- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT06311682
Próba oceny skuteczności i bezpieczeństwa stosowania tralokinumabu w skojarzeniu z miejscowymi kortykosteroidami u dzieci i niemowląt z umiarkowanym do ciężkiego atopowym zapaleniem skóry (TRAPEDS 2)
Wieloośrodkowe badanie fazy III mające na celu ocenę skuteczności i bezpieczeństwa stosowania tralokinumabu w skojarzeniu z miejscowo stosowanymi kortykosteroidami u dzieci (w wieku od 2 do
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.
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Typ studiów
Zapisy (Szacowany)
Faza
- Faza 3
Kontakty i lokalizacje
Kontakt w sprawie studiów
- Nazwa: Clinical Disclosure
- Numer telefonu: +45 4494 5888
- E-mail: disclosure@leo-pharma.com
Lokalizacje studiów
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Brussels, Belgia, 1020
- Wycofane
- Leo Pharma Investigational site
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Ghent, Belgia, 9000
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Leuven, Belgia, 3000
- Wycofane
- Leo Pharma Investigational site
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Liège, Belgia, 4000
- Wycofane
- Leo Pharma Investigational site
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Rijeka, Chorwacja, 51000
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Zagreb, Chorwacja, 10000
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Zagreb, Chorwacja, 10000
- Wycofane
- Leo Pharma Investigational site
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Alicante, Hiszpania, 03010
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Madrid, Hiszpania, 28046
- Wycofane
- Leo Pharma Investigational site
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Valencia, Hiszpania, 46014
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Utrecht, Holandia, 3584 CW
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Cork, Irlandia, T12 DFK4
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Crumlin, Irlandia, D12N512
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Burlington, Kanada, L7L 6W6
- Rekrutacyjny
- Leo Pharma Investigational site
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Calgary, Kanada, Calgary
- Wycofane
- Leo Pharma Investigational site
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Calgary, Kanada, T2J 7E1
- Rekrutacyjny
- Leo Pharma Investigational site
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Edmonton, Kanada, T5J 3S9
- Rekrutacyjny
- Leo Pharma Investigational site
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Edmonton, Kanada, T6G 1C3
- Rekrutacyjny
- Leo Pharma Investigational site
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Hamilton, Kanada, L8S 1G5
- Rekrutacyjny
- Leo Pharma Investigational site
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Niagara Falls, Kanada, L2H 1H5
- Rekrutacyjny
- Leo Pharma Investigational site
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Saskatoon, Kanada, S7K 2C1
- Rekrutacyjny
- Leo Pharma Investigational site
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Windsor, Kanada, N8X2G1
- Rekrutacyjny
- Leo Pharma Investigational site
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Winnipeg, Kanada, R3M 3Z4
- Rekrutacyjny
- Leo Pharma Investigational site
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Ansan-si, Korea Południowa, 15355
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Gwangju, Korea Południowa, 61453
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Seoul, Korea Południowa, 02447
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Seoul, Korea Południowa, 03080
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Seoul, Korea Południowa, 03722
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Seoul, Korea Południowa, 05030
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Seoul, Korea Południowa, 06273
- Wycofane
- Leo Pharma Investigational site
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Seoul, Korea Południowa, 06591
- Wycofane
- Leo Pharma Investigational site
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Seoul, Korea Południowa, 139-711
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Buxtehude, Niemcy, 21614
- Wycofane
- Leo Pharma Investigational site
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Dresden, Niemcy, 01307
- Wycofane
- Leo Pharma Investigational site
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Mainz, Niemcy, 55131
- Wycofane
- Leo Pharma Investigational site
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Osnabrück, Niemcy, 49074
- Wycofane
- Leo Pharma Investigational site
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Tübingen, Niemcy, 72076
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Wuppertal, Niemcy, 42283
- Wycofane
- Leo Pharma Investigational site
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Gdansk, Polska, 80-546
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Krakow, Polska, 30-002
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Lodz, Polska, 90-436
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Ostrowiec Świętokrzyski, Polska, 27-400
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Rzeszów, Polska, 35-055
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Tarnów, Polska, 33-100
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Warsaw, Polska, 02-953
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Warsaw, Polska, 02-962
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Brasov, Rumunia, 500091
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Iași, Rumunia, 700259
