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Searched for action. Results 41 to 50 of 329 total matches.
Ensifentrine (Ohtuvayre) for COPD
The Medical Letter on Drugs and Therapeutics • Aug 19, 2024 (Issue 1709)
of PDE3 and PDE4 to be
approved by the FDA, and the first inhaled drug
with a new mechanism of action ...
The FDA has approved ensifentrine (Ohtuvayre –
Verona), an inhaled phosphodiesterase (PDE) 3 and
4 inhibitor, for maintenance treatment of chronic
obstructive pulmonary disease (COPD) in adults.
It is the first dual inhibitor of PDE3 and PDE4 to be
approved by the FDA, and the first inhaled drug
with a new mechanism of action to be approved for
treatment of COPD in more than 20 years.
Med Lett Drugs Ther. 2024 Aug 19;66(1709):131-3 doi:10.58347/tml.2024.1709b | Show Introduction Hide Introduction
Suzetrigine (Journavx) — A Sodium Channel Blocker for Acute Pain
The Medical Letter on Drugs and Therapeutics • Mar 03, 2025 (Issue 1723)
state of the channel, suzetrigine inhibits the
generation of action potentials that act as pain signals ...
The FDA has approved suzetrigine (Journavx –
Vertex), a selective sodium channel blocker, for oral
treatment of moderate to severe acute pain in adults.
Suzetrigine is the first sodium channel blocker to be
approved in the US for this indication and the first oral
nonopioid drug to be approved for treatment of pain
in over 25 years.
Med Lett Drugs Ther. 2025 Mar 3;67(1723):33-5 doi:10.58347/tml.2025.1723a | Show Introduction Hide Introduction
In Brief: Expanded Indication for Elevidys
The Medical Letter on Drugs and Therapeutics • Aug 19, 2024 (Issue 1709)
.
MECHANISM OF ACTION — Delandistrogene
moxeparvovec is a nonreplicating, recombinant
AAV vector-based ...
The adeno-associated virus (AAV) vector-based
gene therapy delandistrogene moxeparvovec-rokl
(Elevidys – Sarepta) received accelerated approval
from the FDA in 2023 for treatment of ambulatory
children 4-5 years old with Duchenne muscular
dystrophy (DMD) who have a confirmed mutation
in the DMD gene. It has now received full approval
for use in ambulatory patients ≥4 years old and
accelerated approval for use in nonambulatory
patients with DMD.
Med Lett Drugs Ther. 2024 Aug 19;66(1709):135-6 doi:10.58347/tml.2024.1709e | Show Introduction Hide Introduction
Timing of Remdesivir for COVID-19
The Medical Letter on Drugs and Therapeutics • Oct 19, 2020 (Issue 1609)
hospitalized with severe disease.1
MECHANISM OF ACTION — Remdesivir is a nucleotide
prodrug of an adenosine ...
Remdesivir (Veklury – Gilead), an investigational
antiviral drug administered by IV infusion, is now
available through an FDA Emergency Use Authorization
(EUA) for treatment of COVID-19 in all hospitalized
patients. An earlier EUA limited use of the drug to
patients hospitalized with severe disease.
In Brief: Adstiladrin – A Gene Therapy for Bladder Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Mar 06, 2023 (Issue 1671)
acquisition cost (WAC) for one 75-mL dose of
Adstiladrin is $60,000.2
MECHANISM OF ACTION — Nadofaragene ...
Nadofaragene firadenovec-vncg (Adstiladrin – Ferring), an adenoviral vector-based gene therapy,
has been approved by the FDA for treatment of adults
with high-risk Bacillus Calmette-Guérin (BCG)-unresponsive non-muscle invasive bladder cancer
(NMIBC) with carcinoma in situ with or without
papillary tumors. It is the first adenoviral vector-based
gene therapy to be approved in the US for
this indication. The immune checkpoint inhibitor
pembrolizumab (Keytruda) was approved for the
same indication in 2021.
