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A Multicenter, Randomized, Blinded, Placebo- and Active-Controlled Phase II Study to Evaluate the Efficacy and Safety of SYH9061 in Adult Patients With Idiopathic Pulmonary Fibrosis

2026年11月8日 更新者:CSPC-NBP Pharmaceutical Co., Ltd.

This is a multicenter, randomized, blinded, placebo- and active-controlled Phase II study to evaluate the efficacy, safety, and pharmacokinetic (PK) profile of SYH9061 at different doses and dosing frequencies in patients with IPF, and to determine the optimal recommended dose for Phase III confirmatory studies.

研究概览

研究类型

介入性

注册 (估计的)

300

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。

学习联系方式

  • 姓名:Clinical Trials Information Group NA officer
  • 电话号码:86-311-69085587
  • 邮箱:ctr-contact@cspc.cn

学习地点

    • Guangdong
      • Guangzhou、Guangdong、中国、510120
        • The First Affiliated Hospital of Guangzhou Medical University
        • 接触:
          • Shiyue NA Li, Medical Doctor
          • 电话号码:86-020-83382991
          • 邮箱:lishiyue@188.com
        • 首席研究员:
          • Shiyue NA Li, Medical Doctor

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

40年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Age ≥ 40 years, male or female;
  2. According to the 2022 guidelines of the American Thoracic Society/European Respiratory Society/Japanese Respiratory Society/Latin American Thoracic Association titled "Idiopathic Pulmonary Fibrosis (an Update) and Progressive Pulmonary Fibrosis in Adults", the investigator confirms that the participant has a clinical diagnosis of IPF based on chest HRCT or surgical lung biopsy or transbronchial lung cryobiopsy (if available) during the screening period or within 1 year prior to screening;
  3. Received a stable dose of a single anti-fibrotic therapy (pirfenidone or namilumab) for at least 8 weeks prior to screening and will continue after randomization, OR have not received stable anti-fibrotic therapy or have discontinued it for at least 8 weeks and do not plan to use anti-fibrotic therapy during the trial; for participants receiving background therapy, their compliance with background therapy within 8 weeks prior to screening must be ≥80% (i.e., the proportion of days the participant actually took the background medication to the days they should have taken it within 8 weeks prior to screening is not less than 80%);
  4. Participants are able to correctly use a DPI for inhalation;
  5. Able to perform acceptable and repeatable pulmonary function tests;
  6. FVCpp ≥ 45% at screening;
  7. Hemoglobin-corrected DLCOpp ≥ 25% and < 90% at screening;
  8. Understand the purpose and risks of this study, understand and are willing to follow all study procedures, agree to participate in the study and sign written informed consent.

Exclusion Criteria:

  1. Interstitial lung diseases other than IPF, including any other type of idiopathic interstitial pneumonia; interstitial lung disease associated with exposure to fibrogenic substances, other environmental toxins, or drugs; other types of occupational interstitial lung disease; granulomatous interstitial lung disease; pulmonary vascular disease; autoimmune-related interstitial lung disease, including vasculitis and connective tissue diseases, etc.;

  2. Presence of airway obstruction (FEV₁/FVC < 0.7) at screening, or emphysema extent greater than pulmonary fibrosis extent on chest HRCT;

  3. Known acute exacerbation of IPF or suspected acute exacerbation of IPF by the investigator within 3 months prior to screening (Definition of acute exacerbation of IPF: primarily assessed by the investigator, acute exacerbation is defined as an acute, clinically significant respiratory deterioration characterized by new widespread alveolar abnormality, accompanied by all of the following: acute worsening or development of dyspnea lasting within one month; new bilateral ground-glass opacities and/or consolidation on CT images consistent with IPF features; deterioration not fully attributable to heart failure or fluid overload);

  4. The investigator judges, based on changes in FVC, DLCO, and/or chest HRCT results, that there has been continuous improvement in the severity of IPF during the 12 months prior to screening;

  5. Presence of other clinically significant respiratory diseases at screening, including diseases of the airways, lung parenchyma, pleural cavity, mediastinum, diaphragm, or chest wall, which, in the investigator's judgment, may affect the study results;

  6. Presence of any severe and/or uncontrolled disease that, in the investigator's judgment, affects drug evaluation, including but not limited to: severe neurological diseases (e.g., epilepsy, dementia, etc.), history of severe mental disorders, major cardiovascular diseases (including but not limited to: myocardial infarction within 6 months prior to screening, unstable angina within 1 month prior to screening), thrombotic events (including but not limited to stroke and transient ischemic attack within 6 months prior to screening), QTcF interval prolongation (males > 450 msec, females > 470 msec) or severe arrhythmias requiring pharmacological intervention, etc.;

