A Multicentre, Randomised, Double-blind, Positive-control Clinical Trial Evaluating Dihydroartemisinin Tablets for the Treatment of Discoid Lupus Erythematosus
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Estimated)
Enrollment
Phase
Phase
- Phase 2
Contacts and Locations
Study Contact
Study Contact
- Name: Duo Gao, bachelor
- Phone Number: 0871-68319868-3052
- Email: GAODUO5@kpc.com.cn
Study Locations
-
-
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
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
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.
|
|
Active Comparator: control group
hydroxychloroquine 200 mg, once daily
|
Hydroxychloroquine 200mg, taken orally once a day, for a treatment period of 24 weeks.
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Percentage change from baseline in the Cutaneous Lupus Erythematosus Area and Severity Index (CLASI-A) score at week 24
Time Frame: Week 24
|
Week 24
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
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
Time Frame: weeks 2, 4, 8, 12, 16 and 20
|
weeks 2, 4, 8, 12, 16 and 20
|
|
Change in CLASI-A score from baseline
Time Frame: 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)
Time Frame: 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
Time Frame: 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
Time Frame: 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')
Time Frame: 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
Time Frame: 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
Time Frame: 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
Time Frame: weeks 2, 4, 8, 12, 16, 20 and 24
|
weeks 2, 4, 8, 12, 16, 20 and 24
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Principal Investigator: Yong Cui, MD, China-Japan Friendship Hospital
Study record dates
Study Major Dates
Study Start (Estimated)
Study Start
Primary Completion (Estimated)
Primary Completion
Study Completion (Estimated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- KPC078-C202
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.