Search Results for "treatment guidelines"
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Searched for treatment guidelines. Results 101 to 110 of 172 total matches.
In Brief: Vybrique — Sildenafil Oral Film for Erectile Dysfunction
The Medical Letter on Drugs and Therapeutics • May 11, 2026 (Issue 1754)
(PDE5) inhibitor sildenafil, for
treatment of erectile dysfunction (ED). Sildenafil oral tablets ...
The FDA has approved Vybrique (IBSA), an oral film
formulation of the phosphodiesterase type 5 (PDE5)
inhibitor sildenafil, for treatment of erectile dysfunction
(ED). Sildenafil oral tablets (Viagra, and generics)
have been available since 1998. The manufacturer is
promoting the new product as a "discreet, on-the-go"
option that can be taken without water.
Med Lett Drugs Ther. 2026 May 11;68(1754):78-9 doi:10.58347/tml.2026.1754e | Show Introduction Hide Introduction
Iloperidone (Fanapt) — A New Indication for Bipolar Disorder
The Medical Letter on Drugs and Therapeutics • Jul 22, 2024 (Issue 1707)
and Anxiety
Treatments (CANMAT) and International Society for Bipolar
Disorders (ISBD) 2018 guidelines ...
The oral second-generation antipsychotic drug
iloperidone (Fanapt – Vanda) has been approved
by the FDA for acute treatment of manic or mixed
episodes associated with bipolar I disorder in adults.
First approved in 2009 for treatment of schizophrenia,
iloperidone is the eighth second-generation antipsychotic
to be approved for acute treatment of manic
or mixed episodes of bipolar I disorder (see Table 1).
Med Lett Drugs Ther. 2024 Jul 22;66(1707):115-6 doi:10.58347/tml.2024.1707c | Show Introduction Hide Introduction
Futibatinib (Lytgobi) for Cholangiocarcinoma (online only)
The Medical Letter on Drugs and Therapeutics • Apr 17, 2023 (Issue 1674)
–
Taiho) has received accelerated approval from the
FDA for treatment of adults with previously treated ...
The oral kinase inhibitor futibatinib (Lytgobi –
Taiho) has received accelerated approval from the
FDA for treatment of adults with previously treated,
unresectable, locally advanced or metastatic
intrahepatic cholangiocarcinoma with fibroblast
growth factor receptor 2 (FGFR2) fusions or other
rearrangements. Accelerated approval was based
on the overall response rate and duration of
response. Futibatinib is the second drug to be
approved for this indication; pemigatinib (Pemazyre)
was approved earlier.
Med Lett Drugs Ther. 2023 Apr 17;65(1674):e69-70 doi:10.58347/tml.2023.1674f | Show Introduction Hide Introduction
In Brief: Twice-Yearly Paliperidone (Invega Hafyera) for Schizophrenia
The Medical Letter on Drugs and Therapeutics • Jan 10, 2022 (Issue 1641)
:160.
2. GA Keepers et al. The American Psychiatric Association
practice guideline for the treatment ...
Invega Hafyera (Janssen), a long-acting, extended-release
(ER) formulation of the second-generation
antipsychotic paliperidone palmitate, has been
approved by the FDA for twice-yearly IM treatment
of schizophrenia in adults who have been adequately
treated with another injectable ER formulation of the
drug (Invega Sustenna or Invega Trinza). It is the first
drug to become available in the US for twice-yearly
treatment of schizophrenia.
Enlicitide (Lipfendra) – An Oral PCSK9 Inhibitor for LDL-Cholesterol Lowering
The Medical Letter on Drugs and Therapeutics • Aug 31, 2026 (Issue 1762)
health priorities.
STANDARD TREATMENT ― Statins are the drugs of choice
for almost all patients who ...
Enlicitide (Lipfendra – Merck), an oral proprotein convertase
subtilisin-kexin type 9 (PCSK9) inhibitor, has been approved
by the FDA to reduce low-density lipoprotein cholesterol
(LDL-C) in adults with hypercholesterolemia, including
heterozygous familial hypercholesterolemia (HeFH). It is the
first oral PCSK9 inhibitor to be approved in the US; the other
FDA-approved PCSK9 inhibitors (alirocumab [Praluent],
evolocumab [Repatha], and lerodalcibep [Lerochol]) and the
PCSK9-directed small interfering RNA inclisiran (Leqvio) are
injected subcutaneously. Lipfendra was approved under...
