Search Results for "Drug"
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Searched for Drug. Results 451 to 460 of 618 total matches.
Valoctocogene Roxaparvovec (Roctavian) – A Gene Therapy for Severe Hemophilia A
The Medical Letter on Drugs and Therapeutics • Oct 02, 2023 (Issue 1686)
has no pronunciation or meaning; such
suffixes are now added to biologic drugs to distinguish reference
products ...
Valoctocogene roxaparvovec-rvox (Roctavian –
Biomarin), an adeno-associated virus (AAV) vector-based
gene therapy, has been approved by the FDA
for one-time treatment of severe hemophilia A
in adults without pre-existing antibodies to AAV
serotype 5. It is the first gene therapy to be approved
in the US for treatment of hemophilia A.
Med Lett Drugs Ther. 2023 Oct 2;65(1686):157-8 doi:10.58347/tml.2023.1686c | Show Introduction Hide Introduction
Isatuximab (Sarclisa) for Multiple Myeloma (online only)
The Medical Letter on Drugs and Therapeutics • Dec 09, 2024 (Issue 1717)
transplantation (ASCT). The drug was approved earlier
for treatment of relapsed or treatment-refractory
multiple ...
Isatuximab-irfc (Sarclisa – Sanofi), a CD38-directed
cytolytic antibody, has been approved by the FDA for
treatment of newly diagnosed multiple myeloma in
adults who are not eligible for autologous stem cell
transplantation (ASCT). The drug was approved earlier
for treatment of relapsed or treatment-refractory
multiple myeloma.
Med Lett Drugs Ther. 2024 Dec 9;66(1717):e200-1 doi:10.58347/tml.2024.1717e | Show Introduction Hide Introduction
Vimseltinib (Romvimza) for Tenosynovial Giant Cell Tumor (online only)
The Medical Letter on Drugs and Therapeutics • Apr 14, 2025 (Issue 1726)
, and peripheral edema,
fatigue, rash, and elevations in AST, ALT, and serum creatinine
can occur.
▶ Drug ...
Vimseltinib (Romvimza – Deciphera), an oral kinase
inhibitor, has been approved by the FDA for treatment
of symptomatic tenosynovial giant cell tumor in adults
for whom surgical resection would cause worsening
functional limitation or severe morbidity. The kinase
inhibitor pexidartinib (Turalio) was approved for a
similar indication in 2019.
Med Lett Drugs Ther. 2025 Apr 14;67(1726):e66-7 doi:10.58347/tml.2025.1726h | Show Introduction Hide Introduction
Telisotuzumab Vedotin (Emrelis) for Non-Small Cell Lung Cancer (online only)
The Medical Letter on Drugs and Therapeutics • Aug 04, 2025 (Issue 1734)
have been
reported. The drug can cause ocular surface disorders
including blurred vision and keratitis.
DRUG ...
Telisotuzumab vedotin-tllv (Emrelis – Abbvie), a
c-Met-directed antibody and microtubule inhibitor
conjugate, has received accelerated approval from the
FDA for treatment of locally advanced or metastatic
nonsquamous non-small cell lung cancer (NSCLC) in
adults with high c-Met protein overexpression [≥50%
of tumor cells with strong (3+) staining] who received
prior systemic therapy. Accelerated approval was
based on the overall response rate and duration of
response.
Med Lett Drugs Ther. 2025 Aug 4;67(1734):e132-3 doi:10.58347/tml.2025.1734e | Show Introduction Hide Introduction
In Brief: Sacubitril/Valsartan (Entresto) Expanded Indication
The Medical Letter on Drugs and Therapeutics • May 03, 2021 (Issue 1623)
normal.
Entresto is the first drug to be approved in the US for
this indication.
TYPES OF HF — Almost ...
The oral fixed-dose combination of the neprilysin
inhibitor sacubitril and the angiotensin receptor
blocker (ARB) valsartan (Entresto – Novartis) was
approved in 2015 to reduce the risk of cardiovascular
death and hospitalization for heart failure in adults with
chronic heart failure (NYHA Class II-IV) and reduced
ejection fraction (HFrEF; LVEF...
