Studio per valutare la farmacocinetica, l'efficacia, la tollerabilità e la sicurezza dell'immunoglobulina umana sottocutanea (Newnorm) in pazienti con malattie da immunodeficienza primaria
Studio prospettico, in aperto, a braccio singolo, multicentrico di fase 3 per valutare la farmacocinetica, l'efficacia, la tollerabilità e la sicurezza dell'immunoglobulina umana sottocutanea (Newnorm) in pazienti con malattie da immunodeficienza primaria
Prospective, open-label, single-arm, multicentre Phase 3 study to evaluate the pharmacokinetics, efficacy, tolerability, and safety of subcutaneous human immunoglobulin (Newnorm) in patients with primary immunodeficiency diseases
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 3
Contatti e Sedi
Luoghi di studio
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Leipzig, Germania, 04129
- Octapharma Research Site
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Munich, Germania, 80337
- Octapharma Research Site
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Naples, Italia, 80131
- Octapharma Research Site
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Roma, Italia, 00161
- Octapharma Research Site
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Roma, Italia, 133
- Octapharma Research Site
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Treviso, Italia, 31100
- Octapharma Research Site
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Krakow, Polonia, 30-663
- Octapharma Research Site
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Bratislava, Slovacchia, 833 40
- Octapharma Research Site
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California
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Irvine, California, Stati Uniti, 92697
- Octapharma Research Site
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Colorado
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Centennial, Colorado, Stati Uniti, 80112
- Octapharma Research Site
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Florida
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Port Saint Lucie, Florida, Stati Uniti, 34986
- Octapharma Research Site
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St. Petersburg, Florida, Stati Uniti, 33701
- Octapharma Research Site
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Illinois
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Chicago, Illinois, Stati Uniti, 60612
- Octapharma Research Site
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Kansas
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Overland Park, Kansas, Stati Uniti, 66211
- Octapharma Research Site
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Kentucky
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Louisville, Kentucky, Stati Uniti, 40217
- Octapharma Research Site
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Maryland
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White Marsh, Maryland, Stati Uniti, 21162
- Octapharma Research Site
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Missouri
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Kansas City, Missouri, Stati Uniti, 64111
- Octapharma Research Site
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Nebraska
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Omaha, Nebraska, Stati Uniti, 68046
- Octapharma Research Site
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Kyiv, Ucraina, 04209
- Octapharma Research Site
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Lviv, Ucraina, 79010
- Octapharma Research Site
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Lviv, Ucraina, 79035
- Octapharma Research Site
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Budapest, Ungheria, 1097
- Octapharma Research Site
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Debrecen, Ungheria, 4032
- Octapharma Research Site
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Age of ≥2 years and ≤75 years
- Documented and confirmed diagnosis of PID as defined by European Society of Immunodeficiencies (ESID) and the Pan American Group for Immune Deficiency (PAGID) and requiring immunoglobulin replacement therapy due to hypogammaglobulinaemia or agammaglobulinaemia. The exact type of PID must be recorded.
- At least 12 weeks of regular treatment before the screening visit (i.e., with a stable dosing interval) with any IVIG, SCIG, or fSCIG, with a stable IgG dose between 200 and 800 mg/kg/month. A stable dose is defined as one that deviates less than ±25% from the mean dose for all infusions within this 12-week period before screening.
- Trough level of IgG ≥5 g/L at screening and documentation of an IgG trough level of ≥5 g/L at least once within the previous 12 weeks.
- Freely given written informed consent from adult patients or freely given written informed consent from the patient's parent(s)/legal guardian(s) and written informed assent from paediatric or adolescent patients in accordance with the applicable regulatory requirements, before any study-specific procedure takes place.
- Willingness to comply with all aspects of the protocol, including blood sampling, for the duration of the study.
Exclusion Criteria:
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Any acute infection requiring IV antibiotic treatment within 2 weeks before the screening visit or during the screening period, or any SBI within the 3 months prior to the screening visit or during the screening period.
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The patient has isolated specific antibody deficiency disorder, isolated IgG subclass deficiency, or transient hypogammaglobulinaemia of infancy.
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Current medical condition or history of condition known to cause secondary immune deficiency, for example, chronic lymphocytic leukaemia, lymphoma, multiple myeloma, or chronic or recurrent neutropenia (absolute neutrophil count <1000/μL).
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Known history of ADRs to IgA contained in other products.
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Body mass index >40 kg/m2.
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Exposure to blood or any blood product or plasma derivative other than IgG for PID within 3 months before the first infusion of Newnorm.
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History of or ongoing severe hypersensitivity, e.g., anaphylaxis or severe systemic response, or persistent reactions to blood or plasma-derived products, or to any component of Newnorm (such as glycine).
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Severe liver dysfunction (alanine aminotransferase [ALT] >3 times the upper limit of normal for the expected normal range for the testing laboratory) at screening.
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Known protein-losing enteropathies or proteinuria (known urinary protein loss of >1 g/24 h, or dipstick proteinuria of ≥3+).
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Moderate to severe renal dysfunction (per investigator discretion based on estimated glomerular filtration rate [eGFR] ≤44 mL/min/1.73 m2, as defined by KDIGO Clinical Practice Guideline) or predisposition to acute renal failure (e.g., any degree of pre-existing renal dysfunction in presence of additional acute renal failure risk factors, e.g. routine treatment with known nephrotoxic drugs).
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Uncontrolled diabetes mellitus (HbA1c > 7% / >53 mmol/mol).
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Uncontrolled arterial hypertension (systolic blood pressure of ≥ 130 mmHg for the subject under 13 years of age, ≥ 140 mmHg for subject 13 to 17 years of age, and > 160 mmHg for adults).
