Journal
JOURNAL OF ASTHMA
Volume 58, Issue 1, Pages 93-101Publisher
TAYLOR & FRANCIS LTD
DOI: 10.1080/02770903.2019.1663428
Keywords
Accessorized prefilled syringe; asthma; at-home use; autoinjector; benralizumab; biologic; interleukin-5 receptor; monoclonal antibody; pharmacokinetics
Categories
Funding
- AstraZeneca
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The pharmacokinetic exposure of benralizumab following subcutaneous administration with either autoinjectors (AI) or accessorized prefilled syringes (APFS) was comparable. There were minor differences in exposure when comparing injection sites or weight classes, but clinically relevant outcomes, such as consistent blood eosinophil count depletion, were achieved with both devices. This suggests that patients and physicians have the flexibility to choose between AI and APFS for at-home delivery of benralizumab.
Objective: We compared the pharmacokinetic exposure following a single subcutaneous dose of benralizumab 30 mg using either autoinjectors (AI) or accessorized prefilled syringes (APFS). APFS and AI functionality and reliability for at-home benralizumab delivery have been demonstrated in the GREGALE and GRECO studies, respectively. Methods: In the open-label AMES study (NCT02968914), 180 healthy adult men and women were randomized to one of two device (AI or APFS) and three injection site (upper arm, abdomen, or thigh) combinations. Randomization was stratified by weight (<70 kg, 70-84.9 kg, and >= 85 kg). Blood eosinophil counts were measured on Days 1, 8, 29, and 57. Results: Benralizumab pharmacokinetic exposure was similar between AI and APFS. Geometric mean ratios (AI/APFS) (90% CI) were 92.8% (87.4-98.6) and 94.5% (88.2-101.2) for two area under the concentration-time curve measurements (AUC(last) and AUC(inf)). Benralizumab exposure was approximately 15-30% greater for thigh vs. abdomen or upper arm administration. Exposure was slightly greater for APFS vs. AI regardless of injection site or weight class. These differences were unlikely to be clinically relevant, as eosinophil depletion was achieved consistently with both devices at all injection sites. No device malfunctions were reported. No new or unexpected safety findings were observed. Conclusion: Benralizumab pharmacokinetic exposure was similar between AI and APFS, with consistent blood eosinophil count depletion observed with both devices. These results support benralizumab administration with either AI or APFS, providing patients and physicians increased choice, flexibility, and convenience for potential at-home delivery.
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