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

22 april 2026 bijgewerkt door: 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).

Studie Overzicht

Gedetailleerde beschrijving

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.

Studietype

Ingrijpend

Inschrijving (Geschat)

100

Fase

  • Fase 2

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Locaties

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

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

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.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Verviervoudigen

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: 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.
Experimenteel: 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.
Actieve vergelijker: control group
hydroxychloroquine 200 mg, once daily
Hydroxychloroquine 200mg, taken orally once a day, for a treatment period of 24 weeks.

Wat meet het onderzoek?

Primaire uitkomstmaten

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

Secundaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
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
Tijdsspanne: weeks 2, 4, 8, 12, 16 and 20
weeks 2, 4, 8, 12, 16 and 20
Change in CLASI-A score from baseline
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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')
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: weeks 2, 4, 8, 12, 16, 20 and 24
weeks 2, 4, 8, 12, 16, 20 and 24

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Yong Cui, MD, China-Japan Friendship Hospital

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Geschat)

30 april 2026

Primaire voltooiing (Geschat)

30 september 2028

Studie voltooiing (Geschat)

30 september 2028

Studieregistratiedata

Eerst ingediend

22 april 2026

Eerst ingediend dat voldeed aan de QC-criteria

22 april 2026

Eerst geplaatst (Werkelijk)

30 april 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

30 april 2026

Laatste update ingediend die voldeed aan QC-criteria

22 april 2026

Laatst geverifieerd

1 april 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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