- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT05004324
Safety and Efficacy of FURESTEM-AD Inj. for Moderate to Severe Atopic Dermatitis (AD) (smart(FURIN))
A Two-stage, Multi-center, Randomized, Double-Blind, Placebo Controlled, Phase 3 Clinical Trial to Evaluate the Efficacy and Safety of FURESTEM-AD Inj. for Moderate to Severe Chronic Atopic Dermatitis
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Studietype
Registrering (Forventet)
Fase
- Fase 3
Kontakter og plasseringer
Studiekontakt
- Navn: Noori Kim
- Telefonnummer: 82 2-888-1590
- E-post: nrkim@kangstem.com
Studer Kontakt Backup
- Navn: Seulbi Lee
- Telefonnummer: 82 2-888-1590
- E-post: sblee@kangstem.com
Studiesteder
-
-
Jeollanam-do
-
Gwangju, Jeollanam-do, Korea, Republikken, 61453
- Rekruttering
- Chosun University Hospital
-
Ta kontakt med:
- Chanho Na, professor
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Adults aged 19 years and older at time of informed consent
- Subjects diagnosed with atopic dermatitis based on the Hanifin and Rajka diagnostic criteria
- Subjects with chronic atopic dermatitis that has been present for at least 1 year before screening
Subjects with moderate to severe atopic dermatitis as indicated by:
- EASI score ≥ 16 points at the time of screening and baseline (Day 1),
- IGA score ≥ 3 points at the time of screening and baseline (Day 1), and
- BSA affected by atopic dermatitis ≥ 10% at the time of screening and baseline (Day 1)
- Subjects who have documented history of insufficient response to stable use of atopic dermatitis treatment within 24 weeks before screening, or inability to receive such treatment because of safety issues
- Subjects who are willing to apply a stable dose of non-medicated topical moisturizer at least twice daily for at least 7 days before the baseline (Day 1) visit and the duration of the study
- Women of childbearing potential who use appropriate contraceptive methods during this trial period
- Subjects who have voluntarily agreed to participate in this trial in writing
Exclusion Criteria:
Subjects with the following history of disease or surgery/procedure at screening
- Malignancy or lympho-proliferative disease within 5 years before screening (except completely treated carcinoma in situ of the cervix, or completely treated and resolved non-metastatic squamous or basal cell carcinoma of the skin)
- organ transplants
- History of mental illness, drug or alcohol abuse within 2 years before screening, as per Investigator's opinion
Subjects with the following underlying disease at screening
- Chronic active, acute infection or superficial skin infections requiring treatment with systemic antibiotics, antivirals, antiparasitics, antiprotozoals or antifungals;
- Skin diseases, pigmentation, or extensive scarring other than atopic dermatitis that may affect the efficacy evaluations of the study
- Renal dysfunction with serum creatinine level > 2.0 mg/dL at screening
- Liver dysfunction with alanine aminotransferase (ALT) or aspartate aminotransferase (AST) levels exceeding 2.5 times the upper limit of the normal range (ULN) at the time of screening
- Subjects with the history of using leukotriene receptor antagonists, systemic steroids, phototherapy, systemic immunosuppressants/modulators including janus kinase (JAK) inhibitors, and/or any other systemic therapy (not mentioned in Exclusion Criteria 6 and 8) to treat atopic dermatitis or symptoms of atopic dermatitis (approved or off-label use) within 4 weeks before baseline (Day 1)
- Subjects with the history of using systemic or topical antihistamines, topical corticosteroids (TCS), topical calcineurin inhibitors (TCIs), or topical phosphodiesterase 4 (PDE4) inhibitors within 2 weeks before baseline (Day 1)
- Allergen immunotherapy within 6 months before baseline (Day 1)
Subjects with the history of receipt of the following treatments before baseline (Day 1)
- B cell-depleting agents including rituximab within 6 months
- Other biologics including dupilumab within 5 half-lives (if known) or 12 weeks, whichever is longer
- Subjects with regular use (more than two times per a week) of a tanning booth/parlor within 4 weeks before screening visit
- Subjects with the history of a live (attenuated) vaccine injection within 12 weeks before baseline (Day 1) or the plan to inject a live (attenuated) vaccine within 24 weeks after randomization
- Subjects who are deemed to require prohibited concomitant medications drug/therapy during the study period
- Subjects with uncontrolled chronic disease that might require administration of oral corticosteroids such as uncontrolled and severe asthma
- Pregnant/lactating women and men and women of childbearing potential who plan to become pregnant or who refuse to use appropriate contraceptive methods during the study period
- Subjects with the history of receipt of any investigational products or devices from another clinical trial within 4 weeks or 5 half-lives (if known) pior to screening
- Positive serology for hepatitis B or C, or for HIV
- Subjects with prior use of FURESTEM-AD
- Subjects with history of anaphylaxis
- Subjects who are deemed to have difficulty in performing this study by the judgment of the Investigator and those with other medical findings that are unsuitable for participation in the study
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Firemannsrom
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Furestem-AD Inj.
