A Study of Telitacicept for the Treatment of Moderately to Severely Active Systemic Lupus Erythematosus (REMESLE-2)

Last updated: September 13, 2024
Sponsor: RemeGen Co., Ltd.
Overall Status: Active - Recruiting

Phase

3

Condition

Bone Diseases

Lupus

Cutaneous Lupus Erythematosus

Treatment

Placebo

Telitacicept

Clinical Study ID

NCT06456567
RC18G002
  • Ages 12-70
  • All Genders

Study Summary

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

Eligibility Criteria

Inclusion

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 definined by the following:

  5. SELENA SLEDAI total score ≥6 points with clinical SLEDAI score ≥4 points atscreening;

  6. BILAG organ system scores of at least 1A or 2B at screening.

  7. Clinical SLEDAI score of ≥4 at Day 0 prior to randomization.

  8. At least one positive serologic parameter within the screening period.

  9. Currently receiving at least one of the SOC SLE medications: oral corticosteroid,antimalarial and/or immunosuppressive agent.

Exclusion

Exclusion Criteria:

  1. Active lupus nephritis undergoing induction therapy or unstable renal diseaseswithin 12 weeks prior to screening.

  2. Active or unstable neuropsychiatric SLE.

  3. Autoimmune or rheumatic disease other than SLE.

  4. History of arterial or venous thromboembolism or microangiopathy within 12 monthsprior to screening.

  5. History of non-SLE disease requiring treatment with oral or parenteral.glucocorticosteroids for more than a total of 2 weeks within the last 24 weeks priorto screening.

Study Design

Total Participants: 350
Treatment Group(s): 2
Primary Treatment: Placebo
Phase: 3
Study Start date:
September 01, 2024
Estimated Completion Date:
May 31, 2027

Study Description

Systemic Lupus Erythematosus (SLE) is a chronic autoimmune disease with heterogeneous manifestations and disease course. Despite advances in medical care, there are still significant unmet needs in SLE with diminished health-related quality of life (HRQoL), persistent disease activity, disease flares, intolerance to standard of care (SOC) therapies, and development of organ damage and co-morbidities.

Telitacicept is a fully human TACI-Fc fusion protein that targets B lymphocyte stimulator (BLyS) and a proliferating-inducing ligand (APRIL). Blocking the interaction of BLyS and APRIL with their cell membrane receptors (TACI, B-cell maturation antigen (BCMA), and B-cell activating factor receptor (BAFF-R) would inhibit B cell proliferation and maturation, suppresses immune responses and may alleviate autoimmune symptoms.

This is a multicenter, randomized, double-blind, placebo-controlled, phase 3 study to evaluate the efficacy and safety of telitacicept added to standard of care (SoC) therapy compared to placebo with SoC therapy in subjects with moderately to severely active SLE.

Connect with a study center

  • Hemet site

    Hemet, California 92543
    United States

    Active - Recruiting

  • Menifee site

    Menifee, California 92586
    United States

    Active - Recruiting

  • Rockford site

    Rockford, Illinois 61114
    United States

    Active - Recruiting

  • Stafford site

    Stafford, Texas 77477
    United States

    Active - Recruiting

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