Efficacy of Molnupiravir in Reducing the Risk of Severe Outcomes in Patients with SARS-CoV-2 Infection: A Real-Life Full-Matched Case–Control Study (SAVALO Study)
Ivan Gentile,
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Riccardo Scotto,
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Maria Michela Scirocco
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et al.
Microorganisms,
Journal Year:
2025,
Volume and Issue:
13(3), P. 669 - 669
Published: March 15, 2025
We
conducted
a
real-life
case–control
study
among
outpatients
with
Omicron
SARS-CoV-2
infection
to
assess
the
effectiveness
of
molnupiravir
(MNP)
in
reducing
hospital
admission,
admission
intensive
care
unit,
and
death
at
day
28.
Cases
were
SARS-CoV-2-positive
patients
seeking
medical
within
five
days
symptom
onset
from
1
January
31
December
2022,
who
received
MNP.
Controls
selected
regional
database
positive
subjects
did
not
receive
antiviral
treatment
for
SARS-CoV-2.
A
total
1382
included
(146
cases,
1236
controls).
Vaccinated
had
lower
risk
mortality
composite
outcome
(hospital
ICU
or
all-cause
death)
than
unvaccinated
ones
(0.6%
vs.
7.8%,
p
<
0.001
2%
=
0.001,
respectively).
After
full-matching
propensity
score
analysis,
MNP-treated
incidence
outcome,
although
no
effect
was
observed
on
individual
outcomes.
In
subgroup
analyses
by
vaccination
status,
MNP
effective
preventing
all
outcomes
reduced
both
vaccinated
patients.
Molnupiravir
effectively
infection,
more
pronounced
benefit
These
findings
highlight
MNP’s
potential
help
prevent
disease
progression
high-risk
patients,
thereby
supporting
its
role
as
an
outpatient
therapeutic
option
COVID-19.
Language: Английский
Cost-effectiveness Analysis of Nirmatrelvir/Ritonavir Compared with Molnupiravir in Patients at High Risk for Progression to Severe COVID-19 in Japan
Journal of health economics and outcomes research,
Journal Year:
2025,
Volume and Issue:
unknown, P. 75 - 85
Published: Jan. 1, 2025
Background:
Nirmatrelvir/ritonavir
(NMV/r)
and
molnupiravir
are
oral
antiviral
drugs
approved
for
the
treatment
of
early
symptomatic
patients
with
mild
to
moderate
COVID-19
at
high
risk
progression
severe
disease
in
Japan.
Objective:
This
study
evaluated,
from
a
Japanese
payer
perspective,
cost-effectiveness
NMV/r
compared
among
COVID-19.
Methods:
model
describes
history
impact
on
short-term
long-term
outcomes.
was
molnupiravir,
scenario
analysis
standard
care
over
lifetime
horizon.
Results:
When
showed
higher
quality-adjusted
life
years
(QALYs)
(15.752
vs
15.739)
total
cost
(¥6
248
014
¥6
245
829
[US
$44
136.86
121.42]).
The
incremental
ratio
¥164
934
(US
$1165.12)
per
QALY
gained,
which
lower
than
willingness-to-pay
(WTP)
threshold
Japan
(¥5
000
000/QALY
$35
320.71/QALY]).
In
analysis,
¥3
646
821
$25
761.66)
gained.
One-way
sensitivity
probabilistic
that
cost-effective
consistently.
All
results
one-way
ratios
were
below
WTP
result
acceptability
curve
probability
¥5
320.71/QALY)
100.00%.
Conclusion:
is
perspective.
provides
evidence
Language: Английский
Cost-effectiveness Analysis of Nirmatrelvir/Ritonavir Compared with Molnupiravir in Patients at High Risk for Progression to Severe COVID-19 in Japan
Journal of health economics and outcomes research,
Journal Year:
2025,
Volume and Issue:
12(1)
Published: Feb. 24, 2025
Background:
Nirmatrelvir/ritonavir
(NMV/r)
and
molnupiravir
are
oral
antiviral
drugs
approved
for
the
treatment
of
early
symptomatic
patients
with
mild
to
moderate
COVID-19
at
high
risk
progression
severe
disease
in
Japan.
Objective:
This
study
evaluated,
from
a
Japanese
payer
perspective,
cost-effectiveness
NMV/r
compared
among
COVID-19.
Methods:
model
describes
history
impact
on
short-term
long-term
outcomes.
was
molnupiravir,
scenario
analysis
standard
care
over
lifetime
horizon.
Results:
When
showed
higher
quality-adjusted
life
years
(QALYs)
(15.752
vs
15.739)
total
cost
(¥6
248
014
¥6
245
829
[US
$44
136.86
121.42]).
The
incremental
ratio
¥164
934
(US
$1165.12)
per
QALY
gained,
which
lower
than
willingness-to-pay
(WTP)
threshold
Japan
(¥5
000
000/QALY
$35
320.71/QALY]).
In
analysis,
¥3
646
821
$25
761.66)
gained.
