- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07630714
A Study to Investigate Pharmacokinetics, Pharmacodynamics, and Safety of Subcutaneous Anifrolumab in Pediatric Participants 5 to < 18 Years of Age With Systemic Lupus Erythematosus
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
Studieoversigt
Status
Betingelser
Intervention / Behandling
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
Tilmelding (Anslået)
Fase
- Fase 2
Kontakter og lokationer
Studiekontakt
- Navn: AstraZeneca Clinical Study Information Center
- Telefonnummer: 1-877-240-9479
- E-mail: information.center@astrazeneca.com
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
Tager imod sunde frivillige
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
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:
|
|
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:
|
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
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Bindevævssygdomme
- Autoimmune sygdomme
- Sygdomme i immunsystemet
- Infektioner
- Gram-positive bakterielle infektioner
- Bakterielle infektioner
- Bakterielle infektioner og mykoser
- Actinomycetales infektioner
- Mycobacterium infektioner
- Hud- og bindevævssygdomme
- Lupus erythematosus, systemisk
- Mycobacterium-infektioner, ikke-tuberkuløse
- Anifrolumab
Andre undersøgelses-id-numre
- D3465C00008
- 2025-524578-41-00 (Ctis)
- EMA/PE/0000246211 (Anden identifikator: Pediatric investigation plan [PIP])
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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
IPD-delingsadgangskriterier
IPD-deling Understøttende informationstype
- STUDY_PROTOCOL
- SAP
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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