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A Phase 1, Randomized, Open-Label, Parallel Group Study to Evaluate the Relative Bioavailability of Subcutaneous Bepirovirsen When Delivered From a Vial or Prefilled Syringe Fitted With a Safety Syringe Device in Healthy Adult Participants

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Trial Profile

A Phase 1, Randomized, Open-Label, Parallel Group Study to Evaluate the Relative Bioavailability of Subcutaneous Bepirovirsen When Delivered From a Vial or Prefilled Syringe Fitted With a Safety Syringe Device in Healthy Adult Participants

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 03 Sep 2024

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At a glance

  • Drugs Bepirovirsen (Primary)
  • Indications Hepatitis B
  • Focus Pharmacokinetics
  • Sponsors GSK

Most Recent Events

  • 30 Aug 2024 Status changed from recruiting to completed.
  • 04 Apr 2024 Planned number of patients changed from 200 to 160.
  • 04 Apr 2024 Planned End Date changed from 30 May 2024 to 15 May 2024.

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