One-way
sensitivity
probabilistic
that
cost-effective
consistently.
All
results
one-way
ratios
were
below
WTP
result
acceptability
curve
probability
¥5
320.71/QALY)
100.00%.
Conclusion:
is
perspective.
provides
evidence
Language: Английский
Leveraging SARS-CoV-2 Main Protease (Mpro) for COVID-19 Mitigation with Selenium-Based Inhibitors
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(2), P. 971 - 971
Published: Jan. 12, 2024
The
implementation
of
innovative
approaches
is
crucial
in
an
ongoing
endeavor
to
mitigate
the
impact
COVID-19
pandemic.
present
study
examines
strategic
application
SARS-CoV-2
Main
Protease
(M
Language: Английский
Nirmatrelvir: From Discovery to Modern and Alternative Synthetic Approaches
Michela Galli,
No information about this author
Francesco Migliano,
No information about this author
Valerio Fasano
No information about this author
et al.
Processes,
Journal Year:
2024,
Volume and Issue:
12(6), P. 1242 - 1242
Published: June 17, 2024
The
global
urgency
in
response
to
the
COVID-19
pandemic
has
catalyzed
extensive
research
into
discovering
efficacious
antiviral
compounds
against
SARS-CoV-2.
Among
these,
Nirmatrelvir
(PF-07321332)
emerged
as
a
promising
candidate,
exhibiting
potent
activity
by
targeting
main
protease
of
SARS-CoV-2,
and
been
marketed
combination
with
ritonavir
first
oral
treatment
for
name
PaxlovidTM.
This
review
outlines
synthetic
approaches
Nirmatrelvir,
ranging
from
Pfizer’s
original
method
newer,
more
sustainable
strategies,
such
flow
chemistry
strategies
multicomponent
reactions.
Each
approach’s
novelty
contributions
yield
purification
processes
are
highlighted.
Additionally,
synthesis
key
fragments
comprising
innovative
optimization
discussed.
Language: Английский
Antiviral combination treatment strategies for SARS-CoV-2 infection in immunocompromised patients
Current Opinion in Infectious Diseases,
Journal Year:
2024,
Volume and Issue:
37(6), P. 506 - 517
Published: Oct. 23, 2024
Purpose
of
review
The
purpose
this
is
to
report
the
available
evidence
regarding
use
combination
regimens
antivirals
and/or
antibody-based
therapy
in
treatment
SARS-CoV-2
immunocompromised
patients.
Recent
findings
Literature
search
identified
24
articles,
excluding
single
case
reports,
which
included
mainly
patients
with
hematological
malignancies
B-cell
depletion.
Data
were
divided
based
on
timing
and
reason
for
administration
treatment,
that
is,
early
prevent
progression
severe
COVID-19
prolonged
or
relapsed
infection.
We
described
treated
populations,
duration
composition
treatment.
briefly
addressed
new
options
we
proposed
an
algorithm
management
infection
affected
by
malignancies.
Summary
Combination
seems
effective
(73–100%)
well
tolerated
(<5%
reported
bradycardia,
hepatotoxicity,
neutropenia)
strategy
treating
prolonged/relapsed
infections
host,
although
its
optimal
cannot
be
defined
currently
evidence.
role
as
at
a
high
risk
disease/persistent
shedding
requires
further
from
comparison
monotherapy,
even
though
efficacy
was
combinations
plus
mAbs
previous
viral
variants.
Language: Английский
Sub-acute toxicity of the standardised extract of Boesenbergia rotunda in rats
Pinnakarn Techapichetvanich,
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Phisit Khemawoot,
No information about this author
Passaraporn Srimangkornkaew
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et al.
ScienceAsia,
Journal Year:
2024,
Volume and Issue:
50(3), P. 1 - 1
Published: Jan. 1, 2024
An
in
vitro
study
of
Thai
medicinal
plants
revealed
anti-SARS-CoV-2
activity
ethanolic
extract
Boesenbergia
rotunda
and
its
bioactive
component
panduratin
A.
The
present
aims
to
evaluate
the
safety
after
28
consecutive
days
oral
doses
according
OECD
GLP
407.The
28-day
repeated
were
performed
both
male
female
Wistar
rats.Three
150,
300
600
mg/kg/day
assigned
as
low,
medium
high
doses,
respectively.During
administration
period,
there
was
no
evidence
morbidity,
mortality,
or
neurological
toxicity
for
gender
all
doses.Weight
food
water
intake
similar
control
group.The
hematological
clinical
biochemistry
parameters
within
normal
ranges
rats.The
oestrous
cycle
animals
groups
vaginal
cytology
investigation
showed
abnormal
cellular
types.The
statistically
significant
difference
weight
organs
no-test
itemrelated
effects
histopathological
examination
remarkable
lesion.The
observed
adverse
effect
level
(NOAEL)
B.
considered
be
mg/kg
body
per
day.These
findings
are
useful
information
developing
a
potential
phytopharmaceutical
product
future
investigation.
Language: Английский