- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT06311682
Un ensayo para evaluar la eficacia y seguridad de tralokinumab en combinación con corticosteroides tópicos en niños y lactantes con dermatitis atópica de moderada a grave (TRAPEDS 2)
Un ensayo multicéntrico de fase 3 para evaluar la eficacia y seguridad de tralokinumab en combinación con corticosteroides tópicos en niños (de 2 a 2 años)
The purpose of this trial is to test whether treatment with tralokinumab (administered subcutaneous injections [SC]) in combination with topical corticosteroids (TCS) is safe and effective to treat moderate-to-severe atopic dermatitis (AD) in children and infants. This will be judged by a range of assessments that rate the severity and extent of atopic dermatitis and its symptoms, as well as general health status and quality of life. The trial will last for up to 4 years. There will be visits every 2 weeks for the first year and every 6 weeks thereafter. Some of the visits will be conducted by phone.
The study involves two different age groups: children aged 2 to under 12 years and infants aged 6 months to under 2 years. This trial compares tralokinumab +TCS to placebo + TCS for children with moderate-to-severe AD and evaluates tralokinumab + TCS for infants with moderate-to-severe AD. Infants will not receive placebo. All subjects will go through a screening process, which is the first part of the trial and will last up to 4 weeks. During this period, it will be checked if the child or infant meets the criteria to participate in the trial.
The children will be randomly assigned to receive tralokinumab + TCS or placebo + TCS for the initial 16 weeks, with the treatment being double-blinded. During the first 16 weeks, children will have a 2 out of 3 chance of getting tralokinumab and a 1 out of 3 chance of getting placebo. Thereafter, all subjects will receive tralokinumab + TCS. The infants will receive tralokinumab + TCS as open-label treatment for the entire treatment period, meaning that the participants will know they are receiving tralokinumab. After stopping treatment, all participants will enter a 4-week safety follow-up period.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 3
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Clinical Disclosure
- Número de teléfono: +45 4494 5888
- Correo electrónico: disclosure@leo-pharma.com
Ubicaciones de estudio
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Buxtehude, Alemania, 21614
- Retirado
- Leo Pharma Investigational site
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Dresden, Alemania, 01307
- Retirado
- Leo Pharma Investigational site
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Mainz, Alemania, 55131
- Retirado
- Leo Pharma Investigational site
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Osnabrück, Alemania, 49074
- Retirado
- Leo Pharma Investigational site
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Tübingen, Alemania, 72076
- Activo, no reclutando
- Leo Pharma Investigational site
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Wuppertal, Alemania, 42283
- Retirado
- Leo Pharma Investigational site
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Brussels, Bélgica, 1020
- Retirado
- Leo Pharma Investigational site
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Ghent, Bélgica, 9000
- Activo, no reclutando
- Leo Pharma Investigational site
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Leuven, Bélgica, 3000
- Retirado
- Leo Pharma Investigational site
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Liège, Bélgica, 4000
- Retirado
- Leo Pharma Investigational site
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Burlington, Canadá, L7L 6W6
- Reclutamiento
- Leo Pharma Investigational site
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Calgary, Canadá, Calgary
- Retirado
- Leo Pharma Investigational site
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Calgary, Canadá, T2J 7E1
- Reclutamiento
- Leo Pharma Investigational site
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Edmonton, Canadá, T5J 3S9
- Reclutamiento
- Leo Pharma Investigational site
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Edmonton, Canadá, T6G 1C3
- Reclutamiento
- Leo Pharma Investigational site
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Hamilton, Canadá, L8S 1G5
- Reclutamiento
- Leo Pharma Investigational site
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Niagara Falls, Canadá, L2H 1H5
- Reclutamiento
- Leo Pharma Investigational site
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Saskatoon, Canadá, S7K 2C1
- Reclutamiento
- Leo Pharma Investigational site
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Windsor, Canadá, N8X2G1
- Reclutamiento
- Leo Pharma Investigational site
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Winnipeg, Canadá, R3M 3Z4
- Reclutamiento
- Leo Pharma Investigational site
