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Searched for action. Results 41 to 50 of 329 total matches.

Ensifentrine (Ohtuvayre) for COPD

   
The Medical Letter on Drugs and Therapeutics • Aug 19, 2024  (Issue 1709)
of PDE3 and PDE4 to be approved by the FDA, and the first inhaled drug with a new mechanism of action ...
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 IntroductionHide Introduction

Suzetrigine (Journavx) — A Sodium Channel Blocker for Acute Pain

   
The Medical Letter on Drugs and Therapeutics • Mar 03, 2025  (Issue 1723)
state of the channel, suzetrigine inhibits the generation of action potentials that act as pain signals ...
The FDA has approved suzetrigine (Journavx – Vertex), a selective sodium channel blocker, for oral treatment of moderate to severe acute pain in adults. Suzetrigine is the first sodium channel blocker to be approved in the US for this indication and the first oral nonopioid drug to be approved for treatment of pain in over 25 years.
Med Lett Drugs Ther. 2025 Mar 3;67(1723):33-5   doi:10.58347/tml.2025.1723a |  Show IntroductionHide Introduction

In Brief: Expanded Indication for Elevidys

   
The Medical Letter on Drugs and Therapeutics • Aug 19, 2024  (Issue 1709)
. MECHANISM OF ACTION — Delandistrogene moxeparvovec is a nonreplicating, recombinant AAV vector-based ...
The adeno-associated virus (AAV) vector-based gene therapy delandistrogene moxeparvovec-rokl (Elevidys – Sarepta) received accelerated approval from the FDA in 2023 for treatment of ambulatory children 4-5 years old with Duchenne muscular dystrophy (DMD) who have a confirmed mutation in the DMD gene. It has now received full approval for use in ambulatory patients ≥4 years old and accelerated approval for use in nonambulatory patients with DMD.
Med Lett Drugs Ther. 2024 Aug 19;66(1709):135-6   doi:10.58347/tml.2024.1709e |  Show IntroductionHide Introduction

Timing of Remdesivir for COVID-19

   
The Medical Letter on Drugs and Therapeutics • Oct 19, 2020  (Issue 1609)
hospitalized with severe disease.1 MECHANISM OF ACTION — Remdesivir is a nucleotide prodrug of an adenosine ...
Remdesivir (Veklury – Gilead), an investigational antiviral drug administered by IV infusion, is now available through an FDA Emergency Use Authorization (EUA) for treatment of COVID-19 in all hospitalized patients. An earlier EUA limited use of the drug to patients hospitalized with severe disease.
Med Lett Drugs Ther. 2020 Oct 19;62(1609):161 |  Show IntroductionHide Introduction

In Brief: Adstiladrin – A Gene Therapy for Bladder Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • Mar 06, 2023  (Issue 1671)
acquisition cost (WAC) for one 75-mL dose of Adstiladrin is $60,000.2 MECHANISM OF ACTION — Nadofaragene ...
Nadofaragene firadenovec-vncg (Adstiladrin – Ferring), an adenoviral vector-based gene therapy, has been approved by the FDA for treatment of adults with high-risk Bacillus Calmette-Guérin (BCG)-unresponsive non-muscle invasive bladder cancer (NMIBC) with carcinoma in situ with or without papillary tumors. It is the first adenoviral vector-based gene therapy to be approved in the US for this indication. The immune checkpoint inhibitor pembrolizumab (Keytruda) was approved for the same indication in 2021.
Med Lett Drugs Ther. 2023 Mar 6;65(1671):e40-1   doi:10.58347/tml.2023.1671e |  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)
≥10 years old.1 MECHANISM OF ACTION ― SGLT2 inhibitors decrease renal glucose reabsorption ...
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: A New Endometrial Cancer Indication for Dostarlimab (Jemperli) (online only)

   
The Medical Letter on Drugs and Therapeutics • Aug 21, 2023  (Issue 1683)
for curative surgery or radiation.1 MECHANISM OF ACTION — Binding of PD-L1 and PD-L2 to programmed death ...
The immune checkpoint inhibitor dostarlimab-gxly (Jemperli – GSK) has been approved by the FDA for use in combination with carboplatin and paclitaxel for treatment of adults with mismatch repair deficient (dMMR) or microsatellite instability-high (MSI-H) primary advanced or recurrent endometrial cancer. Dostarlimab was recently granted regular approval for treatment of adults with dMMR recurrent or advanced endometrial cancer that progressed on or following a prior platinum-containing regimen in any setting and who are not candidates for curative surgery or radiation.
Med Lett Drugs Ther. 2023 Aug 21;65(1683):e138   doi:10.58347/tml.2023.1683f |  Show IntroductionHide Introduction

In Brief: Anktiva for Bladder Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • Jun 24, 2024  (Issue 1705)
acquisition cost (WAC) for one dose of Anktiva is $35,800.2 MECHANISM OF ACTION — Nogapendekin alfa ...
Nogapendekin alfa inbakicept-pmln (Anktiva – ImmunityBio), a first-in-class interleukin-15 (IL15) receptor agonist, has been approved by the FDA for use with Bacillus Calmette-Guérin (BCG) for treatment of patients with BCG-unresponsive nonmuscle invasive bladder cancer (NMIBC) with carcinoma in situ with or without papillary tumors. Such patients generally undergo bladder tumor resection, followed by intravesical BCG treatment, but treatment failure and cancer recurrence are common. The adenoviral vector-based intravesical gene therapy nadofaragene firadenovec-vncg (Adstiladrin)...
Med Lett Drugs Ther. 2024 Jun 24;66(1705):e105-6   doi:10.58347/tml.2024.1705e |  Show IntroductionHide Introduction

Cenobamate (Xcopri) for Focal Seizures

   
The Medical Letter on Drugs and Therapeutics • Aug 24, 2020  (Issue 1605)
OF ACTION — Cenobamate's precise mechanism of action is unknown. It enhances fast and slow sodium channel ...
The FDA has approved cenobamate (Xcopri – SK Life Science) for oral treatment of partial-onset (focal) seizures in adults.
Med Lett Drugs Ther. 2020 Aug 24;62(1605):134-6 |  Show IntroductionHide Introduction

Osilodrostat (Isturisa) for Cushing's Disease

   
The Medical Letter on Drugs and Therapeutics • Feb 08, 2021  (Issue 1617)
effective for treatment of Cushing's disease, but it has a slow onset of action and very long half-life ...
The FDA has approved osilodrostat (Isturisa – Recordati), a cortisol synthesis inhibitor, for oral treatment of adults with Cushing's disease when surgical resection of the pituitary adenoma is not an option or has not been curative. Osilodrostat is the first cortisol synthesis inhibitor to be approved in the US for this indication. Other oral steroidogenesis inhibitors such as ketoconazole and metyrapone have been used off-label for this indication for many years.
Med Lett Drugs Ther. 2021 Feb 8;63(1617):21-3 |  Show IntroductionHide Introduction