Aurélie Du-Thanh is an expert in Dermatology at University Hospital of Montpellier (France). As of October 2026, ScienceLeadR ranks Aurélie Du-Thanh in the top 1% of experts worldwide for Hypersensitivity and Skin Diseases, Vascular. Aurélie Du-Thanh has authored 241 publications, the most recent in 2026, and is an investigator in 13 clinical trials, 6 of them ongoing. SLR score: 839 (community average: 125). How the SLR is computed.

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Aurélie Du-Thanh University Hospital of Montpellier France
839 ScienceLeadR Reputation 839
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Dermatology

Subspecialties: Immunology

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Expert Rankings

Top experts on the MeSH terms this expert works on

Organizations

Career arc: 2006 - 2026

Source: PubMed

University Hospital of Montpellier

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 241

Citations

Citations: 2 066 1st author: 52 Last author: 29 Unique author: 4


Best Journals

Breakdown by type

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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Berotralstat Tolerability and Effectiveness in Hereditary Angioedema: Berolife Study Results.
PMID 42603305 — pain, angioedemas, hereditary, therapeutics, angioedema, abdominal pain
Clin Transl Allergy20260
Oral deucrictibant for on-demand treatment of hereditary angioedema attacks (RAPIDe-1): a randomised, double-blind, placebo-controlled, phase 2 trial.
PMID 41865747 — skin, safety, pain, pharmaceutical preparations, angioedemas, hereditary, drug-related side effects and adverse reactions, capsules, bradykinin, therapeutics, angioedema, hematologic diseases
Lancet Haematol20260
Integrated Clinical Trial and Molecular Profiling Reveals Immune Drivers of Chronic Hand Eczema.
PMID 41705342 — skin, dermatitis, hypersensitivity, eczema, immunity, therapeutics, psoriasis, dermatitis, atopic, dermatitis, contact
Allergy20260
The International Guideline for the Definition, Classification, Diagnosis and Management of Urticaria.
PMID 41649409 — cells, hypersensitivity, urticaria, classification, work, diagnosis, therapeutics, angioedema, mast cells
Allergy20262
Diagnostic Delay in Patients With Chronic Urticaria: Results From the Chronic Urticaria Registry (CURE).
PMID 41532284 — registries, chronic urticaria, hypersensitivity, urticaria, diagnosis, chronic inducible urticaria
Clin Exp Allergy20261

Clinical Studies 13

Sources: ClinicalTrials, EU CTIS

Synthesis

Principal Investigator: 2 Study Director: 1

By phase:

Phase 3 6
N/A 4
Phase 2 3

By status:

Completed 5
Recruiting 3
Active not recruiting 2
Not yet recruiting 1
Unknown 1
Withdrawn 1

By type:

Interventional 10
Observational 3

By Monocentric/Multicentric:

monocentric 4
multicentric2to4 0
multicentric5to9 0
multicentricup10 9

Main Topics

Cohort/Consortium Investigators 2

Ongoing Clinical Trials

6 ongoing trials started since 2021, where this expert is an investigator

Source: ClinicalTrials

Study Phase Status Start
A 52 week multi center randomized double blind placebo controlled basket study with an open label extension to investigate the efficacy safety and tolerability of remibrutinib (LOU064) in Chronic Inducible Urticaria (CINDU) in adults inadequately controlled by H1 antihistamines
2023-505739-12-01 — histamine antagonists, safety, urticaria, multiple chronic conditions, chronic inducible urticaria
Phase 3Active not recruiting2024
STOP HAE A Phase 3 Study of ADX 324 in HAE
2025-521352-38-00 — rna, small interfering, angioedemas, hereditary, prekallikrein, therapeutics, angioedema
Phase 3Recruiting2026
Effectiveness and Safety of Lebrikizumab Treatment in Adults and Adolescents with Moderate to Severe Atopic Dermatitis
2023-508235-31-00 — safety, dermatitis, signs and symptoms, adolescent, therapeutics, dermatitis, atopic
Phase 3Active not recruiting2024
A clinical trial to provide continued access to remibrutinib (LOU064) for people who are benefiting from it in a previous remibrutinib trial
2025-524078-40-00 — urticaria, multiple chronic conditions, therapeutics
Phase 3Recruiting2026
A 12 week randomized participant and investigator blinded placebo controlled exploratory study in adult participants with Chronic Urticaria to assess the efficacy and safety and explore the Mechanism of Action of remibrutinib (LOU064)
2024-516355-41-00 — chronic urticaria, safety, urticaria, chronic inducible urticaria
Phase 2Recruiting2025

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