Evidence map›Paper›PMID 41176291›Full record

ReviewThe Journal of infection2025

Target product profile and discovery and development path for novel cryptococcal disease treatments.

David B Meya, Manu De Rycker, Ian H Gilbert, William Hope, Justine Jelagat Odionyi, Michael Keegan, Angela Loyse, Pablo Moral-Lopez, Peter R Williamson, Lionel K Tan and 2 more

Abstract readReview
In one paragraph

Review in The Journal of infection, 2025. 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

12 authors.

David B MeyaDepartment of Internal Medicine, College of Health Sciences, Makerere University, Kampala, Uganda. Electronic address: dmeya@idi.ac.ug.
Manu De RyckerUniversity of Dundee, Dundee, UK. Electronic address: M.DeRycker@dundee.ac.uk.
Ian H GilbertUniversity of Dundee, Dundee, UK. Electronic address: I.H.Gilbert@dundee.ac.uk.
William HopeUniversity of Liverpool, Antimicrobial Pharmacodynamics and Therapeutics, Liverpool, UK. Electronic address: william.hope@liverpool.ac.uk.
Justine Jelagat OdionyiDrugs for Neglected Diseases Initiative (DNDi), Geneva, Switzerland. Electronic address: jodionyi@dndi.org.
Michael KeeganViiV Healthcare Ltd., London, UK. Electronic address: michael.r.keegan@viivhealthcare.com.
Angela LoyseCity St George's University of London, London, UK. Electronic address: aloyse@sgul.ac.uk.
Pablo Moral-LopezGSK, Tres Cantos, Spain. Electronic address: pablo.x.moral@gsk.com.
Peter R WilliamsonLaboratory of Clinical Immunology and Microbiology (LCIM), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD, USA. Electronic address: peter.williamson2@nih.gov.
Lionel K TanViiV Healthcare Ltd., London, UK. Electronic address: lionel.x.tan@viivhealthcare.com.
Isabela RibeiroDrugs for Neglected Diseases Initiative (DNDi), Geneva, Switzerland. Electronic address: iribeiro@dndi.org.
Timothy J MilesGSK, Tres Cantos, Spain. Electronic address: tim.j.miles@gsk.com.

Funding

Intramural NIH HHS Z99 AI999999
6 · The paper itself

Abstract

Cryptococcus neoformans and Cryptococcus gattii are World Health Organization critical and medium priority pathogens, respectively. These mainly impact people with human immunodeficiency virus residing in low- and middle-income countries, but other patient groups and settings are also affected. The high global morbidity and mortality and the limitations of current treatments provided an impetus for the development of a target product profile (TPP) for new anti-cryptococcal agents. Key attributes of the TPP include improved safety, superior (or at least comparable) activity to current treatments against all syndromes across the full disease spectrum (cryptococcal meningitis, cryptococcal pneumonia, etc.), relevance for C. neoformans and C. gattii, suitability for all age groups, oral and intravenous formulations, an acceptable treatment regimen, minimal/manageable drug-drug interactions, thermostability, and a barrier to resistance at least as high as current options. The aim of this TPP, along with the suggested discovery and development paths, is to assist all stakeholders in the development of novel cryptococcal disease treatments.

Indexed as

Antifungal AgentsCryptococcosisCryptococcus gattiiCryptococcus neoformansDrug DevelopmentDrug DiscoveryHumansAntifungal AgentsCryptococcal meningitisCryptococcus neoformansDrug developmentHuman immunodeficiency virusLow- and middle-income countries

Identifiers

PMID41176291
PMCPMC13195516

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.