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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.
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.
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.
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.
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).
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.
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.
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...
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 Introduction Hide 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.