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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

8 novembre 2026 mis à jour par: 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.

Aperçu de l'étude

Statut

Pas encore de recrutement

Les conditions

Intervention / Traitement

Type d'étude

Interventionnel

Inscription (Estimé)

300

Phase

  • Phase 2

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

  • Nom: Clinical Trials Information Group NA officer
  • Numéro de téléphone: 86-311-69085587
  • E-mail: ctr-contact@cspc.cn

Lieux d'étude

    • Guangdong
      • Guangzhou, Guangdong, Chine, 510120
        • The First Affiliated Hospital of Guangzhou Medical University
        • Contact:
          • Shiyue NA Li, Medical Doctor
          • Numéro de téléphone: 86-020-83382991
          • E-mail: lishiyue@188.com
        • Chercheur principal:
          • Shiyue NA Li, Medical Doctor

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

40 ans et plus (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

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.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Quadruple

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Group A1

Group SYH9061 4 mg

Administered at the dose specified in the protocol.

Comparateur placebo: Group A2

Group Placebo

Administered at the dose specified in the protocol.

Expérimental: Group B1

Group SYH9061 6 mg

Administered at the dose specified in the protocol.

Comparateur placebo: Group B2

Group Placebo

Administered at the dose specified in the protocol.

Expérimental: Group C1

Group SYH9061 4 mg

Administered at the dose specified in the protocol.

Comparateur placebo: Group C2

Group Placebo

Administered at the dose specified in the protocol.

Comparateur actif: Group D1

Group Ofev®

Administered at the dose specified in the protocol.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change in FVC from baseline (mL)
Délai: Week 12

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

Week 12

Mesures de résultats secondaires

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

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Les enquêteurs

  • Chaise d'étude: Shiyue NA Li, Medical Doctor, The First Affiliated Hospital of Guangzhou Medical University

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 décembre 2026

Achèvement primaire (Estimé)

1 avril 2029

Achèvement de l'étude (Estimé)

1 février 2030

Dates d'inscription aux études

Première soumission

2 novembre 2026

Première soumission répondant aux critères de contrôle qualité

8 novembre 2026

Première publication (Réel)

12 novembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

12 novembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

8 novembre 2026

Dernière vérification

1 novembre 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • SYH9061-002

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .