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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. juni 2026 opdateret af: 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.

Studieoversigt

Status

Ikke rekrutterer endnu

Detaljeret beskrivelse

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.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

24

Fase

  • Fase 2

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Barn

Tager imod sunde frivillige

Ingen

Beskrivelse

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).

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Ikke-randomiseret
  • Interventionel model: Sekventiel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: 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.
Andre navne:
  • MEDI-546
  • SAPHNELO™
Eksperimentel: 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.
Andre navne:
  • MEDI-546
  • SAPHNELO™

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Maximum observed serum (peak) concentration (Cmax)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: At Week 12
To characterize PK (Ctrough,ss) of anifrolumab in pediatric participants with SLE following SC administration.
At Week 12

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Suppression of type I IFN 21-gene signature
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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

Andre resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Number with participants with adverse events (AEs), serious adverse events (SAEs) and adverse events of special interest (AESIs)
Tidsramme: 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)

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

28. juli 2026

Primær færdiggørelse (Anslået)

3. september 2030

Studieafslutning (Anslået)

5. september 2031

Datoer for studieregistrering

Først indsendt

2. juni 2026

Først indsendt, der opfyldte QC-kriterier

2. juni 2026

Først opslået (Faktiske)

5. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

5. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

2. juni 2026

Sidst verificeret

1. maj 2026

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

JA

IPD-planbeskrivelse

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.

IPD-delingstidsramme

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.

IPD-delingsadgangskriterier

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.

IPD-deling Understøttende informationstype

  • STUDY_PROTOCOL
  • SAP

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ja

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ja

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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