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Ansan-si, Corea del Sur, 15355
- Activo, no reclutando
- Leo Pharma Investigational site
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Gwangju, Corea del Sur, 61453
- Activo, no reclutando
- Leo Pharma Investigational site
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Seoul, Corea del Sur, 02447
- Activo, no reclutando
- Leo Pharma Investigational site
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Seoul, Corea del Sur, 03080
- Activo, no reclutando
- Leo Pharma Investigational site
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Seoul, Corea del Sur, 03722
- Activo, no reclutando
- Leo Pharma Investigational site
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Seoul, Corea del Sur, 05030
- Activo, no reclutando
- Leo Pharma Investigational site
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Seoul, Corea del Sur, 06273
- Retirado
- Leo Pharma Investigational site
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Seoul, Corea del Sur, 06591
- Retirado
- Leo Pharma Investigational site
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Seoul, Corea del Sur, 139-711
- Activo, no reclutando
- Leo Pharma Investigational site
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Rijeka, Croacia, 51000
- Activo, no reclutando
- Leo Pharma Investigational site
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Zagreb, Croacia, 10000
- Activo, no reclutando
- Leo Pharma Investigational site
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Zagreb, Croacia, 10000
- Retirado
- Leo Pharma Investigational site
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Alicante, España, 03010
- Activo, no reclutando
- Leo Pharma Investigational site
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Madrid, España, 28046
- Retirado
- Leo Pharma Investigational site
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Valencia, España, 46014
- Activo, no reclutando
- Leo Pharma Investigational site
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Alabama
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Birmingham, Alabama, Estados Unidos, 35209
- Reclutamiento
- Leo Pharma Investigational site
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Arkansas
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North Little Rock, Arkansas, Estados Unidos, 72117
- Reclutamiento
- Leo Pharma Investigational site
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California
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Palo Alto, California, Estados Unidos, 94304
- Reclutamiento
- Leo Pharma Investigational site
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Sacramento, California, Estados Unidos, 95816
- Reclutamiento
- Leo Pharma Investigational site
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San Diego, California, Estados Unidos, 92108
- Retirado
- Leo Pharma Investigational site
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San Diego, California, Estados Unidos, 92123
- Reclutamiento
- Leo Pharma Investigational site
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Florida
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Jacksonville, Florida, Estados Unidos, 32256
- Reclutamiento
- Leo Pharma Investigational site
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Miami, Florida, Estados Unidos, 33156
- Reclutamiento
- Leo Pharma Investigational site
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Tampa, Florida, Estados Unidos, 33613
- Reclutamiento
- Leo Pharma Investigational site
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Georgia
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Macon, Georgia, Estados Unidos, 31217
- Reclutamiento
- Leo Pharma Investigational site
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Michigan
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Waterford, Michigan, Estados Unidos, 48328
- Reclutamiento
- Leo Pharma Investigational site
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Oklahoma
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Tulsa, Oklahoma, Estados Unidos, 74136
- Reclutamiento
- Leo Pharma Investigational site
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Oregon
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Portland, Oregon, Estados Unidos, 97239
- Reclutamiento
- Leo Pharma Investigational site
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South Carolina
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Charleston, South Carolina, Estados Unidos, 27420
- Reclutamiento
- Leo Pharma Investigational site
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Virginia
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Norfolk, Virginia, Estados Unidos, 23502
- Reclutamiento
- Leo Pharma Investigational site
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Cork, Irlanda, T12 DFK4
- Activo, no reclutando
- Leo Pharma Investigational site
