Use of Dupilumab in Asthma in Real-world Setting

Use of Dupilumab in Asthma in Real-world Setting: Analysis of the SNDS Database

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT07637292

Acronym

DUPILUMAB

Enrollment

35000

Registered

2026-06-09

Start date

2025-01-02

Completion date

2026-12-31

Last updated

2026-06-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma Acute

Keywords

Recombinant human monoclonal antibody, SNDS database, Real-life setting

Brief summary

The main objective of asthma pharmacological management in adults and teenagers is to maintain long-term control of the disease, including symptom relief, the prevention of exacerbations, the improvement of pulmonary function, the reduction of limitations in daily life and side effects of pharmacological treatments. Dupilumab is a recombinant human monoclonal antibody that inhibits signalling of both IL-4 and IL-13, two Type 2 cytokines involved in inflammatory pathway. Dupixent obtained a European Marketing Authorization in September 2017 and was reimbursed in France from March 5, 2019 in adults with moderate-to-severe atopic dermatitis. On November 10, 2020, the reimbursement of Dupixent was extended to adults and adolescents aged 12 and over as add-on maintenance treatment for severe asthma with type 2 inflammation characterised by raised blood eosinophils (≥ 0.150 g/L) and/or raised fraction of exhaled nitric oxide (FeNO ≥ 20 ppb), who are inadequately controlled with high dose inhaled corticosteroids (ICS) plus another medicinal product for maintenance treatment. Lastly, on July 22, 2021, Dupixent was also reimbursed in patients with severe nasal polyposis. Primary objective: To describe the characteristics of patients using dupilumab for severe asthma in a real-world setting. Secondary objectives: * To describe the Health Care Resource Use (HCRU) and associated costs of severe asthmatic patients using dupilumab. * To describe the use of corticosteroids (oral and inhaled) before and after dupilumab initiation. * To study persistence with dupilumab in real-world

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

12 Years to No maximum

Healthy volunteers

Inclusion criteria

* At least one reimbursement of dupilumab during the inclusion period from November 10, 2020 to December 31, 2023 * At least one of the following asthma markers: * at least one reimbursement of inhaled corticosteroids (ICS and fixed-dose combination ICS/LABA inhalers) in a 3-month time-window before and after one of the reimbursement of dupilumab * A Long-Term Disease (LTD) for asthma in the 12 months before dupilumab initiation or over follow-up. * An hospital admission for asthma in the 12 months before dupilumab initiation or over follow-up.

Exclusion criteria

Design outcomes

Primary

Measure	Time frame	Description
Patient's characteristics	At index date, i.e. at the date of the 1st reimbursement of Dupilumab over the inclusion period (betw Nov 10, 2020 and Dec 31, 2023)	Age at index date * Sex * Affiliation of Complementary universal healthcare coverage (CMU-C) * Comorbidities in the 12 months before dupilumab initiation, from diagnoses recorded during hospitalization or LTD status and medications : * Diabetes * Cardiovascular diseases * disabling stroke, * chronic arterial diseases, * heart failure, arrhythmias, valvular and severe congenital heart disease, * severe hypertension, * coronary heart disease, * Mental illness, including depression/anxiety * Eosinophilic Esophagitis * Nodular prurigo * Atopic dermatitis * Osteoporosis The characteristics of patients will be described in the overall cohort and in age subgroups (\[12-18\[ and ≥ 18 years old).

Countries

France

Outcome results