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UnknownNCT05398718

Study on Sotrovimab and Its Impact on the Immune Response to COVID-19 Infection in Real-life in the UAE and Bahrain

Bi-directional Real-world Cohort Study on Sotrovimab and Its Impact on the Strength and Duration of the Immune Response to Natural SARS-CoV-2 Infection in Real-life Setting in the UAE and the Kingdom of Bahrain

Status
Unknown
Phase
Study type
Observational
Enrollment
20,000 (estimated)
Sponsor
Abu Dhabi Health Services Company · Other Government
Sex
All
Age
12 Years
Healthy volunteers
Not accepted

Summary

The United Arab Emirates (UAE), the Kingdom of Bahrain, Kuwait, Oman, and Qatar have authorised sotrovimab for emergency use. Local experience among physicians include recent successful COVID-19 vaccine pivotal studies supported by the authorities' willingness to expedite understanding of the role of monoclonal antibodies such as sotrovimab in the management of COVID-19 and expertise to integrate the latest knowledge into the local or regional COVID-19 management guidelines. The aim of this study is to collect local clinical evidence for sotrovimab effect in the real-life setting in the UAE and the Kingdom of Bahrain. Overall study population is 20,000 and the duration of the study will be approximately six months from recruitment date.

Conditions

Interventions

TypeNameDescription
DRUGSotrovimabcollect local clinical evidence for sotrovimab effect in the real-life setting

Timeline

Start date
2022-05-12
Primary completion
2022-12-15
Completion
2022-12-31
First posted
2022-06-01
Last updated
2022-06-01

Locations

1 site across 1 country: Bahrain

Source: ClinicalTrials.gov record NCT05398718. Inclusion in this directory is not an endorsement.