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Searched for f. Results 21 to 30 of 58 total matches.
Imetelstat (Rytelo) for Myelodysplastic Syndromes (online only)
The Medical Letter on Drugs and Therapeutics • Sep 30, 2024 (Issue 1712)
of beta-thalassemia and its
treatment strategies. Mol Genet Genomic Med 2021; 9:e1788.
3. F Locatelli et ...
The FDA has approved imetelstat (Rytelo – Geron),
a first-in-class telomerase inhibitor, for treatment
of low- to intermediate-1 risk myelodysplastic
syndromes (MDS) in adults with transfusion-dependent
anemia requiring 4 or more red blood cell
(RBC) units over 8 weeks who have not responded
to, are no longer responding to, or are ineligible for
erythropoiesis-stimulating agents (ESAs).
Med Lett Drugs Ther. 2024 Sep 30;66(1712):e169-70 doi:10.58347/tml.2024.1712d | Show Introduction Hide Introduction
Aprocitentan (Tryvio) for Hypertension
The Medical Letter on Drugs and Therapeutics • Jun 10, 2024 (Issue 1704)
of resistant and refractory
hypertension. Circ Res 2019; 124:1061. 3. F Angeli et al. Aprocitentan, a dual ...
The FDA has approved the dual endothelin receptor
antagonist aprocitentan (Tryvio – Idorsia) for
use in combination with other antihypertensive
drugs to treat hypertension in adults whose blood
pressure is not adequately controlled on other drugs.
Three other dual endothelin receptor antagonists,
ambrisentan (Volibris, and generics), bosentan
(Tracleer, and generics), and macitentan (Opsumit),
are available in the US for treatment of pulmonary
arterial hypertension.
Med Lett Drugs Ther. 2024 Jun 10;66(1704):92-3 doi:10.58347/tml.2024.1704b | Show Introduction Hide Introduction
Tarlatamab (Imdelltra) for Small Cell Lung Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Jul 08, 2024 (Issue 1706)
toxicity can occur.
1. F Rojo et al. International real-world study of DLL3 expression
in patients ...
Tarlatamab-dlle (Imdelltra – Amgen), a first-in-class
bispecific delta-like ligand 3 (DLL3)-directed CD3
T-cell engager, has received accelerated approval
from the FDA for treatment of extensive-stage
small cell lung cancer (SCLC) in adults who had
disease progression on or after platinum-based
chemotherapy. It is the first bispecific DLL3-directed
CD3 T-cell engager to be approved in the US for this
indication. Most patients with SCLC have a response
to initial treatment, but progression generally
occurs within a few months and overall survival is
usually less than 8 months....
Med Lett Drugs Ther. 2024 Jul 8;66(1706):e113-4 doi:10.58347/tml.2024.1706c | Show Introduction Hide Introduction
COVID-19 Update: New Novavax Vaccine Formulation for 2023-2024
The Medical Letter on Drugs and Therapeutics • Nov 13, 2023 (Issue 1689)
formulations for 2023-2024. Med Lett Drugs Ther 2023;
65:167.
3. F Dubovsky. Data in support of Novavax XBB ...
A new 2023-2024 formulation of the adjuvanted
protein subunit COVID-19 vaccine manufactured by
Novavax that was developed to more closely target
currently circulating SARS-CoV-2 variants has been
made available in the US under an FDA Emergency Use Authorization (EUA) for use in persons ≥12
years old. The original formulation of the Novavax
vaccine is no longer authorized for use in the US.
In September, updated formulations of the mRNA
COVID-19 vaccines manufactured by Pfizer/BioNTech (Comirnaty) and Moderna (Spikevax) were
licensed by the FDA for use in persons ≥12 years old
and...
Med Lett Drugs Ther. 2023 Nov 13;65(1689):182-3 doi:10.58347/tml.2023.1689b | Show Introduction Hide Introduction
Toripalimab (Loqtorzi) for Nasopharyngeal Carcinoma (online only)
The Medical Letter on Drugs and Therapeutics • Jan 22, 2024 (Issue 1694)
or metastatic nasopharyngeal carcinoma: the JUPITER-02
randomized clinical trial. JAMA 2023; 330:1961.
