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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.

調査の概要

状態

まだ募集していません

条件

介入・治療

研究の種類

介入

入学 (推定)

300

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

  • 名前:Clinical Trials Information Group NA officer
  • 電話番号:86-311-69085587
  • メール:ctr-contact@cspc.cn

研究場所

    • Guangdong
      • Guangzhou、Guangdong、中国、510120
        • The First Affiliated Hospital of Guangzhou Medical University
        • コンタクト:
          • Shiyue NA Li, Medical Doctor
          • 電話番号:86-020-83382991
          • メール:lishiyue@188.com
        • 主任研究者:
          • Shiyue NA Li, Medical Doctor

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

40年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:4倍

武器と介入

参加者グループ / アーム
介入・治療
実験的:Group A1

Group SYH9061 4 mg

Administered at the dose specified in the protocol.

プラセボコンパレーター:Group A2

Group Placebo

Administered at the dose specified in the protocol.

実験的:Group B1

Group SYH9061 6 mg

Administered at the dose specified in the protocol.

プラセボコンパレーター:Group B2

Group Placebo

Administered at the dose specified in the protocol.

実験的:Group C1

Group SYH9061 4 mg

Administered at the dose specified in the protocol.

プラセボコンパレーター:Group C2

Group Placebo

Administered at the dose specified in the protocol.

アクティブコンパレータ:Group D1

Group Ofev®

Administered at the dose specified in the protocol.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Change in FVC from baseline (mL)
時間枠:Week 12

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

Week 12

二次結果の測定

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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • スタディチェア:Shiyue NA Li, Medical Doctor、The First Affiliated Hospital of Guangzhou Medical University

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年12月1日

一次修了 (推定)

2029年4月1日

研究の完了 (推定)

2030年2月1日

試験登録日

最初に提出

2026年11月2日

QC基準を満たした最初の提出物

2026年11月8日

最初の投稿 (実際)

2026年11月12日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月12日

QC基準を満たした最後の更新が送信されました

2026年11月8日

最終確認日

2026年11月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • SYH9061-002

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。