Investigational product name: FURESTEM-AD® inj. 5.0 X 10^7 cells/1.5 mL baseline (0week) Experimental group will receive Investigational product (FURESTEM-AD® inj. 5.0 X 10^7 cells/1.5 mL). After 12 weeks, Experimental group will receive placebo. |
the following study drug is injected respectively into both upper arms, both thighs, and abdomen (total of 5 regions)
the following study drug is injected respectively into both upper arms, both thighs, and abdomen (total of 5 regions)
|
|
Placebo komparator: Placebo
Placebo baseline (0week) Placebo comparator group will receive placebo. After 12 weeks, Placebo comparator group will receive Investigational product (FURESTEM-AD® inj. 5.0 X 10^7 cells/1.5 mL). |
the following study drug is injected respectively into both upper arms, both thighs, and abdomen (total of 5 regions)
the following study drug is injected respectively into both upper arms, both thighs, and abdomen (total of 5 regions)
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
EASI(Eczema Area and Severity Index)-50
Tidsramme: 12 weeks
|
Ratio of subject whose Eczema Area and Severity Index (EASI) decreased over 50% as contrasted with baseline value
|
12 weeks
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
EASI(Eczema Area and Severity Index)-75
Tidsramme: 2,4,8,12 weeks
|
Ratio of subjects whose Eczema Area and Severity Index (EASI) decreased over 75% as contrasted with baseline value
|
2,4,8,12 weeks
|
|
EASI(Eczema Area and Severity Index)-50
Tidsramme: 2,4,8 weeks
|
Ratio of subjects whose Eczema Area and Severity Index (EASI) decreased over 50% as contrasted with baseline value
|
2,4,8 weeks
|
|
EASI(Eczema Area and Severity Index) index
Tidsramme: 2,4,8,12 weeks
|
Change and rate of change in Eczema Area and Severity Index (EASI) index as contrasted with baseline value
|
2,4,8,12 weeks
|
|
IGA(Investigator's Global Assessment) Score
Tidsramme: 2,4,8,12 weeks
|
Proportion of subjects who Investigator's Global Assessment (IGA) score 0 or 1 and at least 2 points reduction in IGA score as contrasted with baseline value
|
2,4,8,12 weeks
|
|
SCORAD(SCORing Atopic Dermatitis)-50
Tidsramme: 2,4,8,12 weeks
|
Ratio of subjects whose SCORing Atopic Dermatitis (SCORAD) decreased over 50% as contrasted with baseline value
|
2,4,8,12 weeks
|
|
SCORAD(SCORing Atopic Dermatitis) index
Tidsramme: 2,4,8,12 weeks
|
Change and rate of change in SCORing Atopic Dermatitis (SCORAD) index as contrasted with baseline value
|
2,4,8,12 weeks
|
|
BSA(Body Surface Area)
Tidsramme: 2,4,8,12 weeks
|
Change and rate of change in Body Surface Area (BSA) as contrasted with baseline value
|
2,4,8,12 weeks
|
|
Worst daily Pruritus NRS(Numerical Rating Scale)
Tidsramme: 2,4,8,12 weeks
|
Rate of change in Worst daily Pruritus Numerical Rating Scale (NRS) as contrasted with baseline value
|
2,4,8,12 weeks
|
|
Average daily Pruritus NRS(Numerical Rating Scale)
Tidsramme: 2,4,8,12 weeks
|
Rate of change in Average daily Pruritus Numerical Rating Scale (NRS) as contrasted with baseline value
|
2,4,8,12 weeks
|
|
Worst daily Pruritus NRS(Numerical Rating Scale) - 4 points
Tidsramme: 2,4,8,12 weeks
|
Proportion of patients at least 4 points reduction in Worst daily Pruritus Numerical Rating Scale (NRS) as contrasted with baseline value
|
2,4,8,12 weeks
|
|
POEM(Patient-Oriented Eczema Measure)
Tidsramme: 2,4,8,12 weeks
|
Change and rate of change in Patient-Oriented Eczema Measure (POEM) as contrasted with baseline value
|
2,4,8,12 weeks
|
|
DLQI(Dermatology Life Quality Index)
Tidsramme: 2,4,8,12 weeks
|
Change and rate of change in Dermatology Life Quality Index (DLQI) as contrasted with baseline value
|
2,4,8,12 weeks
|
|
Rescue medicine
Tidsramme: up to 12, 24 weeks
|
Total number of use and consumed amount of rescue medicine
|
up to 12, 24 weeks
|
Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Hovedetterforsker: Yeonglib Park, professor (CI), Bucheon Hospital, Soonchunhyang University
- Hovedetterforsker: Yangwon Lee, professor, Konkuk University Hospital
- Hovedetterforsker: Sanguk Son, professor, Korea University
- Hovedetterforsker: Bakrin Yoo, professor, Gangdong Kyunghee University Hospital
- Hovedetterforsker: Jihyun Lee, professor, Seoul St. Mary'S Hospital
- Hovedetterforsker: Donghoon Lee, professor, Seoul National University Hospital
- Hovedetterforsker: Chanho Na, professor, Chosun University Hospital
- Hovedetterforsker: Yooin Bae, professor, Hallym University Dongtan Seongsim Hospital
- Hovedetterforsker: Hyunchang Ko, professor, Yangsan Pusan National University Hospital
- Hovedetterforsker: Younghyun Jang, professor, Kyungpook National University Hospital
- Hovedetterforsker: Jeongeun Kim, professor, The Catholic University of Korea Eunpyeong St. Mary's Hospital
- Hovedetterforsker: Minkyung Shin, professor, KyungHee University Hospital
- Hovedetterforsker: Sanghyun Cho, professor, Catholic University Incheon St. Mary's Hospital
- Hovedetterforsker: Cheonuk Park, professor, Hallym University Gangnam Seongsim Hospital
- Hovedetterforsker: Jooyeon Ko, professor, Hanyang University
- Hovedetterforsker: Taeyoung Han, professor, Nowon Eulji University Hospital
- Hovedetterforsker: Jiyoung Ahn, professor, National Medical Center
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Forventet)
Studiet fullført (Forventet)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- K0106
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .