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Searched for vol. Results 851 to 860 of 1617 total matches.
Donanemab (Kisunla) for Alzheimer's Disease
The Medical Letter on Drugs and Therapeutics • Aug 19, 2024 (Issue 1709)
of this material is strictly prohibited.
For further information call: 800-211-2769
The Medical Letter ® Vol. 66 ...
Donanemab-azbt (Kisunla – Lilly), an IV amyloid beta-directed
monoclonal antibody, has been approved by
the FDA for treatment of Alzheimer's disease (AD).
The label states that the drug should only be started
in patients with mild cognitive impairment (MCI) or
mild dementia. Donanemab is the third IV amyloid
beta-directed monoclonal antibody to be marketed
in the US. Lecanemab (Leqembi – Biogen/Eisai) was
approved by the FDA in 2023 for the same indication
as donanemab. Aducanumab (Aduhelm – Lilly)
was granted accelerated approval in 2021, but it
was withdrawn from the market...
Med Lett Drugs Ther. 2024 Aug 19;66(1709):129-31 doi:10.58347/tml.2024.1709a | Show Introduction Hide Introduction
Ensifentrine (Ohtuvayre) for COPD
The Medical Letter on Drugs and Therapeutics • Aug 19, 2024 (Issue 1709)
The Medical Letter ® Vol. 66 (1709) August 19, 2024
132
69% of patients in ENHANCE-1 and 55% of those ...
The FDA has approved ensifentrine (Ohtuvayre –
Verona), an inhaled phosphodiesterase (PDE) 3 and
4 inhibitor, for maintenance treatment of chronic
obstructive pulmonary disease (COPD) in adults.
It is the first dual inhibitor of PDE3 and PDE4 to be
approved by the FDA, and the first inhaled drug
with a new mechanism of action to be approved for
treatment of COPD in more than 20 years.
Med Lett Drugs Ther. 2024 Aug 19;66(1709):131-3 doi:10.58347/tml.2024.1709b | Show Introduction Hide Introduction
Risankizumab (Skyrizi) for Ulcerative Colitis
The Medical Letter on Drugs and Therapeutics • Nov 11, 2024 (Issue 1715)
: 260 mg;
>55-85 kg: 390 mg; >85 kg: 520 mg.
The Medical Letter ® Vol. 66 (1715) November 11, 2024 ...
The injectable interleukin (IL)-23 antagonist
risankizumab-rzza (Skyrizi – Abbvie), previously
approved by the FDA for treatment of Crohn's disease
(CD), has now been approved for treatment of
moderately to severely active ulcerative colitis (UC)
in adults. Risankizumab is the first IL-23 antagonist
to be approved for treatment of both CD and UC. It is
also approved for treatment of plaque psoriasis and
psoriatic arthritis.
Med Lett Drugs Ther. 2024 Nov 11;66(1715):182-4 doi:10.58347/tml.2024.1715d | Show Introduction Hide Introduction
Capvaxive – A 21-Valent Pneumococcal Conjugate Vaccine
The Medical Letter on Drugs and Therapeutics • Oct 14, 2024 (Issue 1713)
. www.fdbhealth.com/drug-pricing-policy. The Medical Letter ® Vol. 66 (1713) October 14, 2024 162 Table 2 ...
The FDA has licensed Capvaxive (PCV21; Merck),
a 21-valent pneumococcal conjugate vaccine, for
prevention of invasive pneumococcal disease (IPD)
and pneumococcal pneumonia in adults. Four other
pneumococcal vaccines are currently available in the
US: Prevnar 20 (PCV20), Vaxneuvance (PCV15), and
Prevnar 13 (PCV13) are conjugate vaccines licensed
for use in persons ≥6 weeks old, and Pneumovax 23
(PPSV23) is a pneumococcal polysaccharide vaccine
licensed for use in persons ≥2 years old (see Table 1).
Med Lett Drugs Ther. 2024 Oct 14;66(1713):161-3 doi:10.58347/tml.2024.1713a | Show Introduction Hide Introduction
Xanomeline/Trospium (Cobenfy) for Schizophrenia
The Medical Letter on Drugs and Therapeutics • Nov 11, 2024 (Issue 1715)
prohibited.
For further information call: 800-211-2769
The Medical Letter ® Vol. 66 (1715) November 11 ...
The FDA has approved Cobenfy (BMS), an oral
fixed-dose combination of the muscarinic agonist
xanomeline and the peripheral muscarinic antagonist
trospium chloride, for treatment of schizophrenia in
adults. It is the first antipsychotic drug to be approved
in the US for treatment of schizophrenia that does not
block dopamine receptors. This is the first approval
for xanomeline; trospium has been available for many
years for treatment of overactive bladder.
