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Oral Fingolimod (Gilenya) for Multiple Sclerosis
The Medical Letter on Drugs and Therapeutics • Dec 13, 2010 (Issue 1353)
to fingolimod phosphate, which interacts with
sphingosine 1-phosphate (S1P) receptors to block lymphocyte ...
The FDA has approved the marketing of fingolimod
(Gilenya – Novartis) to reduce the frequency of clinical
exacerbations and delay the accumulation of physical
disability in patients with relapsing forms of multiple
sclerosis (MS). Fingolimod is the first oral drug
approved for this indication.
Tirzepatide (Zepbound) for Obstructive Sleep Apnea
The Medical Letter on Drugs and Therapeutics • Feb 17, 2025 (Issue 1722)
The injectable glucose-dependent insulinotropic
polypeptide (GIP)/glucagon-like peptide-1 (GLP-1)
receptor ...
The injectable glucose-dependent insulinotropic
polypeptide (GIP)/glucagon-like peptide-1 (GLP-1)
receptor agonist tirzepatide (Zepbound) has been
approved by the FDA for treatment of moderate to
severe obstructive sleep apnea (OSA) in adults with
obesity. It is the first drug to be approved in the US for
this indication. Zepbound is also approved for chronic
weight management in adults with obesity and in those
who are overweight and have at least one weightrelated
comorbidity. Tirzepatide is also available as
Mounjaro for treatment of type 2 diabetes.
Med Lett Drugs Ther. 2025 Feb 17;67(1722):29-31 doi:10.58347/tml.2025.1722c | Show Introduction Hide Introduction
In Brief: Widaplik — Another Three-Drug Combination for Hypertension
The Medical Letter on Drugs and Therapeutics • Jun 22, 2026 (Issue 1757)
and Tribenzor) have
been available for years
(see Table 1).1
Table 1. ARB/Calcium Channel Blocker/Diuretic ...
The FDA has approved Widaplik (Azurity), a fixed-dose
combination of the angiotensin receptor blocker (ARB)
telmisartan, the dihydropyridine calcium channel blocker
amlodipine, and the thiazide-like diuretic indapamide, for
treatment of hypertension in adults. Telmisartan, amlodipine,
and indapamide are also available alone and in various
combinations for treatment of hypertension. Two three-drug
combinations containing an ARB, amlodipine, and the thiazide
diuretic hydrochlorothiazide (Exforge HCT and Tribenzor) have
been available for years
(see Table 1).
Med Lett Drugs Ther. 2026 Jun 22;68(1757):101-2 doi:10.58347/tml.2026.1757d | Show Introduction Hide Introduction
Paxlovid for Treatment of COVID-19
The Medical Letter on Drugs and Therapeutics • Jan 24, 2022 (Issue 1642)
Authorization (EUA) for the investigational
antiviral drug nirmatrelvir copackaged with the HIV-1
protease ...
On December 22, 2021, the FDA issued an Emergency
Use Authorization (EUA) for the investigational
antiviral drug nirmatrelvir copackaged with the HIV-1
protease inhibitor ritonavir (Paxlovid – Pfizer) for
oral treatment of mild to moderate COVID-19 in
outpatients ≥12 years old who weigh at least 40 kg
and are at high risk of progressing to severe disease,
including hospitalization or death. Paxlovid was the
first oral antiviral drug to be authorized in the US for
treatment of COVID-19; Merck's oral antiviral drug
molnupiravir was granted an EUA for treatment of
COVID-19 on...
Bunavail: Another Buprenorphine/Naloxone Formulation for Opioid Dependence
The Medical Letter on Drugs and Therapeutics • Feb 02, 2015 (Issue 1461)
sublingual tablet.1
CLINICAL STUDIES — An unpublished, 12-week, openlabel,
uncontrolled trial conducted ...
The FDA has approved a buccal film formulation of the
partial opioid agonist buprenorphine combined with
the opioid antagonist naloxone (Bunavail – BioDelivery
Sciences) for maintenance treatment of opioid
dependence. Sublingual tablet and film formulations
of the same combination were approved earlier. The
manufacturer of Bunavail claims that the new product
is superior to sublingual formulations because of
the convenience of buccal administration and better
absorption into the blood, permitting use of lower doses.
An EUA for Bamlanivimab - A Monoclonal Antibody for COVID-19
The Medical Letter on Drugs and Therapeutics • Nov 30, 2020 (Issue 1612)
to severe disease and/or hospitalization (see Table 1).1 Monoclonal antibodies, such as bamlanivimab ...
The investigational neutralizing IgG1 monoclonal
antibody bamlanivimab (LY-CoV555; Lilly) has
been granted an FDA Emergency Use Authorization
(EUA) for treatment of recently diagnosed mild
to moderate COVID-19 in patients who are ≥12
years old, weigh at least 40 kg, and are at high
risk for progressing to severe disease and/or
hospitalization (see Table 1).
A Dexamethasone Ophthalmic Insert (Dextenza) for Allergic Conjunctivitis
The Medical Letter on Drugs and Therapeutics • Mar 20, 2023 (Issue 1672)
of allergic conjunctivitis was based
on the results of 3 randomized, double-masked
trials (1 published; 2 ...
The FDA has approved Dextenza (Ocular Therapeutix),
a dexamethasone ophthalmic insert, for
treatment of ocular itching associated with allergic
conjunctivitis. Dextenza was approved earlier for
treatment of ocular inflammation and pain following
ophthalmic surgery.
Med Lett Drugs Ther. 2023 Mar 20;65(1672):45-6 doi:10.58347/tml.2023.1672b | Show Introduction Hide Introduction
Retifanlimab (Zynyz) for Anal Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Jul 21, 2025 (Issue 1733)
(Zynyz – Incyte), a programmed
death receptor-1 (PD-1)-blocking antibody, has been
approved by the FDA ...
Retifanlimab-dlwr (Zynyz – Incyte), a programmed
death receptor-1 (PD-1)-blocking antibody, has been
approved by the FDA for use in combination with
carboplatin and paclitaxel for first-line treatment of
unresectable locally recurrent or metastatic squamous
cell carcinoma of the anal canal (SCAC) and as
monotherapy in patients who had disease progression
or intolerance to platinum-based chemotherapy. The
drug received accelerated approval for treatment of
recurrent locally advanced or metastatic Merkel cell
carcinoma in 2023.
Med Lett Drugs Ther. 2025 Jul 21;67(1733):e126-7 doi:10.58347/tml.2025.1733m | Show Introduction Hide Introduction
In Brief: An Expanded Indication for Afrezza
The Medical Letter on Drugs and Therapeutics • Oct 26, 2026 (Issue 1766)
-acting inhaled human insulin Afrezza (MannKind),
which was approved in 2014 for treatment of type 1 ...
The rapid-acting inhaled human insulin Afrezza (MannKind),
which was approved in 2014 for treatment of type 1 or type
2 diabetes in adults, has now been approved by the FDA for
use in children ≥6 years old.
Med Lett Drugs Ther. 2026 Oct 26;68(1766):174-5 doi:10.58347/tml.2026.1766d | Show Introduction Hide Introduction
Fluticasone Furoate (Veramyst) for Allergic Rhinitis
The Medical Letter on Drugs and Therapeutics • Nov 05, 2007 (Issue 1273)
for the glucocorticoid receptor is
1.7 times that of fluticasone propionate, and it is a
more potent inhibitor ...
Fluticasone furoate nasal spray (Veramyst - GSK) is now available for once-daily treatment of seasonal and perennial allergic rhinitis in adults and children ≥2 years old. It is similar to fluticasone propionate nasal spray (Flonase, and others), which is now available generically.