Med Lett Drugs Ther. 2026 Aug 31;68(1762):137-9 doi:10.58347/tml.2026.1762a | Show Introduction Hide Introduction
Belimumab (Benlysta) for Lupus Nephritis (online only)
The Medical Letter on Drugs and Therapeutics • Sep 23, 2021 (Issue 1634)
. BH Hahn et al. American College of Rheumatology guidelines for
screening, treatment, and management ...
The B-lymphocyte stimulator (BLyS)-specific inhibitor
belimumab (Benlysta – GSK), which was approved
earlier for treatment of active, autoantibody-positive,
nonrenal, systemic lupus erythematosus (SLE), has
now been approved for use in addition to standard
therapy for treatment of active lupus nephritis in
adults. Belimumab is the first drug to be approved in
the US for treatment of both SLE and lupus nephritis.
Taletrectinib (Ibtrozi) — Another Kinase Inhibitor for Non-Small Cell Lung Cancer (NSCLC) (online only)
The Medical Letter on Drugs and Therapeutics • Aug 04, 2025 (Issue 1734)
, has been approved by the FDA for treatment
of locally advanced or metastatic ROS1-positive nonsmall
cell lung ...
Taletrectinib (Ibtrozi – Nuvation Bio), an oral kinase
inhibitor, has been approved by the FDA for treatment
of locally advanced or metastatic ROS1-positive non-small
cell lung cancer (NSCLC) in adults. It is the fourth
oral kinase inhibitor to be approved in the US for this
indication; crizotinib (Xalkori), entrectinib (Rozlytrek),
and repotrectinib (Augtyro) were approved earlier.
Med Lett Drugs Ther. 2025 Aug 4;67(1734):e130-1 doi:10.58347/tml.2025.1734d | Show Introduction Hide Introduction
Datopotamab Deruxtecan (Datroway) for Advanced Breast Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Mar 03, 2025 (Issue 1723)
antibody
and topoisomerase inhibitor conjugate, for treatment
of adults with unresectable or metastatic ...
The FDA has approved datopotamab deruxtecan
(Datroway – Daiichi Sankyo/AstraZeneca), a trophoblast
cell-surface antigen-2 (Trop-2)-directed antibody
and topoisomerase inhibitor conjugate, for treatment
of adults with unresectable or metastatic hormone
receptor (HR)-positive, human epidermal growth factor
receptor 2 (HER2)-negative breast cancer who received
prior endocrine-based therapy and chemotherapy for
unresectable or metastatic disease.
Med Lett Drugs Ther. 2025 Mar 3;67(1723):e41-2 doi:10.58347/tml.2025.1723e | Show Introduction Hide Introduction
In Brief: Three New Injectable Antipsychotic Drugs
The Medical Letter on Drugs and Therapeutics • Dec 25, 2023 (Issue 1692)
Keepers et al. The American Psychiatric Association
practice guideline for the treatment of patients ...
Three extended-release injectable formulations of
second-generation antipsychotic drugs — two of
risperidone (Rykindo, Uzedy) and one of aripiprazole
(Abilify Asimtufii) — have been approved by the FDA
for treatment of schizophrenia in adults. Rykindo and
Abilify Asimtufii are also approved for maintenance
treatment of bipolar I disorder in adults. Other
extended-release injectable formulations of
risperidone and aripiprazole have been available in
the US for years (see Table 1).
Med Lett Drugs Ther. 2023 Dec 25;65(1692):207-8 doi:10.58347/tml.2023.1692d | Show Introduction Hide Introduction
Upadacitinib (Rinvoq) for Giant Cell Arteritis
The Medical Letter on Drugs and Therapeutics • Jul 21, 2025 (Issue 1733)
Janus kinase (JAK) inhibitor upadacitinib
(Rinvoq – Abbvie) has been approved by the FDA
for treatment ...
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 Introduction Hide Introduction
