Evidence map›Paper›PMID 42339080›Full record

ArticleInfection and drug resistance2026

Effect of Early Administration of Casirivimab and Imdevimab in Hospitalized Patients with COVID-19: A Post Hoc Analysis.

Eleftherios Mylonakis, Amy Sullivan, Selin Somersan-Karakaya, Xiaojun You, Jiangnan Lyu, Fadi Shehadeh, Gregory P Geba

Abstract read
In one paragraph

Article in Infection and drug resistance, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Eleftherios MylonakisDepartment of Medicine, Houston Methodist Hospital, Houston, TX, USA.
Amy SullivanGlobal Development, Regeneron Pharmaceuticals, Inc, Tarrytown, NY, USA.
Selin Somersan-KarakayaGlobal Development, Regeneron Pharmaceuticals, Inc, Tarrytown, NY, USA.
Xiaojun YouGlobal Development, Regeneron Pharmaceuticals, Inc, Tarrytown, NY, USA.
Jiangnan LyuGlobal Development, Regeneron Pharmaceuticals, Inc, Tarrytown, NY, USA.ORCID 0009-0001-4661-9154
Fadi ShehadehDepartment of Medicine, Houston Methodist Hospital, Houston, TX, USA.
Gregory P GebaGlobal Development, Regeneron Pharmaceuticals, Inc, Tarrytown, NY, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Casirivimab and imdevimab (CAS+IMD) has been shown to improve clinical outcomes (death/mechanical ventilation) in seronegative hospitalized patients with COVID-19. The objective of the current analysis was to assess whether time to administration of CAS+IMD, from the start of COVID-19 symptoms, influenced these outcomes. Patients and Methods: This was a post hoc analysis of Study 2066 (conducted between 10 June 2020 and 9 April 2021), a Phase I/II/III trial investigating the safety and efficacy of CAS+IMD (single intravenous dose) vs placebo in hospitalized adult patients with COVID-19. The primary outcome in this analysis was death or mechanical ventilation. Two populations of patients were assessed: efficacy (n = 738) and exploratory (full analysis set-exploratory data analysis [FAS-EDA]; n = 1115). Time to administration was defined as the number of days of COVID-19 prior to treatment, 4 days being the first quartile, which was considered early treatment administration of CAS+IMD. Results: Odds of death or mechanical ventilation were higher in those aged 50-70 years (odds ratio [OR]: 2.98; 95% confidence interval [CI], 1.62-5.91; Conclusion: Early monoclonal antibody treatment is associated with better outcomes in hospitalized patients with severe COVID-19.

Indexed as

casirivimabCOVID-19imdevimabmonoclonal antibodytime to treatment

Identifiers

PMID42339080
PMCPMC13285929

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.