Med Lett Drugs Ther. 2024 Nov 11;66(1715):177-9 doi:10.58347/tml.2024.1715a | Show Introduction Hide Introduction
Oral Semaglutide (Wegovy) for Weight Loss
The Medical Letter on Drugs and Therapeutics • Feb 02, 2026 (Issue 1747)
to injectable drugs used for this indication.
The Medical Letter ® Vol. 68 (1747) February 2, 2026
DOSAGE ...
The FDA has approved an oral tablet formulation of
the glucagon-like peptide-1 (GLP-1) receptor agonist
semaglutide (Wegovy) for chronic weight management
in adults. It is the first oral GLP-1 receptor agonist to
be approved in the US for weight management. An
injectable formulation of Wegovy was approved for
the same indication in 2021.1 The injectable GLP-1
receptor agonist liraglutide (Saxenda, and generic)
and the injectable glucose-dependent insulinotropic
polypeptide (GIP)/GLP-1 receptor agonist tirzepatide
(Zepbound) are also FDA-approved for chronic weight
management (see...
Med Lett Drugs Ther. 2026 Feb 2;68(1747):17-8 doi:10.58347/tml.2026.1747a | Show Introduction Hide Introduction
A Treprostinil Inhaler (Yutrepia) for Pulmonary Hypertension
The Medical Letter on Drugs and Therapeutics • Feb 16, 2026 (Issue 1748)
Letter ® Vol. 68 (1748) February 16, 2026
28
PREGNANCY AND LACTATION — Treprostinil ...
Yutrepia (Liquidia), a dry powder inhaler formulation of
the prostacyclin analog treprostinil, has been approved
by the FDA to improve exercise ability in adults with
pulmonary arterial hypertension (PAH; WHO Group 1)
or pulmonary hypertension associated with interstitial
lung disease (PH-ILD; WHO Group 3). Tyvaso DPI,
another treprostinil dry powder inhaler, was approved
earlier for the same indication.
Med Lett Drugs Ther. 2026 Feb 16;68(1748):27-8 doi:10.58347/tml.2026.1748b | Show Introduction Hide Introduction
Leucovorin for Cerebral Folate Deficiency
The Medical Letter on Drugs and Therapeutics • May 11, 2026 (Issue 1754)
with autism could benefit from
leucovorin treatment remains to be determined.
76
The Medical Letter ® Vol ...
The FDA has approved use of oral leucovorin calcium (folinic
acid) for treatment of cerebral folate transport deficiency in
patients who have a confirmed variant in the folate receptor 1
gene (FOLR1-CFTD). It is the first drug to be approved for this
extremely rare disorder.
Med Lett Drugs Ther. 2026 May 11;68(1754):75-7 doi:10.58347/tml.2026.1754b | Show Introduction Hide Introduction
Aficamten (Myqorzo) for Obstructive Hypertrophic Cardiomyopathy
The Medical Letter on Drugs and Therapeutics • May 25, 2026 (Issue 1755)
ejection fraction (LVEF) ≥60%, and left ventricular
The Medical Letter ® Vol. 68 (1755) May 25, 2026 ...
Aficamten (Myqorzo – Cytokinetics), an oral cardiac myosin
inhibitor, has been approved by the FDA to improve functional
capacity and symptoms in adults with symptomatic obstructive
hypertrophic cardiomyopathy (HCM). It is the second cardiac
myosin inhibitor to be approved in the US for this indication;
mavacamten (Camzyos) was approved in 2022.
Med Lett Drugs Ther. 2026 May 25;68(1755):85-7 doi:10.58347/tml.2026.1755c | Show Introduction Hide Introduction
Baxdrostat (Baxfendy) — An Aldosterone Synthase Inhibitor for Hypertension
The Medical Letter on Drugs and Therapeutics • Jul 06, 2026 (Issue 1758)
-2769
106
The Medical Letter ® Vol. 68 (1758) July 6, 2026
to receive once-daily add-on treatment ...
The FDA has approved baxdrostat (Baxfendy – AstraZeneca),
an oral aldosterone synthase inhibitor, for add-on treatment
of hypertension in adults whose blood pressure is not
adequately controlled on other drugs. Baxdrostat is the first
aldosterone synthase inhibitor to become available in the US.
Med Lett Drugs Ther. 2026 Jul 6;68(1758):105-6 doi:10.58347/tml.2026.1758a | Show Introduction Hide Introduction
