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

Abstract 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.

with bronchiectasis. 7 For patients who experience ≥3 exacerbations annually, guidelines recommend longterm antibiotics; however, antibiotic resistance is a common hurdle in effective bronchiectasis management. 7 Although use of inhaled corticosteroids to manage inflammation of bronchiectasis is widespread, data regarding the efficacy of their use are limited, and longterm treatment is not currently recommended. 8 Thus, treatments that target inflammation in bronchiectasis represent an important unmet need.
Deficits in both the innate and adaptive immune systems, particularly dysfunctional neutrophilic response, contribute to bronchiectasis pathophysiology, anatomic damage to the bronchi, and bacterial infection and colonization. 1 Sputum neutrophils have been correlated with pulmonary function decline, bacterial colonization, and severe disease and contribute to the functional changes and inflammatory-associated morbidity seen in patients with bronchiectasis. 4 Neutrophil elastase, a neutrophil serine protease found within cytoplasmic granules, is associated with exacerbations 7 and may represent a prospective biomarker for disease severity, a predictor of clinical outcomes, and a therapeutic target. 4 Neutrophil elastase contributes to extracellular matrix degradation, mucus gland hyperplasia, increased mucus production, ciliary beating rate reduction, and direct damage to the epithelium. 4 Neutrophil elastase inhibitors for the treatment of bronchiectasis have been investigated in phase 2 studies but have failed to produce a clinically significant benefit. 4 Activation of neutrophil elastase and other neutrophil serine proteases, including proteinase 3 and cathepsin G, occurs during neutrophil maturation in the bone marrow through the action of dipeptidyl peptidase 1 (DPP1; also known as cathepsin C). 9,10 Brensocatib (INS1007, formerly AZD7896 11 ) is a firstin-class, small-molecule, orally bioavailable, selective, and reversible inhibitor of DPP1 that is under investigation for the treatment of bronchiectasis. Brensocatib is a cytochrome P450 (CYP) 3A4, P-glycoprotein (Pgp), and breast cancer resistance protein substrate. It is highly permeable in Caco-2 monolayers (with an apparent permeability from apical side to basolateral side of 9.03 × 10 -6 cm/s) and subject to minimal degradation in human intestinal microsomes and hepatocytes (unpublished data). Following oral or intravenous administration of 14 C-brensocatib to intact and bile duct-cannulated rats, brensocatib was moderately metabolized, mainly via oxidation, N-demethylation, hydrolysis, N-formylation, oxidative dealkylation, and hydration. Brensocatib was the major component in plasma, urine, and feces, but not in bile. In plasma, 5 metabolites were detected, with the most abundant metabolite being ≈3% of total radioactivity exposure and brensocatib as the predominant radioactivity component (>80% of total radioactivity exposure) (unpublished data). In healthy adults, ≈20% of brensocatib was excreted in urine as unchanged (unpublished data). A mass balance and metabolic profiling study is ongoing. Brensocatib is not a significant CYP inhibitor (half maximal inhibitory concentration >30 μM for CYP2B6, CYP2D6, and CYP3A4/5; no effect on CYP1A2, CYP2A6, CYP2C8, CYP2C9, CYP2C19, and CYP2E1) or a significant inducer for CYP1A2, CYP2B6, and CYP3A4. In addition, it is not a significant inhibitor of P-gp, breast cancer resistance protein, organic anion and cation transporters, organic anion transporting polypeptides, or multidrug and toxin extrusion transporters (half maximal inhibitory concentration >11 μM; unpublished data), suggesting that brensocatib is unlikely to modulate the activity of CYP isozymes and transporters at clinically relevant dose levels. In the presence of CYP3A4 and P-gp inhibitors of verapamil (240 mg once daily for 5 days) or itraconazole (200 mg twice daily for 6 days) (unpublished data), brensocatib area under the plasma concentration-time curve (AUC) increased by ≈14% to 32% in healthy participants, 12 indicating a mild effect of CYP3A4 and P-gp inhibitors on brensocatib exposure. Brensocatib also has been shown to inhibit the activity of neutrophil elastase in blood in an exposure-dependent manner. 9 A previously conducted phase 1 study of brensocatib in healthy adult male participants revealed dose-dependent increases in plasma levels with increasing single doses of brensocatib 5, 15, 35, 50, or 65 mg, with maximum concentrations observed at 0.5 to 1.5 hours after dosing; terminal half-life was 20 to 26 hours with single dosing and 26 to 34 hours with daily dosing (10, 25, or 40 mg for 21-28 days); furthermore, single oral brensocatib administration (5-65 mg) or once-daily dosing (10-40 mg) for 28 days also resulted in dose-dependent brensocatib exposure and inhibitory effects on neutrophil elastase activity in the blood. 9 In a phase 2 randomized, double-blind, placebo-controlled trial that assessed the effect of brensocatib on time to first exacerbation, rate of exacerbations, and sputum neutrophil activity (the WILLOW study; Clinical-Trials.gov identifier: NCT03218917), brensocatib 10 and 25 mg reduced neutrophil elastase and improved clinical outcomes in patients with non-cystic fibrosis bronchiectasis. 3 In this phase 1 study, we evaluated the safety and pharmacokinetics (PK) of brensocatib in healthy Japanese and White adults following single and multiple oral administration. In addition, food effect on brensocatib PK was assessed.