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Dysrhythmia/Tachycardia (resting heart rate > 100 bpm for adults/adolescents and > 120 bpm for children) and symptomatic bradycardia (resting heart rate < 60 bpm for adults, < 50 bpm for adolescents, and < 75 bpm for children in presence of symptoms e.g., low blood pressure, abnormal rhythm, chest discomfort, shortness of breath). Physiological sinus bradycardia in physically active adults/children/athletes is NOT an exclusion criterion).
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The subject has a history of or current diagnosis of deep venous thrombosis or thromboembolism (e.g. myocardial infarction, cerebrovascular accident, or transient ischemic attack); history refers to an incident in the year prior to screening or 2 episodes over lifetime.
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The subject is currently receiving anti-coagulation therapy which would make SC administration inadvisable (vitamin K antagonist, nonvitamin K antagonist oral anticoagulants [e.g. dabigatran etexilate targeting Factor IIa, rivaroxaban, edoxaban, and apixaban targeting Factor Xa], parenteral anticoagulants [e.g. fondaparinux]).
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Treatment with oral or parenteral steroids either
- at daily doses >0.3 mg/kg of prednisone (or equivalent) within the last 12 weeks before screening or
- bolus treatment of a daily dose greater than 1 mg/kg of prednisone (or equivalent) for longer than 10 days within the last 12 weeks before screening. Courses of corticosteroids (intermittent) of not more than 10 days would not exclude a patient. Inhaled or topical corticosteroids are allowed.
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Treatment with systemic immunosuppressants including chemotherapeutic agents 1 year before screening or immunomodulatory drugs 12 weeks before the screening visit.
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Live viral vaccination (such as measles, rubella, mumps, or varicella) within 1 month before the first infusion of Newnorm, during the study period, and within 3 months after last infusion of Newnorm. Note: Seasonal inactivated (killed) influenza vaccines (incl. H1N1) are allowed. COVID vaccines (mRNA vaccine and a non-replicating viral vector vaccine) are allowed.
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Treatment with any investigational medicinal product (IMP) within 3 months before the screening visit.
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Presence of any condition likely to interfere with the evaluation of Newnorm or with the compliant conduct of the study.
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Known or suspected abuse of alcohol, drugs, and/or psychotropic agents within 12 months before screening.
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Known human immunodeficiency virus (HIV)-1/2, hepatitis B virus (HBV), or hepatitis C virus (HCV) infection or positive for HIV-1/2, HBV, or HCV at screening.
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Women who are breast feeding, pregnant, or planning to become pregnant, or are unwilling to use an effective birth control method (refer to protocol Section 7.4.10.b) while on study and for 30 days following the last dose of study drug.
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Men who are unwilling to use birth control to prevent pregnancy for the duration of the study (unless the female partner
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
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Sperimentale: Newnorm
Newnorm is a 20% human normal immunoglobulin for SC infusion |
Newnorm is a 20% human normal immunoglobulin for SC infusion. |
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Rate of Serious Bacterial Infections
Lasso di tempo: 52 weeks
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Rate of SBIs (defined as bacteraemia/sepsis, bacterial meningitis, osteomyelitis/septic arthritis, bacterial pneumonia, and visceral abscess) per person-year on treatment. |
52 weeks
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Average total IgG concentration
Lasso di tempo: 16 weeks
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Average total IgG concentration (Cav) on steadystate dosing. |
16 weeks
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Infections of any type of seriousness
Lasso di tempo: 52 weeks
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Infections of any type or seriousness (including acute sinusitis, exacerbation of chronic sinusitis, acute otitis media, acute bronchitis, infectious diarrhoea, etc) (total and by category, annual rate) |
52 weeks
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Time to resolution of infections
Lasso di tempo: 52 weeks
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Time to resolution of infections |
52 weeks
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Use of antibiotics
Lasso di tempo: 52 weeks
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Use of antibiotics (number of days on antibiotics and annual rate of treatment episodes) characterised as therapeutic or prophylactic use |
52 weeks
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Hospitalisations due to infection
Lasso di tempo: 52 weeks
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Hospitalisations due to infection (number of days and annual rate) |
52 weeks
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Episodes of fever
Lasso di tempo: 52 weeks
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Episodes of fever |
52 weeks
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Days lost from work, school, kindergarten, or day care due to infection
Lasso di tempo: 52 weeks
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Days lost from work, school, kindergarten, or day care due to infection |
52 weeks
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Child Health Questionnaire-Parent Form
Lasso di tempo: 52 weeks
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Child Health Questionnaire-Parent Form (CHQPF50) for patients <14 years |
52 weeks
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SF-36 Health Survey
Lasso di tempo: 52 weeks
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SF-36 Health Survey for patients ≥ 14 of age |
52 weeks
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Non-compartmental PK analyses of all available PK profiles (IVIG and SCIG)
Lasso di tempo: 16 weeks
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Total IgG, IgG subclasses (IgG1, IgG2, IgG3, and IgG4), and antigen specific antibodies against Haemophilus influenzae B (capsular polysaccharide), Streptococcus pneumoniae (serotypes 4, 6B, 9V, 14, 18C, 19F, 23F), cytomegalovirus (CMV), tetanus, and measles |
16 weeks
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IgG Levels
Lasso di tempo: 16 weeks
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Trough and peak levels of total IgG and IgG subclasses for weekly Newnorm relative to 3- or 4-weekly IVIG dosing |
16 weeks
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Collaboratori e investigatori
Sponsor
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
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
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- NORM-01
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
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 .