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Localized Aeroallergen Exposure in Atopic Dermatitis

Pilot Study to Assess the Localized Aeroallergen Exposure Induced Skin Reaction in Patients With Atopic Dermatitis

This pilot study evaluates skin reactions following localized aeroallergen exposure in adults with atopic dermatitis.

Studieoversikt

Studietype

Intervensjonell

Registrering (Antatt)

15

Fase

  • Ikke aktuelt

Kontakter og plasseringer

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

Studiekontakt

Studiesteder

    • Lower Saxony
      • Hanover, Lower Saxony, Tyskland, 30625
        • Fraunhofer Institute for Toxicology and Experimental Medicine ITEM, Clinical Airway Research
        • Ta kontakt med:
      • Hanover, Lower Saxony, Tyskland, 30625
        • Hannover Medical School, Department of Dermatology and Allergy
        • Ta kontakt med:

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

18 år til 65 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  1. Able and willing to give written informed consent.

  2. Male and female subjects, aged 18-65 years. Women will be considered for inclusion if they are:

    • Not pregnant, as confirmed by pregnancy test (see flow chart), and not nursing.
    • Of non-child bearing potential (i.e. physiologically incapable of becoming pregnant, including any female who is pre-menarchial or post-menopausal, with documented proof of hysterectomy or tubal ligation, or meets clinical criteria for menopause and has been amenorrhoeic for more than 1 year prior to the screening visit).
    • Of childbearing potential and using a highly effective method of contraception during the entire study (vasectomised partner, sexual abstinence - the lifestyle of the female should be such that there is complete abstinence from intercourse from two weeks prior to the start of the study until at least 72 hours after the last study visit -, implants, injectables, combined oral contraceptives, hormonal IUDs or double-barrier methods, i.e. any double combination of IUD, condom with spermicidal gel, diaphragm, sponge, and cervical cap).
  3. Positive IgE level for grass pollen (Phadia g6, Lieschgras) of at least CAP FEIA class 3 (≥3,50 kU/l) at screening or in previous year.

  4. Atopic dermatitis fulfilling the UK criteria of AD.

  5. Local SCORAD for erythema domain 1 or 2 in exposed area (cubital fossa / lower arm).

  6. Local IGA 1 or 2.

  7. Difference of Local SCORAD between both arms ≤ 2.

  8. BMI ≥18 and ≤ 40.

Exclusion Criteria:

  1. Any clinically relevant abnormal findings in physical examination, clinical chemistry, hematology, vital signs at screening visit, which, in the opinion of the investigator, may either put the subject at risk because of participation in the study or may influence the results of the study, or the subject's ability to participate in the study.
  2. Past or present disease, which as judged by the investigator, may affect the outcome of this study. These diseases include, but are not limited to, cardiovascular disease, malignancy, hepatic disease, renal disease, hematological disease, neurological disease, endocrine disease or pulmonary disease.
  3. Positive HIV-1/2Ab, hepatitis B surface antigen (HBsAg) or hepatitis C virus antibodies (HCVAb) test at screening or test not performed.
  4. Treatment with medication that might interfere with rescue medication for the management of allergic reactions (e.g. beta blocker).
  5. Topical (skin) steroid treatment (wash out phase: 2 weeks before day 1).
  6. Topical calcineurin inhibitor treatment (wash out phase 2 weeks before day 1).
  7. UV radiation treatment (wash out phase 4 weeks before day 1).
  8. Systemic immunosuppression treatment (steroids, biologics, e.g. dupilumab, JAK-Inhibitors, cyclosporine, azathioprine, Mycophenolat Mofetil (MMF); wash out phase 3 months, before day 1.
  9. Treatment with high dose inhaled corticosteroids.
  10. Treatment with antihistamines (wash out phase 1 week before day 1).
  11. Unstable AD during Screening (SCORAD difference of >15 points from Visit 1 to Visit 2).
  12. Diastolic blood pressure above 95 mmHg.
  13. Acute respiratory infection 2 weeks prior to screening visit.
  14. Alcohol or drug abuse within 12 months prior to screening.
  15. Regular daily consumption of more than 1 liter of usual beer or the equivalent quantity of approximately 40 g of alcohol in another form.
  16. Participation in another clinical trial 30 days prior to enrollment.
  17. There is a risk of non-compliance with study procedures.
  18. Suspected inability to understand the protocol requirements, instructions and study-related restrictions, the nature, scope, and possible consequences of the study.
  19. History of an acute infection four weeks prior to the informed consent visit.
  20. Subject has received previous immunotherapy treatment with any grass pollen allergen within 2 years prior to screening.
  21. Subject is receiving ongoing treatment with any specific immunotherapy for other allergies.

