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Synonyms: F027400161 [2] | SAR-443765 | SAR443765
Compound class:
Antibody
Comment: Lunsekimig (SAR443765) is a single chain nanobody that is constructed of five linked antibody (VHH) domains that simultaneously bind the inflammatory targets thymic stromal lymphopoietin (TSLP) and IL-13, and human serum albumin (ALB). The peptide sequence provided in the INN record matches SEQ ID No 1 in patent US11208476 [2], which equates to clone F027400161 therein.
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| No information available. |
Summary of Clinical Use ![]() |
| Lunsekimig (SAR443765) is a clinical candidate for the treatment of chronic inflammaroty diseases. Efficacy has been noted in respiratory diseases [1], but the phase 2b Velvet study in atopic dermatitis missed its primary endpoint (reduction in disease severity; April 2026). |
| Clinical Trials | |||||
| Clinical Trial ID | Title | Type | Source | Comment | References |
| NCT06676319 | Study of Lunsekimig (SAR443765) Compared With Placebo in Adults With High-risk Asthma | Phase 2 Interventional | Sanofi | ||
| NCT06914908 | Long-term Safety and Efficacy Evaluation of Lunsekimig in Adult Participants With Chronic Rhinosinusitis With Nasal Polyps (CRSwNP) Who Completed a Previous Lunsekimig CRSwNP Study | Phase 2 Interventional | Sanofi | ||
| NCT07190222 | Efficacy, Safety, and Tolerability Study of Lunsekimig Compared With Placebo in Adult Participants With Inadequately Controlled Chronic Obstructive Pulmonary Disease (COPD), Characterized by an Eosinophilic Phenotype | Phase 3 Interventional | Sanofi | ||
| NCT06790121 | A Study to Investigate the Efficacy and Safety of Subcutaneous Lunsekimig (SAR443765) Compared With Placebo in Adult Participants With Moderate-to-severe Atopic Dermatitis | Phase 2 Interventional | Sanofi | The VELVET study. | |