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A Phase 1 Study Evaluating the Safety, Tolerability, and Pharmacokinetics of Intranasal Plus Intraoral IGM-6268 in Healthy Adults and Patients With Mild to Moderate COVID-19

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Trial Profile

A Phase 1 Study Evaluating the Safety, Tolerability, and Pharmacokinetics of Intranasal Plus Intraoral IGM-6268 in Healthy Adults and Patients With Mild to Moderate COVID-19

Status: Discontinued
Phase of Trial: Phase I

Latest Information Update: 18 Oct 2022

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At a glance

  • Drugs IGM-6268 (Primary) ; IGM-6268 (Primary)
  • Indications COVID 2019 infections
  • Focus Adverse reactions
  • Sponsors IGM Biosciences

Most Recent Events

  • 12 Oct 2022 Status changed from recruiting to discontinued.
  • 09 Feb 2022 According to an IGM Biosciences media release, IGM-6268 is been administered intranasally first in healthy volunteers, once an appropriate dose cohort has been cleared, in outpatients with mild to moderate COVID-19. The first dose cohort of healthy volunteers has been cleared in the South Africa study, and data from the study are expected in mid-2022.
  • 24 Jan 2022 Status changed from not yet recruiting to recruiting.

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