Studieplan

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

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Grunnvitenskap
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Allocation A

Localized grass pollen allergen exposure on the left forearm and localized placebo exposure on the right forearm.

Localized grass pollen allergen exposure on two consecutive days.

Localized placebo exposure on two consecutive days.

Eksperimentell: Allocation B

Localized placebo exposure on the left forearm and localized grass pollen allergen exposure on the right forearm.

Localized grass pollen allergen exposure on two consecutive days.

Localized placebo exposure on two consecutive days.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Difference in the change of local SCORAD
Tidsramme: Baseline to Day 3

The primary endpoint is defined as the difference in the change of local SCORAD between the grass pollen-exposed arm and the placebo-exposed arm from baseline to post-provocation assessment. For each subject, the change in local SCORAD will be calculated separately for each arm as follows: ΔSCORAD_grass = local SCORAD_grass (Day 3) - local SCORAD_grass (Baseline); ΔSCORAD_placebo = local SCORAD_placebo (Day 3) - local SCORAD_placebo (Baseline). The primary endpoint is then calculated as: Primary endpoint = ΔSCORAD_grass - ΔSCORAD_placebo.

Baseline to Day 3

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in total SCORAD
Tidsramme: Baseline to Day 3

Assess the change in total SCORAD between pre-provocation baseline and one day after the second exposure (day 3).

Baseline to Day 3
Change in EASI
Tidsramme: Baseline to Day 3

Assess the change in EASI between pre-provocation baseline and one day after the second exposure (day 3). EASI assesses the extent and severity of atopic dermatitis based on erythema, infiltration/papulation, excoriation, and lichenification. Total scores range from 0 to 72, with higher scores indicating greater disease severity.

Baseline to Day 3
Change in local IGA
Tidsramme: Baseline to Day 3

Evaluate disease severity by the change in local IGA between baseline and one day after the second exposure (day 3).

Baseline to Day 3
Change in itch intensity
Tidsramme: Baseline to Day 3

Evaluate itch intensity related to provocation by the change in itch VAS between baseline and one day after the second exposure (day 3).

Baseline to Day 3
Proportion of local responders
Tidsramme: Baseline to Day 3

Determine the proportion of local responders, defined as patients with a worsening of local SCORAD ≥25% over baseline at one day after the second exposure (day 3).

Baseline to Day 3
Rescue medication use in relation to provocation
Tidsramme: Baseline to Day 3

Assess rescue medication use in relation to provocation (change in use of topical or systemic rescue medication between the pre-provocation period and the period including and following the two exposure days).

Baseline to Day 3
Safety and tolerability
Tidsramme: From first exposure through follow-up on Day 7

Assess the safety and tolerability of local aeroallergen application in adults with atopic dermatitis by determining the number of participants with at least one adverse event related to the local aeroallergen provocation.

From first exposure through follow-up on Day 7

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Changes in skin microbiome composition over time
Tidsramme: Baseline to Day 3

Exploratory analyses will be performed to characterize biological changes associated with localized grass pollen provocation at the skin level. Skin swabs: Exploratory microbiome endpoints include changes in skin microbiome composition over time, assessed by beta-diversity metrics. For each subject, within-site changes in microbial community composition from baseline to Day 3 will be determined separately for the grass pollen and placebo sites, and the difference in these changes between the two sites will be analyzed. Additional exploratory microbiome endpoints include changes in alpha diversity and exploratory analyses of differential abundance of selected bacterial taxa, where technically feasible.

Baseline to Day 3
Changes in selected serum proteins
Tidsramme: Baseline to Day 3

Blood samples: Exploratory endpoints include changes in selected serum proteins associated with allergic inflammation and AD from baseline to Day 3. Serum proteins will be measured using the Olink Inflammation Panel and reported as NPX (Normalized Protein Expression).

Baseline to Day 3

Samarbeidspartnere og etterforskere

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

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 (Antatt)

1. desember 2026

Primær fullføring (Antatt)

1. april 2027

Studiet fullført (Antatt)

1. april 2027

Datoer for studieregistrering

Først innsendt

20. oktober 2026

Først innsendt som oppfylte QC-kriteriene

30. oktober 2026

Først lagt ut (Faktiske)

5. november 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

5. november 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

30. oktober 2026

Sist bekreftet

1. oktober 2026

Mer informasjon

Begreper knyttet til denne studien

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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