Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

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

5. august 2021 oppdatert av: 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.

Studieoversikt

Studietype

Intervensjonell

Registrering (Forventet)

308

Fase

  • Fase 3

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

Studiesteder

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

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

19 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

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

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

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

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

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

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

29. juni 2021

Primær fullføring (Forventet)

1. januar 2023

Studiet fullført (Forventet)

1. april 2023

Datoer for studieregistrering

Først innsendt

4. juli 2021

Først innsendt som oppfylte QC-kriteriene

5. august 2021

Først lagt ut (Faktiske)

13. august 2021

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

13. august 2021

Siste oppdatering sendt inn som oppfylte QC-kriteriene

5. august 2021

Sist bekreftet

1. juli 2021

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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. .

Abonnere