Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: June 12, 2024
Abstract
There
have
been
774,075,242
cases
of
COVID-19
and
7,012,986
deaths
worldwide
as
January
2024.
In
the
early
stages
pandemic,
there
was
an
urgent
need
to
reduce
severity
disease
prevent
for
hospitalization
avoid
stress
on
healthcare
systems
worldwide.
The
repurposing
drugs
clinical
deterioration
patients
trialed
in
many
studies
using
different
drugs.
Fluvoxamine
(an
SSRI
sigma-1
receptor
agonist)
initially
identified
potentially
provide
beneficial
effects
COVID-19-infected
patients,
preventing
hospitalization.
Fourteen
carried
out
date,
with
seven
those
being
randomized
placebo-controlled
studies.
This
systematic
review
meta-analysis
covers
literature
from
outbreak
SARS-CoV-2
late
2019
until
Search
terms
related
fluvoxamine,
such
its
trade
names
chemical
names,
along
words
COVID-19,
coronavirus,
were
used
databases
including
PubMed,
Google
Scholar,
Scopus,
ClinicalTrials.gov
database
NIH,
identify
trials
subsequent
analysis.
Clinical
death
data
extracted
these
where
available
meta-analysis.
A
total
7153
studied
across
14
(both
open-label
double-blind
placebo-controlled).
681
3553
(19.17%)
standard
care
group
255
3600
(7.08%)
fluvoxamine-treated
experienced
deterioration.
estimated
average
log
odds
ratio
1.087
(95%
CI
0.200
1.973),
which
differed
significantly
zero
(z
=
2.402,
p
0.016).
resulted
a
0.359
0.1111
0.5294),
3.103,
0.002).
results
this
study
fluvoxamine
effective
deterioration,
subgrouping
analysis
suggests
that
earlier
treatment
dose
200
mg
or
above
provides
best
outcomes.
We
hope
outcomes
can
help
design
future
into
respiratory
viral
infections
improve
Pathogens,
Journal Year:
2022,
Volume and Issue:
11(2), P. 275 - 275
Published: Feb. 20, 2022
COVID-19
is
caused
by
a
novel
coronavirus
(2019-nCoV),
which
was
declared
as
pandemic
after
it
emerged
in
China
2019.
A
vast
international
effort
has
been
conducted
to
prevent
and
treat
due
its
high
transmissibility
severe
morbidity
mortality
rates,
particularly
individuals
with
chronic
co-morbidities.
In
addition,
polymorphic
variants
increased
the
need
for
proper
vaccination
overcome
infectivity
of
new
that
are
emerging
across
globe.
Many
treatment
options
have
proposed
more
than
25
vaccines
various
stages
development;
however,
infection
peaks
oscillating
periodically,
raises
significant
question
about
effectiveness
prevention
measures
persistence
this
disease.
review,
we
exploring
most
recent
knowledge
advances
well
2019-nCoV
possible
mitigation
one
aggressive
pandemics
last
centuries.
Antiviral Research,
Journal Year:
2022,
Volume and Issue:
209, P. 105492 - 105492
Published: Dec. 16, 2022
Molnupiravir
(EIDD-2801)
is
a
prodrug
of
ribonucleoside
analogue
that
currently
being
used
under
US
FDA
emergency
use
authorization
for
the
treatment
mild
to
moderate
COVID-19.
We
evaluated
molnupiravir
efficacy
as
an
oral
in
rhesus
macaque
model
SARS-CoV-2
infection.
Twenty
non-human
primates
(NHPs)
were
challenged
with
and
treated
75
mg/kg
(n
=
8)
or
250
twice
daily
by
gavage
7
days.
The
NHPs
observed
14
days
post-challenge
monitored
clinical
signs
disease.
After
challenge,
all
groups
showed
trend
toward
increased
respiration
rates.
Treatment
significantly
reduced
viral
RNA
levels
bronchoalveolar
lavage
(BAL)
samples
at
Days
10.
Considering
nature
infection
model,
this
study
highlights
importance
monitoring
load
lung
indicator
pharmaceutical
COVID-19
treatments.
Additionally,
provides
evidence
which
supplements
current
ongoing
trials
drug.
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
25(1), P. 354 - 354
Published: Dec. 26, 2023
The
coronavirus
disease
2019
(COVID-19)
pandemic
has
claimed
over
7
million
lives
worldwide,
providing
a
stark
reminder
of
the
importance
preparedness.
Due
to
lack
approved
antiviral
drugs
effective
against
coronaviruses
at
start
pandemic,
world
largely
relied
on
repurposed
efforts.
Here,
we
summarise
results
from
randomised
controlled
trials
date,
as
well
selected
in
vitro
data
directly
acting
antivirals,
host-targeting
and
immunomodulatory
drugs.
Overall,
repurposing
efforts
evaluating
antivirals
targeting
other
viral
families
were
unsuccessful,
whereas
several
led
clinical
improvement
hospitalised
patients
with
severe
disease.
In
addition,
accelerated
drug
discovery
during
progressed
multiple
novel
efficacy,
including
small
molecule
inhibitors
monoclonal
antibodies.
We
argue
that
large-scale
investment
is
required
prepare
for
future
pandemics;
both
develop
an
arsenal
broad-spectrum
beyond
build
worldwide
trial
networks
can
be
rapidly
utilised.
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: June 12, 2024
Abstract
There
have
been
774,075,242
cases
of
COVID-19
and
7,012,986
deaths
worldwide
as
January
2024.
In
the
early
stages
pandemic,
there
was
an
urgent
need
to
reduce
severity
disease
prevent
for
hospitalization
avoid
stress
on
healthcare
systems
worldwide.
The
repurposing
drugs
clinical
deterioration
patients
trialed
in
many
studies
using
different
drugs.
Fluvoxamine
(an
SSRI
sigma-1
receptor
agonist)
initially
identified
potentially
provide
beneficial
effects
COVID-19-infected
patients,
preventing
hospitalization.
Fourteen
carried
out
date,
with
seven
those
being
randomized
placebo-controlled
studies.
This
systematic
review
meta-analysis
covers
literature
from
outbreak
SARS-CoV-2
late
2019
until
Search
terms
related
fluvoxamine,
such
its
trade
names
chemical
names,
along
words
COVID-19,
coronavirus,
were
used
databases
including
PubMed,
Google
Scholar,
Scopus,
ClinicalTrials.gov
database
NIH,
identify
trials
subsequent
analysis.
Clinical
death
data
extracted
these
where
available
meta-analysis.
A
total
7153
studied
across
14
(both
open-label
double-blind
placebo-controlled).
681
3553
(19.17%)
standard
care
group
255
3600
(7.08%)
fluvoxamine-treated
experienced
deterioration.
estimated
average
log
odds
ratio
1.087
(95%
CI
0.200
1.973),
which
differed
significantly
zero
(z
=
2.402,
p
0.016).
resulted
a
0.359
0.1111
0.5294),
3.103,
0.002).
results
this
study
fluvoxamine
effective
deterioration,
subgrouping
analysis
suggests
that
earlier
treatment
dose
200
mg
or
above
provides
best
outcomes.
We
hope
outcomes
can
help
design
future
into
respiratory
viral
infections
improve