Update on Early Combination Therapy with Lastest Monoclonal Antibodies and Antivirals as HIV, HCV, Influenza in Extremely Vulnerable Persons with Sars-Cov-2: A Literature Review and Clinical Experience
Weimer LE
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Journal of Clinical Medical Research,
Journal Year:
2025,
Volume and Issue:
unknown, P. 1 - 28
Published: Jan. 31, 2025
The
emergence
of
new
variants
concern
in
immunocompromised
persons
with
SARS-CoV-2,
particularly
those
mutations
the
spike
protein,
has
complicated
treatment
strategies.
Some
Therapies
focused
only
on
viral
clearance
effects
and
not
major
clinical
outcomes.
As
virus
continues
to
evolve,
development
broad-spectrum
therapies,
along
personalized
approaches
treatment,
will
be
crucial
managing
COVID-19
.
After
first
year
period
which
several
treatments
were
employed
early
intervention
strategies,
including
use
antiretrovirals
monoclonal
antibodies,
have
emerged
as
promising
mitigate
severity
fragile
individuals
prevent
disease
progression,
hospitalization
death
even
recent
time
less
aggressive
SARS-CoV-2
variants.
Guidelines,
high-quality
data
for
combination
exploiting
antivirals
neutralizing
antibodies
do
exist
outpatient
setting,
especially
severe
individuals.
Nevertheless,
studies
attempted
investigate
efect
this
approach
although
these
are
often
observational
without
control
groups,
generally
no
adverse
reactions
from
therapy
been
reported.
potential
efficacy
therapy,
based
an
antiviral
plus
a
antibody,
severely
patients
is
matter
literature
debate
scientific
word.
To
date,
information
concerning
using
combined
therapies
limited.
In
Literature
Review
we
explain
Last
variant
updates
vulnerable
Sars-Cov-2.
Language: Английский
Efficacy and safety of antiviral treatments for symptomatic COVID-19 outpatients: network meta-analysis and budget impact analysis
Giacomo Berti,
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Daniele Mengato,
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Honoria Ocagli
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et al.
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 16, 2025
Introduction
Remdesivir
(RDV)
and
nirmatrelvir/ritonavir
(NRM/RTV)
are
two
antiviral
agents
for
treating
outpatient
adults
with
mild
to
moderate
symptomatic
COVID-19
at
high
risk
of
developing
a
severe
disease.
The
review
objectives
compare
the
efficacy
safety
these
antivirals
based
on
published
RCT
real-world
data,
evaluate
costs
from
healthcare
perspective.
Methods
This
study
provides
network
meta-analysis
RDV
NRM/RTV
early
treatment
COVID-19.
outcomes
analysed
were
hospitalisation
any
cause
serious
adverse
events.
A
cost-analysis
was
performed
incorporating
drug
costs,
administration,
hospitalisations,
management
budget
impact
analysis
estimated
University
Hospital
Padua.
Results
Our
results
indicated
that
showed
trend
towards
lower
compared
(RR
1.59,
95%
CI:
0.60–4.20),
though
this
not
statistically
significant.
For
safety,
demonstrated
slightly
events
0.92,
0.31–2.74),
but
without
statistical
significance.
cost
could
save
€550,854.46
per
1,000
patients.
Finally,
data
Padua
annual
savings
€210,977.25
if
all
treatments
administered
instead
RDV.
Discussion
comparison
therapies
did
yield
significant
differences
in
potential
prevent
or
However,
saving
favour
NRM/RTV.
Language: Английский
Early combination of sotrovimab with nirmatrelvir/ritonavir or remdesivir is associated with low rate of persisting SARS CoV-2 infection in immunocompromised outpatients with mild-to-moderate COVID-19: a prospective single-centre study
Ivan Gentile,
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Giulio Viceconte,
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F. M. Cuccurullo
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et al.
Annals of Medicine,
Journal Year:
2024,
Volume and Issue:
57(1)
Published: Dec. 11, 2024
Immunocompromised
patients
are
at
high
risk
of
developing
persisting/prolonged
COVID-19.
Data
on
the
early
combined
use
antivirals
and
monoclonal
antibodies
in
this
population
scarce.
Language: Английский
Impact of oral early antiviral therapies for mild–moderate COVID-19 in the outpatient’s setting during Omicron era: a pharmacoeconomic analysis
Vincenzo Scaglione,
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Samuele Gardin,
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Lolita Sasset
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et al.
European journal of medical research,
Journal Year:
2024,
Volume and Issue:
29(1)
Published: Dec. 19, 2024
Molnupiravir
(MOL)
and
nirmatrelvir/ritonavir
(NIR)
decreased
mortality
hospital
admissions
in
high-risk
patients
with
mild
to
moderate
COVID-19.
Nevertheless,
there
is
a
lack
of
data
about
the
pharmacoeconomic
impact
these
antivirals
Omicron
era.
We
conducted
analysis
assessing
medical
costs
use
compared
those
occurred
people
who
refused
treatment.
The
study
included
first
50
vaccinated
against
SARS-CoV-2
each
month
experienced
COVID-19
were
consecutively
treated
oral
at
Padua
University
Hospital
between
February
1,
2022,
June
30,
2022.
In
addition,
all
consecutive
met
criteria
for
antiviral
therapy
during
this
period
but
opted
not
receive
treatment
as
control
group.
two
groups
terms
associated
emergency
department
visits
hospitalizations,
which
identified
primary
outcomes
study.
Nine-hundred-sixty-one
analysed,
mean
age
was
67.72
±
15.19
years
49%
males.
most
prevalent
comorbidities
cardiovascular
disease
(57%),
obesity
(18)
diabetes
mellitus
(18%).
Two-hundred-fifty-one
(26%)
MOL
(group
A),
252/961
NIR
B)
458/961
(48%)
C).
While
generally
more
favourable
observed
early
group,
no
statistically
significance
differences
hospitalization
or
found
group
A
C
B
C.
Total
direct
significantly
higher
both
comparing
(671.42
460€)
vs.
(1008.42
1562€)
(446.58
4977€).
main
cost
driver
increased
therapy.
average
19,334.3
27,030€
C,
8956.2
7412€
10,267.2€
A.
context
variant
pandemic,
agents
individuals
be
expensive
avoid
treatment,
primarily
due
high
it.
To
enhance
efficiency
resource
allocation,
it
essential
pursue
policies
aimed
reducing
drug
costs,
along
conducting
further
pharmaco-economic
studies.
Language: Английский