Bioavailability, Biotransformation, and Excretion of the Covalent Bruton Tyrosine Kinase Inhibitor Acalabrutinib in Rats, Dogs, and Humans

• Published in: Drug metabolism and disposition Vol. 47; no. 2; pp. 145 - 154
• Main Authors: Podoll, Terry, Pearson, Paul G., Evarts, Jerry, Ingallinera, Tim, Bibikova, Elena, Sun, Hao, Gohdes, Mark, Cardinal, Kristen, Sanghvi, Mitesh, Slatter, J. Greg
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.02.2019; American Society for Pharmacology and Experimental Therapeutics, Inc
• Subjects: Absorption; Acrylamide; Administration, Oral; Adult; Agammaglobulinaemia Tyrosine Kinase - antagonists & inhibitors; Animals; Antineoplastic Agents - analysis; Antineoplastic Agents - metabolism; Antineoplastic Agents - pharmacology; Benzamide; Benzamides - analysis; Benzamides - metabolism; Benzamides - pharmacology; Bioavailability; Biological Availability; Biotransformation; Blood cells; Bruton's tyrosine kinase; Carbon 14; Conjugation; Covalence; Cytochrome P-450 CYP3A - metabolism; Dogs; Economic conditions; Enzyme inhibitors; Excretion; Feces - chemistry; Female; Glutathione; Half-Life; Healthy Volunteers; Humans; Hydrolysis; Inhibitors; Intestinal Absorption; Intravenous administration; Kinases; Liquid chromatography; Low concentrations; Lymphoma, Mantle-Cell - drug therapy; Male; Mass spectrometry; Mass spectroscopy; Metabolism; Metabolites; Middle Aged; Occupancy; Oxidation; Oxidation-Reduction; Peripheral blood; Protein Kinase Inhibitors - analysis; Protein Kinase Inhibitors - metabolism; Protein Kinase Inhibitors - pharmacology; Pyrazines - analysis; Pyrazines - metabolism; Pyrazines - pharmacology; Pyrrolidine; Radioactive half-life; Radioactivity; Rats; Rats, Sprague-Dawley; Thioethers; Tyrosine; Tyrosine kinase inhibitors; Urine; Urine - chemistry; Young Adult; FDA; MS/MS; AUC; t1/2; ACP-5862; ACP-5461; GSH; LSC; HPLC; BCRP; ADME; MS; AMS; CL; GST; PBMC; CV; HER; LC; Tmax; ACP-5530; ACP-5134; BTK; ACP-5531; PK; TCI; ACP-5197
• ISSN: 0090-9556; 1521-009X; 1521-009X
• DOI: 10.1124/dmd.118.084459

Acalabrutinib is a targeted, covalent inhibitor of Bruton tyrosine kinase (BTK) with a unique 2-butynamide warhead that has relatively lower reactivity than other marketed acrylamide covalent inhibitors. A human [14C] microtracer bioavailability study in healthy subjects revealed moderate intravenous clearance (39.4 l/h) and an absolute bioavailability of 25.3% ± 14.3% (n = 8). Absorption and elimination of acalabrutinib after a 100 mg [14C] microtracer acalabrutinib oral dose was rapid, with the maximum concentration reached in <1 hour and elimination half-life values of <2 hours. Low concentrations of radioactivity persisted longer in the blood cell fraction and a peripheral blood mononuclear cell subfraction (enriched in target BTK) relative to plasma. [14C]Acalabrutinib was metabolized to more than three dozen metabolites detectable by liquid chromatography–tandem mass spectrometry, with primary metabolism by CYP3A-mediated oxidation of the pyrrolidine ring, thiol conjugation of the butynamide warhead, and amide hydrolysis. A major active, circulating, pyrrolidine ring-opened metabolite, ACP-5862 (4-[8-amino-3-[4-(but-2-ynoylamino)butanoyl]imidazo[1,5-a]pyrazin-1-yl]-N-(2-pyridyl)benzamide), was produced by CYP3A oxidation.Novel enol thioethers from the 2-butynamide warhead arose from glutathione and/or cysteine Michael additions and were subject to hydrolysis to a β-ketoamide. Total radioactivity recovery was 95.7% ± 4.6% (n = 6), with 12.0% of dose in urine and 83.5% in feces. Excretion and metabolism characteristics were generally similar in rats and dogs. Acalabrutinib’s highly selective, covalent mechanism of action, coupled with rapid absorption and elimination, enables high and sustained BTK target occupancy after twice-daily administration.