- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica 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
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
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.
Tipo di studio
Iscrizione (Stimato)
Fase
- Fase 2
Contatti e Sedi
Contatto studio
- Nome: AstraZeneca Clinical Study Information Center
- Numero di telefono: 1-877-240-9479
- Email: information.center@astrazeneca.com
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Bambino
Accetta volontari sani
Descrizione
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).
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Non randomizzato
- Modello interventistico: Assegnazione sequenziale
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: 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.
Altri nomi:
|
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Sperimentale: 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.
Altri nomi:
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Maximum observed serum (peak) concentration (Cmax)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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
|
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Apparent total body clearance of drug from plasma (CL/F)
Lasso di tempo: 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)
Lasso di tempo: At Week 12
|
To characterize PK (Ctrough,ss) of anifrolumab in pediatric participants with SLE following SC administration.
|
At Week 12
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Suppression of type I IFN 21-gene signature
Lasso di tempo: At Week 12 and 52
|
To characterize PD of anifrolumab in pediatric participants with SLE following SC administration.
|
At Week 12 and 52
|
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Change from baseline in anti-double-stranded deoxyribonucleic acid (dsDNA) antibodies
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: At Week 12 and 52
|
To characterize PD of anifrolumab in pediatric participants with SLE following SC administration.
|
At Week 12 and 52
|
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Number and percentage of participants who develop anti drug antibody (ADA) against anifrolumab
Lasso di tempo: 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
|
Altre misure di risultato
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Number with participants with adverse events (AEs), serious adverse events (SAEs) and adverse events of special interest (AESIs)
Lasso di tempo: 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.
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Up to follow-up visit (12 weeks post last dose of study intervention) (approximately 64 weeks)
|
Collaboratori e investigatori
Sponsor
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Malattie del tessuto connettivo
- Malattie autoimmuni
- Malattie del sistema immunitario
- Infezioni
- Infezioni batteriche Gram-positive
- Infezioni batteriche
- Infezioni batteriche e micosi
- Infezioni da actinomiceti
- Infezioni da micobatteri
- Malattie della pelle e del tessuto connettivo
- Lupus Eritematoso, Sistemico
- Infezioni da micobatteri, non tubercolari
- Anifrolumab
Altri numeri di identificazione dello studio
- D3465C00008
- 2025-524578-41-00 (Ctis)
- EMA/PE/0000246211 (Altro identificatore: Pediatric investigation plan [PIP])
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
Descrizione del piano 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.
Periodo di condivisione IPD
Criteri di accesso alla condivisione IPD
Tipo di informazioni di supporto alla condivisione IPD
- STUDIO_PROTOCOLLO
- LINFA
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su Lupus eritematoso sistemico
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Ruitherapeutics Co., LTDNon ancora reclutamentoLupus systemic Lupus Erthematosus (SLE)Cina
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Vanderbilt University Medical CenterNational Heart, Lung, and Blood Institute (NHLBI)Reclutamento
-
CytoCares IncReclutamentoLES - Lupus Eritematoso Sistemico | Miopatie infiammatorie idiopatiche | Sclerosi SSC-systemicCina
-
McGill University Health Centre/Research Institute...The Arthritis Society, CanadaReclutamentoMalattie reumatiche | Vasculite | Artrite infiammatoria | Malattie muscoloscheletriche | Malattie autoimmuni sistemiche | Lupus systemic Lupus Erthematosus (SLE)Canada
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Hinge BioReclutamentoNefrite lupica (LN) | Lupus systemic Lupus Erthematosus (SLE) | Lupus Extra-renale (ERL)Australia
-
University of PatrasReclutamentoSclerosi SSC-systemicGrecia
-
Union Hospital, Tongji Medical College, Huazhong...CARsgen Therapeutics Co., Ltd.Reclutamento
-
Institute of Hematology & Blood Diseases Hospital...Shanghai Xiniao Biotech Co., Ltd.ReclutamentoLES - Lupus Eritematoso Sistemico | Vasculite associata ad ANCA (AAV) | Miopatie infiammatorie idiopatiche | Sclerosi SSC-systemic | Trombocitopenia associata al tessuto connettivo | SLE-ITPCina
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The Children's Hospital of Zhejiang University...ReclutamentoMalattie autoimmuni | Nefropatia da IgA (IgAN) | Vasculite sistemica associata ad ANCA | Sclerosi sistemica (SSc) | Sindrome nefrosica multiresistente | Lupus systemic Lupus Erthematosus (SLE)Cina
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Beijing GoBroad HospitalMagicTime MedicineNon ancora reclutamentoSclerosi multipla | Artrite reumatoide (AR) | Nefrite lupica (LN) | Malattie correlate alle IgG4 | Lupus systemic Lupus Erthematosus (SLE) | Miastenia Gravis (MG)Cina
Prove cliniche su Anifrolumab + APFS
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AstraZenecaParexelCompletatoPartecipanti saniGermania, Stati Uniti, Regno Unito
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National and Kapodistrian University of AthensAstraZenecaReclutamentoSindrome da antifosfolipidi (APS)Grecia
-
AstraZenecaCompletato
-
National Institute of Arthritis and Musculoskeletal...ReclutamentoMalattia cardiovascolare | Lupus eritematoso sistemico | Aterosclerosi precoceStati Uniti
-
AstraZenecaCompletatoSoggetti sani | Farmacocinetica | SicurezzaStati Uniti
-
AstraZenecaCompletatoLupus Eritematoso Sistemico AttivoTailandia, Filippine, Cina, Taiwan, Hong Kong, Corea del Sud
-
AstraZenecaCompletato
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AstraZenecaPRA Health SciencesCompletatoLupus Eritematoso Sistemico AttivoStati Uniti, Francia, Germania, Spagna, Belgio, Federazione Russa, Giappone, Corea, Repubblica di, Argentina, Bulgaria, Sud Africa, Messico, Canada, Brasile, Lituania
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University Hospital, BordeauxAstraZenecaReclutamento
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University of North Carolina, Chapel HillAstraZenecaAttivo, non reclutanteIdradenite Suppurativa | Idradenite | Acne InversaStati Uniti