drugset / Trial / NCT05648110

Parent Study: Study Understanding Pre-Exposure pRophylaxis of NOvel Anitbodies (SUPERNOVA) Sub-study: Study Understanding Pre-Exposure pRophylaxis of NOvel Anitbodies (SUPERNOVA Sub-study)

NCT05648110

Phase 2/3 Completed 3882 enrolled AstraZeneca
RandomizedParallel-groupQuadruple-blindPrevention

Summary

AZD3152, a single mAb, is being developed to have broad neutralizing activity across known SARS-CoV-2 variants of concern for pre-exposure prophylaxis of COVID-19. The aim of the Phase I/III study (Parent Study) will be to evaluate the safety, efficacy and neutralizing activity of AZD3152 compared with comparator for pre exposure prophylaxis of COVID-19, and separately evaluate the safety and PK of AZD5156, a combination of AZD3152 and AZD1061. Sub-study: This Phase II sub-study of SUPERNOVA will assess the safety, PK, and predicted neutralizing activity of AZD3152 compared with EVUSHELD for pre-exposure prophylaxis of COVID-19.

Timeline

Start
2022-12-16
Primary completion
2024-03-29
Completion
2025-02-11

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Sipavibart Monoclonal antibody 300 mg Intramuscular
Subject Sipavibart Monoclonal antibody 1200 mg Intramuscular
Subject cilgavimab Monoclonal antibody 300 mg Intramuscular
Comparator tixagevimab Monoclonal antibody 300 mg Intramuscular

Indications