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A Study for AR100DP1 in Mild to Moderate Atopic Dermatitis

29 octobre 2026 mis à jour par: Arjil Pharmaceuticals LLC

A Phase II Double-Blind Study to Evaluate the Safety, Tolerability, and Efficacy of AR100DP1 in Subjects With Mild to Moderate Atopic Dermatitis

This study is composed of a two-arm, double-blind, randomized, placebo-controlled, Phase II study to evaluate the efficacy of AR100DP1 compared to placebo on AD lesion area(s) in subjects with mild to moderate AD.

Aperçu de l'étude

Statut

Recrutement

Les conditions

Description détaillée

Eligible subjects with mild to moderate AD will have 14 days of treatment with 0.5% AR100DP1 or placebo on all AD lesion area(s). At Screening Visit, all AD lesions will be measured and recorded in cm², and the investigator will identify one or multiple patches of AD lesions with an Investigator's Global Assessment (IGA) score of 1 to 3, and a maximum total treated area of 1,050 cm². For topical administration of IP, AR100DP1 will be applied on all AD lesion area(s) two times a day for 14 days. At subsequent visits, the lesion regions of all applied study IP will be traced, measured, and recorded. If any existing AD lesion expands or a new AD lesion with an IGA score of 1 to 3 is detected during the study period, the investigational product (IP) may continue to be applied, provided that the total treated area does not exceed 1.5 times the total AD lesion area defined on Day 1.

Type d'étude

Interventionnel

Inscription (Estimé)

40

Phase

  • Phase 2

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

    • Taiwan
      • Taipei, Taiwan, Taïwan, 110
        • Recrutement
        • Taipei Medical University Hospital
        • Contact:
      • Taoyuan, Taiwan, Taïwan, 333
        • Pas encore de recrutement
        • Chang Gung Memorial Hospital-Linkou
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans et plus (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  1. Dated and signed informed consent
  2. Either gender, ≥ 18 years old (the legal age of consent majority is 18 years old in Taiwan)
  3. Confirmed clinical diagnosis of atopic dermatitis (based on the criteria of Hanifin and Rajka for AD)
  4. Clinical diagnosis of AD with clinically consistent and stable disease status, defined as AD lesions with the Investigator's Global Assessment (IGA) score of 1(almost clear) to 3(moderate) for at least 4 weeks prior to Screening Visit, at the investigator's discretion
  5. Not expected to require regular AD maintenance therapy during the study period, at the investigator's discretion
  6. Have AD lesion area(s) with an IGA score of 1 to 3 at the Screening Visit and Day 1, with a maximum total treated area of 1,050 cm², as judged by the Investigator.
  7. Have a pruritus NRS score of ≥ 2 for both the average itch and the worst itch in the past 24 hours, as assessed at Screening Visit and Day 1 prior to randomization
  8. Subject of childbearing potential must agree to use abstinence to intercourse, or highly effective contraceptives from signing informed consent to 14 days after the last dose of study drug administration

Exclusion Criteria:

  1. Fluctuating or actively infected AD judged by the investigator

  2. Have any AD lesion with an IGA score of 4 at the Screening Visit or Day 1, as judged by the Investigator

  3. History of the following conditions, including irritant contact dermatitis, allergic contact dermatitis, skin infections (such as scabies), or other autoimmune skin diseases

  4. Active or potentially recurrent dermatologic condition other than atopic dermatitis that may confound evaluation (e.g. fungal infection), judged by the investigator

  5. Received systemic medication including immunosuppressant, phototherapy, or other therapy, which could affect AD within 4 weeks before Day 1

  6. Received systemic antihistamine within 5 half-lives (see Appendix 1 for half-lives of common antihistamine) prior to Day 1 (except for permitted background medication, Fexofenadine)

  7. Received systemic corticosteroid within 2 days or 5 half-lives, whichever is longer, prior to Day 1

  8. Received topical medication including corticosteroid, immunosuppressant, anti-histamine, phototherapy, calcineurin inhibitors, or other therapy for AD lesion area(s) within 1 week before Day 1

  9. Plan to receive immunosuppressive agents (including azathioprine, mycophenolate, cyclophosphamide, chlorambucil, methotrexate, cyclosporine)

  10. Unwilling or unable to comply with the criteria in Life Style Guidelines (Section 5.3) during the study

  11. History of use of biologic therapy (including intravenous immunoglobulin) within 12 weeks or 5 half-lives (whichever is longer) prior to Day 1

  12. Received any other investigational drug within 4 weeks prior to Day 1

  13. Required or received systemic CYP3A4 inhibitors with strong potency within 1 week prior to Day 1, including but not limited to clarithromycin, itraconazole, nefazodone, and atazanavir, evaluated by the investigator

  14. Treatment for any type of cancer (except squamous cell carcinoma, basal cell carcinoma, or carcinoma in situ of the skin, curatively treated with cryosurgery or surgical excision only) within 5 years before Day 1

  15. Had surgery within 4 weeks prior to Day 1, or plan to have surgery during the study.

  16. Known hypersensitivity to any of the components of the study drug

  17. Active clinically serious infection or any known history of immunodeficiency, including human immunodeficiency virus (HIV) infection