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Crumlin, Irlanda, D12N512
- Activo, no reclutando
- Leo Pharma Investigational site
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Ancona, Italia, 60126
- Retirado
- Leo Pharma Investigational site
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Brescia, Italia, 25123
- Activo, no reclutando
- Leo Pharma Investigational site
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Padova, Italia, 35128
- Activo, no reclutando
- Leo Pharma Investigational site
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Roma, Italia, 00168
- Activo, no reclutando
- Leo Pharma Investigational site
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Rome, Italia, 00165
- Activo, no reclutando
- Leo Pharma Investigational site
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Utrecht, Países Bajos, 3584 CW
- Activo, no reclutando
- Leo Pharma Investigational site
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Gdansk, Polonia, 80-546
- Activo, no reclutando
- Leo Pharma Investigational site
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Krakow, Polonia, 30-002
- Activo, no reclutando
- Leo Pharma Investigational site
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Lodz, Polonia, 90-436
- Activo, no reclutando
- Leo Pharma Investigational site
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Ostrowiec Świętokrzyski, Polonia, 27-400
- Activo, no reclutando
- Leo Pharma Investigational site
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Rzeszów, Polonia, 35-055
- Activo, no reclutando
- Leo Pharma Investigational site
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Tarnów, Polonia, 33-100
- Activo, no reclutando
- Leo Pharma Investigational site
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Warsaw, Polonia, 02-953
- Activo, no reclutando
- Leo Pharma Investigational site
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Warsaw, Polonia, 02-962
- Activo, no reclutando
- Leo Pharma Investigational site
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Lincoln, Reino Unido, LN2 5QY
- Activo, no reclutando
- Leo Pharma Investigational site
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London, Reino Unido, WC1N 3JH
- Activo, no reclutando
- Leo Pharma Investigational site
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Sheffield, Reino Unido, S10 2TH
- Activo, no reclutando
- Leo Pharma Investigational site
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Southampton, Reino Unido, SO16 6YD
- Activo, no reclutando
- Leo Pharma Investigational site
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Brasov, Rumania, 500091
- Activo, no reclutando
- Leo Pharma Investigational site
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Iași, Rumania, 700259
- Activo, no reclutando
- Leo Pharma Investigational site
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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:
- Age 6 months to <12 years at screening.
- Body weight ≥9 kg at screening.
- Diagnosis of AD as defined by the Hanifin and Rajka (1980) criteria for AD.
- History of AD for: ≥12 months for subjects aged ≥6 years at screening and ≥3 months for subjects aged 6 months to <6 years at screening.
- Documented inadequate response to mid-strength TCS within 6 months before the screening visit.
- AD involvement of ≥10% body surface area at screening and baseline according to component A of SCORAD.
- An EASI score of ≥16 at screening and baseline.
- An IGA score of ≥3 at screening and baseline.
- A Child Worst Itch NRS average score of ≥4 (subjects aged ≥6 years at screening) or a Scratch ObsRO average score of ≥4 (subjects aged <6 years at screening) during the week prior to baseline.
Exclusion Criteria:
- Treatment with the topical corticosteroids (TCS), topical calcineurin inhibitors (TCI), topical phosphodiesterase-4 inhibitors (PDE-4), and topical Janus kinase inhibitors (JAK) within 1 week prior to baseline.
- Treatment with bleach baths within 1 week prior to baseline.
- Treatment with the immunomodulatory medications systemic immunosuppressive/immunomodulating drugs (e.g. methotrexate, cyclosporine, azathioprine, mycophenolate mofetil, Janus kinase inhibitors) and systemic corticosteroids (excludes inhaled, ophthalmic, or intranasal delivery) within 4 weeks prior to baseline.
- Use of tanning beds or phototherapy within 4 weeks prior to baseline.
- Treatment with a live (attenuated) or non-live vaccine within 30 days prior to the baseline visit.
- Active dermatologic conditions that may confound the diagnosis of AD or would interfere with assessment of treatment such as seborrheic dermatitis, active skin infection, scabies, cutaneous T cell lymphoma, or psoriasis.
- Clinically significant active chronic or acute infection requiring treatment with systemic antibiotics, antivirals, antifungals or antiprotozoal within 2 weeks before the baseline visit.
