Search Results for "treatment guidelines"
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Searched for treatment guidelines. Results 101 to 110 of 172 total matches.

In Brief: Vybrique — Sildenafil Oral Film for Erectile Dysfunction

   
The Medical Letter on Drugs and Therapeutics • May 11, 2026  (Issue 1754)
(PDE5) inhibitor sildenafil, for treatment of erectile dysfunction (ED). Sildenafil oral tablets ...
The FDA has approved Vybrique (IBSA), an oral film formulation of the phosphodiesterase type 5 (PDE5) inhibitor sildenafil, for treatment of erectile dysfunction (ED). Sildenafil oral tablets (Viagra, and generics) have been available since 1998. The manufacturer is promoting the new product as a "discreet, on-the-go" option that can be taken without water.
Med Lett Drugs Ther. 2026 May 11;68(1754):78-9   doi:10.58347/tml.2026.1754e |  Show IntroductionHide Introduction

Iloperidone (Fanapt) — A New Indication for Bipolar Disorder

   
The Medical Letter on Drugs and Therapeutics • Jul 22, 2024  (Issue 1707)
and Anxiety Treatments (CANMAT) and International Society for Bipolar Disorders (ISBD) 2018 guidelines ...
The oral second-generation antipsychotic drug iloperidone (Fanapt – Vanda) has been approved by the FDA for acute treatment of manic or mixed episodes associated with bipolar I disorder in adults. First approved in 2009 for treatment of schizophrenia, iloperidone is the eighth second-generation antipsychotic to be approved for acute treatment of manic or mixed episodes of bipolar I disorder (see Table 1).
Med Lett Drugs Ther. 2024 Jul 22;66(1707):115-6   doi:10.58347/tml.2024.1707c |  Show IntroductionHide Introduction

Futibatinib (Lytgobi) for Cholangiocarcinoma (online only)

   
The Medical Letter on Drugs and Therapeutics • Apr 17, 2023  (Issue 1674)
– Taiho) has received accelerated approval from the FDA for treatment of adults with previously treated ...
The oral kinase inhibitor futibatinib (Lytgobi – Taiho) has received accelerated approval from the FDA for treatment of adults with previously treated, unresectable, locally advanced or metastatic intrahepatic cholangiocarcinoma with fibroblast growth factor receptor 2 (FGFR2) fusions or other rearrangements. Accelerated approval was based on the overall response rate and duration of response. Futibatinib is the second drug to be approved for this indication; pemigatinib (Pemazyre) was approved earlier.
Med Lett Drugs Ther. 2023 Apr 17;65(1674):e69-70   doi:10.58347/tml.2023.1674f |  Show IntroductionHide Introduction

In Brief: Twice-Yearly Paliperidone (Invega Hafyera) for Schizophrenia

   
The Medical Letter on Drugs and Therapeutics • Jan 10, 2022  (Issue 1641)
:160. 2. GA Keepers et al. The American Psychiatric Association practice guideline for the treatment ...
Invega Hafyera (Janssen), a long-acting, extended-release (ER) formulation of the second-generation antipsychotic paliperidone palmitate, has been approved by the FDA for twice-yearly IM treatment of schizophrenia in adults who have been adequately treated with another injectable ER formulation of the drug (Invega Sustenna or Invega Trinza). It is the first drug to become available in the US for twice-yearly treatment of schizophrenia.
Med Lett Drugs Ther. 2022 Jan 10;64(1641):7-8 |  Show IntroductionHide Introduction

Enlicitide (Lipfendra) – An Oral PCSK9 Inhibitor for LDL-Cholesterol Lowering

   
The Medical Letter on Drugs and Therapeutics • Aug 31, 2026  (Issue 1762)
health priorities. STANDARD TREATMENT ― Statins are the drugs of choice for almost all patients who ...
Enlicitide (Lipfendra – Merck), an oral proprotein convertase subtilisin-kexin type 9 (PCSK9) inhibitor, has been approved by the FDA to reduce low-density lipoprotein cholesterol (LDL-C) in adults with hypercholesterolemia, including heterozygous familial hypercholesterolemia (HeFH). It is the first oral PCSK9 inhibitor to be approved in the US; the other FDA-approved PCSK9 inhibitors (alirocumab [Praluent], evolocumab [Repatha], and lerodalcibep [Lerochol]) and the PCSK9-directed small interfering RNA inclisiran (Leqvio) are injected subcutaneously. Lipfendra was approved under...
Med Lett Drugs Ther. 2026 Aug 31;68(1762):137-9   doi:10.58347/tml.2026.1762a |  Show IntroductionHide Introduction

