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A Multicentre, Randomised, Double-blind, Positive-control Clinical Trial Evaluating Dihydroartemisinin Tablets for the Treatment of Discoid Lupus Erythematosus

22 de abril de 2026 actualizado por: Kunming Pharmaceuticals, Inc.
This study is a multicentre, randomised, double-blind, double-dummy, phase II clinical trial with a positive-control group, designed to evaluate the efficacy and safety of dihydroartemisinin tablets in the treatment of discoid lupus erythematosus (DLE).

Descripción general del estudio

Descripción detallada

Participants are screened during the screening phase, and those meeting the inclusion criteria are enrolled in the study. Enrolled participants were randomised in a 2:2:1 ratio to Treatment Group 1 (dihydroartemisinin 40 mg, twice daily), Treatment Group 2 (dihydroartemisinin 60 mg, twice daily) or the control group (hydroxychloroquine 200 mg, once daily). Participants in all groups will receive treatment for 24 weeks, during which efficacy and safety will be monitored at regular intervals.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

100

Fase

  • Fase 2

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

  • Nombre: Duo Gao, bachelor
  • Número de teléfono: 0871-68319868-3052
  • Correo electrónico: GAODUO5@kpc.com.cn

Ubicaciones de estudio

    • Anhui
      • Hefei, Anhui, Porcelana
        • The First Affiliated Hospital of Anhui Medical University
    • Beijing Municipality
      • Beijing, Beijing Municipality, Porcelana
        • Peking University People's Hospital
      • Beijing, Beijing Municipality, Porcelana
        • China-Japan Friendship Hospital
    • Chongqing Municipality
      • Chongqing, Chongqing Municipality, Porcelana
        • The First Affiliated Hospital of Chongqing Medical University
    • Guangdong
      • Guangzhou, Guangdong, Porcelana
        • Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University
      • Guangzhou, Guangdong, Porcelana
        • Nanfang Hospital, Southern Medical University
    • Hunan
      • Changsha, Hunan, Porcelana
        • The Second Xiangya Hospital of Central South University
    • Liaoning
      • Shenyang, Liaoning, Porcelana
        • The First Affiliated Hospital of China Medical University
    • Yunnan
      • Kunming, Yunnan, Porcelana
        • The Second Affiliated Hospital of Kunming Medical University
    • Zhejiang
      • Hangzhou, Zhejiang, Porcelana
        • Hangzhou Third People's Hospital

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:

  1. Participants are able to understand the purpose and risks of the study and voluntarily sign an informed consent form;
  2. Aged between 18 and 65 years (inclusive);
  3. Body weight ≥ 45 kg;
  4. Diagnosed with discoid lupus erythematosus (DLE) at the screening visit (refer to the '2021 Guidelines for the Diagnosis, Treatment and Long-term Management of Cutaneous Lupus Erythematosus'); new patients must undergo a skin biopsy and provide a pathology report, whilst existing patients must provide a biopsy pathology report dated within the last 5 years;
  5. At the time of screening, the Cutaneous Lupus Erythematosus Area and Severity Index (CLASI-A) must be ≥4.

Exclusion Criteria:

  1. Patients with systemic lupus erythematosus (SLE) or those at high risk of developing SLE;
  2. Drug-induced lupus;
  3. Patients with a history of resistance to antimalarial treatment;
  4. At screening, aspartate transaminase (AST) or alanine transaminase (ALT) or gamma-glutamyltransferase (GGT) levels exceeding twice the upper limit of normal (ULN); or alkaline phosphatase (ALP) or total bilirubin levels exceeding 1.5 times the upper limit of normal (ULN); or serum creatinine (Cr) or urea (UREA) levels exceeding 1.5 times the upper limit of normal (ULN);
  5. Patients diagnosed with anaemia within 3 months prior to randomisation, or patients with haemoglobin levels below 110 g/L at screening;
  6. Patients who have used any antimalarial drug (hydroxychloroquine sulphate, chloroquine phosphate or chloroquine) within 4 weeks prior to randomisation;
  7. Patients who have used topical corticosteroids (e.g. mometasone furoate cream or others) or topical calcineurin inhibitors (e.g. tacrolimus ointment or others) within 2 weeks prior to randomisation;
  8. Patients treated with biologics (e.g. adalimumab, secukinumab or others) within 12 weeks prior to randomisation;
  9. Patients treated with immunomodulators (e.g. thalidomide, lenalidomide or others) within 4 weeks prior to randomisation;
  10. Patients who have received live vaccines (e.g. measles vaccine, varicella vaccine or others) within 4 weeks prior to randomisation;
  11. Patients who have used traditional Chinese medicinal preparations with lupus-modulating effects within 4 weeks prior to randomisation, such as Tripterygium preparations (e.g. Tripterygium glycosides), Paeonia lactiflora total glycosides capsules, Zhengqing Fengtongning, or Euphorbia root tablets;
  12. History of malignant tumours within the 5 years prior to screening;
  13. History of acute myocardial infarction, unstable angina, or severe arrhythmias (multifocal frequent premature ventricular contractions, ventricular tachycardia, ventricular fibrillation) within the 6 months prior to screening, or New York Heart Association (NYHA) Class III-IV;
  14. Conditions not effectively controlled at the time of screening or markedly unstable diseases (such as acute pneumonia, pulmonary arterial hypertension, diabetic ketoacidosis, acute pancreatitis, etc.), which, in the investigator's judgement, may confound the study results or expose the participant to undue risk;
  15. Patients with a history of major organ transplantation (e.g., heart, lung, kidney, liver) or haematopoietic stem cell and/or bone marrow transplantation within the 5 years prior to screening;
  16. A history of chronic, recurrent (three or more episodes of the same type of infection within 52 weeks) or recent severe infections (e.g. pneumonia, sepsis), including viral infections (particularly varicella and herpes zoster), or requiring anti-infective treatment during the screening period;
  17. Patients who have undergone any major surgery within 6 weeks prior to randomisation, such as abdominal, thoracic or joint replacement surgery, or who are scheduled to undergo major surgery during the study (including follow-up);
  18. Patients for whom the investigator, based on an ophthalmological examination prior to randomisation, considers the findings to be clinically significant and unsuitable for participation in this clinical trial, or who have diseases associated with retinal pathology;
  19. Pregnant or breastfeeding women, or women of childbearing potential who do not agree to use effective contraception during the clinical trial;
  20. Patients with known hypersensitivity to artemisinin-based drugs, hydroxychloroquine or excipients (lactose, microcrystalline cellulose, sodium carboxymethyl starch, sodium dodecyl sulphate, polyvinylpyrrolidone, magnesium stearate);
  21. Any other circumstances, as determined by the investigator, that may interfere with the assessment of efficacy.
  22. Individuals who abuse drugs or alcohol;
  23. Participants who have taken part in any clinical trial within the three months prior to screening (excluding those who underwent safety checks only and did not receive any substantive medication or therapeutic.