Methods
The clinical study protocol, participant information sheet, informed consent form, and relevant study documentation were reviewed and approved by the local independent review board (Aspire IRB, LLC) for the study site, Parexel International Early Phase Clinical Unit (Los Angeles, California). The study was performed in accordance with the ethical principles of the Declaration of Helsinki, the Good Clinical Practice guidelines of the International Council for Harmonisation, and applicable regulatory requirements, including the Health Insurance Portability and Accountability Act. All participants provided written informed consent.

Study Design
The study was conducted sequentially in 2 parts. Part A was a randomized, double-blind, placebo-controlled, dose-escalation study in which healthy Japanese and White adults were randomized 4:1 to receive single (day 1) and multiple (days 3-30) oral doses of brensocatib (10, 25, or 40 mg) or placebo (10 Japanese and 10 White participants per dose group). Eligible participants were admitted to the clinical unit for single-dose evaluation from days −2 to 2 and from days 29 to 31 for steady-state PK and safety evaluation. Participants self-administered daily doses after an overnight fast of at least 10 hours on days 4 to 30, with outpatient visits on days 3, 4, 7, 14, 21, 32, 33, and 61 ( Figure S1). Brensocatib 10-and 25-mg dosing was conducted in parallel, whereas dosing of the 40-mg group initiated after at least 12 participants (6 Japanese, 6 White) in the 25-mg group were evaluated following completion of active treatment. Dosing of the 40-mg group commenced when the safety of 25 mg was deemed acceptable by both the investigator and the sponsor's (Insmed Incorporated, Bridgewater, New Jersey) medical monitor.
Part B was an open-label, 2-period, 2-sequence crossover study in which 20 healthy Japanese and White participants were randomized 1:1 (10 per group/sequence) to receive a single dose of brensocatib 40 mg under either fasted or fed (high-fat, high-calorie breakfast) conditions ( Figure S1). Participants were admitted to the clinical unit the day before doses were administered on days 1 and 8 and discharged on days 2 and 9, after collection of the 36-hour postdose PK sample. The washout period between doses was 7 days. For fed conditions, brensocatib was administered ≈30 minutes after the start of breakfast and within 5 minutes of completion. After dosing, participants were required to remain upright for at least 2 hours and refrain from food and drink for at least 4 hours; water was allowed after 2 hours. For fasted conditions, brensocatib was administered after an overnight fast of at least 10 hours.

