Search Results for "Metabolic"
Search again or select article below to purchase. Single article price: $45. Order 3 or more at one time and receive a 10% discount.
Sort by relevance | Sort by date
Searched for Metabolic. Results 481 to 490 of 1047 total matches.

Neratinib (Nerlynx) for Metastatic HER2-Positive Breast Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • Nov 14, 2022  (Issue 1663)
infection, and upper respiratory tract infection. DRUG INTERACTIONS — Neratinib is metabolized primarily ...
The oral tyrosine kinase inhibitor neratinib (Nerlynx – Puma Biotechnology) has been approved by the FDA for use in combination with capecitabine (Xeloda, and generics) for treatment of advanced or metastatic human epidermal growth factor receptor 2 (HER2)-positive breast cancer in adults who received ≥2 prior anti-HER2-based regimens for metastatic disease. It was previously approved for use as monotherapy for extended adjuvant treatment of adults with early-stage, HER2-positive breast cancer following adjuvant trastuzumab (Herceptin)-based therapy. HER2 is overexpressed in...
Med Lett Drugs Ther. 2022 Nov 14;64(1663):e192-3 |  Show IntroductionHide Introduction

In Brief: A Second Indication for Tucatinib (Tukysa) (online only)

   
The Medical Letter on Drugs and Therapeutics • Feb 20, 2023  (Issue 1670)
starting tucatinib and every 3 weeks during treatment. DRUG INTERACTIONS — Tucatinib is metabolized ...
The oral kinase inhibitor tucatinib (Tukysa – Seagen) has received accelerated approval from the FDA for use in combination with trastuzumab (Herceptin) for treatment of adults with RAS wild-type human epidermal growth factor receptor 2 (HER2)-positive unresectable or metastatic colorectal cancer that has progressed following treatment with fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy regimens. Tucatinib was approved in 2020 for use in combination with trastuzumab and capecitabine (Xeloda, and generics) for treatment of adults with advanced unresectable or...
Med Lett Drugs Ther. 2023 Feb 20;65(1670):e37-8   doi:10.58347/tml.2023.1670g |  Show IntroductionHide Introduction

In Brief: A New Breast Cancer Indication for Sacituzumab Govitecan (Trodelvy) (online only)

   
The Medical Letter on Drugs and Therapeutics • Mar 06, 2023  (Issue 1671)
INTERACTIONS — SN-38 is metabolized by uridine diphosphate-glucuronosyl transferase 1A1 (UGT1A1). Patients ...
Sacituzumab govitecan-hziy (Trodelvy – Gilead) has been approved for treatment of unresectable locally advanced or metastatic hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative breast cancer in adults who received prior endocrine therapy and ≥2 additional systemic therapies for metastatic disease. It was previously approved for treatment-refractory metastatic triplenegative breast cancer and for treatment of locally advanced or metastatic urothelial cancer in adults who received platinum-based chemotherapy and a programmed death receptor-1...
Med Lett Drugs Ther. 2023 Mar 6;65(1671):e43-4   doi:10.58347/tml.2023.1671g |  Show IntroductionHide Introduction

Linaclotide (Linzess) for Functional Constipation

   
The Medical Letter on Drugs and Therapeutics • Aug 21, 2023  (Issue 1683)
limit of quantitation1 Metabolism Proteolysis to smaller peptides and amino acids 1. Linaclotide ...
The guanylate cyclase-C receptor agonist linaclotide (Linzess – Abbvie/Ironwood) was first approved by the FDA in 2012 for treatment of chronic idiopathic constipation and irritable bowel syndrome with constipation in adults. The drug has now been approved for treatment of functional constipation in patients 6-17 years old. Linaclotide is the only drug to be approved in the US for treatment of functional constipation.
Med Lett Drugs Ther. 2023 Aug 21;65(1683):135-6   doi:10.58347/tml.2023.1683d |  Show IntroductionHide Introduction

Clonidine Oral Suspension (Onyda XR) for ADHD

   
The Medical Letter on Drugs and Therapeutics • Dec 23, 2024  (Issue 1718)
Formulation 0.1 mg/mL oral suspension Route Oral Tmax 7.5 hrs (single 0.2-mg dose, fasting) Metabolism 50 ...
The FDA has approved Onyda XR (Tris), an extended-release (ER) oral suspension formulation of the alpha2-adrenergic agonist clonidine, for use as monotherapy or as an adjunct to stimulant therapy for treatment of attention-deficit/hyperactivity disorder (ADHD) in children ≥6 years old. Clonidine ER tablets have been available for years for treatment of ADHD in children 6-17 years old.
Med Lett Drugs Ther. 2024 Dec 23;66(1718):205-6   doi:10.58347/tml.2024.1718d |  Show IntroductionHide Introduction

