EHS-Strategy: Insight Into the UAE Experience With Monoclonal Antibodies (Sotrovimab )

Sponsor
Emirates Health Services (EHS) (Other)
Overall Status
Recruiting
CT.gov ID
NCT05144178
Collaborator
(none)
3,500
1
2.9
1224.5

Study Details

Study Description

Brief Summary

Sotrovimab is a newly developed monoclonal antibody for the treatment of mild and moderate COVID-19 patient, who are at high risk for progression to severe COVID-19, including hospitalization or death. This includes, for example, individuals who are 65 years of age and older or individuals who have certain medical conditions.

The safety and effectiveness of this investigational therapy continues to be evaluated for treatment of COVID-19. Sotrovimab is not authorized for patients who are hospitalized due to COVID-19 or require oxygen therapy due to COVID-19.

As the clinical trial results are too preliminary for the drug to enter routine use in UAE the drug approved only for emergency use, until further evidence shows Sotrovimab is effective, so we thought about this study as a tool to assess the success of Emirats Health service (EHS) strategy for fighting against COVID-19 outside the hospital setting.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    May 26, 2021, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for the treatment of mild-to-moderate coronavirus disease 2019 (COVID-19), as described in the Scope of Authorization (Section II) of this letter, pursuant to Section 564 of the Federal Food, Drug, and Cosmetic Act (the Act) (21 U.S.C. ยง360bbb-3).

    May 28,2021 the UAE Ministry of Health and Prevention approved the investigational drug for emergency use, and Emirats health service considered strategy for fighting against COVID-19 outside the hospital setting, based on this strategy ,special protocol was finalized and approved including initiation of infusion units for the drug in EHS hospital and primary health care centers, all Infection Prevention and Control Precautions were taken inconsideration .

    The overall aim of this study is to determine the effectiveness of Sotrovimab infusion in cohort of ambulatory patients with early symptomatic COVID-19 at high risk for hospitalization, in UAE. We expect to assess the Proportion of patients who have progression of COVID-19 through 28 days as defined by visit to a hospital emergency room for management or illness, or hospitalization more than 24 h for acute management of illness or death. files of patients treated from June 2021 till October 2021 will be reviewed and data will be collected based on the protocol approved from MOHAP ethical committee.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    3500 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Insight Into the UAE Experience With Monoclonal Antibodies (Sotrovimab ) as Part of Emirats Health Service (EHS)Fighting Strategy Against COVID-19.
    Actual Study Start Date :
    Nov 14, 2021
    Anticipated Primary Completion Date :
    Jan 30, 2022
    Anticipated Study Completion Date :
    Feb 9, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    Mild and moderated COVID -19 patient treated out side the hospital sitting

    Reviewing files of such group that had been received Sotrovimab

    Outcome Measures

    Primary Outcome Measures

    1. percent of hospital admission from total number of reviewed patient [10 days]

      Admission to hospital with progressive COVID -19 more than 24h

    2. percent of Death among total number of reviewed patient [28 days]

      mortality post treatment

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    13 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • All cases received Sotrovimab according the EUA protocol.

    • All patient aged 13 and above

    Exclusion Criteria:
    • Sever form of the COVID-19 disease

    • Hospitalized patient

    • Age less than 13 years old

    • BMI less than 25 and no risk factors

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Emirats Health Service Dubai United Arab Emirates

    Sponsors and Collaborators

    • Emirates Health Services (EHS)

    Investigators

    • Principal Investigator: sumaya abdalateef, Emirats Health Service (EHS)

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Dr. Sumaya Abdalateef, Clinical Director, Emirates Health Services (EHS)
    ClinicalTrials.gov Identifier:
    NCT05144178
    Other Study ID Numbers:
    • No.108/ 2021.EHS
    First Posted:
    Dec 3, 2021
    Last Update Posted:
    Jan 3, 2022
    Last Verified:
    Dec 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Dr. Sumaya Abdalateef, Clinical Director, Emirates Health Services (EHS)
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 3, 2022