Participants
Participants in both parts A and B were healthy Japanese and White adults (18-50 years old) with no clinically important abnormalities on a 12-lead electrocardiogram (ECG). Japanese participants had to meet the following criteria: born in Japan, both parents and all 4 grandparents of Japanese descent, and lived <10 years outside of Japan with no significant change in lifestyle (including diet). White participants were required to verbally identify as White and have 4 White grandparents. Eligible participants were nonsmokers with a body mass index (BMI) between 18.0 and 30.0 kg/m 2 and weighing 45 to 100 kg. Female participants were required to be postmenopausal, surgically sterile, or actively using highly effective contraception methods. Male participants were required to be nonfertile or actively practicing effective contraceptive methods.
Participants were excluded if they had a clinically significant history or evidence of cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, neurological, immunological, or psychiatric disorder(s) or a serious, chronic, or recurring infection within 6 months before screening. Additional exclusion criteria include any disorder that would interfere with absorption, distribution, metabolism, or excretion of drugs; clinically significant abnormal findings in vital signs; a history of multiple or severe allergies to prescription or nonprescription drugs or foods; and use of over-the-counter medications within 7 days before the screening visit (use of 1000 mg/day of paracetamol/acetaminophen or ibuprofen was permitted) or prescription medications within 30 days before the screening visit. Throughout the study, participants were monitored for infections and had regular complete blood counts performed, including differential white blood cell count.

Pharmacokinetic and Pharmacodynamic Assessments
For part A, blood samples for PK assessments were collected following administration on days 1 and 30 at 0 (predose), 0.5, 0.75, 1, 1.5, 2, 3, 4, 8, 12, 24, 48, and 72 hours after dosing. In addition, predose PK samples were collected on days 4, 7, 14, and 21. PK parameters following single and multiple once-daily dosing were evaluated using noncompartmental analysis, including the AUC over a dosing interval (AUC τ ), AUC from time 0 to the last time with quantifiable concentration (AUC last ), AUC from time 0 to infinite time (AUC ∞ ), maximum plasma concentration (C max ), minimum plasma concentration, time to maximum plasma concentration (t max ), terminal elimination halflife (t 1/2 ), apparent total drug clearance following oral administration (CL/F), and predose concentration. Plasma concentrations of brensocatib were analyzed using a validated liquid chromatography-tandem mass spectrometry (LC-MS/MS) with a quantification range of 0.250 to 150 ng/mL.

Safety
Safety was assessed from the signing of informed consent until the end of study and included the following variables: treatment-emergent adverse events (TEAEs), serious adverse events (SAEs), clinical laboratory tests (clinical chemistry, hematology, coagulation [part A only], and urinalysis), vital signs, 12-lead ECG, primary Holter monitoring, and physical examinations (including evaluation of teeth and gingiva, and evaluation of palms and soles). Because of the mechanism of action of brensocatib, findings of hyperkeratosis, periodontitis/gingivitis, and other infections were reported as adverse events of special interest (AE-SIs). Renal function (part A only) was monitored by measuring serum creatinine and blood urea nitrogen, performing routine urinalysis, and measuring neutrophil gelatinase-associated lipocalin and cystatin.
Adverse events (AEs) observed before the first dosing were recorded as medical history. All medical history and AEs were coded using the Medical Dictionary for Regulatory Activities (version 21.1 or higher). A TEAE was defined as an AE that began or worsened in severity after at least 1 dose of study drug was administered. All AEs experienced by a participant were monitored until the event had resolved, any abnormal laboratory values returned to baseline or stabilized, a satisfactory explanation for the changes was identified, or the participant was lost to follow-up.

Analytical Methods
The plasma concentrations of brensocatib were analyzed using a validated LC-MS/MS with dipotassium ethylenediaminetetraacetic acid as an anticoagulant. The chromatographic method consisted of a Pursuit C18 column (Agilent Technologies, Santa Clara, California) and a gradient mobile phase of 0.1% formic acid in acetonitrile/water, with 13 C6-brensocatib as an internal standard. Brensocatib and the internal standard were monitored by the precursor and product ions of m/z 421.2→100.1 for brensocatib and m/z 427.2→100.1 for the internal standard using an API 5000 or API 5500 LC-MS/MS (Sciex, Framingham, Massachusetts). The assay range was 0.250 to 150 ng/mL, with overall precision and accuracy for intraand interassays of 2.2% to 5.9% and −2.7% to 0.3%, respectively.