- History of past or current hepatitis B or C including a positive hepatitis B or C test at screening.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Triple
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Tralokinumab + TCS for subjects aged 2 to <12 years
Dose and dosing frequency for each subject will depend on the subject's body weight. |
The trial medication will be given under the skin (SC). Dose and dosing frequency for each subject will depend on the subject's body weight. Subjects who will receive treatment every two weeks will receive a loading dose corresponding to a double dose at baseline. Subjects who will receive treatment every 4 weeks will receive a staggered loading dose at baseline and Week 2. After the loading dose, they will continue to receive treatment every 4 weeks. The dose and dosing frequency will be adjusted according to the subject's body weight at weeks 16, 32, 52, 64, 88, 112, 136, 160, and 184. |
|
Experimental: Placebo + TCS for subjects aged 2 to <12 years
Dose and dosing frequency for each subject will depend on the subject's body weight. |
The trial medication will be given under the skin (SC). Dose and dosing frequency for each subject will depend on the subject's body weight. Subjects who will receive treatment every two weeks will receive a loading dose corresponding to a double dose at baseline. Subjects who will receive treatment every 4 weeks will receive a staggered loading dose at baseline and Week 2. After the loading dose, they will continue to receive treatment every 4 weeks. The dose and dosing frequency will be adjusted according to the subject's body weight at weeks 16, 32, 52, 64, 88, 112, 136, 160, and 184. |
|
Experimental: Tralokinumab + TCS for subjects aged 6 months to <2 years
Dose and dosing frequency for each subject will depend on the subject's body weight. |
The trial medication will be given under the skin (SC). Dose and dosing frequency for each subject will depend on the subject's body weight. Subjects who will receive treatment every two weeks will receive a loading dose corresponding to a double dose at baseline. Subjects who will receive treatment every 4 weeks will receive a staggered loading dose at baseline and Week 2. After the loading dose, they will continue to receive treatment every 4 weeks. The dose and dosing frequency will be adjusted according to the subject's body weight at weeks 16, 32, 52, 64, 88, 112, 136, 160, and 184. |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 2 to <12 years at screening.
Periodo de tiempo: At week 16
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The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 16
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Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Periodo de tiempo: At week 16
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The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 16
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Presencia de anticuerpos antidrogas emergentes del tratamiento (sí/no) en sujetos de 2 a <12 años en el momento de la selección.
Periodo de tiempo: Desde el inicio hasta la semana 16
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Desde el inicio hasta la semana 16
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Presencia de anticuerpos antidrogas emergentes del tratamiento (sí/no) en sujetos de 6 meses a <2 años en el momento de la selección.
Periodo de tiempo: Desde el inicio hasta la semana 16
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Desde el inicio hasta la semana 16
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Uso de tratamiento de rescate (sí/no) en sujetos de 2 a <12 años en el momento del cribado.
Periodo de tiempo: Desde el inicio hasta la semana 16
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Desde el inicio hasta la semana 16
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Uso de tratamiento de rescate (sí/no) en sujetos de 6 meses a <2 años en el momento de la selección.
Periodo de tiempo: Desde el inicio hasta la semana 16
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Desde el inicio hasta la semana 16
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Cambio porcentual en la superficie corporal afectada (BSA) en sujetos de 2 a <12 años en el momento de la selección.
Periodo de tiempo: Desde el inicio hasta la semana 52
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Desde el inicio hasta la semana 52
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Cambio porcentual en la superficie corporal afectada (BSA) en sujetos de 6 meses a <2 años en el momento de la selección.
Periodo de tiempo: Desde el inicio hasta la semana 52
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Desde el inicio hasta la semana 52
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Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Periodo de tiempo: At week 16
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The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 16
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Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: At week 16
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The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 16
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Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: At week 16
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The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 16
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Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: At week 16
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 16
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Having at least 50% reduction in EASI score in subjects aged 2 to <12 years at screening.
Periodo de tiempo: At week 16
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 16
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Having at least 50% reduction in EASI score in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: At week 16
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The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 16
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Percent change in EASI in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 16
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 16
|
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Percent change in EASI in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 16
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 16
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 16
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The SCORAD is a validated tool to evaluate the extent and severity of atopic dermatitis. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 16
|
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Percent change in Scoring Atopic Dermatitis (SCORAD) in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 16
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The SCORAD is a validated tool to evaluate the extent and severity of atopic dermatitis. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 16
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Percent change in affected BSA in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 16
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BSA is a body surface area. |
From baseline to week 16
|
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Percent change in affected BSA in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 16
|
BSA is a body surface area. |
From baseline to week 16
|
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Percent change in Children's Dermatology Life Quality Index (CDLQI) for subjects aged 4 to <12 years at screening.
Periodo de tiempo: From baseline to Week 16
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to Week 16
|
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Reduction in Child Worst Itch numeric rating score (NRS) (weekly average) ≥4 for subjects aged 6 to <12 years at screening.