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: Cuadruplicar

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Treatment Group 1
dihydroartemisinin 40 mg, twice daily
Dihydroartemisinin 40mg, taken orally twice a day, for a treatment period of 24 weeks.
Dihydroartemisinin 60mg, taken orally twice a day, for a treatment period of 24 weeks.
Experimental: Treatment Group 2
dihydroartemisinin 60 mg, twice daily
Dihydroartemisinin 40mg, taken orally twice a day, for a treatment period of 24 weeks.
Dihydroartemisinin 60mg, taken orally twice a day, for a treatment period of 24 weeks.
Comparador activo: control group
hydroxychloroquine 200 mg, once daily
Hydroxychloroquine 200mg, taken orally once a day, for a treatment period of 24 weeks.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Percentage change from baseline in the Cutaneous Lupus Erythematosus Area and Severity Index (CLASI-A) score at week 24
Periodo de tiempo: Week 24
Week 24

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
Percentage change from baseline in the Cutaneous Lupus Erythematosus Area and Severity Index (CLASI-A) score at weeks 2, 4, 8, 12, 16 and 20
Periodo de tiempo: weeks 2, 4, 8, 12, 16 and 20
weeks 2, 4, 8, 12, 16 and 20
Change in CLASI-A score from baseline
Periodo de tiempo: weeks 2, 4, 8, 12, 16, 20 and 24
weeks 2, 4, 8, 12, 16, 20 and 24
Percentage of participants with a ≥50% reduction in CLASI-A score from baseline (CLASI-50)
Periodo de tiempo: weeks 2, 4, 8, 12, 16, 20 and 24
weeks 2, 4, 8, 12, 16, 20 and 24
Percentage of participants with a ≥20% reduction in CLASI-A score from baseline
Periodo de tiempo: weeks 2, 4, 8, 12, 16, 20 and 24
weeks 2, 4, 8, 12, 16, 20 and 24
Percentage of participants with a 4-point reduction in CLASI-A activity score from baseline
Periodo de tiempo: weeks 2, 4, 8, 12, 16, 20 and 24
weeks 2, 4, 8, 12, 16, 20 and 24
Percentage of participants achieving a complete response (CR) in CLASI-A (defined as a score of '0')
Periodo de tiempo: weeks 2, 4, 8, 12, 16, 20 and 24
weeks 2, 4, 8, 12, 16, 20 and 24
Proportion of participants with a post-treatment DLQI (Dermatology Life Quality Index) score reduced by 2 points or more compared to baseline
Periodo de tiempo: weeks 2, 4, 8, 12, 16, 20 and 24
weeks 2, 4, 8, 12, 16, 20 and 24
Mean change in post-treatment DLQI (Dermatology Life Quality Index) score compared to baseline
Periodo de tiempo: weeks 2, 4, 8, 12, 16, 20 and 24
weeks 2, 4, 8, 12, 16, 20 and 24
Mean change in post-treatment PGA (Physician Global Assessment) score compared to baseline
Periodo de tiempo: weeks 2, 4, 8, 12, 16, 20 and 24
weeks 2, 4, 8, 12, 16, 20 and 24

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Yong Cui, MD, China-Japan Friendship Hospital

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 (Estimado)

30 de abril de 2026

Finalización primaria (Estimado)

30 de septiembre de 2028

Finalización del estudio (Estimado)

30 de septiembre de 2028

Fechas de registro del estudio

Enviado por primera vez

22 de abril de 2026

Primero enviado que cumplió con los criterios de control de calidad

22 de abril de 2026

Publicado por primera vez (Actual)

30 de abril de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

30 de abril de 2026

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

22 de abril de 2026

Última verificación

1 de abril de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

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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