A Phase III Open-label Study in Adults to Determine the Safety and Immunogenicity of AZD1222, a Non-replicating ChAdOx1 Vector Vaccine, for the Prevention of COVID-19
Latest Information Update: 08 Oct 2021
At a glance
- Drugs AZD 1222 (Primary)
- Indications COVID 2019 infections; SARS-CoV-2 acute respiratory disease
- Focus Adverse reactions; Registrational
- Sponsors AstraZeneca
- 27 Sep 2021 Planned End Date changed from 11 May 2021 to 11 May 2022.
- 27 Sep 2021 Planned primary completion date changed from 11 May 2021 to 4 Dec 2020.
- 27 Sep 2021 Status changed from suspended to withdrawn prior to enrolment due to The study was put on hold in September 2020 due to a safety concern in another trial but neverrestarted. In the meantime our clinical development program now includes a similar study with adifferent design, which we prefer to complete now. .