Sağlıklı katılımcılarda tek doz inhalasyon, intravenöz ve oral uygulamadan sonra londamocitinib'in emilimi, dağılımı, metabolizması ve atılımı

Özet (abstract)

Aim 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). Methods 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 [ 14 C]londamocitinib (NMT 37.0 kBq [ 14 C]) in Part 1 and an intravenous 30‐μg dose of [ 14 C]londamocitinib (NMT 37.0 kBq [ 14 C]), followed by a single inhaled dose of 3‐mg londamocitinib in Part 2. Results 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. Conclusion 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.

Yazarların özeti; kaynağından alınmıştır. British Journal of Clinical Pharmacology, 2026 · DOI ↗