Search Results for "type 2 diabetes"
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Searched for type 2 diabetes. Results 31 to 40 of 57 total matches.
In Brief: Semaglutide (Wegovy) for Weight Loss in Children
The Medical Letter on Drugs and Therapeutics • Feb 20, 2023 (Issue 1670)
as Ozempic and
Rybelsus for treatment of type 2 diabetes in adults.2
GUIDELINES — Recently published ...
The injectable glucagon-like peptide-1 (GLP-1)
receptor agonist semaglutide (Wegovy), which was
approved by the FDA in 2021 for chronic weight
management in adults, has now been approved for
chronic weight management in children ≥12 years old
with an initial BMI in the ≥95th percentile for age and
sex.Semaglutide is also available as Ozempic and
Rybelsus for treatment of type 2 diabetes in adults.
Med Lett Drugs Ther. 2023 Feb 20;65(1670):31-2 doi:10.58347/tml.2023.1670d | Show Introduction Hide Introduction
Teplizumab (Tzield) to Delay Onset of Type 1 Diabetes
The Medical Letter on Drugs and Therapeutics • Jan 09, 2023 (Issue 1667)
≥8 years old who have stage 2 type 1
diabetes. It is the first drug to become available ...
Teplizumab-mzwv (Tzield – Provention Bio), an anti-CD3 monoclonal antibody, has been approved by the
FDA to delay the onset of stage 3 type 1 diabetes
in patients ≥8 years old who have stage 2 type 1
diabetes. It is the first drug to become available in the
US that delays the onset of type 1 diabetes.
Med Lett Drugs Ther. 2023 Jan 9;65(1667):7-8 doi:10.58347/tml.2023.1667c | Show Introduction Hide Introduction
In Brief: Merilog — A NovoLog Biosimilar
The Medical Letter on Drugs and Therapeutics • Jun 23, 2025 (Issue 1731)
of an open-label trial (GEMELLI 1)
in 597 patients with type 1 or type 2 diabetes. Patients
were randomized ...
The FDA has approved Merilog (Sanofi), a biosimilar to
rapid-acting insulin aspart (NovoLog), for treatment of
patients with type 1 or type 2 diabetes. Merilog is the
first rapid-acting insulin biosimilar product to become
available in the US.
Med Lett Drugs Ther. 2025 Jun 23;67(1731):104 doi:10.58347/tml.2025.1731c | Show Introduction Hide Introduction
Metoclopramide Nasal Spray (Gimoti) for Diabetic Gastroparesis
The Medical Letter on Drugs and Therapeutics • Jan 11, 2021 (Issue 1615)
)
with type 1 or 2 diabetes and symptoms of gastroparesis,
intranasal metoclopramide 10 and 20 mg reduced ...
The FDA has approved Gimoti (Evoke), a nasal
spray formulation of the dopamine-2 (D2) receptor
antagonist metoclopramide, for relief of symptoms in
adults with acute and recurrent diabetic gastroparesis.
Metoclopramide (Reglan, and generics) has been
available for years in conventional and orally-disintegrating
tablets and in an injectable formulation.
It is the only drug that is FDA-approved for treatment
of diabetic gastroparesis.
Comparison Table: Some FDA-Approved Drugs for Weight Management (online only)
The Medical Letter on Drugs and Therapeutics • May 30, 2022 (Issue 1651)
weeks: up
to 8%
▶ Improved cardiovascular outcomes in patients with
type 2 diabetes
$1174.00 ...
View the Comparison Table: Some FDA-Approved Drugs for Weight Management
Vazalore - A New Aspirin Formulation
The Medical Letter on Drugs and Therapeutics • May 02, 2022 (Issue 1649)
CLINICAL STUDIES — A randomized, single-blind,
crossover trial in 40 obese patients with type 2
diabetes ...
The FDA has approved an over-the-counter (OTC)
liquid-filled capsule formulation of aspirin (Vazalore –
PLx Pharma). The manufacturer has been heavily
promoting Vazalore with claims of fast, predictable
absorption and antiplatelet activity and improved
gastrointestinal safety compared to existing OTC
aspirin formulations.
Tirzepatide (Zepbound) for Obstructive Sleep Apnea
The Medical Letter on Drugs and Therapeutics • Feb 17, 2025 (Issue 1722)
for treatment of type 2 diabetes.2
STANDARD TREATMENT ― OSA is common in
patients who are overweight ...
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
Dasiglucagon (Zegalogue) for Severe Hypoglycemia
The Medical Letter on Drugs and Therapeutics • Aug 23, 2021 (Issue 1631)
trials in patients with type 1 diabetes, 2 of which
have been published.5,6 Two of the trials enrolled ...
The FDA has approved dasiglucagon (Zegalogue –
Zealand) for subcutaneous (SC) treatment of severe
hypoglycemia in patients ≥6 years old with diabetes.
Dasiglucagon is the third glucagon product to be
marketed in the US that does not require reconstitution
before administration; Gvoke, a SC formulation approved for use in patients ≥2 years old, and Baqsimi,
an intranasal powder approved for use in patients
≥4 years old, have been available since 2019.
Injectable glucagon emergency kits (GlucaGen
HypoKit, and generics) have been available for years,
but they require...
Drugs for Chronic Heart Failure
The Medical Letter on Drugs and Therapeutics • May 26, 2025 (Issue 1729)
-approved to reduce renal function decline and
cardiovascular events in patients with type 2 diabetes ...
Pharmacologic management of chronic heart failure
(HF) is primarily determined by the patient's left
ventricular ejection fraction (LVEF) and severity of
symptoms. Patients with chronic HF who have an
LVEF ≤40% are considered to have heart failure with
reduced ejection fraction (HFrEF) and those with an
LVEF ≥50% are considered to have heart failure with
preserved ejection fraction (HFpEF). Patients with an
LVEF of 41-49% have heart failure with mildly reduced
or mid-range ejection fraction.
Med Lett Drugs Ther. 2025 May 26;67(1729):81-8 doi:10.58347/tml.2025.1729a | Show Introduction Hide Introduction
Inclisiran (Leqvio) for LDL-Cholesterol Lowering
The Medical Letter on Drugs and Therapeutics • Mar 21, 2022 (Issue 1646)
(type 2 diabetes, familial
hypercholesterolemia, or a 10-year risk of a cardiovascular event of
≥20 ...
The FDA has approved inclisiran (Leqvio – Novartis),
a small interfering RNA (siRNA) directed to proprotein
convertase subtilisin/kexin type 9 (PCSK9) mRNA,
as an adjunct to diet and maximally tolerated statin
therapy for subcutaneous (SC) treatment of adults
with heterozygous familial hypercholesterolemia
(HeFH) or clinical atherosclerotic cardiovascular
disease (ASCVD) who require additional lowering
of low-density lipoprotein cholesterol (LDL-C).
Inclisiran is the first FDA-approved PCSK9-directed
siRNA therapeutic agent.