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Obtaining Descriptive Classifications of Pruritus and Assessing Change in Pruritus Over Time in Atopic Dermatitis Patients Using Topical Roflumilast Cream.

2026年8月11日 更新者:Integrative Skin Science and Research

A Phase 4, Open Label Study to Assess Descriptive Classification of Pruritus Over Time With Roflumilast 0.15% Cream in Patients With Atopic Dermatitis

This study is being done to obtain descriptive classifications of pruritus using a patient directed survey system and assess change in pruritus over time in patients with Atopic Dermatitis over 4 weeks with use of topical Roflumilast cream 0.15% QD.

調査の概要

研究の種類

介入

入学 (推定)

40

段階

  • フェーズ 4

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

研究場所

    • California
      • Sacramento、California、アメリカ、95815
        • 募集
        • Integrative Skin Science and Research
        • 主任研究者:
          • Raja Sivamani, MD
        • コンタクト:

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

  • 子
  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  1. Male or female subjects aged 12 years or older
  2. Participants and/or legal guardians are legally competent to sign and give informed consent.
  3. Clinically confirmed diagnosis of active mild to moderate AD according to Hanifin and Rajka criteria (1980).
  4. History of AD for at least 6 months as determined by the Investigator using information from the subject's medical chart, from the subject's physician, or through subject/caregiver interview. Stable disease for the past 4 weeks with no significant flares in atopic dermatitis before screening
  5. At least 3 months of chronic pruritus related to AD before the screening visit.
  6. EASI Score ≥5 at Baseline. EASI is evaluated for the entire body except the scalp, palms, and soles.
  7. vIGA-AD score of 'Mild' (2') or 'Moderate' (3') at Baseline. The vIGA-AD is evaluated for the entire body except the scalp, palms, and soles.
  8. Has AD involvement of ≥3% BSA (excluding the scalp, palms, soles) at Baseline.
  9. Participants must have access to a device and be willing to download the ExpiWell app and able to complete the associated questionnaires once daily at approximately the same time each day throughout participation in the study.
  10. Prior to the first application of study drug, participant has a baseline WI-NRS (24-hour recall period) and mItch-NRS score ≥ 4.0.
  11. Females of childbearing potential (FOCBP) must have a negative urine pregnancy test at Screening and Baseline/Day 1. In addition, sexually active FOCBP must agree to use at least one form of a highly effective or barrier method of contraception throughout the trial. The use of abstinence as a contraceptive measure is acceptable if this is a consistent part of a lifestyle choice and an acceptable backup method has been identified if the subject becomes sexually active.
  12. Females of non-childbearing potential should be post-menopausal with spontaneous amenorrhea for at least 12 months (post-menopausal status should be confirmed with FSH testing) or have undergone surgical sterilization (permanent sterilization methods include hysterectomy, bilateral oophorectomy, hysteroscopic sterilization, bilateral tubal ligation or bilateral salpingectomy).
  13. In good health as judged by the Investigator, based on medical history, targeted physical examination, and vital signs. Subjects and parent(s)/legal guardian(s) are considered reliable and capable of adhering to the Protocol and visit schedule, according to the judgment of the Investigator.

Exclusion Criteria:

  1. Subjects with any medical condition or physical examination abnormality that would prevent study participation or place the subject at significant risk, as judged by the Investigator.
  2. Subjects who cannot discontinue medications and treatments prior to the Baseline visit and during the study according to Excluded Medications and Treatments.
  3. Participant had significant flares or unstable course in AD (i.e., condition worsened significantly or required significant change in medications, as per medical judgment) in the previous 4 weeks before screening or any consistent requirement for high potency topical steroids to manage AD signs or symptoms.
  4. Participant has significant active systemic or localized infection, like clinically infected AD, or has used antibiotics (systemic or topical), antifungal or antiviral agents within 2 weeks prior to the run-in period.
  5. Participant with a history or presence of a condition that, in the opinion of the investigator, would interfere with the study assessments (e.g., generalized erythroderma, Netherton syndrome, psoriasis, or any skin condition other than AD that may risk inducing a pruritus flare/worsening).
  6. Subjects who are unwilling to refrain from prolonged sun exposure and from using a tanning bed or other artificial light emitting devices (LEDs) for 4 weeks prior to Baseline/Day 1 and during the study.
  7. Participants have tattoos, scratches, open sores, excessive hair, or skin damage that, in the opinion of the investigator, may interfere with study evaluations.
  8. Subjects with known genetic dermatological conditions that overlap with AD, such as Netherton syndrome.
  9. Known allergies to roflumilast or to the excipients in Roflumilast cream (petrolatum, isopropyl palmitate, methylparaben, propylparaben, diethylene glycol monoethyl ether, hexylene glycol, cetylstearyl alcohol, dicetyl phosphase and ceteth-10 phosphate).
  10. Participant has a clearly defined etiology for pruritus other than AD, including but not limited to urticaria, psoriasis, or other nonatopic dermatologic conditions; hepatic or renal disease; psychogenic pruritus; drug reaction; uncontrolled hyperthyroidism; and infection.
  11. Subjects who have received oral roflumilast (Daxas®, Daliresp®) within 4 weeks prior to Baseline/ Day 1.
  12. History of severe depression, suicidal ideation or behavior at Baseline/Screening indicative of suicidal ideation or behavior, whether lifetime or recent/current.
  13. Subjects currently undergoing allergy testing (eg, food allergy testing or skin prick testing), patch testing, food challenges, or allergy desensitization, or plan to do so during the study.
  14. Subjects with any serious medical condition (eg, uncontrolled hypo- or hyper-thyroidism) or clinically significant laboratory abnormality that would prevent study participation or place the subject at significant risk, as determined by the Investigator.
  15. Previous treatment with Roflumilast cream or foam (any potency) or current Roflumilast use for any indication at the baseline visit that would be expected to continue during the trial.
  16. Subjects with a history of major surgery within 4 weeks prior to Baseline/Day 1 or subjects who have major surgery planned during the study.
  17. Subjects with a history of chronic alcohol or drug abuse within 6 months prior to Screening.
  18. Subjects who are family members of the clinical study site, clinical study staff, or sponsor, or family members of enrolled subjects living in the same house.
  19. Subjects with known or suspected severe renal insufficiency or moderate to severe liver impairment (Child-Pugh B or C) as determined by the clinical investigator based upon subject's medical history and physical exam.

