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Searched for days. Results 281 to 290 of 477 total matches.
Cantharidin Topical Solution (Ycanth) for Molluscum Contagiosum
The Medical Letter on Drugs and Therapeutics • Feb 19, 2024 (Issue 1696)
achieved complete clearance of
all molluscum contagiosum lesions by day 84, compared to
15-20 ...
The FDA has approved cantharidin 0.7% solution
(Ycanth – Verrica) for topical treatment of molluscum
contagiosum in patients ≥2 years old. Ycanth
was the first drug to be approved in the US for this
indication. A 10.3% gel formulation of berdazimer
(Zelsuvmi), a nitric oxide-releasing agent, has
also been approved by the FDA for treatment of
molluscum contagiosum (in patients ≥1 year old); it
will be reviewed in a future issue.
Med Lett Drugs Ther. 2024 Feb 19;66(1696):27-9 doi:10.58347/tml.2024.1696b | Show Introduction Hide Introduction
Tovorafenib (Ojemda) for Pediatric Low-Grade Glioma (online only)
The Medical Letter on Drugs and Therapeutics • Jun 10, 2024 (Issue 1704)
Tovorafenib (Ojemda) for Pediatric Low-Grade Glioma
Tovorafenib (Ojemda – Day One), a type II RAF ...
Tovorafenib (Ojemda – Day One), a type II RAF kinase
inhibitor, has received accelerated approval from the
FDA for treatment of patients ≥6 months old with
relapsed or refractory pediatric low-grade glioma
harboring a BRAF fusion or rearrangement or a BRAF
V600 mutation. Tovorafenib is the first systemic
treatment to be approved in the US for pediatric
low-grade gliomas with BRAF fusions. Accelerated
approval of tovorafenib was based on response rates
and duration of response.
Med Lett Drugs Ther. 2024 Jun 10;66(1704):e97-8 doi:10.58347/tml.2024.1704f | Show Introduction Hide Introduction
Comparison Chart: Some Inhaled Drugs for Treatment of Asthma (online only)
The Medical Letter on Drugs and Therapeutics • Nov 25, 2024 (Issue 1716)
mcg/d
High: 200 mcg/d
5-11 yrs: 50 mcg once/day 208.505
Fluticasone propionate –
authorized ...
View the Comparison Chart: Some Inhaled Drugs for Treatment of Asthma
Med Lett Drugs Ther. 2024 Nov 25;66(1716):e192-5 doi:10.58347/tml.2024.1716b | Show Introduction Hide Introduction
COVID-19 Update: Novavax Vaccine Authorized for Adolescents 12-17 Years Old (online only)
The Medical Letter on Drugs and Therapeutics • Oct 03, 2022 (Issue 1660)
with that in
415 adults 18-25 years old. At 14 days after the
second dose, the geometric mean anti-SARS-CoV-2 ...
The FDA has expanded its Emergency Use
Authorization for the adjuvanted protein subunit
COVID-19 vaccine manufactured by Novavax to
include use of the vaccine as a two-dose primary
series in adolescents 12-17 years old. The vaccine
was authorized for primary immunization of adults in
July 2022.
Empagliflozin (Jardiance) for Type 2 Diabetes in Children (online only)
The Medical Letter on Drugs and Therapeutics • Aug 21, 2023 (Issue 1683)
daily
dose is 25 mg/2000 mg. The wholesale acquisition
cost for a 30-day supply of Jardiance ...
The sodium-glucose cotransporter 2 (SGLT2)
inhibitor empagliflozin has been available for years
alone (Jardiance – Boehringer Ingelheim) and in
combination with metformin (Synjardy) to improve
glycemic control in adults with type 2 diabetes. Both
products have now been approved for use in children
≥10 years old. Empagliflozin is the second oral drug
to become available in the US for treatment of type
2 diabetes in children; metformin has been available
since 2000 for this indication. The injectable
glucagon-like peptide-1 (GLP-1) receptor agonists
liraglutide (Victoza) and...
Med Lett Drugs Ther. 2023 Aug 21;65(1683):e137 doi:10.58347/tml.2023.1683e | Show Introduction Hide Introduction
In Brief: New FDA Warning of Pulmonary Aspiration with GLP-1 Receptor Agonists
The Medical Letter on Drugs and Therapeutics • Dec 23, 2024 (Issue 1718)
recommended
withholding GLP-1 receptor agonists on the day
of elective surgery for those ...
