BiotechTube

Evusheld

Pre-clinicalCompleted
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23
Hype Score

Development Stage

1
Pre-clinical
2
Phase 1
3
Phase 2
4
Phase 3
5
Approved
Indication / Disease

SARS-CoV-2, COVID-19

Conditions

SARS-CoV-2, COVID-19

Trial Timeline

Jan 4, 2023 → Sep 1, 2023

NCT ID
NCT05663957

About Evusheld

Evusheld is a pre-clinical stage product being developed by AstraZeneca for SARS-CoV-2, COVID-19. The current trial status is completed. This product is registered under clinical trial identifier NCT05663957. Target conditions include SARS-CoV-2, COVID-19.

Hype Score Breakdown

Clinical
5
Activity
2
Company
10
Novelty
2
Community
1

Clinical Trials (7)

NCT IDPhaseStatus
NCT06156982Pre-clinicalCompleted
NCT05465876Phase 2Withdrawn
NCT05569408Pre-clinicalCompleted
NCT05712096Pre-clinicalCompleted
NCT05667116Pre-clinicalCompleted
NCT05663957Pre-clinicalCompleted
NCT05461378Pre-clinicalCompleted

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S-268019-b + PlaceboShionogiPhase 3
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S-217622 + PlaceboShionogiPhase 3
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S-217622 + PlaceboShionogiPhase 3
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FOY-305 + PlaceboOno PharmaceuticalPhase 3
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Nitric OxideGlenmark PharmaceuticalsPhase 3
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Mesenchymal stem cell + PlaceboRohto PharmaceuticalPhase 2
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Biological: AZD3152 + Biological: PlaceboAstraZenecaPhase 2
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AZD5156 (Parent study Sentinel Safety Cohort) + Placebo (Parent study Sentinel Safety Cohort) + EVUSHELD™ (Parent study Main Cohort) + AZD3152 (Parent study Main Cohort) + Placebo (Parent study Main Cohort) + AZD3152 (Sub-study) + AZD7442 - EVUSHELD™ (Sub-study) + AZD7442 (EVUSHELD™) (Sub-study) Immunocompromised participants offered AZD3152AstraZenecaPhase 2/3
65
EVUSHELDAstraZenecaPre-clinical
23
AZD1222AstraZenecaApproved
85
AZD3152 (Cohort 1) + Placebo (Cohort 1) + AZD3152 (Cohort 2) + Placebo (Cohort 2) + AZD3152 (Cohort 3) + Placebo (Cohort 3)AstraZenecaPhase 1
33
EVUSHELDAstraZenecaPre-clinical
23
AZD7442AstraZenecaPhase 1
33
EVUSHELDAstraZenecaPre-clinical
23
Molnupiravir 200 mg + Molnupiravir 400 mg + Molnupiravir 800 mg + Placebo (PBO)MerckPhase 2
52
Tocilizumab (TCZ) + PlaceboRochePhase 2
52

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