Drugs / Lunsekimig
last change Apr 2026 re-read 2 minutes ago

Lunsekimig

also known as SAR443765

Monoclonal antibody

Developed for
asthma · chronic obstructive pulmonary disease · chronic rhinosinusitis · atopic eczema
Investigated by
Sanofi

Trials 9 · a red edge is where a trial was stopped

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 11 trial
Phase 1 NCT05366764 Jun 2022 → Feb 2023 asthma Sanofi Completed No outcome recorded
Phase 26 trials
Phase 2 NCT06914908 May 2025 → Jan 2031 expected chronic rhinosinusitis Sanofi Enrolling by invitation No outcome recorded
Phase 2 NCT06790121 Jan 2025 → Feb 2026 atopic eczema Sanofi Completed No outcome recorded
Phase 2 NCT06676319 Nov 2024 → Jun 2027 expected asthma Sanofi Active not recruiting No outcome recorded
Phase 2 NCT06609239 Sep 2024 → Jan 2031 expected asthma Sanofi Enrolling by invitation No outcome recorded
Phase 2 NCT06454240 Jul 2024 → Jan 2026 chronic rhinosinusitis Sanofi Completed No outcome recorded
Phase 2 NCT06102005 Oct 2023 → Feb 2026 asthma Sanofi Completed No outcome recorded
Phase 32 trials
Phase 3 NCT07190222 Sep 2025 → Nov 2029 expected chronic obstructive pulmonary disease Sanofi Recruiting No outcome recorded
Phase 3 NCT07190209 Sep 2025 → Nov 2029 expected chronic obstructive pulmonary disease Sanofi Recruiting No outcome recorded

Press releases naming this drug 1 release

DateIssuerRelease
2026-04-07 Sanofi Press Release: Sanofi’s lunsekimig met primary and key secondary endpoints in phase 2 respiratory studies in asthma and CRSwNP sanofi.com

Evidence & citations 6 cited values

Every value below carries the sentence it was read from. 11 sources stand behind the page.

FieldValueCited text
Known as Lunsekimig ClinicalTrials.gov intervention name — accepted as the source's own label NCT06790121
7

NCT06454240

NCT07190222

NCT06676319

NCT07190209

NCT06102005

NCT06914908

NCT06609239

Known as SAR443765 “Study of Lunsekimig (SAR443765) Compared With Placebo in Adults With High-risk Asthma” NCT06676319
1

NCT05366764

Action Inhibit inhibits both thymic stromal lymphopoietin (TSLP) and interleukin (IL)-13” PMID 38924698 Jun 2024
Modality Monoclonal antibody CHEMBL5314848
Route Intravenous “10-400 mg intravenous [IV] or 400 mg subcutaneous [SC]” PMID 38924698 Jun 2024
Route Subcutaneous “10-400 mg intravenous [IV] or 400 mg subcutaneous [SC]” PMID 38924698 Jun 2024