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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 IntroductionHide 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 IntroductionHide 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 IntroductionHide 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.
Med Lett Drugs Ther. 2022 Oct 3;64(1660):e160 |  Show IntroductionHide Introduction

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 IntroductionHide 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 IntroductionHide 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.
Med Lett Drugs Ther. 2022 Dec 12;64(1665):e205-6 |  Show IntroductionHide Introduction

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 IntroductionHide 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 IntroductionHide 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 IntroductionHide Introduction