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To compare the immunogenicity and safety of an intradermal (ID) fractional third dose of AZD1222 vaccine compared with those of a standard intramuscular (IM) third dose volunteers who previously received two doses of CoronaVac

Trial Profile

To compare the immunogenicity and safety of an intradermal (ID) fractional third dose of AZD1222 vaccine compared with those of a standard intramuscular (IM) third dose volunteers who previously received two doses of CoronaVac

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 04 Mar 2022

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At a glance

  • Drugs AZD 1222 (Primary) ; AZD 1222 (Primary)
  • Indications COVID 2019 infections
  • Focus Pharmacodynamics

Most Recent Events

  • 04 Mar 2022 New trial record
  • 12 Feb 2022 Primary endpoint (Geometric mean ratio of anti-receptor binding domain antibody in the ID1/ID2 vs. the IM groups 14 days post-vaccination) has been met according to the results published in the Vaccine
  • 12 Feb 2022 Results published in the Vaccine

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