Periodo de tiempo: From baseline to Week 16
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The Child Worst Itch NRS assesses 'worst itch today' and 'worst itch last night' using a numerical rating scale from 0 to 10, where 0 represents 'Not itchy at all' and 10 represents 'Very itchy'. |
From baseline to Week 16
|
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Reduction in Scratch Observer-Reported Outcome (ObsRO) (weekly average) ≥4 for subjects aged 2 to <6 years at screening.
Periodo de tiempo: From baseline to week 16
|
The Scratch ObsRO NRS assesses 'worst scratching during the past 24 hours' using a numerical rating scale from 0 to 10, where 0 represents 'No scratching' and 10 represents 'Worst scratching possible'. |
From baseline to week 16
|
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Reduction in Scratch Observer-Reported Outcome (ObsRO) (weekly average) ≥4 for subjects aged 6 months to <2 years years at screening.
Periodo de tiempo: From baseline to week 16
|
The Scratch ObsRO NRS assesses 'worst scratching during the past 24 hours' using a numerical rating scale from 0 to 10, where 0 represents 'No scratching' and 10 represents 'Worst scratching possible'. |
From baseline to week 16
|
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Reduction of ≥4 in Child Worst Itch NRS (weekly average) for subjects aged 6 to <12 years at screening or Scratch ObsRO (weekly average) for subjects aged 2 to <6 years at screening.
Periodo de tiempo: From baseline to week 16
|
The Child Worst Itch NRS assesses 'worst itch today' and 'worst itch last night' using a numerical rating scale from 0 to 10, where 0 represents 'Not itchy at all' and 10 represents 'Very itchy'. The Scratch ObsRO NRS assesses 'worst scratching during the past 24 hours' using a numerical rating scale from 0 to 10, where 0 represents 'No scratching' and 10 represents 'Worst scratching possible'. |
From baseline to week 16
|
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Percent change in Patient-Oriented Eczema Measure (POEM) in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 16
|
The POEM is a validated questionnaire used to assess disease symptoms in atopic eczema patients in both clinical practice and clinical trials. The tool consists of 7 items each addressing a specific symptom (itching, sleep, bleeding, weeping, cracking, flaking, and dryness). Subjects will score how often they have experienced each symptom over the previous week on a 5-point categorical response scale (0 = 'no days'; 1 = '1 to 2 days'; 2 = '3 to 4 days'; 3 = '5 to 6'days; 4 = 'every day'). The total score is the sum of the 7 items (range 0 to 28) and reflects disease-related morbidity; a high score is indicative of a worse disease severity. |
From baseline to week 16
|
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Percent change in Patient-Oriented Eczema Measure (POEM) in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 16
|
The POEM is a validated questionnaire used to assess disease symptoms in atopic eczema patients in both clinical practice and clinical trials. The tool consists of 7 items each addressing a specific symptom (itching, sleep, bleeding, weeping, cracking, flaking, and dryness). Subjects will score how often they have experienced each symptom over the previous week on a 5-point categorical response scale (0 = 'no days'; 1 = '1 to 2 days'; 2 = '3 to 4 days'; 3 = '5 to 6'days; 4 = 'every day'). The total score is the sum of the 7 items (range 0 to 28) and reflects disease-related morbidity; a high score is indicative of a worse disease severity. |
From baseline to week 16
|
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Reduction of in Patient-Oriented Eczema Measure (POEM) ≥6 in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 16
|
The POEM is a validated questionnaire used to assess disease symptoms in atopic eczema patients in both clinical practice and clinical trials. The tool consists of 7 items each addressing a specific symptom (itching, sleep, bleeding, weeping, cracking, flaking, and dryness). Subjects will score how often they have experienced each symptom over the previous week on a 5-point categorical response scale (0 = 'no days'; 1 = '1 to 2 days'; 2 = '3 to 4 days'; 3 = '5 to 6'days; 4 = 'every day'). The total score is the sum of the 7 items (range 0 to 28) and reflects disease-related morbidity; a high score is indicative of a worse disease severity. |
From baseline to week 16
|
|
Reduction of in Patient-Oriented Eczema Measure (POEM) ≥6 in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 16
|
The POEM is a validated questionnaire used to assess disease symptoms in atopic eczema patients in both clinical practice and clinical trials. The tool consists of 7 items each addressing a specific symptom (itching, sleep, bleeding, weeping, cracking, flaking, and dryness). Subjects will score how often they have experienced each symptom over the previous week on a 5-point categorical response scale (0 = 'no days'; 1 = '1 to 2 days'; 2 = '3 to 4 days'; 3 = '5 to 6'days; 4 = 'every day'). The total score is the sum of the 7 items (range 0 to 28) and reflects disease-related morbidity; a high score is indicative of a worse disease severity. |
From baseline to week 16
|
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Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 16
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 16
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Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 16
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 16
|
|
Change in Child Worst Itch NRS (weekly average) for subjects aged 6 to <12 years at screening.
