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Safety and Tolerability of Manual Push Administration of Subcutaneous IgPro20 at High Infusion Rates in Patients with Primary Immunodeficiency: Findings from the Manual Push Administration Cohort of the HILO Study.

Publication ,  Journal Article
Cowan, J; Bonagura, VR; Lugar, PL; Maglione, PJ; Patel, NC; Vinh, DC; Hofmann, JH; Praus, M; Rojavin, MA
Published in: J Clin Immunol
January 2021

PURPOSE: To evaluate the safety and tolerability of IgPro20 manual push (also known as rapid push) infusions at flow rates of 0.5-2.0 mL/min. METHODS: Patients with primary immunodeficiency (PID) with previous experience administering IgPro20 (Hizentra®, CSL Behring, King of Prussia, PA, USA) were enrolled in the Hizentra® Label Optimization (HILO) study (NCT03033745) and assigned to Pump-assisted Volume Cohort, Pump-assisted Flow Rate Cohort, or Manual Push Flow Rate Cohort; this report describes the latter. Patients administered IgPro20 via manual push at 0.5, 1.0, and 2.0 mL/min/site for 4 weeks each. Responder rates (percentage of patients who completed a predefined minimum number of infusions), safety outcomes, and serum immunoglobulin G (IgG) trough levels were evaluated. RESULTS: Sixteen patients were treated; 2 patients (12.5%) discontinued at the 1.0-mL/min level (unrelated to treatment). Responder rates were 100%, 100%, and 87.5% at 0.5-, 1.0-, and 2.0-mL/min flow rates, respectively. Mean weekly infusion duration decreased from 103-108 to 23-28 min at the 0.5- and 2.0-mL/min flow rates, respectively. Rates of treatment-related treatment-emergent adverse events (TEAEs) per infusion were 0.023, 0.082, and 0.025 for the 0.5-, 1.0-, and 2.0-mL/min flow rates, respectively. Most TEAEs were mild local reactions and tolerability (infusions without severe local reactions/total infusions) was 100% across flow rate levels. Serum IgG levels (mean [SD]) were similar at study start (9.36 [2.53] g/L) and end (9.58 [2.12] g/L). CONCLUSIONS: Subcutaneous IgPro20 manual push infusions at flow rates up to 2.0 mL/min were well tolerated and reduced infusion time in treatment-experienced patients with PID. TRIAL REGISTRATION: NCT03033745.

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Published In

J Clin Immunol

DOI

EISSN

1573-2592

Publication Date

January 2021

Volume

41

Issue

1

Start / End Page

66 / 75

Location

Netherlands

Related Subject Headings

  • Young Adult
  • Treatment Outcome
  • Primary Immunodeficiency Diseases
  • Patient Compliance
  • Middle Aged
  • Male
  • Injections, Subcutaneous
  • Infusions, Subcutaneous
  • Infusion Pumps
  • Immunology
 

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Cowan, J., Bonagura, V. R., Lugar, P. L., Maglione, P. J., Patel, N. C., Vinh, D. C., … Rojavin, M. A. (2021). Safety and Tolerability of Manual Push Administration of Subcutaneous IgPro20 at High Infusion Rates in Patients with Primary Immunodeficiency: Findings from the Manual Push Administration Cohort of the HILO Study. J Clin Immunol, 41(1), 66–75. https://doi.org/10.1007/s10875-020-00876-6
Cowan, Juthaporn, Vincent R. Bonagura, Patricia L. Lugar, Paul J. Maglione, Niraj C. Patel, Donald C. Vinh, Jutta H. Hofmann, Michaela Praus, and Mikhail A. Rojavin. “Safety and Tolerability of Manual Push Administration of Subcutaneous IgPro20 at High Infusion Rates in Patients with Primary Immunodeficiency: Findings from the Manual Push Administration Cohort of the HILO Study.J Clin Immunol 41, no. 1 (January 2021): 66–75. https://doi.org/10.1007/s10875-020-00876-6.
Journal cover image

Published In

J Clin Immunol

DOI

EISSN

1573-2592

Publication Date

January 2021

Volume

41

Issue

1

Start / End Page

66 / 75

Location

Netherlands

Related Subject Headings

  • Young Adult
  • Treatment Outcome
  • Primary Immunodeficiency Diseases
  • Patient Compliance
  • Middle Aged
  • Male
  • Injections, Subcutaneous
  • Infusions, Subcutaneous
  • Infusion Pumps
  • Immunology