Belimumab (Benlysta) for Lupus Nephritis (online only)

   
The Medical Letter on Drugs and Therapeutics • Sep 23, 2021  (Issue 1634)
. BH Hahn et al. American College of Rheumatology guidelines for screening, treatment, and management ...
The B-lymphocyte stimulator (BLyS)-specific inhibitor belimumab (Benlysta – GSK), which was approved earlier for treatment of active, autoantibody-positive, nonrenal, systemic lupus erythematosus (SLE), has now been approved for use in addition to standard therapy for treatment of active lupus nephritis in adults. Belimumab is the first drug to be approved in the US for treatment of both SLE and lupus nephritis.
Med Lett Drugs Ther. 2021 Sep 23;63(1634):e3-4 |  Show IntroductionHide Introduction

Taletrectinib (Ibtrozi) — Another Kinase Inhibitor for Non-Small Cell Lung Cancer (NSCLC) (online only)

   
The Medical Letter on Drugs and Therapeutics • Aug 04, 2025  (Issue 1734)
, has been approved by the FDA for treatment of locally advanced or metastatic ROS1-positive nonsmall cell lung ...
Taletrectinib (Ibtrozi – Nuvation Bio), an oral kinase inhibitor, has been approved by the FDA for treatment of locally advanced or metastatic ROS1-positive non-small cell lung cancer (NSCLC) in adults. It is the fourth oral kinase inhibitor to be approved in the US for this indication; crizotinib (Xalkori), entrectinib (Rozlytrek), and repotrectinib (Augtyro) were approved earlier.
Med Lett Drugs Ther. 2025 Aug 4;67(1734):e130-1   doi:10.58347/tml.2025.1734d |  Show IntroductionHide Introduction

Datopotamab Deruxtecan (Datroway) for Advanced Breast Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • Mar 03, 2025  (Issue 1723)
antibody and topoisomerase inhibitor conjugate, for treatment of adults with unresectable or metastatic ...
The FDA has approved datopotamab deruxtecan (Datroway – Daiichi Sankyo/AstraZeneca), a trophoblast cell-surface antigen-2 (Trop-2)-directed antibody and topoisomerase inhibitor conjugate, for treatment of adults with unresectable or metastatic hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative breast cancer who received prior endocrine-based therapy and chemotherapy for unresectable or metastatic disease.
Med Lett Drugs Ther. 2025 Mar 3;67(1723):e41-2   doi:10.58347/tml.2025.1723e |  Show IntroductionHide Introduction

In Brief: Three New Injectable Antipsychotic Drugs

   
The Medical Letter on Drugs and Therapeutics • Dec 25, 2023  (Issue 1692)
Keepers et al. The American Psychiatric Association practice guideline for the treatment of patients ...
Three extended-release injectable formulations of second-generation antipsychotic drugs — two of risperidone (Rykindo, Uzedy) and one of aripiprazole (Abilify Asimtufii) — have been approved by the FDA for treatment of schizophrenia in adults. Rykindo and Abilify Asimtufii are also approved for maintenance treatment of bipolar I disorder in adults. Other extended-release injectable formulations of risperidone and aripiprazole have been available in the US for years (see Table 1).
Med Lett Drugs Ther. 2023 Dec 25;65(1692):207-8   doi:10.58347/tml.2023.1692d |  Show IntroductionHide Introduction

Upadacitinib (Rinvoq) for Giant Cell Arteritis

   
The Medical Letter on Drugs and Therapeutics • Jul 21, 2025  (Issue 1733)
Janus kinase (JAK) inhibitor upadacitinib (Rinvoq – Abbvie) has been approved by the FDA for treatment ...
The oral Janus kinase (JAK) inhibitor upadacitinib (Rinvoq – Abbvie) has been approved by the FDA for treatment of giant cell arteritis. Upadacitinib was approved earlier for treatment of rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, nonradiographic axial spondyloarthritis, atopic dermatitis, ulcerative colitis, and Crohn's disease.
Med Lett Drugs Ther. 2025 Jul 21;67(1733):114-5   doi:10.58347/tml.2025.1733b |  Show IntroductionHide Introduction