Periodo de tiempo: From baseline to week 16
|
The Scratch ObsRO NRS assesses 'worst scratching during the past 24 hours' using a numerical rating scale from 0 to 10, where 0 represents 'No scratching' and 10 represents 'Worst scratching possible'. |
From baseline to week 16
|
|
Change in Scratch Observer-Reported Outcome (ObsRO) (weekly average) in subjects aged 2 to <6 years at screening.
Periodo de tiempo: From baseline to week 16
|
The Scratch ObsRO NRS assesses 'worst scratching during the past 24 hours' using a numerical rating scale from 0 to 10, where 0 represents 'No scratching' and 10 represents 'Worst scratching possible'. |
From baseline to week 16
|
|
Change in Scratch Observer-Reported Outcome (ObsRO) (weekly average) in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 16
|
The Scratch ObsRO NRS assesses 'worst scratching during the past 24 hours' using a numerical rating scale from 0 to 10, where 0 represents 'No scratching' and 10 represents 'Worst scratching possible'. |
From baseline to week 16
|
|
Reduction in Children's Dermatology Life Quality Index (CDLQI) ≥6 for subjects aged 4 to <12 years at screening.
Periodo de tiempo: From baseline to week 16
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 16
|
|
Number of treatment-emergent adverse events (AEs) per subject aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 16
|
An adverse event (AE) is any unexpected medical issue that happens to a person who is taking a medication or participating in a study. It could be a symptom, disease, or abnormal test result, even if it's not necessarily caused by the medication being used. |
From baseline to week 16
|
|
Number of treatment-emergent adverse events (AEs) per subject aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 16
|
An adverse event (AE) is any unexpected medical issue that happens to a person who is taking a medication or participating in a study. It could be a symptom, disease, or abnormal test result, even if it's not necessarily caused by the medication being used. |
From baseline to week 16
|
|
Number of TCS free days in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 16
|
TCS- tropical corticosteroids. |
From baseline to week 16
|
|
Number of TCS free days in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 16
|
TCS- tropical corticosteroids. |
From baseline to week 16
|
|
Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 2 to <12 years at screening.
Periodo de tiempo: At week 52
|
The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 52
|
|
Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: At week 52
|
The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 52
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: At week 52
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 52
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Periodo de tiempo: At week 52
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 52
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: At week 52
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 52
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Periodo de tiempo: At week 52
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 52
|
|
Percent change in EASI in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 52
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 52
|
|
Percent change in EASI in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 52
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 52
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 52
|
The SCORAD is a validated tool to evaluate the extent and severity of atopic dermatitis. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 52
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 52
|
The SCORAD is a validated tool to evaluate the extent and severity of atopic dermatitis. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 52
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 52
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 52
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 52
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 52
|
|
Percent change in Children's Dermatology Life Quality Index (CDLQI) in subjects aged 4 to <12 years at screening.
Periodo de tiempo: From baseline to week 52
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 52
|
|
Reduction in Children's Dermatology Life Quality Index (CDLQI) ≥6 for subjects aged 4 to <12 years at screening.
