Cette page a été traduite automatiquement et l'exactitude de la traduction n'est pas garantie. Veuillez vous référer au version anglaise pour un texte source.

A Study to Investigate Pharmacokinetics, Pharmacodynamics, and Safety of Subcutaneous Anifrolumab in Pediatric Participants 5 to < 18 Years of Age With Systemic Lupus Erythematosus

2 juin 2026 mis à jour par: AstraZeneca

A Multicenter, Open-Label, Phase II Study to Evaluate the Pharmacokinetics, Pharmacodynamics, and Safety of Subcutaneous Anifrolumab in Pediatric Participants 5 to < 18 Years of Age With Systemic Lupus Erythematosus

The purpose of this study is to characterize the pharmacokinetics (PK), pharmacodynamics (PD), and safety of subcutaneous (SC) anifrolumab in pediatric participants with moderate to severe systemic lupus erythematosus (SLE) while on background standard of care (SoC) therapy.

Aperçu de l'étude

Statut

Pas encore de recrutement

Intervention / Traitement

Description détaillée

This is an open-label, multicenter study.

The study includes -

  • Screening Period of up to 35 days
  • Period A (12-week, open-label treatment period)
  • Period B (a possible 12-week dosing regimen adjustment period, if required)
  • Treatment Extension Period (up-to-40-week, optional)
  • Period C (a 12-week safety follow-up period)

The study intervention (anifrolumab) will be administered subcutaneously using an accessorized pre-filled syringe (APFS) in 2 cohorts.

Type d'étude

Interventionnel

Inscription (Estimé)

24

Phase

  • Phase 2

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Enfant

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  • Diagnosis of SLE.
  • Must be receiving at least one of the following SoC regimens for ≥ 4 weeks: oral glucocorticoids (≤1.0 mg/kg/day or ≤ 40 mg/day prednisone equivalent), antimalarials (hydroxychloroquine, chloroquine, or quinacrine), or a single permitted immunosuppressant (azathioprine, mycophenolate mofetil/mycophenolic acid, methotrexate, mizoribine, or tacrolimus) within specified dose limits.
  • Participant must have moderate to severe active SLE disease defined as Systemic lupus erythematosus disease activity index 2000 (SLEDAI-2K) ≥ 6 total points.
  • Body weight ≥ 15 kg.
  • Participants must agree to follow study specific contraception requirements as per local regulations.

Exclusion Criteria:

  • Known diagnosis of an IFN mediated autoinflammatory interferonopathy.
  • History of, or current diagnosis of, clinically significant non-SLE related vasculitides.
  • Active, severe SLE-driven renal disease with significant proteinuria.
  • Active severe or unstable neuropsychiatric SLE including but not limited to aseptic meningitis; cerebral vasculitis; myelopathy; demyelination syndromes (ascending, transverse, acute inflammatory demyelinating polyradiculopathy); acute confusional state; impaired level of consciousness; psychosis; acute stroke or stroke syndrome; cranial neuropathy; status epilepticus; cerebellar ataxia; and mononeuritis multiplex.
  • In participants ≥ 11 years of age, a history or evidence of suicidal ideation (severity of 4 [active: method and intent, but no plan] or 5 [active: method, intent, and plan]) within the past 6 months; or any suicidal behavior within the past 12 months or recurrent suicidal behavior in the lifetime of the participant based on an assessment with the Columbia suicide severity rating scale (C-SSRS).
  • History of, or current diagnosis of, catastrophic antiphospholipid syndrome (APS).
  • History of recurrent or opportunistic infection requiring hospitalization and intravenous (IV) antibiotics.
  • Known history of a primary immunodeficiency, splenectomy, or any underlying condition that predisposes the participant to infection, or a positive result for human immunodeficiency virus (HIV) infection.
  • Active hepatitis B and C infection.
  • Any active or recent herpes zoster (HZ) infection that has not completely resolved within 12 weeks prior to study entry or that emerges between screening and Day 1.
  • Any history of severe or recurrent HZ, including non-cutaneous HZ, herpes encephalitis, ophthalmic herpes, or 2 or more prior HZ episodes.
  • Any cytomegalovirus (CMV) or Epstein Barr virus (EBV) infection that has not completely resolved.
  • History of cancer.
  • Prior receipt of anifrolumab.
  • Prior treatment with directly acting cytotoxic B-cell depleting therapeutics.
  • A known history of allergy or reaction to any component of the study intervention formulation or history of anaphylaxis to any human gamma globulin therapy, human proteins, or monoclonal antibodies (mAbs).

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Non randomisé
  • Modèle interventionnel: Affectation séquentielle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Cohort 1 (body weight > 40 kg)
Participants with body weight > 40 kg will receive anifrolumab as an injection in APFS.
Anifrolumab will be administered as a SC injection using an APFS.
Autres noms:
  • MEDI-546
  • SAPHNELO™
Expérimental: Cohort 2 (body weight ≥ 15 to ≤ 40 kg)
Participants with body weight ≥ 15 to ≤ 40 kg will receive anifrolumab as an injection in APFS.
Anifrolumab will be administered as a SC injection using an APFS.
Autres noms:
  • MEDI-546
  • SAPHNELO™

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Maximum observed serum (peak) concentration (Cmax)
Délai: Cohort 1: From Day 1 to Day 8; Cohort 2: From Day 1 to Day 11
To characterize PK (Cmax) of anifrolumab in pediatric participants with SLE following SC administration.
Cohort 1: From Day 1 to Day 8; Cohort 2: From Day 1 to Day 11
Area under the serum concentration-time curve (AUC)
Délai: Cohort 1: From Day 1 to Day 8; Cohort 2: From Day 1 to Day 11
To characterize PK (AUC) of anifrolumab in pediatric participants with SLE following SC administration.
Cohort 1: From Day 1 to Day 8; Cohort 2: From Day 1 to Day 11
Time to maximum plasma concentration (tmax)
Délai: Cohort 1: From Day 1 to Day 8; Cohort 2: From Day 1 to Day 11
To characterize PK (tmax) of anifrolumab in pediatric participants with SLE following SC administration.
Cohort 1: From Day 1 to Day 8; Cohort 2: From Day 1 to Day 11
Apparent total body clearance of drug from plasma (CL/F)
Délai: Cohort 1: From Day 1 to Day 8; Cohort 2: From Day 1 to Day 11
To characterize PK (CL/F) of anifrolumab in pediatric participants with SLE following SC administration.
Cohort 1: From Day 1 to Day 8; Cohort 2: From Day 1 to Day 11
Trough drug concentration at steady state (Ctrough,ss)
Délai: At Week 12
To characterize PK (Ctrough,ss) of anifrolumab in pediatric participants with SLE following SC administration.
At Week 12

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Suppression of type I IFN 21-gene signature
Délai: At Week 12 and 52
To characterize PD of anifrolumab in pediatric participants with SLE following SC administration.
At Week 12 and 52
Change from baseline in anti-double-stranded deoxyribonucleic acid (dsDNA) antibodies
Délai: At Week 12 and 52
To characterize PD of anifrolumab in pediatric participants with SLE following SC administration.
At Week 12 and 52
Change from baseline in complement component 3 (C3) levels
Délai: At Week 12 and 52
To characterize PD of anifrolumab in pediatric participants with SLE following SC administration.
At Week 12 and 52
Change from baseline in complement component 4 (C4) levels
Délai: At Week 12 and 52
To characterize PD of anifrolumab in pediatric participants with SLE following SC administration.
At Week 12 and 52
Change from baseline in total hemolytic complement (CH50) levels
Délai: At Week 12 and 52
To characterize PD of anifrolumab in pediatric participants with SLE following SC administration.
At Week 12 and 52
Number and percentage of participants who develop anti drug antibody (ADA) against anifrolumab
Délai: From Day 1 to Week 52
To evaluate the immunogenicity of anifrolumab in pediatric participants with SLE following SC administration.
From Day 1 to Week 52

Autres mesures de résultats

Mesure des résultats
Description de la mesure
Délai
Number with participants with adverse events (AEs), serious adverse events (SAEs) and adverse events of special interest (AESIs)
Délai: Up to follow-up visit (12 weeks post last dose of study intervention) (approximately 64 weeks)
To evaluate the safety and tolerability of anifrolumab in pediatric participants with SLE following SC administration.
Up to follow-up visit (12 weeks post last dose of study intervention) (approximately 64 weeks)

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

28 juillet 2026

Achèvement primaire (Estimé)

3 septembre 2030

Achèvement de l'étude (Estimé)

5 septembre 2031

Dates d'inscription aux études

Première soumission

2 juin 2026

Première soumission répondant aux critères de contrôle qualité

2 juin 2026

Première publication (Réel)

5 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

5 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

2 juin 2026

Dernière vérification

1 mai 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

OUI

Description du régime IPD

Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal Vivli.org. All requests will be evaluated as per the AZ disclosure commitment:

https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.

Yes, indicates that AZ are accepting requests for IPD, but this does not mean all requests will be shared.

Délai de partage IPD

AstraZeneca will meet or exceed data availability as per the commitments made to the EFPIA PhRMA Data Sharing Principles. For details of our timelines, please rerefer to our disclosure commitment at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.

Critères d'accès au partage IPD

When a request has been approved AstraZeneca will provide access to the anonymized individual patient-level data via secure research environment Vivli.org. Signed Data Usage Agreement (non-negotiable contract for data accessors) must be in place before accessing requested information.

Type d'informations de prise en charge du partage d'IPD

  • PROTOCOLE D'ÉTUDE
  • SÈVE

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Oui

Étudie un produit d'appareil réglementé par la FDA américaine

Oui

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

S'abonner