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Thank you for visiting the mAb Âé¶¹´«Ã½¸ßÇå Website!

On this website you will find the archive of products and research findings from the mAb Âé¶¹´«Ã½¸ßÇå project. However, as of May 2022 only the "Research" tab will be updated. Please contact your healthcare provider if you are trying to find monoclonal antibody treatment for COVID-19.


Published mAb Âé¶¹´«Ã½¸ßÇå RWE and D&I Findings

mAb RWE Published Manuscripts

  • Mar 1, 2024
    Conclusion: COVID-19 vaccination, but not mAb therapy, was associated with a shorter time to symptom resolution. Both were associated with lower 28-day hospitalization.
  • Feb 21, 2024
    Conclusions: Among ED patients who presented for symptomatic COVID-19 during the Delta variant phase, ED subcutaneous casirivimab/imdevimab treatment was not associated with a decrease in hospitalizations. However, treatment was associated with lower mortality at 28 and 90 days, hospital LOS, and overall severity of illness.
  • Feb 1, 2024
    Interpretation: Real-world evidence from major US healthcare systems suggests ongoing NMV-r effectiveness in preventing hospitalisation during a BQ.1/BQ.1.1/XBB.1.5-predominant phase in the U.S, supporting its continued use in similar patient populations.
  • Apr 16, 2023
    Conclusion: During the Omicron BA.2/BA.2.12.1/BA.4/BA.5 variant phase, bebtelovimab was associated with lower hospitalization.
  • Feb 10, 2023
    Interpretation: Real-world evidence reported during a BA.2, BA2.12.1, BA.4, and BA.5 omicron surge showed an association between nirmatrelvir-ritonavir treatment and reduced 28-day all-cause hospitalisation, all-cause mortality, and visits to the emergency department. With results that are among the first to suggest effectiveness of nirmatrelvir-ritonavir for non-hospitalised patients during an omicron period inclusive of BA.4 and BA.5 subvariants, these data support nirmatrelvir-ritonavir as an ongoing first-line treatment for adults acutely infected with SARS-CoV-2.
  • Jan 25, 2023
    Summary: Real-world evidence demonstrates that the neutralizing monoclonal antibody sotrovimab was not associated with lower 28-day hospitalization and mortality rates when administered to high-risk outpatients recently infected with SARS-CoV-2 during the Omicron variant phase, compared to a propensity-matched cohort of untreated outpatients.
  • Nov 7, 2022
    Conclusions: Comorbidities, lack of prior SARS-CoV-2 vaccination, non-Hispanic black race/ethnicity, obesity, age ≥ 65 years, and male sex are associated with treatment failure of mAbs.
  • Dec 13, 2022
    Conclusion: Real-world evidence demonstrated sotrovimab effectiveness in reducing hospitalization and all-cause 28-day mortality among COVID-19 outpatients during the Delta variant phase.
  • Oct 28, 2022
    Objective: To evaluate the effectiveness of mAb treatment in preventing progression to severe disease during the Delta phase of the pandemic and based on key baseline risk factors.

mAb D&I Published Manuscripts

  • Nov 13, 2023
    Conclusion: Real-world data can be used to estimate population impact of multi-level dissemination strategies.
  • Feb 10, 2023
    Discussion: Implementation of multiple systematic strategies to administer COVID-19 monoclonal antibodies resulted in an equitable race/ethnic distribution of treatment.
  • Nov 23, 2022
    Objective: This study assessed mAbs community awareness and opportunities for improving equitable mAb access.
  • Dec 16, 2022
    Objective: To understand, from the clinician perspective, the factors facilitating or hindering monoclonal antibody referrals, patient access, and equity to inform development of clinician-focused messages, materials, and processes for improving access to therapeutics for COVID-19 in Âé¶¹´«Ã½¸ßÇå.
  • Oct 1, 2022
    Objective: To assess clinician knowledge, beliefs, and experiences regarding obtaining mAb treatment for eligible patients.

 

This project was funded by a grant from the National Institutes of Health (NIH) and National Center for Advancing Translational Sciences (NCATS) (award number UL1-TR002535-03S3).

Âé¶¹´«Ã½¸ßÇå Clinical and Translational Sciences Institute (CCTSI)

CU Anschutz

Leprino Building

12401 East 17th Avenue

3rd Floor

Aurora, CO 80045


 

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