4. F-H ...
Toripalimab-tpzi (Loqtorzi – Coherus Biosciences),
a programmed death receptor-1 (PD-1)-blocking
antibody, has been approved by the FDA for use
in combination with cisplatin and gemcitabine for
first-line treatment of recurrent locally advanced or
metastatic nasopharyngeal carcinoma and for use as
monotherapy for treatment of recurrent unresectable
or metastatic nasopharyngeal carcinoma in adults
with disease progression on or after platinum-based
chemotherapy. It is the first immune checkpoint
inhibitor to be approved in the US for treatment of
nasopharyngeal carcinoma.
Med Lett Drugs Ther. 2024 Jan 22;66(1694):e16-7 doi:10.58347/tml.2024.1694e | Show Introduction Hide Introduction
Antibiotic Prophylaxis for Dental Procedures
The Medical Letter on Drugs and Therapeutics • Apr 29, 2024 (Issue 1701)
2021; 143:e963.
3. F Sperotto et al. Antibiotic prophylaxis and infective endocarditis
incidence ...
Since 2007, antimicrobial prophylaxis for dental
procedures has been recommended to prevent
viridans group streptococcal infective endocarditis
only for patients at highest risk of an adverse
outcome. Limiting use to such patients does not
appear to have led to an increased incidence of
infective endocarditis or increased mortality due to
infective endocarditis.
Med Lett Drugs Ther. 2024 Apr 29;66(1701):71-2 doi:10.58347/tml.2024.1701e | Show Introduction Hide Introduction
Comparison Table: Some Drugs for Maintenance Treatment of Opioid Use Disorder (online only)
The Medical Letter on Drugs and Therapeutics • Sep 04, 2023 (Issue 1684)
>77°F)
53.40
extended-release –
Vivitrol (Alkermes)
380 mg extended-release
suspension
380 mg IM ...
View Comparison Table: Some Drugs for Maintenance Treatment of Opioid Use Disorder
Med Lett Drugs Ther. 2023 Sep 4;65(1684):e144-5 doi:10.58347/tml.2023.1684b | Show Introduction Hide Introduction
Vamorolone (Agamree) for Duchenne Muscular Dystrophy
The Medical Letter on Drugs and Therapeutics • May 28, 2024 (Issue 5072)
Lett Drugs Ther 2017; 59:153.
2. F Fortunato et al. Innovative therapeutic approaches for
Duchenne ...
The FDA has approved vamorolone (Agamree –
Catalyst), an oral corticosteroid, for treatment of
Duchenne muscular dystrophy (DMD) in patients
≥2 years old. Vamorolone is the second oral
corticosteroid to be approved in the US for treatment
of DMD; deflazacort (Emflaza) was approved in 2017.
Med Lett Drugs Ther. 2024 May 28;66(5072):1-2 doi:10.58347/tml.2024.5072a | Show Introduction Hide Introduction
Givinostat (Duvyzat) for Duchenne Muscular Dystrophy
The Medical Letter on Drugs and Therapeutics • Dec 23, 2024 (Issue 1718)
Ther 2024 May 28 (epub).
3. F Fortunato et al. Innovative therapeutic approaches for
Duchenne ...
Givinostat (Duvyzat – Italfarmaco), an oral histone
deacetylase inhibitor, has been approved by the FDA
for treatment of patients ≥6 years old with Duchenne
muscular dystrophy (DMD), regardless of the DMD-causing
mutation. It is the first nonsteroidal drug to be
approved for this indication. The oral corticosteroids
deflazacort (Emflaza) and vamorolone (Agamree)
are also approved for treatment of patients with all
genetic variants of DMD.
Med Lett Drugs Ther. 2024 Dec 23;66(1718):204-5 doi:10.58347/tml.2024.1718c | Show Introduction Hide Introduction
Drugs for Opioid Use Disorder
The Medical Letter on Drugs and Therapeutics • Sep 04, 2023 (Issue 1684)
as it is not exposed to temperatures
>77°F (25°C).
ALTERNATIVES — Limited data suggest that 24-hour
extended-release ...
Opioid use disorder is a chronic, relapsing disease with
physical and psychiatric components. It is associated
with economic hardship, social isolation, incarceration,
increased rates of blood-borne infections such as HIV
and viral hepatitis, adverse pregnancy outcomes, and
increased mortality. According to the NIH, there were
80,411 deaths involving an opioid in the US in 2021,
more than in any previous year. Several guidelines on
the management of opioid use disorder are available;
all recommend maintenance pharmacotherapy as the
standard of care.
Med Lett Drugs Ther. 2023 Sep 4;65(1684):137-44 doi:10.58347/tml.2023.1684a | Show Introduction Hide Introduction