Safety, Tolerability, and Pharmacokinetic Evaluation of Single and Multiple Doses of the Dipeptidyl Peptidase 1 Inhibitor Brensocatib in Healthy Japanese and White Adults

Brensocatib, an investigational first‐in‐class, small‐molecule, orally bioavailable, selective, and reversible dipeptidyl peptidase 1 inhibitor that blocks activation of neutrophil serine proteases, is currently under clinical development for the treatment of bronchiectasis and other chronic inflammatory diseases. In a 2‐part phase 1 study, the safety, tolerability, and pharmacokinetics of brensocatib were evaluated in healthy Japanese and White adults. In part A, participants received single and multiple once‐daily doses of brensocatib (10, 25, or 40 mg) or placebo after an overnight fast. In part B, participants received a single oral dose of brensocatib 40 mg on days 1 and 8, with or without food in a crossover fashion. Following a single dose and at steady state, brensocatib exposure was dose dependent, with low to moderate interindividual variability; systemic exposure between Japanese and White participants was similar. Elimination half‐life of brensocatib ranged from 22 to 28 hours, resulting in ≈2‐fold accumulation in maximum plasma concentration and area under the plasma concentration–time curve at steady state. In both ethnic groups, the presence of food slightly delayed brensocatib absorption with time to maximum plasma concentration increased by 0.7 to 1.7 hours, but it had no significant effect on brensocatib exposure (maximum plasma concentration and area under the plasma concentration–time curve). Brensocatib was well tolerated in Japanese and White participants. The most frequently reported treatment‐emergent adverse events were headache and skin exfoliation. No clinically significant vital signs, laboratory abnormalities, or evidence of renal toxicity were observed. The results from this study demonstrate that brensocatib can be administered with or without food and that dose adjustment is unnecessary for Japanese patients when receiving brensocatib treatment.

[1]  A. O'donnell,et al.  Phase 2 Trial of the DPP-1 Inhibitor Brensocatib in Bronchiectasis. , 2020, The New England journal of medicine.

[2]  J. Elborn,et al.  INVITED REVIEW SERIES: PAEDIATRIC AND ADULT BRONCHIECTASIS , 2018 .

[3]  J. Chalmers,et al.  Geographic variation in the aetiology, epidemiology and microbiology of bronchiectasis , 2018, BMC Pulmonary Medicine.

[4]  A. Jauhiainen,et al.  Dipeptidyl Peptidase 1 Inhibitor AZD7986 Induces a Sustained, Exposure‐Dependent Reduction in Neutrophil Elastase Activity in Healthy Subjects , 2018, Clinical pharmacology and therapeutics.

[5]  F. Blasi,et al.  Neutrophil elastase in bronchiectasis , 2017, Respiratory Research.

[6]  A. Jauhiainen,et al.  Effect of CYP3A4 inhibitors verapamil and itraconazole on the pharmacokinetics of AZD7986, an oral DPP1 inhibitor , 2017 .

[7]  T. Welte,et al.  European Respiratory Society guidelines for the management of adult bronchiectasis , 2017, European Respiratory Journal.

[8]  D. Weycker,et al.  Prevalence and incidence of noncystic fibrosis bronchiectasis among US adults in 2013 , 2017, Chronic respiratory disease.

[9]  S. Connolly,et al.  Discovery of Second Generation Reversible Covalent DPP1 Inhibitors Leading to an Oxazepane Amidoacetonitrile Based Clinical Candidate (AZD7986). , 2016, Journal of medicinal chemistry.

[10]  W. Guan,et al.  Inflammatory Responses, Spirometry, and Quality of Life in Subjects With Bronchiectasis Exacerbations , 2015, Respiratory Care.

[11]  M. Horwitz,et al.  Neutrophil Elastase, Proteinase 3, and Cathepsin G as Therapeutic Targets in Human Diseases , 2010, Pharmacological Reviews.

[12]  L. Dupont,et al.  Non-cystic fibrosis bronchiectasis: diagnosis and management in 21st century , 2010, Postgraduate Medical Journal.

[13]  L Zhang,et al.  The Role of Ethnicity in Variability in Response to Drugs: Focus on Clinical Pharmacology Studies , 2008, Clinical pharmacology and therapeutics.

[14]  Christine T. N. Pham,et al.  Neutrophil serine proteases: specific regulators of inflammation , 2006, Nature Reviews Immunology.