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Safety and Efficacy of FURESTEM-AD Inj. for Moderate to Severe Atopic Dermatitis (AD) (smart(FURIN))

5. august 2021 opdateret af: Kang Stem Biotech Co., Ltd.

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

This clinical trial study is 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.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Forventet)

308

Fase

  • Fase 3

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

Studiesteder

    • Jeollanam-do
      • Gwangju, Jeollanam-do, Korea, Republikken, 61453
        • Rekruttering
        • Chosun University Hospital
        • Kontakt:
          • Chanho Na, professor

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

19 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  1. Adults aged 19 years and older at time of informed consent
  2. Subjects diagnosed with atopic dermatitis based on the Hanifin and Rajka diagnostic criteria
  3. Subjects with chronic atopic dermatitis that has been present for at least 1 year before screening
  4. 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)
  5. 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
  6. 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
  7. Women of childbearing potential who use appropriate contraceptive methods during this trial period
  8. Subjects who have voluntarily agreed to participate in this trial in writing

Exclusion Criteria:

  1. Subjects with the following history of disease or surgery/procedure at screening

    1. 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)
    2. organ transplants
    3. History of mental illness, drug or alcohol abuse within 2 years before screening, as per Investigator's opinion
  2. Subjects with the following underlying disease at screening

    1. Chronic active, acute infection or superficial skin infections requiring treatment with systemic antibiotics, antivirals, antiparasitics, antiprotozoals or antifungals;
    2. Skin diseases, pigmentation, or extensive scarring other than atopic dermatitis that may affect the efficacy evaluations of the study
  3. Renal dysfunction with serum creatinine level > 2.0 mg/dL at screening
  4. 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
  5. 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)
  6. 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)
  7. Allergen immunotherapy within 6 months before baseline (Day 1)
  8. Subjects with the history of receipt of the following treatments before baseline (Day 1)

    1. B cell-depleting agents including rituximab within 6 months
    2. Other biologics including dupilumab within 5 half-lives (if known) or 12 weeks, whichever is longer
  9. Subjects with regular use (more than two times per a week) of a tanning booth/parlor within 4 weeks before screening visit
  10. 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
  11. Subjects who are deemed to require prohibited concomitant medications drug/therapy during the study period
  12. Subjects with uncontrolled chronic disease that might require administration of oral corticosteroids such as uncontrolled and severe asthma
  13. 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
  14. 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
  15. Positive serology for hepatitis B or C, or for HIV
  16. Subjects with prior use of FURESTEM-AD
  17. Subjects with history of anaphylaxis
  18. 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

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Firedobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: 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)

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
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
Foranstaltningsbeskrivelse
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

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Yeonglib Park, professor (CI), Bucheon Hospital, Soonchunhyang University
  • Ledende efterforsker: Yangwon Lee, professor, Konkuk University Hospital
  • Ledende efterforsker: Sanguk Son, professor, Korea University
  • Ledende efterforsker: Bakrin Yoo, professor, Gangdong Kyunghee University Hospital
  • Ledende efterforsker: Jihyun Lee, professor, Seoul St. Mary'S Hospital
  • Ledende efterforsker: Donghoon Lee, professor, Seoul National University Hospital
  • Ledende efterforsker: Chanho Na, professor, Chosun University Hospital
  • Ledende efterforsker: Yooin Bae, professor, Hallym University Dongtan Seongsim Hospital
  • Ledende efterforsker: Hyunchang Ko, professor, Yangsan Pusan National University Hospital
  • Ledende efterforsker: Younghyun Jang, professor, Kyungpook National University Hospital
  • Ledende efterforsker: Jeongeun Kim, professor, The Catholic University of Korea Eunpyeong St. Mary's Hospital
  • Ledende efterforsker: Minkyung Shin, professor, KyungHee University Hospital
  • Ledende efterforsker: Sanghyun Cho, professor, Catholic University Incheon St. Mary's Hospital
  • Ledende efterforsker: Cheonuk Park, professor, Hallym University Gangnam Seongsim Hospital
  • Ledende efterforsker: Jooyeon Ko, professor, Hanyang University
  • Ledende efterforsker: Taeyoung Han, professor, Nowon Eulji University Hospital
  • Ledende efterforsker: Jiyoung Ahn, professor, National Medical Center

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

29. juni 2021

Primær færdiggørelse (Forventet)

1. januar 2023

Studieafslutning (Forventet)

1. april 2023

Datoer for studieregistrering

Først indsendt

4. juli 2021

Først indsendt, der opfyldte QC-kriterier

5. august 2021

Først opslået (Faktiske)

13. august 2021

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

13. august 2021

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

5. august 2021

Sidst verificeret

1. juli 2021

Mere information

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