Study Understanding Pre-Exposure pRophylaxis of NOvel Anitbodies (SUPERNOVA)
et al., NCT05648110, SUPERNOVA, NCT05648110, Jun 2026
42nd treatment shown to reduce risk in
May 2022, now with p = 0.026 from 20 studies, recognized in 33 countries.
Efficacy is variant dependent.
Lower risk for hospitalization and cases.
No treatment is 100% effective. Protocols
combine treatments.
6,600+ studies for
220+ treatments. c19early.org
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RCT 1,663 immunocompromised patients showing higher mortality with tixagevimab/cilgavimab, without statistical significance. Tixagevimab/cilgavimab may have lost efficacy with variants at the time but retain side effects.
Efficacy is variant dependent. In Vitro research suggests a lack of efficacy for omicron BA.2.75.2, BA.4.6, BQ.1.11, BA.5, BA.2.75, XBB2,3, XBB.1.53, ХВВ.1.9.13, XBB.1.9.3, XBB.1.5.24, XBB.1.16, XBB.2.9, BQ.1.1.45, CL.1, and CH.1.14.
Study covers AZD5156 and tixagevimab/cilgavimab.
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risk of death, 103.6% higher, RR 2.04, p = 0.12, treatment 24 of 1,102 (2.2%), control 6 of 561 (1.1%), all-cause mortality, day 451, registry.
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| Effect extraction follows pre-specified rules prioritizing more serious outcomes. Submit updates |
1.
Planas et al., Resistance of Omicron subvariants BA.2.75.2, BA.4.6 and BQ.1.1 to neutralizing antibodies, bioRxiv, doi:10.1101/2022.11.17.516888.
2.
Haars et al., Prevalence of SARS-CoV-2 Omicron Sublineages and Spike Protein Mutations Conferring Resistance against Monoclonal Antibodies in a Swedish Cohort during 2022–2023, Microorganisms, doi:10.3390/microorganisms11102417.
Haidar et al., 18 Jun 2026, Double Blind Randomized Controlled Trial, placebo-controlled, multiple countries, preprint, 1 author, trial NCT05648110 (history) (SUPERNOVA).
Contact: taylor.cohen@astrazeneca.com.