  18. Current uncontrolled asthma

  19. Any of the following serum test abnormalities:

    • Total bilirubin > 1.5 × ULN
    • AST or ALT > 3.0 × ULN
    • Serum albumin < 2.5 g/dL
    • Creatinine > 1.5 × ULN
    • Any other ≥ Grade 2 (grading of NCI-CTCAE v6.0) laboratory abnormality at baseline (other than those listed above)
  20. With ongoing acute diseases or within the past 2 years serious medical conditions (e.g. concomitant illness) such as cardiovascular (e.g. New York Heart Association (NYHA) grade III or IV), hepatic (e.g. Child-Pugh Class C), psychiatric condition (e.g. alcoholism, drug abuse), medical history, physical findings, or laboratory abnormality that in the investigators' opinion could interfere with the results of the trial or adversely affect the safety of the subject

  21. Female subject who is lactating or has positive urine pregnancy test at Screening and Day 1

  22. Other conditions not suitable for participating in this study judged by the investigator

  23. Plan to donate blood, sperm, or eggs from Screening Visit until Final Visit

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Quadruple

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 0.5% AR100DP1

AD subjects receive 0.5% AR100DP1

Investigational drug administered according to the protocol schedule.

Comparateur placebo: Placebo

AD subjects receive placebo

Visually identical placebo containing no active ingredient

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
The change of IGA to 0 or 1 at visit 4 after 14 days treatment
Délai: From Visit 2 (Day 1) to Visit 4 (Day 15) (14 days treatment)

Proportion of subjects with the Investigator's Global Assessment (IGA) score of 0 or 1 at Visit 4 (Day 15).

From Visit 2 (Day 1) to Visit 4 (Day 15) (14 days treatment)

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Efficacy - the change of IGA
Délai: Evaluated at Visit 3 (Day 8), Visit 5 (Day 22), and Visit 6 (Day 29)

Proportion of subjects achieving the Investigator's Global Assessment (IGA) score of 0 (clear) or 1 (almost clear) at Visit 3 (Day 8), Visit 5 (Day 22), and Visit 6 (Day 29)

Evaluated at Visit 3 (Day 8), Visit 5 (Day 22), and Visit 6 (Day 29)
Efficacy - the change of lesion area(s) (cm²)
Délai: Evaluated at Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)

Change from baseline (Visit 2) of lesion area(s) to Visit 3-6

Evaluated at Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)
Efficacy - the change of pruritus NRS
Délai: Evaluated at Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)

Change from baseline (Visit 2) in pruritus NRS(Numerical Rating Scale) of itch level on lesion area(s) to Visit 3-6

Evaluated at Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)
Efficacy - the change ≥ 2 points of reduction of pruritus NRS
Délai: Evaluated at Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)

Proportion of subjects having ≥ 2 points of reduction from baseline (Visit 2) in pruritus NRS for worst itch in the past 24 hours on lesion area(s) to Visit 3-6

Evaluated at Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)
Efficacy - the change of signs of atopic dermatitis
Délai: Evaluated at Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)

Change from baseline (Visit 2) in signs of atopic dermatitis (erythema, edema/papulation, excoriation, and lichenification) with grading from 0(none) to 3(severe) on lesion area(s) to Visit 3-6

Evaluated at Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)
Safety- AE and SAE
Délai: Evaluated at Visit 2 (Day 1), Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)

Incidence of AE and SAE during Visit 2-6 and AE will be categorized by severity (toxicity grade) and relationship to the study intervention

Evaluated at Visit 2 (Day 1), Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)
Safety - change of vital sign
Délai: Evaluated at Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)

Change from baseline (Visit 2) in vital signs to Visit 3-6

Evaluated at Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)
Safety - abnormality in physical examination occurred
Délai: Evaluated at Visit 2 (Day 1), Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)

Abnormality in physical examination at Visit 2-6

Evaluated at Visit 2 (Day 1), Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)
Safety - ECG result
Délai: Evaluated at Visit 2 (Day 1), Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)

Transition of ECG result from normal to abnormal findings from baseline (Visit 2) to Visit 3-6

Evaluated at Visit 2 (Day 1), Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)
Safety - Lab parameters
Délai: Evaluated at Visit 1 (-14 to -1 Day), (Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)

Change from baseline (Visit 1) in laboratory parameters to Visit 3-6

Evaluated at Visit 1 (-14 to -1 Day), (Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)
Safety - assessment of local tolerability
Délai: Evaluated at Visit 2 (Day 1), Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)

Proportion of subjects with scores of 0 and 1 in each symptom of assessment of local tolerability (erythema, edema, vesiculation, and excoriation) with grading from 0 (none) to 3 (severe) at Visit 2-6

Evaluated at Visit 2 (Day 1), Visit 3 (Day 8), Visit 4 (Day 15), Visit 5 (Day 22) and Visit 6 (Day 29)

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

21 octobre 2026

Achèvement primaire (Estimé)

30 décembre 2027

Achèvement de l'étude (Estimé)

30 décembre 2027

Dates d'inscription aux études

Première soumission

7 octobre 2026

Première soumission répondant aux critères de contrôle qualité

29 octobre 2026

Première publication (Réel)

3 novembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

3 novembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

29 octobre 2026

Dernière vérification

1 octobre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Oui

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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