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Alabama
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Birmingham, Alabama, Stany Zjednoczone, 35209
- Rekrutacyjny
- Leo Pharma Investigational site
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Arkansas
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North Little Rock, Arkansas, Stany Zjednoczone, 72117
- Rekrutacyjny
- Leo Pharma Investigational site
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California
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Palo Alto, California, Stany Zjednoczone, 94304
- Rekrutacyjny
- Leo Pharma Investigational site
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Sacramento, California, Stany Zjednoczone, 95816
- Rekrutacyjny
- Leo Pharma Investigational site
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San Diego, California, Stany Zjednoczone, 92108
- Wycofane
- Leo Pharma Investigational site
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San Diego, California, Stany Zjednoczone, 92123
- Rekrutacyjny
- Leo Pharma Investigational site
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Florida
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Jacksonville, Florida, Stany Zjednoczone, 32256
- Rekrutacyjny
- Leo Pharma Investigational site
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Miami, Florida, Stany Zjednoczone, 33156
- Rekrutacyjny
- Leo Pharma Investigational site
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Tampa, Florida, Stany Zjednoczone, 33613
- Rekrutacyjny
- Leo Pharma Investigational site
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Georgia
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Macon, Georgia, Stany Zjednoczone, 31217
- Rekrutacyjny
- Leo Pharma Investigational site
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Michigan
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Waterford, Michigan, Stany Zjednoczone, 48328
- Rekrutacyjny
- Leo Pharma Investigational site
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Oklahoma
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Tulsa, Oklahoma, Stany Zjednoczone, 74136
- Rekrutacyjny
- Leo Pharma Investigational site
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Oregon
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Portland, Oregon, Stany Zjednoczone, 97239
- Rekrutacyjny
- Leo Pharma Investigational site
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South Carolina
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Charleston, South Carolina, Stany Zjednoczone, 27420
- Rekrutacyjny
- Leo Pharma Investigational site
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Virginia
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Norfolk, Virginia, Stany Zjednoczone, 23502
- Rekrutacyjny
- Leo Pharma Investigational site
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Ancona, Włochy, 60126
- Wycofane
- Leo Pharma Investigational site
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Brescia, Włochy, 25123
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Padova, Włochy, 35128
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Roma, Włochy, 00168
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Rome, Włochy, 00165
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Lincoln, Zjednoczone Królestwo, LN2 5QY
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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London, Zjednoczone Królestwo, WC1N 3JH
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Sheffield, Zjednoczone Królestwo, S10 2TH
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Southampton, Zjednoczone Królestwo, SO16 6YD
- Aktywny, nie rekrutujący
- Leo Pharma Investigational site
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
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 studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Potroić
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Eksperymentalny: 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. |
|
Eksperymentalny: 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. |
|
Eksperymentalny: 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. |
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
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.
Ramy czasowe: At week 16
|
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
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Ramy czasowe: 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
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Obecność powstałych podczas leczenia przeciwciał przeciwlekowych (tak/nie) u osób w wieku od 2 do <12 lat w momencie badania przesiewowego.
Ramy czasowe: Od wartości początkowej do tygodnia 16
|
Od wartości początkowej do tygodnia 16
|
|
|
Obecność powstałych podczas leczenia przeciwciał przeciwlekowych (tak/nie) u pacjentów w wieku od 6 miesięcy do <2 lat w momencie badania przesiewowego.
Ramy czasowe: Od wartości początkowej do tygodnia 16
|
Od wartości początkowej do tygodnia 16
|
|
|
Stosowanie leczenia doraźnego (tak/nie) u osób w wieku od 2 do <12 lat w momencie badania przesiewowego.
Ramy czasowe: Od wartości początkowej do tygodnia 16
|
Od wartości początkowej do tygodnia 16
|
|
|
Zastosowanie w leczeniu doraźnym (tak/nie) u pacjentów w wieku od 6 miesięcy do <2 lat w momencie badania przesiewowego.
Ramy czasowe: Od wartości początkowej do tygodnia 16
|
Od wartości początkowej do tygodnia 16
|
|
|
Procentowa zmiana dotkniętej powierzchni ciała (BSA) u osób w wieku od 2 do <12 lat w momencie badania przesiewowego.
