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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.

Descripción general del estudio

Estado

Reclutamiento

Tipo de estudio

Intervencionista

Inscripción (Estimado)

300

Fase

  • Fase 4

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

      • Shanghai, Porcelana
        • Reclutamiento
        • Guanghua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

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 de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Triple

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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;
Comparador de placebos: 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;

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
the ACR20 response rate at week 12
Periodo de tiempo: 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.

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

15 de octubre de 2025

Finalización primaria (Estimado)

15 de marzo de 2028

Finalización del estudio (Estimado)

15 de marzo de 2028

Fechas de registro del estudio

Enviado por primera vez

26 de marzo de 2026

Primero enviado que cumplió con los criterios de control de calidad

19 de julio de 2026

Publicado por primera vez (Actual)

22 de julio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

22 de julio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

19 de julio de 2026

Última verificación

1 de marzo de 2026

Más información

Términos relacionados con este estudio

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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