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

22 avril 2026 mis à jour par: 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).

Aperçu de l'étude

Description détaillée

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.

Type d'étude

Interventionnel

Inscription (Estimé)

100

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: Duo Gao, bachelor
  • Numéro de téléphone: 0871-68319868-3052
  • E-mail: GAODUO5@kpc.com.cn

Lieux d'étude

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

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:

  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 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: 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.
Expérimental: 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.
Comparateur actif: control group
hydroxychloroquine 200 mg, once daily
Hydroxychloroquine 200mg, taken orally once a day, for a treatment period of 24 weeks.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
Percentage change from baseline in the Cutaneous Lupus Erythematosus Area and Severity Index (CLASI-A) score at week 24
Délai: Week 24
Week 24

Mesures de résultats secondaires

Mesure des résultats
Délai
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
Délai: weeks 2, 4, 8, 12, 16 and 20
weeks 2, 4, 8, 12, 16 and 20
Change in CLASI-A score from baseline
Délai: 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)
Délai: 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
Délai: 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
Délai: 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')
Délai: 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
Délai: 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
Délai: 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
Délai: weeks 2, 4, 8, 12, 16, 20 and 24
weeks 2, 4, 8, 12, 16, 20 and 24

Collaborateurs et enquêteurs

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

Les enquêteurs

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

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)

30 avril 2026

Achèvement primaire (Estimé)

30 septembre 2028

Achèvement de l'étude (Estimé)

30 septembre 2028

Dates d'inscription aux études

Première soumission

22 avril 2026

Première soumission répondant aux critères de contrôle qualité

22 avril 2026

Première publication (Réel)

30 avril 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

30 avril 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

22 avril 2026

Dernière vérification

1 avril 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

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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