Periodo de tiempo: From baseline to week 52
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 52
|
|
Reduction of in Patient-Oriented Eczema Measure (POEM) ≥6 in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 52
|
The POEM is a validated questionnaire used to assess disease symptoms in atopic eczema patients in both clinical practice and clinical trials. The tool consists of 7 items each addressing a specific symptom (itching, sleep, bleeding, weeping, cracking, flaking, and dryness). Subjects will score how often they have experienced each symptom over the previous week on a 5-point categorical response scale (0 = 'no days'; 1 = '1 to 2 days'; 2 = '3 to 4 days'; 3 = '5 to 6'days; 4 = 'every day'). The total score is the sum of the 7 items (range 0 to 28) and reflects disease-related morbidity; a high score is indicative of a worse disease severity. |
From baseline to week 52
|
|
Reduction of in Patient-Oriented Eczema Measure (POEM) ≥6 in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 52
|
The POEM is a validated questionnaire used to assess disease symptoms in atopic eczema patients in both clinical practice and clinical trials. The tool consists of 7 items each addressing a specific symptom (itching, sleep, bleeding, weeping, cracking, flaking, and dryness). Subjects will score how often they have experienced each symptom over the previous week on a 5-point categorical response scale (0 = 'no days'; 1 = '1 to 2 days'; 2 = '3 to 4 days'; 3 = '5 to 6'days; 4 = 'every day'). The total score is the sum of the 7 items (range 0 to 28) and reflects disease-related morbidity; a high score is indicative of a worse disease severity. |
From baseline to week 52
|
|
Number of treatment-emergent adverse events (AEs) per subject aged 2 to <12 years at screening.
Periodo de tiempo: From week 16 to 52
|
An adverse event (AE) is any unexpected medical issue that happens to a person who is taking a medication or participating in a study. It could be a symptom, disease, or abnormal test result, even if it's not necessarily caused by the medication being used. |
From week 16 to 52
|
|
Number of treatment-emergent adverse events (AEs) per subject aged 6 month to <2 years at screening.
Periodo de tiempo: From week 16 to 52
|
An adverse event (AE) is any unexpected medical issue that happens to a person who is taking a medication or participating in a study. It could be a symptom, disease, or abnormal test result, even if it's not necessarily caused by the medication being used. |
From week 16 to 52
|
|
Presence of treatment-emergent anti-drug antibodies (yes/no) in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From week 16 to 52
|
It measures whether the developed antibodies in response to the treatment have any effect on the safety and effectiveness of the treatment. |
From week 16 to 52
|
|
Presence of treatment-emergent anti-drug antibodies (yes/no) in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From week 16 to 52
|
It measures whether the developed antibodies in response to the treatment have any effect on the safety and effectiveness of the treatment. |
From week 16 to 52
|
|
Number of treatment-emergent adverse events (AEs) per subject aged 2 to <12 years at screening.
Periodo de tiempo: From week 52 to end of treatment
|
An adverse event (AE) is any unexpected medical issue that happens to a person who is taking a medication or participating in a study. It could be a symptom, disease, or abnormal test result, even if it's not necessarily caused by the medication being used. |
From week 52 to end of treatment
|
|
Number of treatment-emergent adverse events (AEs) per subject aged 6 month to <2 years at screening.
Periodo de tiempo: From week 52 to end of treatment
|
An adverse event (AE) is any unexpected medical issue that happens to a person who is taking a medication or participating in a study. It could be a symptom, disease, or abnormal test result, even if it's not necessarily caused by the medication being used. |
From week 52 to end of treatment
|
|
Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 2 to <12 years at screening.
Periodo de tiempo: At week 100
|
The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 100
|
|
Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: At week 100
|
The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 100
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Periodo de tiempo: At week 100
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 100
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: At week 100
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 100
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Periodo de tiempo: At week 100
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 100
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: At week 100
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 100
|
|
Percent change in EASI in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 100
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 100
|
|
Percent change in EASI in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 100
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 100
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 100
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 100
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 100
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 100
|
|
Percent change in Children's Dermatology Life Quality Index (CDLQI) for subjects aged 4 to <12 years at screening.
Periodo de tiempo: From baseline to week 100
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 100
|
|
Reduction in Children's Dermatology Life Quality Index (CDLQI) ≥ 6 for subjects aged 4 to <12 years at screening.
Periodo de tiempo: From baseline to week 100
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 100
|
|
Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 2 to <12 years at screening.
