Study on Amlitelimab for Patients Aged 12 and Older with Moderate to Severe Atopic Dermatitis Using Topical Corticosteroids and Inadequate Response to Previous Treatments

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What is this study about?

This clinical trial is focused on studying the effects of a medication called amlitelimab in people aged 12 years and older who have moderate to severe atopic dermatitis, commonly known as eczema. Atopic dermatitis is a skin condition that causes red, itchy, and inflamed skin. The study is designed for participants who have not responded well to previous treatments, such as biologic therapies or oral medications known as Janus Kinase (JAK) inhibitors. Participants will continue using their usual topical treatments, like corticosteroids, which are creams or ointments applied to the skin to reduce inflammation.

The purpose of the study is to evaluate how effective and safe amlitelimab is when given as a subcutaneous injection, which means it is injected under the skin. The study will compare the effects of amlitelimab to a placebo, which is a substance with no active medication. Participants will be randomly assigned to receive either amlitelimab or the placebo. The study will last for a period of 36 weeks, during which participants will receive regular injections and attend scheduled visits to monitor their progress and any changes in their condition.

Throughout the study, researchers will assess various aspects of the participants’ skin condition, including the severity of eczema symptoms and the overall impact on their quality of life. The study aims to provide valuable information on whether amlitelimab can offer a new treatment option for those with moderate to severe atopic dermatitis who have not found relief with other therapies. Participants will be closely monitored for any side effects or adverse reactions to ensure their safety during the trial.

1 joining the study

Upon joining the study, eligibility is confirmed based on specific criteria such as age, diagnosis of atopic dermatitis (AD) for at least one year, and previous inadequate response to certain treatments.

Participants must be at least 12 years old and have a body weight of 25 kg or more.

2 initial assessment

An initial assessment is conducted to evaluate the severity of atopic dermatitis using scales like the Eczema Area and Severity Index (EASI) and the Investigator Global Assessment scale for Atopic Dermatitis (vIGA-AD).

The assessment includes measuring the percentage of body surface area affected by AD and the intensity of symptoms such as itching.

3 treatment phase

Participants receive subcutaneous injections of amlitelimab or a placebo. The injections are administered using a pre-filled syringe.

The treatment is given alongside background topical corticosteroids, which are applied to the skin as part of the standard care for AD.

4 monitoring and follow-up

Regular follow-up visits are scheduled to monitor the participant’s response to the treatment. These visits include assessments of skin condition, symptom severity, and any side effects.

The primary goal is to observe improvements in the skin condition and overall quality of life over a 36-week period.

5 end of study evaluation

At the end of the study, a final evaluation is conducted to measure the overall effectiveness of the treatment.

The evaluation focuses on achieving clear or almost clear skin and a significant reduction in symptoms compared to the baseline measurements.

Who Can Join the Study?

  • Participants must be at least 12 years old.
  • Must have been diagnosed with atopic dermatitis (a type of skin condition) for at least 1 year.
  • Must have a documented history of not responding well to a previous biologic medication for atopic dermatitis or an oral JAK inhibitor (a type of medication).
  • Must have a v-IGA-AD score of 3 or 4 at the start of the study. This is a way to measure the severity of the skin condition.
  • Must have an EASI score of 16 or higher at the start of the study. This score measures the extent and severity of the skin condition.
  • The skin condition must cover 10% or more of the body surface area (BSA) at the start of the study.
  • Must have a weekly average of daily PP-NRS of 4 or higher at the start of the study. This is a way to measure itchiness.
  • Must be able and willing to attend study visits and follow study procedures.
  • Must weigh at least 25 kg (about 55 pounds).

Who Cannot Join the Study?

  • Participants who have a history of severe allergic reactions to any of the ingredients in the study medication.
  • Individuals with other skin conditions that might interfere with the study results.
  • Patients who have used certain medications recently that could affect the study outcomes.
  • People with certain infections that are not well controlled.
  • Participants who are pregnant or breastfeeding.
  • Individuals with a history of certain types of cancer.
  • Patients with significant health issues that could make participation unsafe.
  • Anyone who has participated in another clinical trial recently.
  • Individuals who are unable to comply with the study procedures.

Where you can join this trial?

