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Exploratory Study of DHA in Systemic Lupus Erythematosus Patients

Phase 2
Conditions
Systemic Lupus Erythematosus
Interventions
Registration Number
NCT03396393
Lead Sponsor
Kunming Pharmaceuticals, Inc.
Brief Summary

The primary objective of the study is to assess the efficacy of DHA in patients with SLE.

Detailed Description

This is a Phase 2, multicentre, randomised, double-blind, placebo-controlled study to evaluate the Safety, Pharmacokinetics and Efficacy of four oral treatment regimens of DHA versus placebo while taking standard of care (SOC) treatment with corticosteroids in adult subjects with Systemic Lupus Erythematosus (SLE).

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
120
Inclusion Criteria
  1. Fulfill at least 4 diagnostic criteria for SLE defined by American College of Rheumatology;
  2. Positive antinuclear antibodies (ANA);
  3. Activity Index (SLEDAI) score must be 6-11 points, inclusive;
  4. Stable dose of prednisone (<30mg/d) for at least one month ;
  5. Active mild to moderate SLE activity as demonstrated by British Isles Lupus Assessment Group Index (BILAG);
  6. Males or females between 18 and 65 years old;
  7. Weight of 45 kg or greater.

Key

Exclusion Criteria
  1. Active Severe Lupus as defined by BILAG Index Level A or two or more of Level B in any body system/organ;
  2. Subjects with concurrent relevant medical conditions like defined chronic infections or high risk of new significant infections;
  3. Presence of active central nervous system (CNS) disease requiring treatment;
  4. Subjects with active, severe SLE disease activity which involves the renal system;
  5. Substance abuse or dependence;
  6. History of malignant cancer within the last 5 years;
  7. Subjects with any other condition which, in the investigator's judgment, would make the subject unsuitable for inclusion;
  8. Subjects received any live vaccination within the 30 days prior to Visit 2;
  9. Subjects received intravenous immunoglobulin (IVIg) or,plasmapheresis,or High dose prednisone or equivalent (> 100 mg/day) within 90 days prior to Visit 2;
  10. Subjects who have had therapy with cyclophosphamide within 180 days prior to Visit 2 .

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Dihydroartemisinin 120mgDihydroartemisinin tabletRandomized 30 patients will be received Dihydroartemisinin tablets 120mg in oral continuously from Week 0 to Week 24 in addition to SOC.
Dihydroartemisinin 40mgDihydroartemisinin tabletRandomized 30 patients will be received Dihydroartemisinin tablets 40mg in oral continuously from Week 0 to Week 24 in addition to SOC.
placeboPlacebo tabletRandomized 30 patients will be received placebo tablets in oral continuously from Week 0 to Week 24 in addition to SOC.
Dihydroartemisinin 80mgDihydroartemisinin tabletRandomized 30 patients will be received Dihydroartemisinin tablets 80mg in oral continuously from Week 0 to Week 24 in addition to SOC.
Primary Outcome Measures
NameTimeMethod
SRI,Response at Week 24 according to a combined response indexweek 24

The combined response index incorporates the Bristish Isles Lupus Assessment Group (BILAG) assessment, the Systemic Lupus Eyrthematosus Disease Activity Index (SLEDAI), a physician's global assessment of disease activity, and treatment failure status.

Secondary Outcome Measures
NameTimeMethod
Change from baseline in SLEDAI scoreweek 4,8,12,16,20,24

Change from baseline in SLEDAI score at week 4,8,12,16,20,24

Change from baseline in PAG scoreweek 4,8,12,16,20,24

Change from baseline in PAG score at week 4,8,12,16,20,24

Number of days of daily prednisone dose Less than or equal to 7.5 mg/dayBaseline, Week 24

Number of days of daily prednisone dose Less than or equal to 7.5 mg/day from baseline over 24 weeks

Percent of subjects with UPRO <0.5g/24hWeek 4,12,24

Percent of subjects with UPRO \<0.5g/24h from baseline at Week 4,12,24

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