Search Results for "treatment guidelines"
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Searched for treatment guidelines. Results 121 to 130 of 172 total matches.
Capivasertib (Truqap) for Breast Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Feb 19, 2024 (Issue 1696)
with the selective estrogen receptor degrader (SERD)
fulvestrant (Faslodex, and generics) for treatment of
hormone ...
The oral kinase inhibitor capivasertib (Truqap –
AstraZeneca), a first-in-class AKT inhibitor, has
been approved by the FDA for use in combination
with the selective estrogen receptor degrader (SERD)
fulvestrant (Faslodex, and generics) for treatment of
hormone receptor (HR)-positive, human epidermal
growth factor receptor 2 (HER2)-negative, locally
advanced or metastatic breast cancer in adults with
one or more PIK3CA/AKT1/PTEN-alterations who had
disease progression on at least one endocrine-based
regimen for metastatic disease or recurrence on or
within 12 months of completing...
Med Lett Drugs Ther. 2024 Feb 19;66(1696):e32-3 doi:10.58347/tml.2024.1696e | Show Introduction Hide Introduction
Drugs for Acne
The Medical Letter on Drugs and Therapeutics • Feb 05, 2024 (Issue 1695)
and adults.
Guidelines for treatment of acne were last published
by the American Academy of Dermatology ...
Acne is common among adolescents and adults.
Guidelines for treatment of acne were last published
by the American Academy of Dermatology in 2016.
Med Lett Drugs Ther. 2024 Feb 5;66(1695):17-20 doi:10.58347/tml.2024.1695a | Show Introduction Hide Introduction
Resmetirom (Rezdiffra) for Metabolic Dysfunction-Associated Steatohepatitis
The Medical Letter on Drugs and Therapeutics • Apr 29, 2024 (Issue 1701)
, has received accelerated
approval from the FDA for treatment of noncirrhotic
nonalcoholic steatohepatitis ...
Resmetirom (Rezdiffra – Madrigal), a thyroid hormone
receptor-beta agonist, has received accelerated
approval from the FDA for treatment of noncirrhotic
nonalcoholic steatohepatitis (NASH) with moderate
to advanced fibrosis in adults. NASH has recently
been renamed metabolic dysfunction-associated
steatohepatitis (MASH). Resmetirom is the first drug
to be approved in the US for this indication.
Med Lett Drugs Ther. 2024 Apr 29;66(1701):65-6 doi:10.58347/tml.2024.1701a | Show Introduction Hide Introduction
COVID-19 Update: Bivalent Pfizer and Moderna COVID-19 Vaccines for Booster Immunization
The Medical Letter on Drugs and Therapeutics • Oct 03, 2022 (Issue 1660)
with the
corresponding monovalent products.3,4
DOSAGE AND ADMINISTRATION – CDC guidelines
recommend that adolescents ...
The FDA has amended its Emergency Use Authorizations
(EUAs) for the mRNA COVID-19 vaccines
manufactured by Pfizer/BioNTech (Comirnaty)
and Moderna (Spikevax) to permit use of bivalent
formulations of the products as a single booster dose
in persons ≥12 years old (Pfizer) or ≥18 years old
(Moderna) whose most recent COVID-19 vaccine dose
was a monovalent product given ≥2 months previously
as a booster or for completion of a primary series. The
bivalent formulations are not authorized for primary
immunization. Monovalent Pfizer and Moderna
COVID-19 vaccines are no longer...
Omalizumab (Xolair) for Food Allergy
The Medical Letter on Drugs and Therapeutics • Apr 01, 2024 (Issue 1699)
monoclonal antibody FDA-approved for
treatment of allergic asthma, chronic rhinosinusitis
with nasal polyps ...
Omalizumab (Xolair – Genentech), a recombinant
anti-IgE monoclonal antibody FDA-approved for
treatment of allergic asthma, chronic rhinosinusitis
with nasal polyps, and chronic urticaria, has now
also been approved for use in conjunction with food
allergen avoidance to reduce IgE-mediated food
allergic reactions caused by accidental exposure in
patients ≥1 year old. Omalizumab is the first drug to
be approved in the US to reduce allergic reactions to
more than one food. Palforzia, an oral peanut allergen
powder, was approved in 2020 to mitigate allergic
reactions caused by...