Verified and Recommended Sites

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Verified Sites

Other Sites

Site Name City Country Status
Centre Hospitalier Universitaire Rouen Rouen France
Azienda Ospedaliero Universitaria Di Modena Modena Italy
Hopital Beaujon Clichy France
Centre Hospitalier Le Mans Le Mans France
Vodevo dnt Rxkjb Uhxconcrpn Hvvvsdsb Sevilla Spain
Uzudwrmaoseuhjjsgjxnm Typllfeem Aps Tuebingen Germany
Utumkyyrzeks Mwuytav Czyzskz Uqvvbpq Utrecht The Netherlands
Cgjgooo Ujcmnfrlsxvvmzpgworx Bakygx Kzi Berlin Germany
Emehbhp Urhvkwpujsjz Mzcajqj Chcsnyw Rhbqpacbk (yrzktfi Mct Rotterdam The Netherlands
Awdpscn Ohcjghigapn Unqxozsbkbqta Cxaayzqxecyr Doskx Sjswyd E Dzzln Svlaeis Dj Toogzj Turin Italy
Anypbon Ootkfuihcye Uknexnltkajlc Fmfkjsmi Im Db Nehgfo Naples Italy
Poxobly Srb z ogmp Katowice Poland
Ihvfeg Iyequksk Fnajryacqnysq Ooimcozancp Rome Italy
Hzmjfl Kqsjainj Bygvadmlmri Gboc Berlin Germany
Hezqifqy Uomhqzqhvbmqq Pdmytk Dm Hdjhkh Dk Mjlyzvdqfpa Majadahonda Spain
Foszqeyqv Pobb Lf Ielkstwewjfhk Byygfifex Dly Hzsdfifr Uaqnddzpzkrhq Ly Pwc Madrid Spain
Csexhlz Bublf Kwieinhpzqn Pyyzndmv Srv z olxw Gdansk Poland
Hmubaibc Uenxjgahscxfj Vrnvpr Dc Lve Nhvoqv Granada Spain
Imvuvualzf Gakvhwf Hgzhutok On Tuqvvoabhkzc Thessaloniki Greece
Crugvei Nhuaxlxgscak Tkqslbw Ddlyy Lfrisy Sos z oreg Cracow Poland
Ufjklwmhew Grvxjnf Hiyyqzml Aigvwip Gubhacv Hqlzyfaa Oa Wplv Akrgey H Ajca Vjmsayb Chaidari Greece
Cqkzfq Hofzykeltee Uctbgkrfkhvhr Dt Lz Rjqfxyd St Denis France
Uhxfxfyhop dnxyz ssdek Gvsxpzgo Dykayyeybs Csqouwkabbougf Czfvcn dd Shetx e tdxsmflitg adsuwksm Chieti Italy
Hpiifpzufidzaf Df Mer Mhvyoxip Hmemcmxr Witten Germany
Hxifwldx Ulgzlcjdugkxy Qtohcjrnzuw Mjigrw Pozuelo De Alarcon Spain
Anxgiwy Skrvqge Hnqdcyrm Ol Vjbafhyh Aya Dgzjzlnnvwyxhw Dkqztduf Athens Greece
Pinyhtvas Iqflqzsz Mzaoamvn Muesnaqqmtpd Sawss Wgezsuzkjsyb I Amziqbmnazheo Warsaw Poland
Kueudw Cpmbdy Kqrqwsoln Spc z opom Zamosc Poland
Gwkrnt Ufmnxwxwei Fuewehagq Frankfurt Germany
Hszmkfyd Ducsa Nsug Romans-Sur-Isere France
Hixztoxc Slzhf Myfxl Dumio Mmjloondhigx Perugia Italy
Uivhjljude Og Lerwttp Luebeck Germany
Ayoxnqh Ubcty Lsjuqy Svwyl Sykawdxbn N 8 Bynbyg Vicenza Italy
Wgcrniglz I Buwqsuuw A Sfcrbifithio soxf Wroclaw Poland
Chophntk Roiayjsv Gpflc Sch z oihu Warsaw Poland
Fjkvkzcxtjuxjj Gwjyliroinlwzukbaoo flxz Dvjzvkafnpte Umd Vmtiutlpdaj Aqyucdmevtyk Uzxpufvenervg Laqqssovyboc Glf Blankenfelde-Mahlow Germany
Ckuqhx Dmksxfpjpscws Dp La Pvtx Eh Dt Couuay Paris France
Hxcjutyt Uivnicgbvdaia Hiilyynl Ttmlw y Povame Iseqcork Cajlgd drdfnnoxotfuqslkv (jijn Badalona Spain

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
France France
Recruiting
28.05.2024
Germany Germany
Recruiting
28.05.2024
Greece Greece
Recruiting
28.05.2024
Italy Italy
Recruiting
28.05.2024
Poland Poland
Recruiting
28.05.2024
Spain Spain
Recruiting
28.05.2024
The Netherlands The Netherlands
Not recruiting
28.05.2024

Trial locations

Amlitelimab is a medication being studied for its effectiveness in treating moderate to severe atopic dermatitis, a type of eczema. It is given by injection under the skin. The trial aims to see how well it works for people who have not had enough improvement with other treatments, such as biologic therapies or oral medications known as Janus Kinase (JAK) inhibitors.

Investigated Diseases:

Atopic Dermatitis – Atopic dermatitis, commonly known as eczema, is a chronic skin condition characterized by dry, itchy, and inflamed skin. It often begins in childhood and can persist into adulthood, though the severity and symptoms can vary over time. The skin may appear red, swollen, and cracked, and it can become thickened from repeated scratching. Flare-ups can occur due to various triggers, including allergens, stress, and changes in weather. The condition is often associated with other allergic disorders such as asthma and hay fever. Managing atopic dermatitis involves identifying and avoiding triggers, as well as maintaining skin hydration.

Trial ID:
2023-508099-12-00
Protocol code:
EFC17599 – AQUA
NCT ID:
NCT06241118
Trial Phase:
Therapeutic confirmatory (Phase III)

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