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Phase 3 N=1,164 Randomized Quadruple-blind Treatment

A Study of LY2127399 in Participants With Systemic Lupus Erythematosus

Systemic Lupus Erythematosus · Connective Tissue Disease · Autoimmune Disease

Enrolled (actual)
1,164
Serious AEs
13.4%
Results posted
Jun 2018
Primary outcome: Primary: Percentage of Participants Achieving an SLE Responder Index Response at Week 52 — 31.8; 35.2; 29.3 percentage of participants

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
LY2127399 (Drug); Placebo every 2 weeks (Drug); Placebo every 4 weeks (Drug); Standard of Care (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Eli Lilly and Company
Primary completion
Jul 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants Achieving an SLE Responder Index Response at Week 52
31.8; 35.2; 29.3
SECONDARY
Percentage Participants Able to Decrease Dose of Prednisone or Equivalent With No Increase in Disease Activity at Week 52
15.5; 17.0; 16.4
SECONDARY
Change From Baseline to 52 Weeks in Anti-double Stranded Deoxyribonucleic Acid (Anti-dsDNA) Level
107.2; 110.4; 107.1
SECONDARY
Change From Baseline to 52 Week Endpoint in Systemic Lupus Erythematosus Disease Activity Index (SLEDAI2K) Score
-4.7; -4.9; -4.6
SECONDARY
Time to First Severe SLE Flare (SFI)
SECONDARY
Percentage of Participants With No Worsening in Physician Global Assessment (PGA) Score at 52 Weeks
64.3; 61.4; 58.0
SECONDARY
Change From Baseline to 52 Week Endpoint in Brief Fatigue Inventory (BFI) Scores
-0.9; -0.9; -0.6
SECONDARY
Change From Baseline to 52 Week Endpoint Lupus Quality of Life (LupusQoL) Domain Scores
73.7; 72.8; 72.8; 75.2; 72.4; 73.1
SECONDARY
Time to First New British Isles Lupus Assessment Group (BILAG A) or 2 New BILAG B SLE Flares
SECONDARY
Change From Baseline to 52 Week Endpoint in PGA
-20.8; -20.8; -20.2
SECONDARY
Percentage of Participants With an Increase in Corticosteroids Dose at 52 Weeks
6.7; 9.1; 8.8
SECONDARY
Change From Baseline to 52 Weeks Endpoint in SELENA-SLEDAI Disease Activity Score
-4.6; -4.7; -4.8
SECONDARY
Percentage of Participants Achieving a Response as Measured by Modified SRI With No BILAG A or No More Than 1 BILAG B Organ Domain Flares at 52 Weeks
31.8; 35.2; 29.6; 68.2; 64.8; 70.4
SECONDARY
Number of Participants With No New BILAG A and No More Than One New BILAG B Disease Activity Scores Compared to Baseline
247; 234; 219

Summary

The purpose of this SLE study is to evaluate the efficacy, safety and tolerability of two different doses of LY2127399 administered in participants with active SLE.

Eligibility Criteria

Inclusion Criteria

  • Clinical diagnosis of SLE by American College of Rheumatology (ACR) criteria
  • Have positive antinuclear antibodies (ANA)
  • Agree not to become pregnant throughout the course of the trial
  • Have a screening SELENA-SLEDAI score ≥6. (The participant must be actively exhibiting all the symptoms scored on the screening SELENA-SLEDAI on the day of screening.)

Exclusion Criteria

  • Have active severe Lupus kidney disease
  • Have active Central Nervous System or peripheral neurologic disease
  • Have received intravenous immunoglobulin (IVIg) within 180 days of randomization
  • Have active or recent infection within 30 days of screening
  • Have had a serious infection within 90 days of randomization
  • Have evidence or test positive for Hepatitis B
  • Have Hepatitis C
  • Are human immunodeficiency virus (HIV) positive
  • Have evidence of active or latent tuberculosis (TB)
  • Presence of significant laboratory abnormalities at screening
  • Have had a malignancy in the past 5 years, except for cervical carcinoma in-situ or basal cell or squamous epithelial skin cell that were completely resected with no reoccurrence in the 3 yrs prior to randomization
  • Have received greater than 40 mgs of prednisone or equivalent in the past 30 days
  • Have changed your dose of antimalarial drug in the past 30 days
  • Have changed your dose of immunosuppressive drug in the past 90 days
  • Have previously received rituximab
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01196091). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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