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

2021年8月5日 更新者: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.

調査の概要

研究の種類

介入

入学 (予想される)

308

段階

  • フェーズ 3

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

研究場所

    • Jeollanam-do
      • Gwangju、Jeollanam-do、大韓民国、61453
        • 募集
        • Chosun University Hospital
        • コンタクト:
          • Chanho Na, professor

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

19年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:4倍

武器と介入

参加者グループ / アーム
介入・治療
実験的: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)
プラセボコンパレーター: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)

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
EASI(Eczema Area and Severity Index)-50
時間枠:12 weeks
Ratio of subject whose Eczema Area and Severity Index (EASI) decreased over 50% as contrasted with baseline value
12 weeks

二次結果の測定

結果測定
メジャーの説明
時間枠
EASI(Eczema Area and Severity Index)-75
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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
時間枠: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)
時間枠: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)
時間枠: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
時間枠:up to 12, 24 weeks
Total number of use and consumed amount of rescue medicine
up to 12, 24 weeks

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

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

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2021年6月29日

一次修了 (予想される)

2023年1月1日

研究の完了 (予想される)

2023年4月1日

試験登録日

最初に提出

2021年7月4日

QC基準を満たした最初の提出物

2021年8月5日

最初の投稿 (実際)

2021年8月13日

学習記録の更新

投稿された最後の更新 (実際)

2021年8月13日

QC基準を満たした最後の更新が送信されました

2021年8月5日

最終確認日

2021年7月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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