Ramy czasowe: Od wartości początkowej do 52. tygodnia
|
Od wartości początkowej do 52. tygodnia
|
|
|
Procentowa zmiana dotkniętej powierzchni ciała (BSA) u osób w wieku od 6 miesięcy do <2 lat w chwili badania przesiewowego.
Ramy czasowe: Od wartości początkowej do 52. tygodnia
|
Od wartości początkowej do 52. tygodnia
|
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 2 to <12 years at screening.
Ramy czasowe: 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
|
|
Having at least 90% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Ramy czasowe: 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
|
|
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.
Ramy czasowe: At week 16
|
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
|
|
Having at least 75% reduction in Eczema Area and Severity Index (EASI) score in subjects aged 6 month to <2 years at screening.
Ramy czasowe: 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
|
|
Having at least 50% reduction in EASI score in subjects aged 2 to <12 years at screening.
Ramy czasowe: 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
|
|
Having at least 50% reduction in EASI score in subjects aged 6 month to <2 years at screening.
Ramy czasowe: 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
|
|
Percent change in EASI in subjects aged 2 to <12 years at screening.
Ramy czasowe: 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 EASI in subjects aged 6 month to <2 years at screening.
Ramy czasowe: 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.
Ramy czasowe: From baseline to week 16
|
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
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) in subjects aged 6 month to <2 years at screening.
Ramy czasowe: From baseline to week 16
|
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
|
|
Percent change in affected BSA in subjects aged 2 to <12 years at screening.
Ramy czasowe: From baseline to week 16
|
BSA is a body surface area. |
From baseline to week 16
|
|
Percent change in affected BSA in subjects aged 6 month to <2 years at screening.
Ramy czasowe: From baseline to week 16
|
BSA is a body surface area. |
From baseline to week 16
|
|
Percent change in Children's Dermatology Life Quality Index (CDLQI) for subjects aged 4 to <12 years at screening.
Ramy czasowe: 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
|
|
Reduction in Child Worst Itch numeric rating score (NRS) (weekly average) ≥4 for subjects aged 6 to <12 years at screening.
Ramy czasowe: 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'. |
From baseline to Week 16
|
|
Reduction in Scratch Observer-Reported Outcome (ObsRO) (weekly average) ≥4 for subjects aged 2 to <6 years at screening.
Ramy czasowe: 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 Scratch Observer-Reported Outcome (ObsRO) (weekly average) ≥4 for subjects aged 6 months to <2 years years at screening.
Ramy czasowe: 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 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.
Ramy czasowe: 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
|
|
Percent change in Patient-Oriented Eczema Measure (POEM) in subjects aged 2 to <12 years at screening.
Ramy czasowe: 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
|
|
Percent change in Patient-Oriented Eczema Measure (POEM) in subjects aged 6 month to <2 years at screening.
Ramy czasowe: 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 2 to <12 years at screening.
Ramy czasowe: 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.
Ramy czasowe: 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
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 2 to <12 years at screening.
Ramy czasowe: 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
|
|
Percent change in Scoring Atopic Dermatitis (SCORAD) sleep loss in subjects aged 6 month to <2 years at screening.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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.
Ramy czasowe: 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
|
Współpracownicy i badacze
Sponsor
Śledczy
- Dyrektor Studium: Medical Expert, LEO Pharma
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Szacowany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Dodatkowe istotne warunki MeSH
- Choroby genetyczne, wrodzone
- Choroby układu odpornościowego
- Nadwrażliwość, natychmiastowa
- Nadwrażliwość
- Choroby skórne
- Choroby skóry, genetyczne
- Choroby skóry, egzema
- Zapalenie skóry
- Wrodzone, dziedziczne i noworodkowe choroby i nieprawidłowości
- Choroby skóry i tkanki łącznej
- Zapalenie skóry, atopowe
- Żywność
- Dieta, żywność i odżywianie
- Zjawiska fizjologiczne
- Jedzenie i napoje
- tralokinumab
- Melasa
Inne numery identyfikacyjne badania
- LP0162-1336
- U1111-1285-6559 (Inny identyfikator: World Health Organization (WHO))
- 2023-503630-44-00 (Ctis)
- 2023 (Grant/umowa NIH USA)
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
produkt wyprodukowany i wyeksportowany z USA
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