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Searched for Drug. Results 171 to 180 of 604 total matches.

Adagrasib (Krazati) for NSCLC (online only)

   
The Medical Letter on Drugs and Therapeutics • Jan 23, 2023  (Issue 1668)
. ▶ Efficacy: In one open-label trial, the drug produced an objective response rate of 42.9%, of which 42 ...
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

In Brief: Off-Label Amitriptyline for Insomnia

   
The Medical Letter on Drugs and Therapeutics • Mar 20, 2023  (Issue 1672)
IN BRIEF Off-Label Amitriptyline for Insomnia In our article on Drugs for Chronic Insomnia, we ...
In our article on Drugs for Chronic Insomnia, we said there is little evidence that antidepressants such as trazodone, mirtazapine, or amitriptyline are effective in treating insomnia not associated with depression. We received a comment from a reader who has prescribed the tricyclic antidepressant amitriptyline for insomnia, particularly for patients with headache disorders, and finds that most patients are satisfied with the treatment.
Med Lett Drugs Ther. 2023 Mar 20;65(1672):48   doi:10.58347/tml.2023.1672d |  Show IntroductionHide Introduction

Upadacitinib (Rinvoq): A Second JAK Inhibitor for Ulcerative Colitis

   
The Medical Letter on Drugs and Therapeutics • Sep 05, 2022  (Issue 1658)
) or a biologic drug can then be used for maintenance of remission. MECHANISM OF ACTION — Like other JAK ...
The FDA has approved the oral Janus kinase (JAK) inhibitor upadacitinib (Rinvoq – Abbvie) for treatment of moderately to severely active ulcerative colitis in adults who have had an inadequate response to or cannot tolerate one or more tumor necrosis factor (TNF) inhibitors. Upadacitinib is the second JAK inhibitor to be approved for this indication; tofacitinib (Xeljanz) was the first. Upadacitinib is also approved for treatment of rheumatoid arthritis, psoriatic arthritis, atopic dermatitis, and ankylosing spondylitis.
Med Lett Drugs Ther. 2022 Sep 5;64(1658):142-4 |  Show IntroductionHide Introduction

Nemolizumab (Nemluvio) for Atopic Dermatitis

   
The Medical Letter on Drugs and Therapeutics • Feb 17, 2025  (Issue 1722)
is not adequately controlled with topical prescription drugs. It is the first IL-31 receptor antagonist ...
Nemolizumab (Nemluvio – Galderma), a subcutaneously injected interleukin-31 (IL-31) receptor antagonist, has been approved by the FDA for use in combination with topical corticosteroids and/or calcineurin inhibitors for treatment of moderate to severe atopic dermatitis in patients ≥12 years old whose disease is not adequately controlled with topical prescription drugs. It is the first IL-31 receptor antagonist to be approved in the US for this indication. Nemolizumab was approved earlier for treatment of prurigo nodularis in adults.
Med Lett Drugs Ther. 2025 Feb 17;67(1722):25-7   doi:10.58347/tml.2025.1722a |  Show IntroductionHide Introduction

In Brief: Higher-Dose Semaglutide (Ozempic) for Type 2 Diabetes

   
The Medical Letter on Drugs and Therapeutics • May 16, 2022  (Issue 1650)
of the drug do not achieve the desired A1C goal.1,2 An oral formulation of semaglutide (Rybelsus ...
The FDA has approved a higher-dose injectable formulation of the long-acting glucagon-like peptide-1 (GLP-1) receptor agonist semaglutide (Ozempic) for treatment of type 2 diabetes in adults. A single SC injection of the new 8 mg/3 mL formulation delivers 2 mg of semaglutide.
Med Lett Drugs Ther. 2022 May 16;64(1650):79 |  Show IntroductionHide Introduction

Tapinarof Cream (Vtama) for Atopic Dermatitis

   
The Medical Letter on Drugs and Therapeutics • Mar 03, 2025  (Issue 1723)
with tapinarof cream than with Table 1. Some Topical Nonsteroidal Drugs for Atopic Dermatitis FDA-Approved ...
Tapinarof 1% cream (Vtama – Dermavant), an aryl hydrocarbon receptor (AhR) agonist, has been approved by the FDA for topical treatment of atopic dermatitis in patients ≥2 years old. Tapinarof is the first AhR agonist to be approved in the US for this indication. It was approved in 2022 for treatment of plaque psoriasis in adults.
Med Lett Drugs Ther. 2025 Mar 3;67(1723):37-8   doi:10.58347/tml.2025.1723c |  Show IntroductionHide Introduction

Teplizumab (Tzield) to Delay Onset of Type 1 Diabetes

   
The Medical Letter on Drugs and Therapeutics • Jan 09, 2023  (Issue 1667)
≥8 years old who have stage 2 type 1 diabetes. It is the first drug to become available ...
Teplizumab-mzwv (Tzield – Provention Bio), an anti-CD3 monoclonal antibody, has been approved by the FDA to delay the onset of stage 3 type 1 diabetes in patients ≥8 years old who have stage 2 type 1 diabetes. It is the first drug to become available in the US that delays the onset of type 1 diabetes.
Med Lett Drugs Ther. 2023 Jan 9;65(1667):7-8   doi:10.58347/tml.2023.1667c |  Show IntroductionHide Introduction

Xanomeline/Trospium (Cobenfy) for Schizophrenia

   
The Medical Letter on Drugs and Therapeutics • Nov 11, 2024  (Issue 1715)
. It is the first antipsychotic drug to be approved in the US for treatment of schizophrenia that does not block ...
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 IntroductionHide Introduction

Glofitamab (Columvi) for Diffuse Large B-Cell Lymphoma (online only)

   
The Medical Letter on Drugs and Therapeutics • Aug 07, 2023  (Issue 1682)
to biologic drugs to distinguish reference products from their biosimilars. STANDARD TREATMENT ― DLBCL ...
Glofitamab-gxbm (Columvi – Genentech), a bispecific CD20-directed CD3 T-cell engager, has received accelerated approval from the FDA for IV treatment of relapsed or refractory diffuse large B-cell lymphoma (DLBCL), not otherwise specified, or large B-cell lymphoma (LBCL) arising from follicular lymphoma after ≥2 lines of systemic therapy. Accelerated approval was based on response rates and durability of response. Glofitamab is the second T-cell-engaging bispecific antibody to be approved in the US for treatment of DLBCL; epcoritamab-bysp (Epkinly), which is given...
Med Lett Drugs Ther. 2023 Aug 7;65(1682):e129-30   doi:10.58347/tml.2023.1682b |  Show IntroductionHide Introduction

Upadacitinib (Rinvoq) for Giant Cell Arteritis

   
The Medical Letter on Drugs and Therapeutics • Jul 21, 2025  (Issue 1733)
is not known. The efficacy of these drugs in preventing the most serious complications of giant cell ...
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