Vorasidenib (Voranigo) for Low-Grade Glioma (online only)

   
The Medical Letter on Drugs and Therapeutics • Nov 11, 2024  (Issue 1715)
treatment and for 2 months after the last dose. DRUG INTERACTIONS ― Vorasidenib is metabolized primarily ...
The FDA has approved vorasidenib (Voranigo – Servier), an oral isocitrate dehydrogenase (IDH) inhibitor, for treatment of grade 2 astrocytoma or oligodendroglioma in patients ≥12 years old with an IDH1 or IDH2 mutation. It is the first systemic treatment to be approved in the US for this indication.
Med Lett Drugs Ther. 2024 Nov 11;66(1715):e188-9   doi:10.58347/tml.2024.1715g |  Show IntroductionHide Introduction

Ensartinib (Ensacove) for Non-Small Cell Lung Cancer (online only)

   
The Medical Letter on Drugs and Therapeutics • Feb 17, 2025  (Issue 1722)
— Ensartinib is primarily metabolized by CYP3A4 and is a substrate of P-glycoprotein (P-gp). Concurrent use ...
The FDA has approved ensartinib (Ensacove – Xcovery), an oral kinase inhibitor, for treatment of anaplastic lymphoma kinase (ALK)-positive, locally advanced or metastatic non-small cell lung cancer (NSCLC) in adults who have not previously received an ALK inhibitor (e.g, crizotinib [Xalkori], certinib [Zykadia], alectinib [Alecensa], brigatinib [Alunbrig], lorlatinib [Lorbrena]). All previously approved ALK inhibitors are also approved for first-line use.
Med Lett Drugs Ther. 2025 Feb 17;67(1722):e34-5   doi:10.58347/tml.2025.1722h |  Show IntroductionHide Introduction

Posaconazole (Noxafil) for Invasive Fungal Infections

   
The Medical Letter on Drugs and Therapeutics • Nov 20, 2006  (Issue 1248)
Metabolism Via UDP glucuronidation; highly protein bound Elimination Primarily fecal (71%), urine (13 ...
Posaconazole (Noxafil - Schering-Plough), an oral azole antifungal with a chemical structure similar to that of itraconazole (Sporanox), has been approved by the FDA to prevent Candida and Aspergillus infections in severely immunocompromised patients and for treatment of oropharyngeal candidiasis. It is likely also to be used off-label for treatment of other fungal infections, including those caused by Mucor and other Zygomycetes.
Med Lett Drugs Ther. 2006 Nov 20;48(1248):93-5 |  Show IntroductionHide Introduction

New Drugs for Multiple Sclerosis

   
The Medical Letter on Drugs and Therapeutics • Nov 12, 2012  (Issue 1403)
to steady state 3 months Metabolism Primarily by hydrolysis; secondarily by oxidation, N-acetylation ...
In recent years, several new drugs have been approved by the FDA for use in multiple sclerosis (MS), and many others are in the pipeline. Most recently, teriflunomide (Aubagio – Genzyme) became the second oral drug to be approved by the FDA for treatment of relapsing forms of MS.
Med Lett Drugs Ther. 2012 Nov 12;54(1403):89-91 |  Show IntroductionHide Introduction

Drugs for Hypertriglyceridemia

   
The Medical Letter on Drugs and Therapeutics • Mar 04, 2013  (Issue 1411)
hypoglycemic drugs. Gemfibrozil can inhibit the metabolism of statins and increase the risk of rhabdomyolysis ...
Fibrates, niacin and fish oil are promoted for treatment of hypertriglyceridemia. HMG-CoA reductase inhibitors (statins) can lower elevated serum concentrations of triglycerides, but less so than fibrates, niacins or fish oil. Lifestyle changes such as weight reduction, exercise and decreasing alcohol intake can also lower serum triglyceride levels and should be tried first.
Med Lett Drugs Ther. 2013 Mar 4;55(1411):17-9 |  Show IntroductionHide Introduction