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Searched for Metabolic. Results 191 to 200 of 249 total matches.

Drugs for Plaque Psoriasis

   
The Medical Letter on Drugs and Therapeutics • Sep 30, 2024  (Issue 1712)
alter the metabolism of CYP substrates; dosage adjustments of substrates with narrow therapeutic ...
Mild to moderate plaque psoriasis can be treated with topical drugs and phototherapy. Patients with moderate to severe disease generally require systemic therapy. Guidelines for the treatment of psoriasis with topical therapy, phototherapy, and systemic drugs have recently been published.
Med Lett Drugs Ther. 2024 Sep 30;66(1712):153-60   doi:10.58347/tml.2024.1712a |  Show IntroductionHide Introduction

Ofatumumab (Kesimpta) for Multiple Sclerosis

   
The Medical Letter on Drugs and Therapeutics • Dec 28, 2020  (Issue 1614)
/0.4 mL single-dose syringes and pens Route Subcutaneous Metabolism Proteolysis Half-life 16 days ...
The FDA has approved a subcutaneous formulation of the recombinant human anti-CD20 antibody ofatumumab (Kesimpta – Novartis) for treatment of adults with relapsing forms of multiple sclerosis (MS), including clinically isolated syndrome (initial neurological episode), relapsing-remitting disease, and active secondary progressive MS (SPMS). Kesimpta is the second anti-CD20 antibody to be approved for these indications; IV ocrelizumab (Ocrevus), which is also approved for treatment of primary progressive MS, was the first. An IV formulation of ofatumumab (Arzerra) has...
Med Lett Drugs Ther. 2020 Dec 28;62(1614):203-5 |  Show IntroductionHide Introduction

Oriahnn for Fibroid-Associated Heavy Menstrual Bleeding

   
The Medical Letter on Drugs and Therapeutics • Apr 05, 2021  (Issue 1621)
, estradiol 1 mg, and Oriahnn norethindrone acetate 0.5 mg PM: elagolix 300 mg Tmax 1.5 hours Metabolism ...
Oriahnn (Abbvie), a fixed-dose combination of the gonadotropin-releasing hormone (GnRH) receptor antagonist elagolix, the estrogen estradiol, and the progestin norethindrone acetate copackaged with elagolix alone, has been approved by the FDA for oral treatment of heavy menstrual bleeding associated with uterine leiomyomas (fibroids) in premenopausal women. It is the first product to be approved in the US for this indication. Elagolix (Orilissa) has been available since 2018 for treatment of moderate to severe pain associated with endometriosis. The GnRH receptor antagonist...
Med Lett Drugs Ther. 2021 Apr 5;63(1621):51-2 |  Show IntroductionHide Introduction

Inhaled Mannitol (Bronchitol) for Cystic Fibrosis

   
The Medical Letter on Drugs and Therapeutics • May 31, 2021  (Issue 1625)
of administration Oral inhalation via handheld inhaler Tmax 1.5 hours Metabolism Dehydrogenation to fructose ...
The FDA has approved mannitol powder for oral inhalation (Bronchitol – Chiesi) as add-on maintenance treatment to improve pulmonary function in adults with cystic fibrosis (CF). This product has been available in Europe for the same indication since 2012. Another formulation of mannitol inhalation powder (Aridol) is approved in the US for assessment of bronchial hyperresponsiveness.
Med Lett Drugs Ther. 2021 May 31;63(1625):85-6 |  Show IntroductionHide Introduction

Cabotegravir (Apretude) for HIV-1 Pre-Exposure Prophylaxis

   
The Medical Letter on Drugs and Therapeutics • Feb 21, 2022  (Issue 1644)
600 mg/3 mL single-dose vials Route Intramuscular Metabolism Primarily by UGT1A1; lesser extent ...
The FDA has approved Apretude (ViiV Healthcare), an IM extended-release (ER) formulation of the integrase strand transfer inhibitor (INSTI) cabotegravir, for use every 2 months to prevent sexually acquired HIV-1 infection in at-risk adolescents and adults. Apretude is the first ER formulation to be FDA-approved for pre-exposure prophylaxis (PrEP) of HIV-1 infection.
Med Lett Drugs Ther. 2022 Feb 21;64(1644):29-31 |  Show IntroductionHide Introduction

