- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT05059509
Evaluate Efficacy of FB825 in Adults With Atopic Dermatitis
An Open Labeled Exploratory Study to Evaluate Efficacy of FB825 in Adults With Atopic Dermatitis
Descripción general del estudio
Tipo de estudio
Inscripción (Actual)
Fase
- Fase 2
Contactos y Ubicaciones
Ubicaciones de estudio
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Taipei, Taiwán
- National Taiwan University Hospital
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Male or female between 20 and 65 years of age, inclusive.
- The subject has a physician confirmed diagnosis of chronic atopic dermatitis based on 3 year history of symptoms defined by the Eichenfield revised criteria of Hannifin and Rajka and supported by positive allergen specific IgE (immunoglobulin E) at the screening visit.
- Eczema Area and Severity Index (EASI) score 16 at the screening and baseline visits.
- Investigator's Global Assessment (IGA) score 3 (5 point scale) at the screening and baseline visits.
- 10 % body surface area (BSA) of AD involvement at the screening and baseline visits.
- History of inadequate response to a stable (1 month) regimen of topical corticosteroids or calcineurin inhibitors as treatment for AD within 3 months before the screening visit. (The regimen of topical corticosteroids means medium to high potency, applied for at least 28 days or for the maximum duration recommended by product prescribing information.)
- Patients must be applying stable doses of emollient provided for atopic dermatitis twice daily for at least 7 days before the baseline visit.
Female subjects of childbearing potential must use at least two forms of birth control. One must be barrier protection (i.e., condom or female condom) and the other is one of acceptable method of birth control (ie, diaphragm, intrauterine device, hormonal contraceptives, or abstinence) throughout the study. Subjects who are surgically sterile (ie, hysterectomy, bilateral tubal ligation, or bilateral oophorectomy), or postmenopausal (defined as amenorrhea for 12 consecutive months and documented serum follicle stimulating hormone level >40 mU/mL) will be considered as no childbearing potential. All female subjects must have a negative serum pregnancy test prior to dosing.
Note: The subject must use the method of contraception mentioned above during study period and in 16 weeks or 5 half lives after the last dosing of FB825.
- The subject has a body weight ≥ 40 kg at screening and a body mass index of 18.0 to 30.0 kg/m2, inclusive.
The subject has a normal, as determined by the investigator, 12 lead electrocardiogram (ECG) with normal cardiac conduction parameters:
- Heart rate between 45 and 100 bpm;
- Fridericia corrected QT interval (QTcF) ≤450 milliseconds (men) or ≤470 milliseconds (women);
- QRS interval lower than 120 milliseconds.
- The subject is healthy, except atopic diseases, as determined by the investigator, on the basis of clinical laboratory test results performed at screening. If the results are outside the normal reference ranges, the subject may be included only if the investigator judges the abnormalities or deviations from normal not to be clinically significant.
- The subject is able to provide written informed consent.
- The subject agrees to comply with all protocol requirements.
Exclusion Criteria:
- Female subjects who are pregnant or lactating.
- The subject is on diet or with poor intake.
- The subject has a history of heart arrhythmias (any clinically relevant).
- The subject has a positive test result for hepatitis B surface antigen, hepatitis C virus antibody,or human immunodeficiency virus antibodies at screening.
- The subject has a history of alcohol or drug abuse that would impair or risk the patients' full participation in the study, in the opinion of the investigator.
- The subject is under judicial supervision or curatorship.
- The subject has a clinically relevant, currently active or underlying gastrointestinal, cardiovascular, nervous system, psychiatric, metabolic, renal, hepatic, respiratory (with the exception of uncomplicated allergic rhinitis), inflammatory, immunological, endocrine, diabetes, or infectious disease and ineligible to participate in the study judged by investigator.
- The subject has any history of a previous anaphylactic reaction.
- The subject has any condition that, in the opinion of the investigator, would compromise the study or the well being of the subject or prevent the subject from meeting or performing study requirements.
- The subject has received any immunoglobulin products or blood products within 3 months prior to dosing.
The subject has received an biologic product:
- The subject has received any cell depleting agents, not only limited to rituximab, within 6 months prior to dosing, or before the lymphocyte count returns to normal, whichever is longer.
- The subject has received other biologics within 5 half lives (if known) or 16 weeks, which is longer, prior to dosing).
The subject has one or more of the following laboratory abnormalities at screening as defined by Division of Microbiology and Infectious Diseases Adult Toxicity Table 2007:
- Aspartate aminotransferase or alanine aminotransferase (>2 × upper limit of normal [ULN]) or higher
- Total bilirubin ≥1.5 × ULN
- Serum creatinine ≥1.6 × ULN
- Any other laboratory abnormality higher than or equal to grade 2 with the exception of IgE level, eosinophil counts, eosinophil cationic protein (ECP) and laboratory values mentioned above.
Note: Laboratory values may be converted to equivalent standard units. Retesting of abnormal laboratory values that may lead to exclusion will be allowed once (without prior sponsor approval). Retesting will take place during an unscheduled visit in the screening phase (before baseline).