Med Lett Drugs Ther. 2024 Apr 1;66(1699):54-6 doi:10.58347/tml.2024.1699b | Show Introduction Hide Introduction
Tapinarof Cream (Vtama) for Atopic Dermatitis
The Medical Letter on Drugs and Therapeutics • Mar 03, 2025 (Issue 1723)
for topical treatment of atopic
dermatitis in patients ≥2 years old. Tapinarof is the
first AhR agonist ...
Tapinarof 1% cream (Vtama – Dermavant), an aryl
hydrocarbon receptor (AhR) agonist, has been
approved by the FDA for topical treatment of atopic
dermatitis in patients ≥2 years old. Tapinarof is the
first AhR agonist to be approved in the US for this
indication. It was approved in 2022 for treatment of
plaque psoriasis in adults.
Med Lett Drugs Ther. 2025 Mar 3;67(1723):37-8 doi:10.58347/tml.2025.1723c | Show Introduction Hide Introduction
Sibeprenlimab (Voyxact) for Primary Immunoglobulin A Nephropathy
The Medical Letter on Drugs and Therapeutics • Aug 03, 2026 (Issue 1760)
renal disease.
STANDARD TREATMENT — Patients with primary IgAN are
generally treated initially ...
Sibeprenlimab (Voyxact – Otsuka), a subcutaneously
injected cytokine A proliferation-inducing ligand (APRIL)
blocker, has been granted accelerated approval by the FDA
to reduce proteinuria in adults with primary immunoglobulin
A nephropathy (IgAN; also called Berger's disease) who are
at risk for disease progression. Sibeprenlimab is the first
APRIL blocker to be approved in the US. Atacicept (Trutakna),
a B-lymphocyte stimulator and APRIL blocker, was recently
granted accelerated FDA approval for the same indication; it
will be reviewed in a future issue.
Med Lett Drugs Ther. 2026 Aug 3;68(1760):126-7 doi:10.58347/tml.2026.1760d | Show Introduction Hide Introduction
Antiviral Drugs for Seasonal Influenza for 2025-2026
The Medical Letter on Drugs and Therapeutics • Oct 27, 2025 (Issue 1740)
,
and outpatients with severe, complicated, or progressive
illness.1,3
Guidelines for treatment of community ...
Influenza is generally a self-limited illness, but complications
including pneumonia, respiratory failure, and
death can occur, especially in persons at increased
risk (see Table 1).
Med Lett Drugs Ther. 2025 Oct 27;67(1740):169-74 doi:10.58347/tml.2025.1740a | Show Introduction Hide Introduction
A New Indication for Bempedoic Acid (Nexletol)
The Medical Letter on Drugs and Therapeutics • May 13, 2024 (Issue 1702)
clinicians use lower doses for initial treatment of patients with only modest elevations of LDL-C ...
The oral adenosine triphosphate-citrate lyase (ACL)
inhibitor bempedoic acid was approved by the FDA
in 2020 for use alone (Nexletol – Esperion) and
in a fixed-dose combination with the cholesterol
absorption inhibitor ezetimibe (Nexlizet) as an adjunct
to maximally tolerated statin therapy in adults with
heterozygous familial hypercholesterolemia (HeFH)
or established atherosclerotic cardiovascular disease
(ASCVD) who require additional LDL-cholesterol
(LDL-C) lowering. The indication has now been
expanded to include reducing the risk of myocardial
infarction (MI) and coronary...
Med Lett Drugs Ther. 2024 May 13;66(1702):75-7 doi:10.58347/tml.2024.1702b | Show Introduction Hide Introduction
Inspire for Obstructive Sleep Apnea
The Medical Letter on Drugs and Therapeutics • Jul 24, 2023 (Issue 1681)
1) for treatment with the surgically
implanted hypoglossal nerve stimulation system
(Inspire Upper ...
The FDA recently expanded the eligibility criteria
(see Table 1) for treatment with the surgically
implanted hypoglossal nerve stimulation system
(Inspire Upper Airway Stimulation – Inspire Medical
Systems). The device has been advertised lately on
radio and television.
Med Lett Drugs Ther. 2023 Jul 24;65(1681):118-20 doi:10.58347/tml.2023.1681d | Show Introduction Hide Introduction
