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Safety, Tolerability, and Patient Satisfaction of 16.5% Subcutaneous Immunoglobulin (cutaquig®) Treatment by Rapid Push in Patients with Primary or Secondary Immunodeficiency (PID or SID)

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Trial Profile

Safety, Tolerability, and Patient Satisfaction of 16.5% Subcutaneous Immunoglobulin (cutaquig®) Treatment by Rapid Push in Patients with Primary or Secondary Immunodeficiency (PID or SID)

Status: Active, no longer recruiting
Phase of Trial: Phase IV

Latest Information Update: 31 Jan 2025

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At a glance

  • Drugs Immune globulin (Primary)
  • Indications Immunodeficiency disorders
  • Focus Adverse reactions

Most Recent Events

  • 28 Jan 2025 Planned End Date changed from 1 Dec 2024 to 1 Sep 2025.
  • 28 Jan 2025 Planned primary completion date changed from 1 Dec 2024 to 1 Sep 2025.
  • 28 Jan 2025 Status changed from recruiting to active, no longer recruiting.

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