Periodo de tiempo: At week 148
|
The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 148
|
|
Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: At week 148
|
The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 148
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Periodo de tiempo: At week 148
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 148
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: At week 148
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 148
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Periodo de tiempo: At week 148
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 148
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: At week 148
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 148
|
|
Percent change in EASI in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 148
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 148
|
|
Percent change in EASI in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 148
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 148
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 148
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 148
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 148
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 148
|
|
Percent change in Children's Dermatology Life Quality Index (CDLQI) for subjects aged 4 to <12 years at screening.
Periodo de tiempo: From baseline to week 148
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 148
|
|
Reduction in Children's Dermatology Life Quality Index (CDLQI) ≥ 6 for subjects aged 4 to <12 years at screening.
Periodo de tiempo: From baseline to week 148
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 148
|
|
Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 2 to <12 years at screening.
Periodo de tiempo: At week 196
|
The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 196
|
|
Investigator's Global Assessment for atopic dermatitis (IGA 0/1) score of 0 (clear) or 1 (almost clear) in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: At week 196
|
The IGA is an instrument used in clinical trials to rate the severity of the subject's global AD and is based on a 5-point scale ranging from 0 (clear) to 4 (severe). |
At week 196
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Periodo de tiempo: At week 196
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 196
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: At week 196
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 196
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Periodo de tiempo: At week 196
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 196
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: At week 196
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
At week 196
|
|
Percent change in EASI in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 196
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 196
|
|
Percent change in EASI in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 196
|
The EASI is a validated measure to assess the severity and extent of atopic dermatitis. The EASI is a composite index with scores ranging from 0 to 72, with higher values indicating more severe and/or more extensive condition. |
From baseline to week 196
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 2 to <12 years at screening.
Periodo de tiempo: From baseline to week 196
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 196
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 6 month to <2 years at screening.
Periodo de tiempo: From baseline to week 196
|
The SCORAD is a validated tool to evaluate the extent and severity of AD lesions, along with subjective symptoms. The maximum total score is 103, with higher values indicating more severe disease. |
From baseline to week 196
|
|
Percent change in Children's Dermatology Life Quality Index (CDLQI) for subjects aged 4 to <12 years at screening.
Periodo de tiempo: From baseline to week 196
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 196
|
|
Reduction in Children's Dermatology Life Quality Index (CDLQI) ≥ 6 for subjects aged 4 to <12 years at screening.
Periodo de tiempo: From baseline to week 196
|
The CDLQI is a validated questionnaire with content specific to those with dermatology conditions. It consists of 10 items addressing the subject's perception of the impact of their skin disease on various aspects of their quality of life over the last week such as dermatology-related symptoms and feelings, leisure, school or holidays, personal relationships, sleep, and the treatment. Each item is scored on a 4-point Likert scale (0 = 'not at all'; 1 = 'only a little'; 2 = 'quite a lot'; 3 = 'very much'). Item 7 (on school time) has one additional response category 'prevented school', which is also scored '3'. The total score of the CDLQI is the sum of the 10 items (0 to 30); a high score is indicative of a poor quality of life. |
From baseline to week 196
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Director de estudio: Medical Expert, LEO Pharma
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Estimado)
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
- Enfermedades Genéticas Congénitas
- Enfermedades del sistema inmunológico
- Hipersensibilidad, Inmediata
- Hipersensibilidad
- Enfermedades de la piel
- Enfermedades De La Piel Genéticas
- Enfermedades De La Piel Eccematosas
- Dermatitis
- Enfermedades y anomalías congénitas, hereditarias y neonatales
- Enfermedades de la piel y del tejido conectivo
- Dermatitis Atópica
- Alimento
- Dieta, alimentos y nutrición
- Fenómeno fisiológico
- Comida y bebidas
- tralokinumab
- Melaza
Otros números de identificación del estudio
- LP0162-1336
- U1111-1285-6559 (Otro identificador: World Health Organization (WHO))
- 2023-503630-44-00 (Ctis)
- 2023 (Subvención/contrato del NIH de EE. UU.)
Plan de datos de participantes individuales (IPD)
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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.
producto fabricado y exportado desde los EE. UU.
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