Search Results for "Immunizations"
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Searched for Immunizations. Results 141 to 150 of 174 total matches.
Drugs for Plaque Psoriasis
The Medical Letter on Drugs and Therapeutics • Sep 30, 2024 (Issue 1712)
of skin cells,
reducing expression of immune markers. Ultraviolet
A (UVA) exposure can inactivate ...
Mild to moderate plaque psoriasis can be treated
with topical drugs and phototherapy. Patients
with moderate to severe disease generally require
systemic therapy. Guidelines for the treatment of
psoriasis with topical therapy, phototherapy, and
systemic drugs have recently been published.
Med Lett Drugs Ther. 2024 Sep 30;66(1712):153-60 doi:10.58347/tml.2024.1712a | Show Introduction Hide Introduction
In Brief: Higher-Dose Naloxone Nasal Spray (Kloxxado) for Opioid Overdose
The Medical Letter on Drugs and Therapeutics • Sep 20, 2021 (Issue 1633)
civil and criminal immunity
to laypersons who administer naloxone and to
healthcare professionals who ...
The FDA has approved a higher-dose intranasal
naloxone formulation (Kloxxado – Hikma) for
emergency treatment of opioid overdose. A single
spray of the new formulation delivers 8 mg of
naloxone; a formulation that delivers 4 mg per spray
(Narcan) was approved in 2015.
Tezepelumab (Tezspire) for Severe Asthma
The Medical Letter on Drugs and Therapeutics • Feb 21, 2022 (Issue 1644)
INTERACTIONS — Use of live-attenuated
vaccines should be avoided during treatment with
tezepelumab ...
Tezepelumab-ekko (Tezspire – AstraZeneca/Amgen),
a subcutaneously administered thymic stromal
lymphopoietin (TSLP) blocker, has been approved
by the FDA for add-on maintenance treatment of
severe asthma in patients ≥12 years old. It is the first
TSLP blocker to become available in the US and the
first biologic drug to be approved for treatment
of severe asthma without phenotypic or biomarker
limitations.
Margetuximab (Margenza) for HER2-Positive Breast Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Nov 28, 2022 (Issue 1664)
to
increase binding to activating Fc receptors, leading to
immune activation.
CLINICAL STUDIES — FDA ...
The FDA has approved margetuximab-cmkb
(Margenza – MacroGenics), a HER2/neu receptor antagonist,
for use in combination with chemotherapy
for treatment of metastatic human epidermal growth
factor receptor 2 (HER2)-positive breast cancer in
adults who received ≥2 prior anti-HER2 regimens, at
least one of which was for metastatic disease.
Lifileucel (Amtagvi): A Cellular Therapy for Melanoma (online only)
The Medical Letter on Drugs and Therapeutics • Apr 29, 2024 (Issue 1701)
lymphocyte (TIL) cell therapy,
in patients with advanced melanoma after progression on
immune checkpoint ...
Lifileucel (Amtagvi – Iovance), a tumor-derived
autologous T-cell immunotherapy, has received
accelerated approval from the FDA for one-time
treatment of adults with unresectable or metastatic
melanoma previously treated with a programmed
death receptor-1 (PD-1) inhibitor, and if BRAF V600
mutation-positive, a BRAF inhibitor with or without
a mitogen-activated kinase (MEK) inhibitor. It is the
first cellular therapy to be approved for use in solid
tumors. Accelerated approval of lifileucel was based
on objective response rates.
Med Lett Drugs Ther. 2024 Apr 29;66(1701):e77-8 doi:10.58347/tml.2024.1701h | Show Introduction Hide Introduction
Tebentafusp (Kimmtrak) for Uveal Melanoma (online only)
The Medical Letter on Drugs and Therapeutics • Jun 24, 2024 (Issue 1705)
disease usually does not respond to systemic
therapy, including immune checkpoint inhibitors ...
The FDA has approved tebentafusp-tebn (Kimmtrak –
Immunocore), a first-in-class bispecific gp100
peptide-HLA-directed CD3 T-cell engager, for
treatment of HLA-A*02:01-positive unresectable or
metastatic uveal melanoma in adults.
Med Lett Drugs Ther. 2024 Jun 24;66(1705):e107-8 doi:10.58347/tml.2024.1705f | 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)
, including immune effector cell-associated
neurotoxicity syndrome (ICANS).
DRUG INTERACTIONS ― Tarlatamab ...
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
Anifrolumab (Saphnelo) for Systemic Lupus Erythematosus
The Medical Letter on Drugs and Therapeutics • Sep 20, 2021 (Issue 1633)
vaccines should not be administered
during treatment with anifrolumab. The cost of one
300 mg/2 mL vial ...
The FDA has approved anifrolumab-fnia (Saphnelo – AstraZeneca), a type I interferon receptor antagonist, for IV treatment of adults with moderate to severe systemic lupus erythematosus (SLE) who are receiving standard treatment. Anifrolumab has not been studied in patients with severe active lupus nephritis or severe active CNS lupus. It is the first type I interferon receptor antagonist to become available
in the US.
Ciltacabtagene Autoleucel (Carvykti) for Multiple Myeloma (online only)
The Medical Letter on Drugs and Therapeutics • Nov 14, 2022 (Issue 1663)
, multiorgan
failure and death, immune effector cell-associated
neurotoxicity syndrome (ICANS), parkinsonism ...
The FDA has approved ciltacabtagene autoleucel
(Carvykti – Janssen), a B-cell maturation antigen
(BCMA)-directed genetically-modified cellular product,
for treatment of relapsed or refractory
multiple myeloma in adults who received ≥4 prior
lines of therapy, including a proteasome inhibitor,
an immunomodulatory drug, and an anti-CD38
monoclonal antibody. Carvykti is an individualized
cellular product prepared from the patient's own
T cells, which are genetically modified to express
chimeric antigen receptors (CAR) and then infused
back into the patient. Idecabtagene...
Dupilumab (Dupixent) for COPD
The Medical Letter on Drugs and Therapeutics • Jan 20, 2025 (Issue 1720)
with placebo) were
viral infection, headache, and nasopharyngitis.
DRUG INTERACTIONS — Use of live vaccines ...
The FDA has approved the subcutaneously injected
interleukin (IL)-4 receptor alpha antagonist dupilumab
(Dupixent – Sanofi/Regeneron) for add-on maintenance
treatment of adults with inadequately controlled
chronic obstructive pulmonary disease (COPD) and an
eosinophilic phenotype. Dupilumab is the first biologic
drug to be approved in the US for this indication. It has
been available for years for treatment of asthma, atopic
dermatitis, chronic rhinosinusitis with nasal polyps,
eosinophilic esophagitis, and prurigo nodularis.
Med Lett Drugs Ther. 2025 Jan 20;67(1720):11-3 doi:10.58347/tml.2025.1720c | Show Introduction Hide Introduction