Informazioni generali
  • Categoria della malattia Malattie della pelle e del tessuto connettivo (non cancro) (BASEC)
  • Stato di reclutamento reclutamento in corso (BASEC/ICTRP)
  • Luogo dello studio
    Basilea, Berna, San Gallo
    (BASEC)
  • Responsabile dello studio Franzisca Rusca medinfo.ch@abbvie.com (BASEC)
  • Fonte dati BASEC: Importato da 07.01.2026 ICTRP: N/A
  • Ultimo aggiornamento 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)

  • Categoria della malattia Malattie della pelle e del tessuto connettivo (non cancro) (BASEC)
  • Stato di reclutamento reclutamento in corso (BASEC/ICTRP)
  • Luogo dello studio
    Basilea, Berna, San Gallo
    (BASEC)
  • Responsabile dello studio Franzisca Rusca medinfo.ch@abbvie.com (BASEC)
  • Fonte dati BASEC: Importato da 07.01.2026 ICTRP: N/A
  • Ultimo aggiornamento 07.01.2026 11:35

Descrizione riassuntiva dello studio

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)

Intervento studiato

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)

Malattie studiate

Systemic lupus erythematosus (SLE)

(BASEC)

Criteri di partecipazione
- 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)

Criteri di esclusione
- 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)

Luogo dello studio

Basilea, Berna, San Gallo

(BASEC)

non disponibile

Sponsor

AbbVie Inc. North Chicago USA AbbVie AG Cham Switzerland

(BASEC)

Contatto per ulteriori informazioni sullo studio

Persona di contatto in Svizzera

Franzisca Rusca

+41 41 399 16 89

medinfo.ch@abbvie.com

AbbVie Medical Information

(BASEC)

Informazioni scientifiche

non disponibile

Nome del comitato etico approvante (per studi multicentrici solo il comitato principale)

Ethikkommission Ostschweiz EKOS

(BASEC)

Data di approvazione del comitato etico

22.08.2023

(BASEC)


ID di studio ICTRP
non disponibile

Titolo ufficiale (approvato dal comitato etico)
A Phase 3 Program to Evaluate the Safety and Efficacy of Upadacitinib in Subjects with Moderately to Severely Active SLE (BASEC)

Titolo accademico
non disponibile

Titolo pubblico
non disponibile

Malattie studiate
non disponibile

Intervento studiato
non disponibile

Tipo di studio
non disponibile

Disegno dello studio
non disponibile

Criteri di inclusione/esclusione
non disponibile

non disponibile

Endpoint primari e secondari
non disponibile

non disponibile

Data di registrazione
non disponibile

Inclusione del primo partecipante
non disponibile

Sponsor secondari
non disponibile

Contatti aggiuntivi
non disponibile

ID secondari
non disponibile

Risultati-Dati individuali dei partecipanti
non disponibile

Ulteriori informazioni sullo studio
non disponibile

Risultati dello studio

Riepilogo dei risultati

non disponibile

Link ai risultati nel registro primario

non disponibile