Absorption, distribution, metabolism and excretion of londamocitinib after single-dose inhaled, intravenous and oral administration in healthy participants.

Authors

Camille Riff, Peter Bold, Maria Heijer, Ryan A Bragg, Danielle Steele, Tina Jellesmark Jensen, Davinder P S Dosanjh, Sabrina I Hanswijk-Bartelds, Esther van Duijn, Elwin R Verheij, Somasekhara Menakuru, Rod Hughes, Helena Dahlbäck

Published in

British journal of clinical pharmacology. Oct 19, 2026. Epub Oct 19, 2026.

Abstract

Londamocitinib (AZD4604) is an inhaled, selective Janus kinase 1 (JAK1) inhibitor in development for asthma. This open-label, two-part, phase I clinical study (NCT06157255) used a radiolabelled microtracer approach to evaluate the absolute bioavailability and the absorption, distribution, metabolism and excretion (ADME) of inhaled londamocitinib after intravenous and oral administration in healthy male and female participants (n = 8).
Pharmacokinetics, safety, metabolic profile and metabolite identification from plasma, urine, and faecal samples were assessed employing highly sensitive accelerator mass spectrometry. Participants received a single oral 4-mg dose of [¹⁴C]londamocitinib (NMT 37.0 kBq [¹⁴C]) in Part 1 and an intravenous 30-μg dose of [¹⁴C]londamocitinib (NMT 37.0 kBq [¹⁴C]), followed by a single inhaled dose of 3-mg londamocitinib in Part 2.
Mean recovery of total radioactive material after oral dosing was 76.3% in faeces and 8.7% in urine. After intravenous dosing, recovery was 67.3% in faeces and 16.0% in urine. Absolute bioavailability of oral londamocitinib was 40.4% and for inhaled administration was 62.5%. Unchanged londamocitinib constituted approximately 70% of circulating radioactivity in plasma and accounted for 47.8% and 28.4% of the administered dose in excreta after oral and intravenous administration respectively. No new safety signals were observed.
Following inhaled and oral dosing, londamocitinib demonstrated rapid absorption, and faecal excretion as the principal route of elimination. Unchanged londamocitinib and metabolite M6 were the major entities present in plasma, urine and faeces. Londamocitinib, at these doses, exhibited an acceptable safety and tolerability profile.

PMID:
42896884
Bibliographic data and abstract were imported from PubMed on 20 Oct 2026.

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