For Healthcare Professionals

A Study of Telitacicept for the Treatment of Moderately to Severely Active Systemic Lupus Erythematosus (REMESLE-1)

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About the study

The purpose of this study is to evaluate the efficacy and safety of telitacicept in the treatment of moderately to severely active SLE.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:


  1. Age 12-70 years at screening.
  2. Has a diagnosis of SLE for at least 6 months prior to the screening visit.
  3. Meets the 2019 EULAR/ACR Classification criteria for SLE.
  4. Moderately to severely active SLE defined by the following:

  1. SELENA SLEDAI total score ≥6 points with clinical SLEDAI score ≥4 points at screening;
  2. BILAG organ system scores of at least 1A or 2B at screening.
  3. Clinical SLEDAI score of ≥4 at Day 0 prior to randomization.
  4. At least one positive serologic parameter within the screening period.
  5. Currently receiving at least one of the SOC SLE medications: oral corticosteroid, antimalarial and/or immunosuppressive agent.

EXCLUSION CRITERIA

Exclusion Criteria:


  1. Active lupus nephritis undergoing induction therapy or unstable renal diseases within 12 weeks prior to screening.
  2. Active or unstable neuropsychiatric SLE.
  3. Autoimmune or rheumatic disease other than SLE

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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.

Study’s details


Contition

Systemic Lupus Erythematosus

Age (in years)

12 - 70

Phase

PHASE3

Participants needed

350

Est. Completion Date

Mar 2, 2027

Treatment type

INTERVENTIONAL


Sponsor

RemeGen Co., Ltd.

ClinicalTrials.gov identifier

NCT05306574

Study number

RC18G001

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