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A New Subcutaneous Immune Globulin (HyQvia) for Primary Immunodeficiency

   
The Medical Letter on Drugs and Therapeutics • Aug 31, 2015  (Issue 1476)
combined immunodeficiencies.1 These disorders are usually congenital or develop in early childhood ...
Immune globulin (IgG) has been available for administration intravenously once every 3-4 weeks or subcutaneously once daily, once weekly, or every 2 weeks for treatment of primary immunodeficiencies. Now the FDA has approved human immune globulin 10% with recombinant human hyaluronidase (HyQvia – Baxter) for subcutaneous administration only every 3-4 weeks in adults with these disorders. The IgG component of HyQvia is identical to Gammagard Liquid, which was approved in 2005 for IV administration and in 2011 for SC administration.
Med Lett Drugs Ther. 2015 Aug 31;57(1476):121-2 |  Show IntroductionHide Introduction

Obeticholic Acid (Ocaliva) for Primary Biliary Cholangitis

   
The Medical Letter on Drugs and Therapeutics • Mar 27, 2017  (Issue 1517)
of the intralobular bile ducts that can lead to fibrosis, cirrhosis, and liver failure.1 It most commonly affects ...
Obeticholic acid (Ocaliva – Intercept), a farnesoid X receptor agonist, has been approved by the FDA for treatment of primary biliary cholangitis; it is indicated for use in combination with ursodeoxycholic acid (ursodiol, UDCA; Urso, and others) in adults with an inadequate response to UDCA and as monotherapy in adults unable to tolerate UDCA. Obeticholic acid is the second drug to be approved for this indication; UDCA was the first.
Med Lett Drugs Ther. 2017 Mar 27;59(1517):53-5 |  Show IntroductionHide Introduction

Dupilumab (Dupixent) for Moderate to Severe Atopic Dermatitis

   
The Medical Letter on Drugs and Therapeutics • Apr 24, 2017  (Issue 1519)
Table 1. Pharmacology Class Human monoclonal antibody Formulation 300 mg/2 mL single-dose ...
The FDA has approved dupilumab (Dupixent – Sanofi/Regeneron), a subcutaneously-injected fully human monoclonal antibody, for treatment of adults with moderate to severe atopic dermatitis (eczema) that has not responded to topical therapies. It can be used with or without topical corticosteroids.
Med Lett Drugs Ther. 2017 Apr 24;59(1519):64-6 |  Show IntroductionHide Introduction

Fostamatinib (Tavalisse) for ITP

   
The Medical Letter on Drugs and Therapeutics • Feb 25, 2019  (Issue 1566)
, intravenous immunoglobulin (IVIG), or both are generally used for first-line treatment.1 Second-line options ...
The FDA has approved fostamatinib disodium hexahydrate (Tavalisse – Rigel), the first spleen tyrosine kinase (SYK) inhibitor, for oral treatment of thrombocytopenia in adults with chronic immune thrombocytopenia (ITP) who have had an insufficient response to a previous treatment.
Med Lett Drugs Ther. 2019 Feb 25;61(1566):28-30 |  Show IntroductionHide Introduction

Low-Dose Colchicine for Coronary Artery Disease

   
The Medical Letter on Drugs and Therapeutics • Apr 05, 2021  (Issue 1621)
Low-Dose Colchicine for Coronary Artery Disease Table 1. Pharmacology Formulations 0.6 mg tabs ...
The centuries-old anti-inflammatory drug colchicine (Colcrys, and others) is FDA-approved for prophylaxis and treatment of gout flares and for treatment of familial Mediterranean fever. It is also used off-label to treat pericarditis, and in recent years has been investigated for reduction of cardiovascular risk in patients with coronary artery disease (CAD).
Med Lett Drugs Ther. 2021 Apr 5;63(1621):54-5 |  Show IntroductionHide Introduction