Med Lett Drugs Ther. 2023 Mar 6;65(1671):e40-1 doi:10.58347/tml.2023.1671e | Show Introduction Hide Introduction
Empagliflozin (Jardiance) for Type 2 Diabetes in Children (online only)
The Medical Letter on Drugs and Therapeutics • Aug 21, 2023 (Issue 1683)
≥10 years old.1
MECHANISM OF ACTION ― SGLT2 inhibitors decrease
renal glucose reabsorption ...
The sodium-glucose cotransporter 2 (SGLT2)
inhibitor empagliflozin has been available for years
alone (Jardiance – Boehringer Ingelheim) and in
combination with metformin (Synjardy) to improve
glycemic control in adults with type 2 diabetes. Both
products have now been approved for use in children
≥10 years old. Empagliflozin is the second oral drug
to become available in the US for treatment of type
2 diabetes in children; metformin has been available
since 2000 for this indication. The injectable
glucagon-like peptide-1 (GLP-1) receptor agonists
liraglutide (Victoza) and...
Med Lett Drugs Ther. 2023 Aug 21;65(1683):e137 doi:10.58347/tml.2023.1683e | Show Introduction Hide Introduction
In Brief: A New Endometrial Cancer Indication for Dostarlimab (Jemperli) (online only)
The Medical Letter on Drugs and Therapeutics • Aug 21, 2023 (Issue 1683)
for curative
surgery or radiation.1
MECHANISM OF ACTION — Binding of PD-L1 and
PD-L2 to programmed death ...
The immune checkpoint inhibitor dostarlimab-gxly
(Jemperli – GSK) has been approved by the FDA for
use in combination with carboplatin and paclitaxel
for treatment of adults with mismatch repair deficient
(dMMR) or microsatellite instability-high (MSI-H)
primary advanced or recurrent endometrial cancer.
Dostarlimab was recently granted regular approval
for treatment of adults with dMMR recurrent or
advanced endometrial cancer that progressed on
or following a prior platinum-containing regimen in
any setting and who are not candidates for curative
surgery or radiation.
Med Lett Drugs Ther. 2023 Aug 21;65(1683):e138 doi:10.58347/tml.2023.1683f | Show Introduction Hide Introduction
In Brief: Anktiva for Bladder Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Jun 24, 2024 (Issue 1705)
acquisition cost
(WAC) for one dose of Anktiva is $35,800.2
MECHANISM OF ACTION — Nogapendekin alfa ...
Nogapendekin alfa inbakicept-pmln (Anktiva –
ImmunityBio), a first-in-class interleukin-15 (IL15)
receptor agonist, has been approved by the FDA for
use with Bacillus Calmette-Guérin (BCG) for treatment
of patients with BCG-unresponsive nonmuscle
invasive bladder cancer (NMIBC) with carcinoma in
situ with or without papillary tumors. Such patients
generally undergo bladder tumor resection, followed
by intravesical BCG treatment, but treatment failure
and cancer recurrence are common. The adenoviral
vector-based intravesical gene therapy nadofaragene
firadenovec-vncg (Adstiladrin)...
Med Lett Drugs Ther. 2024 Jun 24;66(1705):e105-6 doi:10.58347/tml.2024.1705e | Show Introduction Hide Introduction
Cenobamate (Xcopri) for Focal Seizures
The Medical Letter on Drugs and Therapeutics • Aug 24, 2020 (Issue 1605)
OF ACTION — Cenobamate's precise
mechanism of action is unknown. It enhances fast
and slow sodium channel ...
The FDA has approved cenobamate (Xcopri – SK Life
Science) for oral treatment of partial-onset (focal)
seizures in adults.
Osilodrostat (Isturisa) for Cushing's Disease
The Medical Letter on Drugs and Therapeutics • Feb 08, 2021 (Issue 1617)
effective for
treatment of Cushing's disease, but it has a slow onset
of action and very long half-life ...
The FDA has approved osilodrostat (Isturisa –
Recordati), a cortisol synthesis inhibitor, for oral
treatment of adults with Cushing's disease when
surgical resection of the pituitary adenoma is not an
option or has not been curative. Osilodrostat is the
first cortisol synthesis inhibitor to be approved in
the US for this indication. Other oral steroidogenesis
inhibitors such as ketoconazole and metyrapone have
been used off-label for this indication for many years.