseline dose during the duration of the study is allowed per medical practice.
  6. On stable doses of Sotatercept therapy for at least 6 months prior to screening, and intended to be continued during the duration of the study.
  7. Screening right heart catheterization mean pulmonary arterial pressure (mPAP) ≥ 25 mmHg at rest; pulmonary wedge pressure (PAWP) ≤ 15 mmHg or left ventricular end diastolic pressure (LVEDP) ≤ 15 mmHg; AND pulmonary vascular resistance (PVR) ≥ 400 dynes•sec/cm5 (5 Wood Units).
  8. If participant is of childbearing potential, willing to use adequate methods of contraception throughout the course of the study. If participant is of childbearing potential (a participant < 55 years of age who has not been postmenopausal for ≥ 5 years or who has not had a bilateral salpingectomy, hysterectomy and/or oophorectomy), need to employ two reliable means of contraception which may include surgical sterilization, barrier methods, spermicidals, intrauterine devices, and/or hormonal contraception, unless the participant chooses abstinence (to avoid heterosexual intercourse completely). If a participant chooses abstinence, then a second reliable means of contraception is not needed.
  9. 6MWD ≥100 and ≤500 meters at screening.
  10. Willing to adhere to study restrictions and examination schedule.

Exclusion Criteria:

  1. Diagnosis of WHO Group 2 - 5 Pulmonary Hypertension.
  2. Participation in another clinical trial, or experimental use, involving a PAH investigational drug or device within the last 3 months.
  3. Total lung capacity (TLC) < 60% predicted; if TLC is ≥ 60% and < 70% predicted, high resolution computed tomography (HRCT) must be available to exclude significant interstitial lung disease.
  4. FEV1 / FVC < 70% predicted and FEV1 < 60% predicted.
  5. Significant left-sided heart disease (based on screening Echocardiogram):

    1. Moderate or severe aortic or mitral valve disease
    2. Diastolic dysfunction ≥ Grade II
    3. LV systolic function < 45%
    4. Pericardial constriction
    5. Restrictive cardiomyopathy
    6. Significant coronary disease with demonstrable ischemia
  6. Chronic renal insufficiency defined as an estimated creatinine clearance < 30 ml/min.
  7. Current atrial arrhythmias not under optimal control.
  8. Uncontrolled systemic hypertension: SBP > 160 mmHg or DBP > 100mmHg.
  9. Severe hypotension: SBP < 80 mmHg.
  10. Pregnant or breast-feeding.
  11. Psychiatric, addictive, or other disorders that compromise the patient's ability to provide informed consent, to follow study protocol, and adhere to treatment instructions.
  12. Known allergy or hypersensitivity to tiprelestat.
  13. Moderate to severe hepatic dysfunction with a Child Pugh score >10.
  14. Hyperkalemia defined as Potassium > 5.1 mEq/L at screening.
  15. Initiation of an exercise program for cardiopulmonary rehabilitation within 90 days prior to screening or planned during the study. Subjects who are already stable in the maintenance phase of an exercise program which will continue for the duration of the study are eligible.
  16. Known active infection requiring antibiotic, antifungal, or antiviral therapies. Patients may be rescreened at physician discretion after the resolution of infection and discontinuation of antibiotic, antifungal, or antiviral therapies.
  17. Co-morbid conditions that would impair a patient's exercise performance and ability to assess WHO functional class, including but not limited to chronic low-back pain or peripheral musculoskeletal problems, other comorbidities expected to alter the patient's clinical course (i.e. active cancer; >3 comorbidities e.g., obesity, systemic HTN, diabetes).

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:三倍

武器和干预

参与者组/臂
干预/治疗
实验性的:Tiprelestat (5 mg)
Participants receive tiprelestat injection daily for 168 days.
5 mg of tiprelestat in 1 mL saline administered as a daily subcutaneous injection for 168 days.
其他名称:
  • Elafin
实验性的:Tiprelestat (10 mg)
Participants receive tiprelestat injection daily for 168 days.
10 mg of tiprelestat in 1 mL saline administered as a daily subcutaneous injection for 168 days.
其他名称:
  • Elafin
安慰剂比较:Placebo (1 mL 0.9% saline solution)
Participants receive placebo injection (matching tiprelestat) daily for 168 days.
Matching 1 mL 0.9% saline solution administered as a daily subcutaneous injection for 168 days.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change in Pulmonary Vascular Resistance (PVR)
大体时间:Baseline to week 24
PVR is calculated based on direct measurements during the right heart catheterization (RHC) procedure. PVR = (mPAP - PAWP) / CO, where mPAP is the mean pulmonary artery pressure, PAWP is the pulmonary wedge arterial pressure, and CO is the cardiac output. These cardiac measures are also obtained from right heart catheterization. PVR is measured in Wood units (WU) or dynes (dynes*sec/cm5), and higher values are associated with more severe disease. Normal range for PVR is 1-3 WU (80-240 dynes*sec/cm5) and can be as high as 30 WU (2,400 80-240 dynes*sec/cm5) in disease.
Baseline to week 24

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Roham T Zamanian, MD、Stanford University

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年7月1日

初级完成 (估计的)

2030年2月1日

研究完成 (估计的)

2030年3月1日

研究注册日期

首次提交

2026年5月15日

首先提交符合 QC 标准的

2026年5月15日

首次发布 (实际的)

2026年5月22日

研究记录更新

最后更新发布 (实际的)

2026年5月22日

上次提交的符合 QC 标准的更新

2026年5月15日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

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