  7. Active peptic ulcer, active gastrointestinal bleeding, hemoptysis, or hematuria within 4 weeks prior to screening;

  8. Received therapeutic doses of anticoagulation (including but not limited to vitamin K antagonists, therapeutic doses of oral anticoagulants, or therapeutic doses of low molecular weight heparin/unfractionated heparin) within 1 week prior to screening, excluding low-dose regimens for prophylactic anticoagulation or catheter locking; received high-dose platelet therapy within 2 weeks prior to screening; received fibrinolytic therapy within 4 weeks prior to screening; known genetic predisposition to bleeding based on the investigator's judgment;

  9. Platelet count < 100×10^9/L, or those with known and potential bleeding risks;

  10. Surgery requiring general anesthesia or hospitalization > 1 day within 8 weeks prior to screening or planned during the study period;

  11. Severe pulmonary hypertension (concomitant use of epoprostenol/treprostinil parenteral therapy, or severe right heart failure);

  12. History of malignancy: Patients with basal cell carcinoma, localized squamous cell carcinoma of the skin, or carcinoma in situ of the cervix can enter this study if at least 12 months have passed since completion of curative treatment prior to signing informed consent; patients with other malignancies can enter this study if at least 5 years have passed since completion of curative treatment prior to signing informed consent;

  13. Clinically significant active bacterial, fungal, or viral infection (defined as requiring oral or intravenous antibacterial, antifungal, or antiviral treatment) from 2 weeks prior to the screening visit until randomization;

  14. Any infectious disease screening indicator at screening meets the following criteria:

    1. HBsAg positive, and HBV DNA test result is above the lower limit of quantification or 1000 copies/mL (500 IU/mL), whichever is lower;
    2. If HBsAg is negative and HBcAb is positive, an additional HBV DNA test is required, and the result is above the lower limit of quantification or 1000 copies/mL (500 IU/mL), whichever is lower;
    3. If the HCV antibody test result is positive, an additional HCV RNA test is required, and the result is above the lower limit of quantification or 1000 copies/mL, whichever is lower;
    4. HIV antibody positive;
    5. Treponema pallidum antibody positive (if the treponemal serological test is positive, a further non-treponemal serological test should be performed; if the latter is negative and the investigator judges it as a past syphilis infection that has been cured, the participant meets the inclusion criteria);
    6. Active tuberculosis infection at screening (if it is old tuberculosis or the tuberculosis screening is positive at screening, but the investigator judges there is no evidence of active infection, this criterion is not applicable);
  15. Use of P-gp inhibitors (e.g., ketoconazole, erythromycin, etc.) or inducers (e.g., rifampicin, carbamazepine, phenytoin, etc.) within 14 days or 5 half-lives (whichever is longer) before the first dose of the investigational drug, or unable to stop taking them during the study period;

  16. Receiving immunomodulatory drugs (except oral corticosteroids) or prednisone > 15 mg/day or equivalent for respiratory or pulmonary reasons during the screening period;

  17. Receiving biologics within 2 months or 5 half-lives (whichever is longer) prior to screening;

  18. Receiving any form of stem cell therapy, immune cell therapy, or other cell therapy products within 6 months prior to screening;

  19. Abnormal liver or kidney function at screening as follows: ALT, AST > 2×ULN, or TBIL > 1.5×ULN, or eGFR < 30 mL/min/1.73 m² (CKD-EPI equation);

  20. Severe, drug-uncontrolled persistent elevation of blood pressure at screening (systolic blood pressure ≥ 180 mmHg or diastolic blood pressure ≥ 100 mmHg);

  21. History of smoking within 3 months prior to screening and unwilling to quit smoking during the study period (including e-cigarettes);

  22. Allergy to SYH9061 or any of its excipients, allergy to nintedanib or nintedanib excipients, allergy to peanuts or soybeans, or a history of severe drug allergy;

  23. Participated in any clinical study within 4 weeks prior to screening (except those who did not receive the investigational drug); or are still in the follow-up period of a clinical study or within 5 half-lives of the investigational drug (whichever is longer) prior to screening;

  24. Use of drugs with the same target (nintedanib) within 8 weeks prior to screening;

  25. Pregnant or lactating women, or women or men of childbearing potential who are unwilling to use strict contraception throughout the entire trial period and for 3 months after receiving the last dose of the investigational drug (including male participants);

  26. Planning to donate sperm during the treatment period or within 3 months after the last dose of the investigational drug;

  27. Other circumstances deemed unsuitable for participation in this clinical trial by the investigator.

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:四人间

武器和干预

参与者组/臂
干预/治疗
实验性的:Group A1

Group SYH9061 4 mg

Administered at the dose specified in the protocol.

安慰剂比较:Group A2

Group Placebo

Administered at the dose specified in the protocol.

实验性的:Group B1

Group SYH9061 6 mg

Administered at the dose specified in the protocol.

