Evidence map›Paper›PMID 41650129›Full record

ArticlePloS one2026

Efficacy evaluation of the S-adenosylhomocysteine hydrolase inhibitor MSD-914 in rhesus macaques (Macaca Mulatta) challenged with Ebola virus by the intramuscular route.

Sara C Johnston, Anthony T Ginnetti, Nancy A Twenhafel, Sarah L W Norris, Shiying Chen, Josh L Moore, Christopher W Boyce, Ondraya M Frick, Dave N Dyer, Donald J Marsh and 19 more

Abstract read
In one paragraph

Article in PloS one, 2026. 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. Biomolecules · 2026
    Review
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

29 authors.

Sara C JohnstonVirology Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
Anthony T GinnettiMerck and Co., Inc., West Point, Pennsylvania, United States of America.
Nancy A TwenhafelPathology Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
Sarah L W NorrisVeterinary Medicine Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
Shiying ChenMerck and Co., Inc., Rahway, New Jersey, United States of America.
Josh L MooreVeterinary Medicine Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
Christopher W BoyceMerck and Co., Inc., West Point, Pennsylvania, United States of America.
Ondraya M FrickVeterinary Medicine Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
Dave N DyerVeterinary Medicine Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
Donald J MarshMerck and Co., Inc., Rahway, New Jersey, United States of America.
Stephen C StevensVeterinary Medicine Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
Walter F KnappMerck and Co., Inc., West Point, Pennsylvania, United States of America.
Kerry L BerrierVeterinary Medicine Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
Hui WanMerck and Co., Inc., West Point, Pennsylvania, United States of America.
Gregory C AdamMerck and Co., Inc., West Point, Pennsylvania, United States of America.
Timothy J HartinghMerck and Co., Inc., West Point, Pennsylvania, United States of America.
Heather L EshamVeterinary Medicine Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
Jimmy O FiallosVeterinary Medicine Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
Eugene L BlueVeterinary Medicine Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
Willie B SiffordVeterinary Medicine Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
Jonathan D LattyVeterinary Medicine Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
Harold L MillsVeterinary Medicine Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
Nazira A AlliVeterinary Medicine Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
Ashley E PiperVirology Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
Aimee I GoodsonResearch Program Office, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
J Matthew MeinigBacteriology Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
David B OlsenMerck and Co., Inc., West Point, Pennsylvania, United States of America.
Linda A LiebermanMerck and Co., Inc., Cambridge, Massachusetts, United States of America.
Rekha G PanchalMolecular Biology Division, United States of America Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.ORCID https://orcid.org/0000-0001-8621-9078

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ebola virus (EBOV) causes a severe and often fatal hemorrhagic fever in humans for which effective postexposure countermeasures are lacking. Herein, we describe the evaluation of an S-adenosylhomocysteine hydrolase inhibitor, MSD-914, using mouse and nonhuman primate (NHP) models of lethal EBOV. Mice were completely protected from severe disease and death at doses as low as 0.31 mg/kg/day administered orally. From the pharmacological data and a toxicokinetic study, a predicted protective dose was selected for rhesus macaques (RMs). Surprisingly, orally administered MSD-914 was unable to protect RMs at doses as high as 0.8 mg/kg/day despite providing similar exposure of the drug to the efficacious dose observed in the mouse model.

Indexed as

AdenosylhomocysteinaseEbolavirusEnzyme InhibitorsHemorrhagic Fever, EbolaAdministration, OralAnimalsDisease Models, AnimalFemaleInjections, IntramuscularMacaca mulattaMiceAdenosylhomocysteinaseEnzyme Inhibitors

Identifiers

PMID41650129
PMCPMC12880677

What OpenQuestion holds

Textmetadata
LicenceCC0
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.