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Searched for activate. Results 1061 to 1070 of 1349 total matches.
Lecanemab (Leqembi) for Alzheimer's Disease
The Medical Letter on Drugs and Therapeutics • Feb 06, 2023 (Issue 1669)
and memantine have produced modest improvements
in cognition, activities of daily living, and behavior ...
Lecanemab-irmb (Leqembi – Biogen/Eisai), an IV
amyloid beta-directed monoclonal antibody, has
received accelerated approval from the FDA for
treatment of Alzheimer's disease. The label states
that treatment with Leqembi should be initiated in
patients with mild cognitive impairment (MCI) or
mild dementia, the population in which the drug was
initiated in clinical trials. Lecanemab is the second
IV amyloid-beta directed monoclonal antibody to be
approved for this indication; aducanumab (Aduhelm)
was approved in 2021 and has the same restrictions
on treatment...
Med Lett Drugs Ther. 2023 Feb 6;65(1669):17-8 doi:10.58347/tml.2023.1669a | Show Introduction Hide Introduction
AD-Detect — A Blood Test for Alzheimer's Disease
The Medical Letter on Drugs and Therapeutics • Oct 30, 2023 (Issue 1688)
), and
glial fibrillary acidic protein (GFAP; a marker of
abnormal activation and proliferation of astrocytes ...
AD-Detect (Quest), a blood test to evaluate
Alzheimer's disease risk, is being marketed directly
to consumers. It has not been cleared or approved
by the FDA (laboratory-developed tests like this
one currently do not need FDA authorization to be
marketed).
Med Lett Drugs Ther. 2023 Oct 30;65(1688):175-6 doi:10.58347/tml.2023.1688b | Show Introduction Hide Introduction
Capivasertib (Truqap) for Breast Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Feb 19, 2024 (Issue 1696)
and antiproliferative antitumor activity.3
CLINICAL STUDIES ― FDA approval of capivasertib
was based on the results ...
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
Resmetirom (Rezdiffra) for Metabolic Dysfunction-Associated Steatohepatitis
The Medical Letter on Drugs and Therapeutics • Apr 29, 2024 (Issue 1701)
(with minimal changes in active
MASH — Nonalcoholic fatty liver disease (recently
renamed metabolic ...
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
Antibiotic Prophylaxis for Dental Procedures
The Medical Letter on Drugs and Therapeutics • Apr 29, 2024 (Issue 1701)
is the antibiotic of
choice in patients without penicillin allergy because
of its bioavailability and activity ...
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
Landiolol (Rapiblyk) for Short-Term Rate Control in Supraventricular Tachycardia
The Medical Letter on Drugs and Therapeutics • May 12, 2025 (Issue 1728)
by pseudocholinesterases and
carboxylesterases to less active metabolite
Elimination Urine (89-99%)
Half-life ~4 minutes ...
The FDA has approved the intravenously administered
beta1-adrenergic blocker landiolol (Rapiblyk – AOP)
for short-term reduction of ventricular rate in adults
with supraventricular tachycardia including atrial
fibrillation and atrial flutter. Esmolol (Brevibloc, and
generics), another IV beta blocker, was approved
earlier for the same indication.
Med Lett Drugs Ther. 2025 May 12;67(1728):75-6 doi:10.58347/tml.2025.1728b | Show Introduction Hide Introduction
Mepolizumab (Nucala) for COPD
The Medical Letter on Drugs and Therapeutics • Aug 18, 2025 (Issue 1735)
is the major cytokine
responsible for the proliferation, differentiation, recruitment,
and activation ...
Mepolizumab (Nucala – GSK), a subcutaneously
injected interleukin-5 (IL-5) antagonist, has been
approved by the FDA for add-on maintenance
treatment of adults who have inadequately controlled
chronic obstructive pulmonary disease (COPD) with an
eosinophilic phenotype. Mepolizumab is also approved
for treatment of asthma, chronic rhinosinusitis with
nasal polyps, eosinophilic granulomatosis with
polyangiitis, and hypereosinophilic syndrome.
Med Lett Drugs Ther. 2025 Aug 18;67(1735):131-2 doi:10.58347/tml.2025.1735b | Show Introduction Hide Introduction
A New Heart Failure Indication for Finerenone (Kerendia)
The Medical Letter on Drugs and Therapeutics • Sep 15, 2025 (Issue 1737)
have been reported. Unlike
spironolactone, finerenone has no significant antiandrogenic
activity.
DOSAGE ...
The FDA has approved the nonsteroidal mineralocorticoid
receptor antagonist (MRA) finerenone
(Kerendia) to reduce the risk of cardiovascular death,
hospitalization for heart failure (HF), and urgent HF
visits in adults with HF with a left ventricular ejection
fraction (LVEF) ≥40%. Finerenone was approved in
2021 to reduce the risk of kidney disease progression
and cardiovascular events in adults with chronic
kidney disease (CKD) associated with type 2 diabetes.
Med Lett Drugs Ther. 2025 Sep 15;67(1737):146-8 doi:10.58347/tml.2025.1737b | Show Introduction Hide Introduction
Aliskiren (Tekturna) for Hypertension
The Medical Letter on Drugs and Therapeutics • Apr 09, 2007 (Issue 1258)
to increase
plasma renin activity (PRA) because it binds renin with
high affinity in plasma.
1,2
In one ...
Aliskiren (ah LIS ker in; Tekturna - Novartis), the first direct renin inhibitor, has been approved by the FDA for treatment of hypertension. It is indicated for oral use either as monotherapy or in combination with other antihypertensive agents.
Drugs for Assisted Reproduction
Treatment Guidelines from The Medical Letter • Oct 01, 2003 (Issue 14)
is generally tried first in anovulatory or oligo-ovulatory
women with endogenous estrogen activity and normal ...
Infertility occurs in about 15% of couples. About one third of infertility is due to problems with ovulation or an anatomic abnormality of the fallopian tube or peritoneum, such as scarring, adhesions or endometriosis. Another third is due to a male infertility factor, most commonly insufficient sperm production or abnormal motility or morphology. The remaining third is unexplained. In older women unexplained infertility is probably caused by diminished quality and quantity of oocytes, decreased implantation and spontaneous pregnancy wastage.