Topical Roflumilast (Zoryve) for Plaque Psoriasis

   
The Medical Letter on Drugs and Therapeutics • Jan 23, 2023  (Issue 1668)
) inhibitor Formulation 0.3% cream Route Topical Metabolism Hepatic by CYP3A4 and CYP1A2 Half-life 4 days ...
The FDA has approved a 0.3% cream formulation of the phosphodiesterase-4 (PDE4) inhibitor roflumilast (Zoryve – Arcutis) for topical treatment of plaque psoriasis in patients ≥12 years old. Roflumilast is the first topical PDE4 inhibitor to be approved by the FDA for this indication; crisaborole (Eucrisa), another topical PDE4 inhibitor, is approved for treatment of atopic dermatitis. Oral roflumilast (Daliresp) is approved for treatment of chronic obstructive pulmonary disease.
Med Lett Drugs Ther. 2023 Jan 23;65(1668):10-2   doi:10.58347/tml.2023.1668b |  Show IntroductionHide Introduction

Deucravacitinib (Sotyktu) for Plaque Psoriasis

   
The Medical Letter on Drugs and Therapeutics • Feb 20, 2023  (Issue 1670)
Oral Tmax 2-3 hours Half-life 10 hours Metabolism Primarily hepatic by CYP1A2 to active metabolite ...
The FDA has approved deucravacitinib (Sotyktu – BMS), an oral tyrosine kinase 2 (TYK2) inhibitor, for once-daily treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy or phototherapy. Deucravacitinib is the first selective TYK2 inhibitor to be approved in the US for any indication.
Med Lett Drugs Ther. 2023 Feb 20;65(1670):29-31   doi:10.58347/tml.2023.1670b |  Show IntroductionHide Introduction

Sotagliflozin (Inpefa) for Heart Failure

   
The Medical Letter on Drugs and Therapeutics • Jul 24, 2023  (Issue 1681)
mg tabs Route Oral Tmax 1.25-3 hrs (single dose); 2.5-4 hrs (multiple doses) Metabolism Primarily ...
The FDA has approved sotagliflozin (Inpefa – Lexicon), an oral sodium-glucose cotransporter 1 and 2 (SGLT1/2) inhibitor, to reduce the risk of hospitalization for heart failure (HF), urgent HF visits, and cardiovascular death in adults with either HF (with any left ventricular ejection fraction [LVEF]) or type 2 diabetes, chronic kidney disease (CKD), and other cardiovascular risk factors. Sotagliflozin is the first dual SGLT1/2 inhibitor to be approved in the US. Unlike SGLT2 inhibitors, it is not FDA-approved to improve glycemic control in adults with type 2 diabetes....
Med Lett Drugs Ther. 2023 Jul 24;65(1681):114-6   doi:10.58347/tml.2023.1681b |  Show IntroductionHide Introduction

Roflumilast Foam (Zoryve) for Seborrheic Dermatitis

   
The Medical Letter on Drugs and Therapeutics • Apr 15, 2024  (Issue 1700)
Phosphodiesterase-4 (PDE4) inhibitor Formulation 0.3% foam Route Topical Metabolism Hepatic by CYP3A4, CYP1A2 ...
The FDA has approved a 0.3% foam formulation of the phosphodiesterase-4 (PDE4) inhibitor roflumilast (Zoryve – Arcutis) for topical treatment of seborrheic dermatitis in patients ≥9 years old. Roflumilast is the first PDE4 inhibitor to be approved in the US for this indication. It is also available in a 0.3% cream formulation (Zoryve) for treatment of plaque psoriasis and in an oral formulation (Daliresp, and generics) for treatment of chronic obstructive pulmonary disease. A 0.15% cream formulation for treatment of atopic dermatitis in patients ≥6 years old will be reviewed...
Med Lett Drugs Ther. 2024 Apr 15;66(1700):57-9   doi:10.58347/tml.2024.1700a |  Show IntroductionHide Introduction

Comparison Table: Drugs for Parkinson's Disease (online only)

   
The Medical Letter on Drugs and Therapeutics • Feb 22, 2021  (Issue 1618)
of this material is strictly prohibited. 4 iCOMT inhibitors can decrease metabolism of COMT substrates ...
View the Comparison Table: Drugs for Parkinson's Disease
Med Lett Drugs Ther. 2021 Feb 22;63(1618):e1-9 |  Show IntroductionHide Introduction