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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 Introduction Hide 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 Introduction Hide 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 Introduction Hide 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 Introduction Hide 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 Introduction Hide 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 Introduction Hide 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 Introduction Hide 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 Introduction Hide 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...
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.