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A Phase 1 study of levothyroxine (XP-8121) to evaluate the pharmacokinetics, safety and tolerability, and potential for weekly dosing of the investigational, novel, subcutaneous (SC) injection for the treatment of hypothyroidism

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Trial Profile

A Phase 1 study of levothyroxine (XP-8121) to evaluate the pharmacokinetics, safety and tolerability, and potential for weekly dosing of the investigational, novel, subcutaneous (SC) injection for the treatment of hypothyroidism

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

Latest Information Update: 02 May 2023

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At a glance

  • Drugs Levothyroxine sodium (Primary) ; Levothyroxine sodium
  • Indications Hypothyroidism
  • Focus Adverse reactions; Pharmacokinetics
  • Sponsors Xeris Biopharma Holdings; XERIS Pharmaceuticals

    • Most Recent Events

    • 24 Mar 2023 Results (n=60) assessing the pharmacokinetics, dose proportionality, safety and tolerability of XP-8121 given subcutaneously (SC) and the relative bioavailability of SC XP-8121 oral (PO) levothyroxine (Synthroid), presented at the 124th Annual Meeting of the American Society for Clinical Pharmacology and Therapeutics.
    • 20 Oct 2022 According to a Xeris Pharmaceuticals media release, Xeris will host a conference call and webcast today, Thursday, October 20, 2022, at 8:30 a.m. Eastern Time. To pre-register for the conference call please use this link: https://www.netroadshow.com/events/login?show=f4a7da25&confId=43411 to discuss this trial results.
    • 20 Oct 2022 Results published in the Xeris Biopharma Media Release

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