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Integrated Clinical Study of Traditional Chinese and Western Medicine for Refractory Rheumatoid Arthritis

Integrated Clinical Study of Traditional Chinese and Western Medicine for the Treatment of Refractory Rheumatoid Arthritis Using Renowned Traditional Chinese Medicines

To evaluate the efficacy and safety of Kunxian Capsule combined with Methotrexate and Tofacitinib in the treatment of difficult-to-treat rheumatoid arthritis through a multicenter, randomized, double-blind, placebo-controlled clinical trial, and to identify the therapeutic advantages of integrated Chinese and Western medicine for optimizing the clinical strategy of D2T RA.

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Estimé)

300

Phase

  • Phase 4

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

Lieux d'étude

      • Shanghai, Chine
        • Recrutement
        • Guanghua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine
        • Contact:

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

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

Inclusion Criteria

Subjects must meet all of the following criteria to be enrolled in this study:

  1. Fully understand the purpose and requirements of the trial, voluntarily participate by signing written informed consent, and be willing and able to complete the study procedures, including medication administration and follow-up assessments;
  2. Male patients aged ≥50 years with no fertility requirements, or postmenopausal female patients, younger than 70 years;
  3. Patients diagnosed with rheumatoid arthritis (RA) according to the 1987 revised criteria of the American College of Rheumatology (ACR), or the 2010 ACR/European League Against Rheumatism (EULAR) classification criteria;
  4. Patients with RA of the "Wind-Damp Bi obstruction" pattern according to traditional Chinese medicine (TCM), defined as:

    • Primary symptoms: joint pain and swelling with a wandering nature; joint pain and swelling with intermittent occurrence.
    • Secondary symptoms: aversion to wind, or spontaneous sweating; headache; heaviness of the limbs.

    Tongue and pulse: pale-red tongue with thin white coating, slippery or floating pulse.Diagnosis requires at least 2 primary symptoms, or 1 primary symptom plus 2 secondary symptoms, in combination with tongue and pulse findings.

  5. Patients with confirmed moderate to severe active RA at screening, defined as ≥6 tender joints (TJC, based on 68-joint count) and ≥6 swollen joints (SJC, based on 66-joint count), with erythrocyte sedimentation rate (ESR) >28 mm/h or C-reactive protein (CRP) >10 mg/L, and DAS28-CRP >3.2;
  6. Prior inadequate response (DAS28-ESR >3.2) to at least two disease-modifying antirheumatic drug (DMARD) regimens (excluding methotrexate + JAK inhibitor + Kunxian capsule), each administered for at least 12 weeks.

Exclusion Criteria

Subjects meeting any of the following conditions will not be eligible for enrollment:

  1. Suspected or confirmed allergy to the investigational drug (including excipients or drugs of the same class), or any other severe allergic disease (excluding RA itself) that, in the investigator's judgment, may compromise subject safety;
  2. Presence of inflammatory diseases other than RA, including but not limited to psoriatic arthritis, ankylosing spondylitis, or systemic lupus erythematosus;
  3. Severe, progressive, or uncontrolled diseases of the kidneys, liver, blood, gastrointestinal tract, endocrine system, lungs, heart, nervous system, psychiatric conditions, or brain; history of venous thromboembolism, diverticulitis, significantly abnormal or poorly controlled blood lipids;
  4. History of lymphoproliferative disorders, or current or past malignancy;
  5. Meeting any of the following criteria for tuberculosis screening, which require exclusion:

    • History of active tuberculosis;
    • Recent close contact with patients with active tuberculosis;
    • Signs or symptoms of active tuberculosis based on medical history and physical examination;
    • Chest CT scan within 3 months prior to enrollment showing evidence of active pulmonary tuberculosis;
    • Positive interferon-gamma release assay (IGRA) within 6 weeks prior to enrollment;
  6. Presence or history of active infections, including:

    • Receipt of systemic anti-infective therapy within 4 weeks prior to randomization;
    • Pharyngalgia, nasal congestion, acute upper respiratory tract infection, or systemic acute infection within 2 weeks prior to randomization;
    • Recurrent, chronic, or other active infections at screening that, in the investigator's judgment, may increase subject risk;
  7. History of recurrent herpes zoster, disseminated herpes zoster, or disseminated herpes simplex, or history of herpes zoster or herpes simplex within 2 months prior to randomization;
  8. Positive hepatitis B surface antigen (HBsAg) and/or HBV DNA >50 IU/mL (or >500 copies/mL) at screening; positive hepatitis C virus antibody, human immunodeficiency virus (HIV) antibody, or Treponema pallidum antibody;
  9. Receipt of, or planned receipt of, live or attenuated vaccines within 3 months prior to the first dose of study medication, during the study, or within 6 months after the last study dose;
  10. Pregnant, breastfeeding, planning pregnancy, or planning fatherhood during the study or within 6 months after the last dose; females or males with fertility requirements;
  11. Clinically significant abnormalities on 12-lead ECG at screening that may increase subject risk, in the investigator's judgment;
  12. Any other disease at screening that may interfere with study assessments;
  13. Laboratory abnormalities at screening, defined as:

    1. Hemoglobin <100.0 g/L in males, or <90.0 g/L in females;
    2. White blood cell (WBC) count <4.0 × 10⁹/L;
    3. Neutrophil count <1.5 × 10⁹/L;
    4. Platelet (PLT) count <100 × 10⁹/L;
    5. Lymphocyte count <0.5 × 10⁹/L;
    6. Aspartate aminotransferase (AST), alanine aminotransferase (ALT), total bilirubin (TBIL), or serum creatinine (Scr) above the upper limit of normal;
    7. Hematology, liver function, or renal function abnormalities that, in combination with medical history and/or additional examinations, are deemed clinically significant by the investigator;
  14. Prior use of any of the following drugs or treatments:

    1. Strong opioids within 1 week prior to randomization;
    2. Any JAK inhibitor within 2 weeks prior to randomization;
    3. Nonsteroidal anti-inflammatory drugs (NSAIDs) at the time of randomization with dosage adjustments within 2 weeks prior;
    4. Prednisone or equivalent corticosteroid >10 mg/day at randomization; or ≤10 mg/day with dosage adjustment within 4 weeks prior to randomization;
    5. Intra-articular, intramuscular, intravenous, trigger-point, bursal, or tendon-sheath corticosteroid injections within 4 weeks prior to randomization or during the study;
  15. Concurrent participation in another drug clinical trial;
  16. Any clinically significant abnormalities in clinical or laboratory examinations, or any other reason deemed inappropriate for study participation 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: Tripler

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Kunxian Capsule group
Kunxian Capsule (0.3 g per capsule, orally, 3 capsules each time, three times daily) combined with Methotrexate (10-15mg/week) and Tofacitinib (5 mg twice daily) for 12 weeks, followed by 12 weeks of maintenance treatment with the same regimen

Experimental Group (Kunxian Capsule Group + MTX + JAKi):

  • Kunxian Capsule Placebo: 3 times daily, 0.3-0.6g each time, taken orally after meals; treatment duration: 12 weeks;
  • Methotrexate: Once weekly, 10-15mg each time, taken orally after meals; treatment duration: 12 weeks;
  • Tofacitinib: 2 times daily, 1 tablet each time, taken orally; treatment duration: 12 weeks;
Comparateur placebo: Placebo group
Kunxian Capsule placebo (identical in appearance and odor, orally, 3 capsules each time, three times daily) combined with Methotrexate (10-15mg/week) and Tofacitinib (5 mg twice daily) for 12 weeks; all participants then switch to Kunxian Capsule plus Methotrexate and Tofacitinib for the following 12 weeks

Placebo Comparator Group (Kunxian Capsule Placebo Group + MTX + JAKi):

  • Kunxian Capsule Placebo: 3 times daily, 0.3-0.6g each time, taken orally after meals; treatment duration: 12 weeks;
  • Methotrexate: Once weekly, 10-15mg each time, taken orally after meals; treatment duration: 12 weeks;
  • Tofacitinib: 2 times daily, 1 tablet each time, taken orally; treatment duration: 12 weeks;

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
the ACR20 response rate at week 12
Délai: To compare the ACR20 response rate at week 12 between the Kunxian Capsule combined with methotrexate (MTX) and JAK inhibitor (JAKi) group and the methotrexate (MTX) plus JAK inhibitor (JAKi) group.
To compare the ACR20 response rate at week 12 between the Kunxian Capsule combined with methotrexate (MTX) and JAK inhibitor (JAKi) group and the methotrexate (MTX) plus JAK inhibitor (JAKi) group.

Collaborateurs et enquêteurs

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

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 (Réel)

15 octobre 2025

Achèvement primaire (Estimé)

15 mars 2028

Achèvement de l'étude (Estimé)

15 mars 2028

Dates d'inscription aux études

Première soumission

26 mars 2026

Première soumission répondant aux critères de contrôle qualité

19 juillet 2026

Première publication (Réel)

22 juillet 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

22 juillet 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

19 juillet 2026

Dernière vérification

1 mars 2026

Plus d'information

Termes liés à cette étude

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 .

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