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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 IntroductionHide 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 IntroductionHide 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 IntroductionHide 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 IntroductionHide 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 IntroductionHide 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 IntroductionHide 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 IntroductionHide 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 IntroductionHide 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.
Med Lett Drugs Ther. 2007 Apr 9;49(1258):29-31 |  Show IntroductionHide Introduction

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.
Treat Guidel Med Lett. 2003 Oct;1(14):89-92 |  Show IntroductionHide Introduction