Evidence map›Paper›PMID 37939024›Full record

ArticlePLOS global public health2023

Data-driven epidemiologic approach to conducting site feasibility for a global phase III tuberculosis vaccine clinical trial.

Wai-Ling Mui, Falgunee K Parekh, Ashley S Tseng, Joy Toro, Taylor Craig, Maggwa Ndugga, Alexander C Schmidt, Alemnew F Dagnew, Craig Penz, Ghiorghis Belai

Abstract read
In one paragraph

Article in PLOS global public health, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Wai-Ling MuiEpiPointe, Cary, North Carolina, United States of America.ORCID https://orcid.org/0009-0002-9932-1594
Falgunee K ParekhEpiPointe, Cary, North Carolina, United States of America.ORCID https://orcid.org/0009-0004-6097-949X
Ashley S TsengEpiPointe, Cary, North Carolina, United States of America.ORCID https://orcid.org/0000-0003-2304-579X
Joy ToroFHI Clinical, Durham, North Carolina, United States of America.ORCID https://orcid.org/0009-0008-3305-508X
Taylor CraigFHI Clinical, Durham, North Carolina, United States of America.ORCID https://orcid.org/0009-0007-8179-8905
Maggwa NduggaFHI Clinical, Durham, North Carolina, United States of America.ORCID https://orcid.org/0009-0007-6089-9643
Alexander C SchmidtBill & Melinda Gates Medical Research Institute, Cambridge, Massachusetts, United States of America.ORCID https://orcid.org/0000-0002-9226-3638
Alemnew F DagnewBill & Melinda Gates Medical Research Institute, Cambridge, Massachusetts, United States of America.
Craig PenzBill & Melinda Gates Medical Research Institute, Cambridge, Massachusetts, United States of America.
Ghiorghis BelaiFHI Clinical, Durham, North Carolina, United States of America.ORCID https://orcid.org/0009-0001-5320-191X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An efficacious tuberculosis (TB) vaccine is critical to reducing the global burden of TB. TB vaccine trials require the identification of multiple sites globally that have both a high incidence of TB and the capacity to conduct a clinical trial. To expand the diversity of potential phase III TB vaccine trial sites to be considered for inclusion, we describe a novel epidemiologic method that incorporates approaches from a variety of public health practices. Our approach incorporates analytic methodology to enable quantification and validation of qualitative information from disparate data sources, and epidemiologic analysis to systematically assess site-specific TB epidemiology. The integration of robust data-driven practices, and more quantitatively focused analysis, allowed for the objective evaluation of sites, which resulted in the identification of sites and catchment areas with high TB burden that may not have been previously considered. This suggests that an integrated epidemiologic methodology, not traditionally utilized for clinical trial site evaluations, could be integrated into site feasibility assessments as it results in more rapid site identification and reduces unintended bias.

Identifiers

PMID37939024
PMCPMC10631637

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.