The package inserts of the GLP-1 receptor agonists
dulaglutide (Trulicity), exenatide (Byetta, Bydureon
BCise), liraglutide (Saxenda, Victoza), and semaglutide
(Ozempic, Rybelsus, Wegovy) and the dual glucosedependent
insulinotropic polypeptide (GIP)/GLP-1
receptor agonist tirzepatide (Mounjaro, Zepbound)
have been updated to include rare postmarketing
reports of pulmonary aspiration associated with their
use in patients undergoing elective surgery or other
procedures requiring general anesthesia or deep
sedation who had residual gastric contents despite
preoperative...
Med Lett Drugs Ther. 2024 Dec 23;66(1718):201-2 doi:10.58347/tml.2024.1718a | Show Introduction Hide Introduction
Mirvetuximab Soravtansine (Elahere) for Ovarian, Fallopian Tube, and Primary Peritoneal Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Dec 12, 2022 (Issue 1665)
for one 21-day treatment cycle for a
patient with an adjusted ideal body weight of 70 kg. WAC ...
Mirvetuximab soravtansine-gynx (Elahere – Immuno-Gen), an antibody-drug conjugate, has received
accelerated approval by the FDA for treatment
of folate receptor (FR) alpha-positive, platinum-resistant
epithelial ovarian, fallopian tube, or primary
peritoneal cancer in adults who received 1-3 prior
lines of systemic therapy. Accelerated approval
was based on the overall response rate and median
duration of response.
Adagrasib (Krazati) for NSCLC (online only)
The Medical Letter on Drugs and Therapeutics • Jan 23, 2023 (Issue 1668)
toxicity occurs.
▶ Cost: A 30-day supply costs $19,750.
▶ Conclusion: Adagrasib was modestly effective ...
Adagrasib (Krazati – Mirati Therapeutics), a RAS
GTPase family inhibitor, has received accelerated
approval from the FDA for oral treatment of KRAS
G12C-mutated locally advanced or metastatic non-small
cell lung cancer (NSCLC) in adults who received
at least one prior systemic therapy. Accelerated
approval was based on the objective response rate
and duration of response.
Med Lett Drugs Ther. 2023 Jan 23;65(1668):e17-8 doi:10.58347/tml.2023.1668f | Show Introduction Hide Introduction
Eflapegrastim (Rolvedon) for Prevention of Chemotherapy-Induced Febrile Neutropenia
The Medical Letter on Drugs and Therapeutics • May 29, 2023 (Issue 1677)
of G-CSF) or pegfilgrastim (6 mg
of G-CSF) SC one day after receiving chemotherapy
in each cycle ...
Eflapegrastim-xnst ((Rolvedon) [Spectrum]; previously
called Rolontis), a granulocyte colony-stimulating
factor (G-CSF) conjugated to an Fc fragment of human
IgG4, has been approved by the FDA to decrease
the incidence of infection, as manifested by febrile
neutropenia, in adults with nonmyeloid malignancies
receiving myelosuppressive chemotherapy that can
cause clinically significant febrile neutropenia.
Med Lett Drugs Ther. 2023 May 29;65(1677):83-4 doi:10.58347/tml.2023.1677b | Show Introduction Hide Introduction
Aprocitentan (Tryvio) for Hypertension
The Medical Letter on Drugs and Therapeutics • Jun 10, 2024 (Issue 1704)
: 12.5 mg PO once/day.
▶ Cost: A 30-day supply costs $775.
▶ Conclusion: Better established, less ...
The FDA has approved the dual endothelin receptor
antagonist aprocitentan (Tryvio – Idorsia) for
use in combination with other antihypertensive
drugs to treat hypertension in adults whose blood
pressure is not adequately controlled on other drugs.
Three other dual endothelin receptor antagonists,
ambrisentan (Volibris, and generics), bosentan
(Tracleer, and generics), and macitentan (Opsumit),
are available in the US for treatment of pulmonary
arterial hypertension.
Med Lett Drugs Ther. 2024 Jun 10;66(1704):92-3 doi:10.58347/tml.2024.1704b | Show Introduction Hide Introduction