Statistical Analyses
All statistical analyses were performed using SAS version 9.3 or higher (SAS Institute Inc., Cary, North Carolina). Analysis of PK data was performed using WinNonlin Professional Software version 8.0 or higher (Certara, LP, Princeton, New Jersey). Continuous data were summarized by race or treatment group (active vs placebo) using descriptive statistics (number of observations, arithmetic mean, standard deviation, minimum, median, and maximum). Categorical data were summarized by race and treatment group in terms of number of participants with data at relevant time points, frequency counts, and percentages. PK concentrations below the limit of quantification (BLQ) at time 0 on days 1 and 30 were considered 0. Postdose BLQ data were considered missing for PK parameter calculation. For mean concentrations and graphic presentation, all BLQ data were imputed as 0.
PK parameters were generated using noncompartmental analysis and were based on the PK population, which included all participants who received at least 1 dose of assigned treatment (safety population) and had evaluable C max and AUC parameters without significant protocol deviations. For part B, the PK population included participants who completed both treatment periods and had sufficient concentration data from both periods to fully derive the PK parameters.
The effect of ethnicity (Japanese vs White) on the PK profile of brensocatib was estimated by determining the geometric mean ratio for each dose-normalized parameter using an analysis of covariance, with AUC (AUC τ , AUC last , and AUC ∞ ) and C max as dependent variables and race and baseline body weight as independent variables.
The effect of food on the PK of brensocatib was assessed separately for Japanese and White participants using an analysis of variance following transformation of the data, with sequence, treatment group, group and period as fixed effects, and participant (sequence) as random effect; group effect was dropped from the analysis of variance if it was nonsignificant at α = 0.05. Estimates and 90% CIs for the differences between treatment means were computed and converted to ratios by antilog transformation. Results for the geometric mean ratio of treatments (fasted vs fed) were tabulated for C max , AUC last , and AUC ∞ .
A formal sample size calculation was not performed. The number of participants was chosen on the basis of feasibility, as is typical and standard for a multipleascending-dose study design and was considered sufficient to meet the study objectives.

Results Participants
A total of 82 participants were enrolled and treated: 62 in part A and 20 in part B. Of the 62 participants who received at least 1 dose of the study drug in part A, 28 (87.5%) Japanese and 30 (100%) White participants completed the study. Four Japanese participants discontinued: 1 treated with brensocatib 40 mg discontinued due to a mild dry throat and mild dyspnea, 1 in the placebo group discontinued due to anemia, and 2 participants withdrew consent (n = 1, placebo; n = 1, brensocatib 25 mg). Age and height were generally consistent between Japanese and White participants across treatment groups (Table 1).
Of the 20 participants enrolled in part B, 9 (90.0%) Japanese and 10 (100%) White participants completed the study. One Japanese participant in the placebo group discontinued the study per protocol before the second dose due to a decrease from baseline in hemoglobin of >2 g/dL. Age, height, body weight, and BMI were generally consistent between Japanese and White participants (Table 1).

Brensocatib Single-and Multiple-Dose PK: Part A
The PK population in part A comprised 49 brensocatibtreated participants (25 Japanese, 24 White). Brensocatib absorption was rapid in all dose groups, with plasma concentrations observed at the first postdose time point (0.5 hour) (Figure 1).
Following single-dose administration, brensocatib was rapidly absorbed, with a median t max of 1 to 1.5 hours (Table 2). Across brensocatib dose groups, C max and AUCs were approximately dose proportional in both Japanese and White participants. Elimination t 1/2 ranged from 18.4 to 22.4 hours in Japanese participants and from 21.5 to 24.5 hours in White participants. The intersubject variability in C max and AUCs was low to moderate (12.4% to 48%) across all groups.
Following once-daily administration, steady-state C max increased 1.2-to 1.7-fold, and AUCτ increased 1.7-to 2.1-fold. T max (1.0-1.8 hours) and elimination t 1/2 (21.7-27.6 hours) were similar to those after a single dose of brensocatib (Table 2). C max and AUC were approximately dose proportional, with linear slopes of 1.08 and 1.05, respectively, in Japanese participants and 1.17 and 1.20, respectively, in White participants. Across the 3 brensocatib dose groups, mean t 1/2 was 21.7 to 23.1 hours in Japanese participants and 22.9 to 27.6 hours in White participants ( Table 2). Mean steady-state CL/F was slightly higher in Japanese participants (10.1, 6.4, and 10.7 L/h in the brensocatib 10-, 25-, and 40-mg groups, respectively) compared with White participants (8.5, 7.0, and 6.5 L/h). The dosedependent systemic exposure and consistent CL/F and apparent volume of distribution after drug administration across the dose groups demonstrated linear PK of brensocatib.
Following single and multiple dosing, C max , AUC τ , AUC last , and AUC ∞ were similar between Japanese and White participants treated with either 10 or 25 mg of brensocatib; for those treated with 40 mg, C max  and AUCs were lower among Japanese participants ( Table 2). Analysis of covariance revealed no differences in C max , AUC τ , AUC last , and AUC ∞ due to either body weight or BMI. Dose-normalized C max was 19.1% lower in Japanese participants than in White participants, and dose-normalized AUCs were ≈25.6% lower in Japanese participants than in White participants (Table 3). Based on body weight-and dosenormalized AUC last , AUC ∞ after a single dose, and AUC τ at steady state, exposure differences observed between Japanese and White participants were likely due to body weight differences between the ethnic groups ( Figure S2).

