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- Klinische proef NCT07557927
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
Toestand
Nog niet aan het werven
Conditie
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
- Naam: Duo Gao, bachelor
- Telefoonnummer: 0871-68319868-3052
- E-mail: GAODUO5@kpc.com.cn
Studie Locaties
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Anhui
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Hefei, Anhui, China
- The First Affiliated Hospital of Anhui Medical University
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Beijing Municipality
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Beijing, Beijing Municipality, China
- Peking University People's Hospital
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Beijing, Beijing Municipality, China
- China-Japan Friendship Hospital
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Chongqing Municipality
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Chongqing, Chongqing Municipality, China
- The First Affiliated Hospital of Chongqing Medical University
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Guangdong
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Guangzhou, Guangdong, China
- Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University
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Guangzhou, Guangdong, China
- Nanfang Hospital, Southern Medical University
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Hunan
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Changsha, Hunan, China
- The Second Xiangya Hospital of Central South University
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Liaoning
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Shenyang, Liaoning, China
- The First Affiliated Hospital of China Medical University
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Yunnan
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Kunming, Yunnan, China
- The Second Affiliated Hospital of Kunming Medical University
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Zhejiang
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Hangzhou, Zhejiang, China
- Hangzhou Third People's Hospital
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-
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:
- Participants are able to understand the purpose and risks of the study and voluntarily sign an informed consent form;
- Aged between 18 and 65 years (inclusive);
- Body weight ≥ 45 kg;
- 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;
- At the time of screening, the Cutaneous Lupus Erythematosus Area and Severity Index (CLASI-A) must be ≥4.
Exclusion Criteria:
- Patients with systemic lupus erythematosus (SLE) or those at high risk of developing SLE;
- Drug-induced lupus;
- Patients with a history of resistance to antimalarial treatment;
- 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);
- Patients diagnosed with anaemia within 3 months prior to randomisation, or patients with haemoglobin levels below 110 g/L at screening;
- Patients who have used any antimalarial drug (hydroxychloroquine sulphate, chloroquine phosphate or chloroquine) within 4 weeks prior to randomisation;
- 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;
- Patients treated with biologics (e.g. adalimumab, secukinumab or others) within 12 weeks prior to randomisation;
- Patients treated with immunomodulators (e.g. thalidomide, lenalidomide or others) within 4 weeks prior to randomisation;
- Patients who have received live vaccines (e.g. measles vaccine, varicella vaccine or others) within 4 weeks prior to randomisation;
- 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;
- History of malignant tumours within the 5 years prior to screening;
- 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;
- 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;
- 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;
- 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;
- 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);
- 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;
- Pregnant or breastfeeding women, or women of childbearing potential who do not agree to use effective contraception during the clinical trial;
- Patients with known hypersensitivity to artemisinin-based drugs, hydroxychloroquine or excipients (lactose, microcrystalline cellulose, sodium carboxymethyl starch, sodium dodecyl sulphate, polyvinylpyrrolidone, magnesium stearate);
- Any other circumstances, as determined by the investigator, that may interfere with the assessment of efficacy.
- Individuals who abuse drugs or alcohol;
- 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
|
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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
|
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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.
Sponsor
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
Aanvullende relevante MeSH-voorwaarden
- Bindweefselziekten
- Huidziektes
- Lupus erythematosus, cutaan
- Huid- en bindweefselaandoeningen
- Lupus Erythematosus, discoïde
- Heterocyclische verbindingen
- Heterocyclische verbindingen, 2-ring
- Heterocyclische verbindingen, gefuseerd ring
- Chinolines
- Aminoquinolines
- Chloroquine
- Hydroxychloroquine
- artenimol
Andere studie-ID-nummers
- KPC078-C202
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 .