Voclosporin (Lupkynis) for Lupus Nephritis

   
The Medical Letter on Drugs and Therapeutics • Aug 23, 2021  (Issue 1631)
% *Statistically significant difference vs placebo 1. BH Bovin et al. Lancet 2021; 397:2070. 2. Primary endpoint ...
Voclosporin (Lupkynis – Aurinia), an oral calcineurin inhibitor, has been approved by the FDA for use in combination with the antimetabolite immunosuppressant mycophenolate mofetil (Cellcept, and generics) and a corticosteroid for treatment of adults with active lupus nephritis. It is the first calcineurin inhibitor to be approved in the US for this indication. Tacrolimus (Prograf, and others) and cyclosporine (Neoral, and others), the other available systemic calcineurin inhibitors, are approved for prophylaxis of organ rejection in transplant patients.
Med Lett Drugs Ther. 2021 Aug 23;63(1631):134-6 |  Show IntroductionHide Introduction

Finerenone (Kerendia) for Chronic Kidney Disease

   
The Medical Letter on Drugs and Therapeutics • Aug 23, 2021  (Issue 1631)
(DKD).1,2 MECHANISM OF ACTION — Finerenone inhibits aldosterone at the mineralocorticoid receptor ...
Finerenone (Kerendia – Bayer), an oral nonsteroidal mineralocorticoid receptor antagonist (MRA), has been approved by the FDA to reduce the risk of sustained eGFR decline, end-stage renal disease, nonfatal MI, hospitalization for heart failure (HF), and cardiovascular death in adults with chronic kidney disease (CKD) associated with type 2 diabetes. It is the first nonsteroidal MRA to be approved in the US.
Med Lett Drugs Ther. 2021 Aug 23;63(1631):131-2 |  Show IntroductionHide Introduction

A Ranibizumab Ocular Implant (Susvimo) for Age-Related Macular Degeneration

   
The Medical Letter on Drugs and Therapeutics • May 02, 2022  (Issue 1649)
for monthly treatment of nAMD.1 The FDA has approved ranibizumab-nuna (Byooviz), a biosimilar of Lucentis ...
The FDA has approved Susvimo (Genentech), a refillable permanent ocular implant containing the vascular endothelial growth factor (VEGF) inhibitor ranibizumab, for treatment of neovascular (wet) age-related macular degeneration (nAMD) in patients who have previously responded to at least two intravitreal injections of a VEGF inhibitor. Ranibizumab intravitreal injection (Lucentis) has been available since 2006 for monthly treatment of nAMD. The FDA has approved ranibizumab-nuna (Byooviz), a biosimilar of Lucentis and the first ophthalmologic biosimilar; it will be available in June...
Med Lett Drugs Ther. 2022 May 2;64(1649):71-2 |  Show IntroductionHide Introduction

Risankizumab (Skyrizi) for Ulcerative Colitis

   
The Medical Letter on Drugs and Therapeutics • Nov 11, 2024  (Issue 1715)
and psoriatic arthritis.1 STANDARD TREATMENT — An aminosalicylate such as mesalamine (Lialda, and others ...
The injectable interleukin (IL)-23 antagonist risankizumab-rzza (Skyrizi – Abbvie), previously approved by the FDA for treatment of Crohn's disease (CD), has now been approved for treatment of moderately to severely active ulcerative colitis (UC) in adults. Risankizumab is the first IL-23 antagonist to be approved for treatment of both CD and UC. It is also approved for treatment of plaque psoriasis and psoriatic arthritis.
Med Lett Drugs Ther. 2024 Nov 11;66(1715):182-4   doi:10.58347/tml.2024.1715d |  Show IntroductionHide Introduction

BiDil for Heart Failure

   
The Medical Letter on Drugs and Therapeutics • Sep 28, 2005  (Issue 1218)
together off-label for many years to treat heart failure in patients not responding to other drugs. 1 ...
BiDil (NitroMed), a fixed-dose combination of isosorbide dinitrate and hydralazine, was approved by the FDA for adjunctive use in the treatment of heart failure in black patients.Both drugs are oral vasodilators that have been used together off-label for many years to treat heart failure in patients not responding to other drugs.
Med Lett Drugs Ther. 2005 Sep 28;47(1218):77-8 |  Show IntroductionHide Introduction