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:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Roflumilast Group
topically applied to the affected areas once daily

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
Number of descriptors (besides itch) used to describe skin sensations associated with AD
時間枠:From enrollment to end of treatment at 4 weeks.
Participants will download and install the ExpiWell app. Descriptive classification of itch will be captured in the app. The number of descriptions selected by the participant will be tabulated to assess if there is more than just a description of itch for their skin sensation.
From enrollment to end of treatment at 4 weeks.

二次結果の測定

結果測定
メジャーの説明
時間枠
Change from baseline in modified Itch Numeric Rating Scale (mItch-NRS) on first day of application.
時間枠:Day of baseline visit
Change from baseline in mItch-NRS at 5, 10, 15, 20, 25, 30, 45, 60, 90, and 120 minutes, and 4, 6, and 8 hours
Day of baseline visit
Change from baseline in Worst Itch Numeric Rating Scale (WI-NRS) at 4 weeks
時間枠:From enrollment to end of treatment at 4 weeks
Change in the Worst Itch Numeric Rating Scale (WI-NRS) response from baseline to week 4
From enrollment to end of treatment at 4 weeks
Change from baseline in Dermatology Life Quality Index (DLQI)
時間枠:From enrollment to end of treatment at 4 weeks
Change from baseline in DLQI at week 2 and week 4
From enrollment to end of treatment at 4 weeks
Change from baseline in Validated Investigator Global Assessment of Atopic Dermatitis (vIGA-AD)
時間枠:From enrollment to the end of treatment at 4 weeks
Change from baseline in vIGA-AD at week 2 and week 4
From enrollment to the end of treatment at 4 weeks
Change from baseline in Eczema Area and Severity Index (EASI)
時間枠:From enrollment to the end of treatment at 4 weeks
Change from baseline in EASI at week 2 and week 4
From enrollment to the end of treatment at 4 weeks
Change from baseline in Body Surface Area (BSA)
時間枠:From enrollment to the end of treatment at 4 weeks
Change from baseline in BSA at week 2 and week 4
From enrollment to the end of treatment at 4 weeks

その他の成果指標

結果測定
メジャーの説明
時間枠
Change from baseline in Treatment Satisfaction Questionnaire (TSQ) outcomes
時間枠:From enrollment to the end of treatment at 4 weeks
Change from baseline in TSQ outcomes at week 2 and week 4
From enrollment to the end of treatment at 4 weeks
Impact assessment question outcome trends
時間枠:From enrollment to the end of treatment at 4 weeks
Assessing Impact assessment question outcomes at baseline and week 4
From enrollment to the end of treatment at 4 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。

捜査官

  • 主任研究者:Raja K Sivamani, MD MS AP、Integrative Skin Science and Research

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)

2026年7月21日

一次修了 (推定)

2027年8月1日

研究の完了 (推定)

2027年8月1日

試験登録日

最初に提出

2026年4月23日

QC基準を満たした最初の提出物

2026年4月23日

最初の投稿 (実際)

2026年5月1日

学習記録の更新

投稿された最後の更新 (実際)

2026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

2026年8月11日

最終確認日

2026年8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

はい

米国FDA規制機器製品の研究

いいえ

米国で製造され、米国から輸出された製品。

はい

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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