Informations générales
  • Catégorie de maladie Maladies de la peau et du tissu conjonctif (hors cancer) (BASEC)
  • État du recrutement recrutement en cours (BASEC/ICTRP)
  • Lieu de l’étude
    Bâle, Berne, St-Gall
    (BASEC)
  • Responsable de l'étude Franzisca Rusca medinfo.ch@abbvie.com (BASEC)
  • Source(s) de données BASEC: Importé de 07.01.2026 ICTRP: N/A
  • Date de mise à jour 07.01.2026 11:35
HumRes63010 | SNCTP000005607 | BASEC2023-01114

Phase III study to assess the safety and efficacy of Upadacitinib in study participants with moderate to severe active systemic lupus erythematosus (SLE)

  • Catégorie de maladie Maladies de la peau et du tissu conjonctif (hors cancer) (BASEC)
  • État du recrutement recrutement en cours (BASEC/ICTRP)
  • Lieu de l’étude
    Bâle, Berne, St-Gall
    (BASEC)
  • Responsable de l'étude Franzisca Rusca medinfo.ch@abbvie.com (BASEC)
  • Source(s) de données BASEC: Importé de 07.01.2026 ICTRP: N/A
  • Date de mise à jour 07.01.2026 11:35

Résumé de l'étude

Systemic lupus erythematosus (SLE) is an immune-mediated disease associated with inflammation of multiple organ systems. This study evaluates the safety and efficacy of Upadacitinib in treating adult study participants with moderate to severe active SLE. Adverse events and changes in disease activity will be assessed. Upadacitinib is a drug approved for rheumatoid arthritis, psoriatic arthritis, and axial spondyloarthritis, and is currently being developed for the treatment of SLE. This study is double-blind, meaning that neither the study participants nor the investigators know who is receiving Upadacitinib and who is receiving placebo (no active ingredient). This study consists of 3 sub-studies. In Study 1 and Study 2, the study doctors assigned participants to one of two so-called treatment arms. Each group receives a different treatment. There is a 1:2 chance that study participants will receive a placebo. Suitable participants from Study 1 and Study 2 will be enrolled in Study 3 at Week 52 and will receive specific doses of Upadacitinib based on disease activity and their original treatment assignment in Study 1 or 2. Approximately 500 patients diagnosed with SLE will be enrolled at about 320 study centers worldwide in Study 1 and Study 2.

(BASEC)

Intervention étudiée

Study participants will receive Upadacitinib tablets to take once daily for 52 weeks or corresponding placebo in Study 1 and Study 2. Suitable participants from Study 1 and Study 2 will receive Upadacitinib tablets to take once daily for 52 weeks in Study 3.

(BASEC)

Maladie en cours d'investigation

Systemic lupus erythematosus (SLE)

(BASEC)

Critères de participation
- Clinical diagnosis of systemic lupus erythematosus (SLE) at least 24 weeks prior to screening according to the definition of the SLE classification criteria of the European Alliance of Associations for Rheumatology (EULAR)/American College of Rheumatology (ACR) 2019 - Meet at least one of the following criteria at screening: 1- Positive antinuclear antibodies (ANA) 2- Positive anti-double-stranded DNA (dsDNA) 3- Positive anti-Smith - hSLEDAI (hybrid systemic lupus erythematosus disease activity index) >= 6, with >= 4 points being clinical (not based on laboratory criteria), independently determined at screening. The clinical hSLEDAI score (not based on laboratory criteria) must be confirmed at the baseline visit as >= 4. Lupus headaches or organic brain syndrome do not count towards the hSLEDAI points required for participation, but should be documented on the hSLEDAI if present. - Physician's global assessment (PhGA) >= 1 in the screening phase - Stable background therapy for >= 30 days prior to baseline (except for oral corticosteroids, which must have a stable dose for at least 14 days prior to baseline) with: a) Antimalarial drug(s) (Hydroxychloroquine <= 400 mg once daily, Chloroquine <= 500 mg once daily, Quinacrine <= 100 mg once daily) and/or Prednisone (or prednisone equivalent) (<= 20 mg once daily) and/or at most one of the following medications: Azathioprine (<= 150 mg once daily) b) Mycophenolate mofetil (<= 2 g once daily), Mycophenolate sodium <= 1,440 mg once daily c) Leflunomide (<= 20 mg once daily) d) Cyclosporine, Tacrolimus, Voclosporin (<= 23.7 mg twice daily) e) Methotrexate (<= 25 mg once weekly) or Mizoribine (<= 150 mg once daily) (BASEC)

Critères d'exclusion
- Clinically relevant or significant abnormalities on ECG at screening. - Planned elective procedure that would affect study procedures or assessments until completion of assessments at Week 52. (BASEC)

Lieu de l’étude

Bâle, Berne, St-Gall

(BASEC)

non disponible

Sponsor

AbbVie Inc. North Chicago USA AbbVie AG Cham Switzerland

(BASEC)

Contact pour plus d'informations sur l'étude

Personne de contact en Suisse

Franzisca Rusca

+41 41 399 16 89

medinfo.ch@abbvie.com

AbbVie Medical Information

(BASEC)

Informations scientifiques

non disponible

Nom du comité d'éthique approbateur (pour les études multicentriques, uniquement le comité principal)

Ethikkommission Ostschweiz EKOS

(BASEC)

Date d'approbation du comité d'éthique

22.08.2023

(BASEC)


Identifiant de l'essai ICTRP
non disponible

Titre officiel (approuvé par le comité d'éthique)
A Phase 3 Program to Evaluate the Safety and Efficacy of Upadacitinib in Subjects with Moderately to Severely Active SLE (BASEC)

Titre académique
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Titre public
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Maladie en cours d'investigation
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Intervention étudiée
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Type d'essai
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Plan de l'étude
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Critères d'inclusion/exclusion
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Critères d'évaluation principaux et secondaires
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Date d'enregistrement
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Inclusion du premier participant
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Sponsors secondaires
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Contacts supplémentaires
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ID secondaires
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Résultats-Données individuelles des participants
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Informations complémentaires sur l'essai
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Résultats de l'essai

Résumé des résultats

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Lien vers les résultats dans le registre primaire

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