安慰剂比较:Group B2

Group Placebo

Administered at the dose specified in the protocol.

实验性的:Group C1

Group SYH9061 4 mg

Administered at the dose specified in the protocol.

安慰剂比较:Group C2

Group Placebo

Administered at the dose specified in the protocol.

有源比较器:Group D1

Group Ofev®

Administered at the dose specified in the protocol.

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 FVC from baseline (mL)
大体时间:Week 12

FVC is one of the pulmonary function indicators; FVC values in patients with IPF tend to decrease.

Week 12

次要结果测量

结果测量
措施说明
大体时间
Change in FVC from baseline (mL)
大体时间:Week 2,4,8,18,24

FVC is one of the pulmonary function indicators; FVC values in patients with IPF tend to decrease.

Week 2,4,8,18,24
Change in FVCpp from baseline
大体时间:Week 12,24
Week 12,24
Proportion of participants with an absolute decrease in FVCpp >10% from baseline
大体时间:Week 12,24
Week 12,24
Adjusted change in DLCOpp from baseline
大体时间:Week 12,24
Week 12,24
Changes in total L-PF score, symptom domain, and impact domain from baseline
大体时间:Week 12,24
Week 12,24
Changes in IPF symptoms (cough, dyspnea, fatigue) assessed by VAS from baseline
大体时间:Week 12,24
Week 12,24
Percent Change from Baseline in the Degree of Quantitative Lung Fibrosis (QLF)
大体时间:Week 24
Week 24
Incidence and severity of adverse events/serious adverse events and adverse reactions/serious adverse reactions during the trial
大体时间:During the trial
During the trial
Proportion of patients with gastrointestinal symptoms (diarrhea, nausea, vomiting, and abdominal pain) during the treatment period
大体时间:During the trial
During the trial
Proportion of participants with dose reduction of the study drug during the extension treatment period
大体时间:During the trial
During the trial
Changes over time in vital signs during the trial
大体时间:During the trial
During the trial
Changes over time in physical examination during the trial
大体时间:During the trial
During the trial
Changes over time in laboratory tests during the trial
大体时间:During the trial
During the trial
Changes over time in 12-lead ECG during the trial
大体时间:During the trial
During the trial
Plasma drug concentrations in participants with sparse sampling
大体时间:Day 1,Week 2
Day 1,Week 2
PK parameters after the first dose in participants with intensive sampling: Cmax
大体时间:Day 1,Week 2
Day 1,Week 2
PK parameters after the first dose in participants with intensive sampling AUC0-12
大体时间:Day 1,Week 2
Day 1,Week 2
PK parameters after the first dose in participants with intensive sampling Tmax
大体时间:Day 1,Week 2
Day 1,Week 2
PK parameters at steady state in participants with intensive sampling Ctau,ss
大体时间:Day 1,Week 2
Day 1,Week 2
PK parameters at steady state in participants with intensive sampling Cmax,ss
大体时间:Day 1,Week 2
Day 1,Week 2
PK parameters at steady state in participants with intensive sampling Cmin,ss
大体时间:Day 1,Week 2
Day 1,Week 2
PK parameters at steady state in participants with intensive sampling Cavg,ss
大体时间:Day 1,Week 2
Day 1,Week 2
PK parameters at steady state in participants with intensive sampling AUC0-tau,ss
大体时间:Day 1,Week 2
Day 1,Week 2
PK parameters at steady state in participants with intensive sampling Tmax,ss
大体时间:Day 1,Week 2
Day 1,Week 2
PK parameters at steady state in participants with intensive sampling DF
大体时间:Day 1,Week 2
Day 1,Week 2
PK parameters at steady state in participants with intensive sampling swing
大体时间:Day 1,Week 2
Day 1,Week 2
PK parameters at steady state in participants with intensive sampling accumulation ratios RAUC
大体时间:Day 1,Week 2
Day 1,Week 2
PK parameters at steady state in participants with intensive sampling RCmax (if data permit), etc
大体时间:Day 1,Week 2
Day 1,Week 2
Change from baseline in blood biomarkers (e.g., KL-6, etc.)
大体时间:Day 1,Week 4,12,24
Day 1,Week 4,12,24

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

  • 学习椅:Shiyue NA Li, Medical Doctor、The First Affiliated Hospital of Guangzhou Medical 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12月1日

初级完成 (估计的)

2029年4月1日

研究完成 (估计的)

2030年2月1日

研究注册日期

首次提交

2026年11月2日

首先提交符合 QC 标准的

2026年11月8日

首次发布 (实际的)

2026年11月12日

研究记录更新

最后更新发布 (实际的)

2026年11月12日

上次提交的符合 QC 标准的更新

2026年11月8日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

其他研究编号

  • SYH9061-002

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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