A Phase 3, Open-label Study to Evaluate Safety of a Booster Dose of S-268019 in Adults and Older Adults Who Have Completed COVID-19 Vaccine as a Primary Series (COVID-19)
Latest Information Update: 25 Oct 2024
At a glance
- Drugs S 268019 (Primary)
- Indications COVID 2019 infections
- Focus Adverse reactions
- 24 Nov 2022 Status changed from not yet recruiting to recruiting, according to Shionogi media release.
- 24 Nov 2022 According to Shionogi media release, company announced that it has filed for manufacturing and sales approval of S-268019, a recombinant protein-based preventive vaccine, for use in priming and booster (3rd) doses, against COVID-19, caused by the novel coronavirus (SA-CoV-2) infection, The filing is based on the positive results of five clinical trials (jRCT2031210383, jRCT2031210269, jRCT2031210470, jRCT2031210613 and jRCT2051210151) conducted in Japan.
- 26 Apr 2022 New trial record