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Searched for vol. Results 361 to 370 of 398 total matches.

In Brief: Finerenone (Kerendia) for Diabetic Kidney Disease

   
The Medical Letter on Drugs and Therapeutics • Jan 23, 2023  (Issue 1668)
Letter ® Vol. 65 (1668) January 23, 2023 CLINICAL STUDIES — The recent recommendations were based ...
Recently published guidelines from the American Diabetes Association (ADA) and the Kidney Disease: Improving Global Outcomes (KDIGO) Diabetes Work Group recommend addition of the oral nonsteroidal mineralocorticoid receptor antagonist (MRA) finerenone (Kerendia) to standard treatment in patients with type 2 diabetes and chronic kidney disease (CKD).
Med Lett Drugs Ther. 2023 Jan 23;65(1668):15-6   doi:10.58347/tml.2023.1668e |  Show IntroductionHide Introduction

Ritlecitinib (Litfulo) for Severe Alopecia Areata

   
The Medical Letter on Drugs and Therapeutics • Nov 27, 2023  (Issue 1690)
Letter® Vol. 65 (1690) drops to ...
The FDA has approved ritlecitinib (Litfulo – Pfizer), an oral JAK and TEC kinase family inhibitor, for treatment of severe alopecia areata in patients ≥12 years old. Ritlecitinib is the second oral drug to be approved in the US for treatment of severe alopecia areata; baricitinib (Olumiant), a JAK inhibitor, is approved only for use in adults.
Med Lett Drugs Ther. 2023 Nov 27;65(1690):185-6   doi:10.58347/tml.2023.1690a |  Show IntroductionHide Introduction

Vonoprazan (Voquezna) for Erosive Esophagitis

   
The Medical Letter on Drugs and Therapeutics • Dec 25, 2023  (Issue 1692)
of a proton-pump inhibitor. Neurogastroenterol Motil 2023; 35:e14468. The Medical Letter ® Vol. 65 (1692 ...
The FDA has approved vonoprazan (Voquezna – Phathom), a potassium-competitive acid blocker, for healing and maintenance of healing of all grades of erosive esophagitis and relief of associated heartburn in adults. Vonoprazan is also available copackaged with amoxicillin (Voquezna Dual Pak) and with amoxicillin and clarithromycin (Voquezna Triple Pak) for treatment of Helicobacter pylori infection in adults.
Med Lett Drugs Ther. 2023 Dec 25;65(1692):203-5   doi:10.58347/tml.2023.1692b |  Show IntroductionHide Introduction

Drugs for Rosacea

   
The Medical Letter on Drugs and Therapeutics • Feb 05, 2024  (Issue 1695)
-skinned patients, and purpura.1,16 The Medical Letter ® Vol. 66 (1695) February 5, 2024 metronidazole ...
Rosacea is a common, chronic inflammatory facial eruption of unknown cause. It is more prevalent in women than in men, and disease onset typically occurs after age 30. Rosacea is characterized by erythema, telangiectasia, and flushing, and sometimes by recurrent, progressive crops of acneiform papules and pustules, usually on the central part of the face. Some patients develop granulomas and tissue hypertrophy, which may lead to rhinophyma (a bulbous nose), particularly in men. Blepharitis and conjunctivitis are common. Keratitis and corneal scarring occur rarely.
Med Lett Drugs Ther. 2024 Feb 5;66(1695):21-2   doi:10.58347/tml.2024.1695b |  Show IntroductionHide Introduction

Qlosi — Pilocarpine 0.4% Ophthalmic Solution for Presbyopia

   
The Medical Letter on Drugs and Therapeutics • Jan 06, 2025  (Issue 1719)
meters on day 8. 3. The primary endpoint.2 The Medical Letter ® Vol. 66 Published online July 15, 2024 ...
The FDA has approved pilocarpine 0.4% preservativefree ophthalmic solution (Qlosi – Orasis) for treatment of presbyopia in adults. Pilocarpine 1.25% ophthalmic solution (Vuity) was approved in 2021 for the same indication. Pilocarpine 1%, 2%, and 4% ophthalmic solutions (Isopto Carpine, and others) have been available for years for treatment of glaucoma, but local (e.g., blurry vision and instillation-site pain) and systemic (e.g., sweating and GI disturbances) adverse effects have limited their use.
Med Lett Drugs Ther. 2025 Jan 6;67(1719):5-6   doi:10.58347/tml.2025.1719b |  Show IntroductionHide Introduction