Brensocatib PK Under Fasted and Fed Conditions: Part B
Following single oral administration of brensocatib 40 mg under fasted conditions, T max was attained at 1.3 hours in both Japanese and White participants ( Table 4). C max , AUC last, and AUC ∞ were 338.4, 4820, and 5183 ng · h/mL, respectively, in Japanese participants and 268.9, 5147, and 6201 ng · h/mL, respectively, in White participants. Elimination t 1/2 was 18.7 and 28.0 hours in Japanese and White participants, respectively, and CL/F was 7.7 and 6.5 L/h in Japanese and White participants, respectively. The presence of food slightly reduced plasma concentrations among both races ( Figure 2) and slightly delayed brensocatib absorption, as the median T max shifted from 1.3 (fasted) to 3.0 (fed) hours in Japanese participants and from 1.3 (fasted) to 2.0 (fed) hours in White participants (Table 4). Mean t 1/2 was consistent at 18 hours among Japanese participants (18.7 fasted, 18.4 fed) and ranged from 27.0 to 28.0 hours among White participants. CL/F was consistent with or without food in both races. Furthermore, food had no effect on brensocatib 40-mg exposure (Table 5). Among Japanese participants, C max was 17.6% lower in the fed state. In White participants, C max , AUC last , and AUC ∞ were similar under fasted and fed conditions. C max and AUC last were comparable between Japanese and White   Table 1). The most frequently reported TEAEs (occurring in ≥2 participants in any treatment group) were headache, skin exfoliation, and nasopharyngitis. In part B, 3 Japanese participants (30.0%) and Mean brensocatib plasma concentration, ng/mL Japanese White Figure 2. Mean brensocatib plasma concentrations in fasted and fed states (PK population). LLOQ, lower limit of quantification; PK, pharmacokinetics. Physical examinations were normal for all but 6 participants in the study. Three participants in part A and 3 in part B had physical examination findings assessed as AEs; however, all were considered mild to moderate, nonserious events and resolved. In part A, 1 participant experienced abnormal palms and soles, 1 experienced abnormal gingiva and teeth, and 1 experienced abnormal skin. In part B, 2 participants experienced abnormal skin, and 1 experienced abnormal palms and soles.