- The subject has received any approved or unapproved (ie, investigational) immunotherapy treatment within the past 3 months.
The subject has used any of the following classes of medication (prescription or over the counter):
- Intranasal corticosteroid (eg, fluticasone propionate) within 30 days prior to dosing.
- Systemic corticosteroids (eg, prednisone) within 30 days prior to dosing.
- Leukotriene modifiers (eg, montelukast) within 30 days prior to dosing.
- Immunosuppressants (eg, gold salts, methotrexate, azathioprine, cyclosporine) within the past 30 days prior to dosing.
- Immunomodulating drugs (eg, interferon-gamma ) within the past 30 days prior to dosing.
- Anti IgE (eg, omalizumab) within the past 1 years prior to dosing
- Allergen immunotherapy within the past 1 years prior to dosing
- Orally inhaled corticosteroids (eg, budesonide) within the past 30 days prior to dosing
- The subject has received phototherapy within 4 weeks prior to dosing.
- The subject has received live vaccine within 12 weeks prior to dosing.
- The subject has known or suspected history of immunosuppression, including history of opportunistic infections (eg, TB) per investigator judgment.
- The subject has history of malignancy within 5 years before the screening period.
High risk of parasite infection.
- Risk factors for parasitic disease (living in an endemic area, chronic gastrointestinal symptoms, travel within the last 6 months to regions where geohelminthic infections are endemic, and/or chronic immunosuppression) AND
- Evidence of parasitic colonization or infection on stool evaluation for ova and parasites.
Note: stool ova and parasite evaluation will only be conducted in patients with risk factors and an eosinophil count more than twice the upper limit of normal
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Experimental: FB825
One dose FB825, 5mg/kg, by 1 hour IV infusion on Day 1
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FB825, 5mg/kg, by 1 hour IV infusion on Day 1
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
---|---|
The mean change in mIgE (Membrane bound Immunoglobulin E) B cell count (absolute and percentage) from baseline
Periodo de tiempo: week 2 and 4
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week 2 and 4
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Medidas de resultado secundarias
Medida de resultado |
Periodo de tiempo |
---|---|
The mean percentage change in Pruritus Visual Analogue Scale (VAS) from baseline
Periodo de tiempo: week 2 and 4
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week 2 and 4
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The mean percentage change in Eczema Area and Severity Index (EASI) from baseline
Periodo de tiempo: week 2 and 4
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week 2 and 4
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The mean percentage change in Severity Scoring of Atopic Dermatitis Index (SCORAD) from baseline
Periodo de tiempo: week 2 and 4
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week 2 and 4
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The mean percentage change in Investigator Global Assessment (IGA) from baseline
Periodo de tiempo: Weeks 2 and 4
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Weeks 2 and 4
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The mean percentage change in Body Surface Area (BSA) involved in atopic dermatitis from baseline to
Periodo de tiempo: Weeks 2 and 4
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Weeks 2 and 4
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The mean change in Dermatology Life Quality Index (DLQI) from baseline
Periodo de tiempo: Weeks 2 and 4
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Weeks 2 and 4
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Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- FB825CLIIS-04-AD
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .
Ensayos clínicos sobre Dermatitis atópica
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Hospices Civils de LyonReclutamientoDermatitis de contacto | Dermatitis de contacto Irritante | Dermatitis de Contacto AlérgicaFrancia
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Steven BakerTerminadoDermatitis de contacto de la manoEstados Unidos
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HealthPartners InstituteTerminadoDermatitis de contacto irritanteEstados Unidos
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Primus PharmaceuticalsTerminadoDermatitis de contacto irritanteEstados Unidos
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University of Split, School of MedicineReclutamientoDermatitis de contactoCroacia
-
University of Split, School of MedicineReclutamientoDermatitis de contacto | Dermatitis de contacto IrritanteCroacia
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University of Split, School of MedicineTerminadoDiferencias regionales de la irritación cutánea y su efecto en la recuperación de la barrera cutáneaDermatitis de contacto irritanteCroacia
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University Ghent3MTerminadoÚlcera de presión | Erupción del pañal | Dermatitis asociada a la incontinencia | Dermatitis de contacto irritante por incontinenciaBélgica
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Herbarium Laboratorio Botanico LtdaTerminado
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Herlev and Gentofte HospitalGöteborg University; University of Copenhagen; Sahlgrenska University Hospital,...TerminadoDermatitis alérgica de contacto por cosméticosDinamarca, Suecia
Ensayos clínicos sobre FB825
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Fountain Biopharma Inc.Terminado
-
Oneness Biotech Co., Ltd.Activo, no reclutandoDermatitis atópicaEstados Unidos
-
Oneness Biotech Co., Ltd.Activo, no reclutandoDermatitis atópicaEstados Unidos
-
Oneness Biotech Co., Ltd.Microbio Shanghai Co., Ltd.Reclutamiento
-
Fountain Biopharma Inc.Terminado