Ganaxolone (Ztalmy) for CDKL5 Deficiency Disorder (online only)

   
The Medical Letter on Drugs and Therapeutics • Aug 19, 2024  (Issue 1709)
on the results of a double-blind trial (Marigold) in 101 patients 2-19 years old e140 The Medical Letter ® Vol ...
The FDA has approved ganaxolone (Ztalmy – Marinus) for oral treatment of seizures associated with cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder in patients ≥2 years old. It is the first drug to be approved in the US for this indication.
Med Lett Drugs Ther. 2024 Aug 19;66(1709):e139-40   doi:10.58347/tml.2024.1709g |  Show IntroductionHide Introduction

Iptacopan (Fabhalta) for Paroxysmal Nocturnal Hemoglobinuria (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 30, 2024  (Issue 1712)
in adult patients with PNH naive to complement inhibitors: the 301 e158 The Medical Letter ® Vol. 66 ...
The FDA has approved the complement factor B inhibitor iptacopan (Fabhalta – Novartis) for treatment of paroxysmal nocturnal hemoglobinuria (PNH) in adults. Iptacopan is the first oral drug to be approved in the US for this indication. Three parenterally administered drugs, the complement C5 inhibitors eculizumab (Soliris) and ravulizumab (Ultomiris) and the complement C3 inhibitor pegcetacoplan (Empaveli), are also approved for treatment of PNH.
Med Lett Drugs Ther. 2024 Sep 30;66(1712):e171-3   doi:10.58347/tml.2024.1712e |  Show IntroductionHide Introduction

A Renal Indication for Semaglutide (Ozempic)

   
The Medical Letter on Drugs and Therapeutics • Mar 03, 2025  (Issue 1723)
BCise were discontinued by the manufacturer in 2024. The Medical Letter ® Vol. 67 (1723) March 3, 2025 ...
The injectable glucagon-like peptide-1 (GLP-1) receptor agonist semaglutide (Ozempic – Novo Nordisk) has been approved by the FDA to reduce the risk of sustained eGFR decline, end-stage kidney disease, and cardiovascular death in adults with type 2 diabetes and chronic kidney disease (CKD). It is the first GLP-1 receptor agonist to be approved in the US for this indication.
Med Lett Drugs Ther. 2025 Mar 3;67(1723):38-40   doi:10.58347/tml.2025.1723d |  Show IntroductionHide Introduction

Rimegepant (Nurtec ODT) for Acute Treatment of Migraine

   
The Medical Letter on Drugs and Therapeutics • May 04, 2020  (Issue 1597)
(see Table 2). These effects persisted for about 48 hours.7,8 71 The Medical Letter ® Vol. 62 (1597 ...
The FDA has approved an orally disintegrating tablet (ODT) formulation of rimegepant (Nurtec ODT – Biohaven), a small-molecule calcitonin gene-related peptide (CGRP) receptor antagonist ("gepant"), for acute treatment of migraine with or without aura in adults. Rimegepant is the second oral gepant to become available in the US; ubrogepant (Ubrelvy), which is approved for the same indication, was the first. Four parenteral CGRP antagonists, erenumab (Aimovig), fremanezumab (Ajovy), galcanezumab (Emgality), and eptinezumab (Vyepti), are approved for prevention of...
Med Lett Drugs Ther. 2020 May 4;62(1597):70-2 |  Show IntroductionHide Introduction

Cetirizine Ophthalmic Solution (Zerviate) for Allergic Conjunctivitis

   
The Medical Letter on Drugs and Therapeutics • Jun 01, 2020  (Issue 1599)
The Medical Letter ® Vol. 62 (1599) June 1, 2020 The ophthalmic mast cell stabilizers cromolyn, lodoxamide ...
A 0.24% ophthalmic solution of the second-generation H1-antihistamine cetirizine (Zerviate – Eyevance) is now available by prescription for treatment of ocular itching associated with allergic conjunctivitis in patients ≥2 years old. Oral cetirizine (Zyrtec, and others), which is used for treatment of allergic conjunctivitis and rhinitis, has been available over the counter (OTC) for years.
Med Lett Drugs Ther. 2020 Jun 1;62(1599):81-3 |  Show IntroductionHide Introduction