Discussion
Because race may be associated with variable drug response, 13,14 the safety, tolerability, and PK of single and once-daily oral doses of brensocatib (10, 25, and 40 mg) were evaluated in Japanese and White participants in this phase 1 study. In addition, the food effect on brensocatib systemic exposure was assessed in Japanese and White participants with a single oral administration of brensocatib 40 mg immediately following a high-fat, high-calorie breakfast.
Following oral brensocatib administration, linear and predictable PK were observed in healthy Japanese and White participants, characterized by rapid oral absorption; dose-proportional exposure; consistent t 1/2 , CL/F, and volume of distribution across doses; and ≈2-fold accumulation at steady state. Based on similar dispositional parameters between a single dose and multiple doses at steady state, brensocatib clearance appeared to be time invariant. When brensocatib was administered with food, its oral absorption was slightly delayed but overall exposure was unchanged, indicating a minimal food effect on oral absorption of brensocatib. Based on these results, brensocatib can be administered with or without food.
Brensocatib exposure following 10-and 25-mg dosing was generally comparable between Japanese and White participants. Following 40-mg dosing, brensocatib exposure in White participants was higher than that in Japanese participants, leading to an overall moderately higher exposure (dose-normalized C max and AUC) in White participants. Since the body weight of Japanese participants was generally lower than that of White participants, exposure differences were evaluated using pooled data from parts A and B. The body weight-and dose-normalized AUC last after single and repeated dosing, AUC ∞ after a single dose, and AUCτ at steady state were nearly comparable between Japanese and White participants, with a mean (median) ng • h/mL of 2.47 (2.04) vs 2.44 (1.96) for AUC last and 2.07 (1.88) vs 2.01 (1.93) for AUC ∞ /AUCτ , indicating that exposure differences between the ethnic groups were due to body weight differences. From a population PK analysis, race was not identified as a significant PK covariate. Preclinical data showed that brensocatib is highly absorbed, minimally metabolized in the liver, and not a significant CYP450 or transporter substrate or modulator (internal unpublished data); therefore, PK polymorphism is not expected for the drug. Investigation of the effect of food on brensocatib PK revealed a negligible food effect in White participants.
Single and multiple administration of brensocatib (10, 25, and 40 mg) for 28 days was well tolerated in healthy Japanese and White participants, with a safety profile that was similar under both fed and fasted conditions. Of 62 participants in part A, only 2 (3.2%; both Japanese) were withdrawn from the study due to the occurrence of mild AEs (mild dyspnea and mild dry throat, n = 1; mild anemia, n = 1). In part B, 1 participant (5.0%) was withdrawn due to a clinically abnormal laboratory finding (low hemoglobin [7.3 g/dL]). Overall, the most frequently reported TEAEs included headache, skin exfoliation, dry skin, upper abdominal pain, and decreased appetite. No deaths or lifethreatening SAEs were reported. Food had no effect on the safety profile of brensocatib.
Because of the mechanism of action of brensocatib (DPP1 inhibition), hyperkeratosis, periodontitis/gingivitis, and other (nonpulmonary) infections were monitored as AESIs. Monitoring for these AE-SIs was informed by the clinical presentation of a rare, autosomal recessive condition, Papillon-Lefèvre syndrome, in which the genetic absence of DPP1 results in diffuse palmoplantar keratoderma and severe periodontitis with premature tooth loss of both deciduous and permanent teeth. 15 None of these AESIs were evident in this study; the few participants with physical examination findings of abnormal skin, gingiva, or palms and soles were not withdrawn, and all events resolved.
The PK results from the current study are generally in agreement with the results from a first-in-human, randomized, placebo-controlled, dose-escalation study conducted in healthy male participants treated with a brensocatib oral solution. 9 After administration of single-oral-dose solutions of brensocatib 5, 15, 35, 50, and 65 mg or once daily at 10, 25, and 40 mg under fasting conditions, AUC and C max increased in a generally dose-proportional manner, and the steady-state AUC and C max were comparable to those from the cur-rent study. Administration of a single 35-mg dose of brensocatib following a high-fat breakfast resulted in delayed absorption (T max of 3.3 hours) and decreased C max and AUC by 36% and 9%, respectively. Like the safety results presented in the current study, both single and multiple ascending doses of brensocatib were well tolerated.

Conclusions
The PK data from this phase 1 study indicate that brensocatib exposure was generally comparable between Japanese and White participants, with linear and predictable PK characteristics. Therefore, no dose adjustment for brensocatib is necessary in Japanese patients. Based on the minimal food effect on brensocatib oral absorption, brensocatib can be administered with or without food. Brensocatib was well tolerated in healthy participants, and the safety profile was similar under fasted and fed conditions. No serious TEAEs occurred, and TEAEs of interest (ie, skin and dental events) were mild or moderate. The PK and safety data from this study support further clinical development of brensocatib.