# Depemokimab and the twice-yearly regimen: pharmacological implications and therapeutic positioning in severe eosinophilic respiratory diseases

**Authors:** A. M. Marra, E. Bizzi, A. Gidaro, F. Bini, S. Rotunno, S. Modica, E. Greco, A. Mauro, R. Mascolo, E. Tombetti, M. Lazzeroni, F. Paciullo, G. Abatianni, C. Gagliardi, S. Damanti, P. Rovere Querini

PMC · DOI: 10.3389/fimmu.2026.1783889 · Frontiers in Immunology · 2026-03-18

## TL;DR

Depemokimab is a new treatment for severe respiratory diseases that reduces inflammation and flare-ups with a dosing schedule only twice a year.

## Contribution

Depemokimab is the first anti-IL-5 monoclonal antibody with a twice-yearly dosing regimen due to its extended half-life.

## Key findings

- Depemokimab significantly reduced asthma exacerbations by 54% compared to placebo.
- It effectively reduced nasal polyp size in patients with chronic rhinosinusitis with nasal polyps.
- The drug offers a convenient dosing schedule, improving patient adherence and chronic disease management.

## Abstract

Type 2 inflammatory diseases (T2D), notably severe eosinophilic asthma (SEA) and chronic rhinosinusitis with nasal polyps (CRSwNP), represent a significant global health burden due to their high morbidity, frequent exacerbations and reliance on systemic glucocorticoids (SGCs). Targeting Interleukin-5 (IL-5), a key driver of eosinophil production and survival, has emerged as a validated therapeutic strategy. Depemokimab is a novel, first-in-class anti-IL-5 monoclonal antibody (mAb) engineered with an extended half-life via the YTE amino acid modification of its Fc region, enabling an unprecedented twice-yearly dosing interval. This review synthesizes clinical data from the Phase III SWIFT (SEA) and ANCHOR (CRSwNP) programs, demonstrating depemokimab’s sustained eosinophil depletion and significant reduction in asthma exacerbation rates (annualized asthma exacerbation rate reduction of approximately 54% versus placebo). While efficacy on secondary endpoints such as lung function (FEV1) and quality of life (QoL) was mixed, the efficacy in reducing nasal polyp size (Nasal Polyp Score and Nasal Congestion) in CRSwNP was clear. The core value proposition of depemokimab is the combination of established IL-5 inhibition efficacy with patient convenience due to its dosing. We discuss its pharmacodynamic profile, safety and pivotal role in shifting the treatment paradigm towards simplified chronic disease management, positioning depemokimab as a novel, patient-centric option in the competitive landscape of T2 biologic therapies.

## Full-text entities

- **Genes:** IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}
- **Diseases:** T2D (MESH:C563310), Congestion (MESH:D002311), chronic rhinosinusitis (MESH:D000092562), eosinophilic respiratory diseases (MESH:D012140), CRSwNP (MESH:D009298), SEA (MESH:D045169), asthma (MESH:D001249)
- **Chemicals:** Depemokimab (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13038953/full.md

## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC13038953/full.md

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Source: https://tomesphere.com/paper/PMC13038953