Evidence map›Paper›PMID 38593352›Full record

ReviewClinical and translational science2024

Molnupiravir: Mechanism of action, clinical, and translational science.

Brian M Maas, Julie Strizki, Randy R Miller, Sushma Kumar, Michelle Brown, Matthew G Johnson, Mickie Cheng, Carisa De Anda, Matthew L Rizk, Julie A Stone

Open access · goldAbstract readReview
In one paragraph

Review in Clinical and translational science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
12.4field-weighted citation impact, top 1% of its field
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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

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  19. Molnupiravir Inhibits Replication of MultiplePathogens (Basel, Switzerland) · 2025
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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 at 1 institution in 1 country.

Brian M MaasMerck & Co., Inc., Rahway, New Jersey, USA.ORCID 0000-0002-2410-4379
Julie StrizkiMerck & Co., Inc., Rahway, New Jersey, USA.ORCID 0009-0002-3893-9374
Randy R MillerMerck & Co., Inc., Rahway, New Jersey, USA.
Sushma KumarMerck & Co., Inc., Rahway, New Jersey, USA.
Michelle BrownMerck & Co., Inc., Rahway, New Jersey, USA.
Matthew G JohnsonMerck & Co., Inc., Rahway, New Jersey, USA.ORCID 0000-0002-6023-1252
Mickie ChengMerck & Co., Inc., Rahway, New Jersey, USA.ORCID 0009-0003-5735-1821
Carisa De AndaMerck & Co., Inc., Rahway, New Jersey, USA.ORCID 0000-0002-6344-8123
Matthew L RizkMerck & Co., Inc., Rahway, New Jersey, USA.ORCID 0009-0005-5009-2139
Julie A StoneMerck & Co., Inc., Rahway, New Jersey, USA.ORCID 0000-0002-4914-4828
Merck & Co., Inc., Rahway, NJ, USA (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molnupiravir is an oral prodrug of the broadly active, antiviral ribonucleoside analog N-hydroxycytidine (NHC). The primary circulating metabolite NHC is taken up into cells and phosphorylated to NHC-triphosphate (NHC-TP). NHC-TP serves as a competitive substrate for viral RNA-dependent RNA polymerase (RdRp), which results in an accumulation of errors in the viral genome, rendering virus replication incompetent. Molnupiravir has demonstrated activity against SARS-CoV-2 both clinically and preclinically and has a high barrier to development of viral resistance. Little to no molnupiravir is observed in plasma due to rapid hydrolysis to NHC. Maximum concentrations of NHC are reached at 1.5 h following administration in a fasted state. The effective half-life of NHC is 3.3 h, reflecting minimal accumulation in the plasma following twice-daily (Q12H) dosing. The terminal half-life of NHC is 20.6 h. NHC-TP exhibits a flatter profile with a lower peak-to-trough ratio compared with NHC, which supports Q12H dosing. Renal and hepatic pathways are not major routes of elimination, as NHC is primarily cleared by metabolism to uridine and cytidine, which then mix with the endogenous nucleotide pools. In a phase III study of nonhospitalized patients with COVID-19 (MOVe-OUT), 5 days of treatment with 800 mg molnupiravir Q12H significantly reduced the incidence of hospitalization or death compared with placebo. Patients treated with molnupiravir also had a greater reduction in SARS-CoV-2 viral load and improved clinical outcomes, compared with those receiving placebo. The clinical effectiveness of molnupiravir has been further demonstrated in several real-world evidence studies. Molnupiravir is currently authorized or approved in more than 25 countries.

Indexed as

RibonucleosidesTranslational Science, BiomedicalCytidineHumansHydroxylaminesSARS-CoV-2CytidineHydroxylaminesmolnupiravirRibonucleosides

Identifiers

PMID38593352
PMCPMC10851176
OpenAlexW4391670547

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.