Anifrolumab (Saphnelo) for Systemic Lupus Erythematosus
The Medical Letter on Drugs and Therapeutics • Sep 20, 2021 (Issue 1633)
;
such suffixes are added to biologic drugs to distinguish reference
products from their biosimilars.
STANDARD ...
The FDA has approved anifrolumab-fnia (Saphnelo – AstraZeneca), a type I interferon receptor antagonist, for IV treatment of adults with moderate to severe systemic lupus erythematosus (SLE) who are receiving standard treatment. Anifrolumab has not been studied in patients with severe active lupus nephritis or severe active CNS lupus. It is the first type I interferon receptor antagonist to become available
in the US.
Opdualag for Metastatic Melanoma (online only)
The Medical Letter on Drugs and Therapeutics • Jan 23, 2023 (Issue 1668)
has no pronunciation or meaning; such
suffixes are added to biologic drugs to distinguish reference products ...
Opdualag (BMS), a fixed-dose combination of two
immune checkpoint inhibitors — nivolumab (Opdivo),
a programmed death receptor-1 (PD-1) inhibitor, and
relatlimab-rmbw, a lymphocyte-activation gene-3
(LAG-3) blocking antibody — has been approved by
the FDA for treatment of unresectable or metastatic
melanoma in patients ≥12 years old. Relatlimab, which
is only available in combination with nivolumab, is
the first LAG-3 blocking antibody to become available
in the US. Immune checkpoint inhibitors, including
the anti-CTLA-4 antibody ipilimumab (Yervoy) and
the PD-1 inhibitors...
Med Lett Drugs Ther. 2023 Jan 23;65(1668):e19-20 doi:10.58347/tml.2023.1668g | Show Introduction Hide Introduction
Live Fecal Microbiota (Rebyota) for Prevention of CDI Recurrence
The Medical Letter on Drugs and Therapeutics • Mar 06, 2023 (Issue 1671)
infection. Med Lett Drugs Ther
2021; 63:137.
6. S Khanna et al. Efficacy and safety of RBX2660 in PUNCH ...
The FDA has approved Rebyota (Ferring), a rectally-administered,
live fecal microbiota suspension, for
prevention of additional recurrences of Clostridioides
difficile infection (CDI) following antibiotic treatment
for a recurrent episode of CDI in adults. Rebyota is
the first microbiome-based treatment to be approved
for this indication. It is not approved for initial
treatment of CDI. Fecal microbiota transplantation
(FMT) has been used in patients with multiple
CDI recurrences.
Med Lett Drugs Ther. 2023 Mar 6;65(1671):35-6 doi:10.58347/tml.2023.1671b | Show Introduction Hide Introduction
In Brief: Expanded Heart Failure Indication for Dapagliflozin (Farxiga)
The Medical Letter on Drugs and Therapeutics • Jun 26, 2023 (Issue 1679)
fraction.
1. Dapagliflozin (Farxiga) – a new indication for heart failure.
Med Lett Drugs Ther 2020; 62 ...
The sodium-glucose cotransporter 2 (SGLT2)
inhibitor dapagliflozin (Farxiga – AstraZeneca) was
approved by the FDA in 2020 to reduce the risk of
cardiovascular death and hospitalization for heart
failure (HF) in adults with heart failure with reduced
ejection fraction (HFrEF). The indication has now
been expanded to include a reduction in the risk
of urgent HF visits and use in adults with any left
ventricular ejection fraction (LVEF).
Med Lett Drugs Ther. 2023 Jun 26;65(1679):101-2 doi:10.58347/tml.2023.1679c | Show Introduction Hide Introduction
Treatment of Common Respiratory Tract Infections
The Medical Letter on Drugs and Therapeutics • Apr 17, 2023 (Issue 1674)
to these drugs.2,3
Fluoroquinolones, tetracyclines, and trimethoprim/
sulfamethoxazole should not be used ...
Most respiratory tract infections are caused by
viruses. Bacterial respiratory tract infections are
usually treated empirically with antibiotic therapy
that targets the most probable causative pathogens.
Recommended antibiotic regimens for outpatient
treatment of some common respiratory tract
infections are listed in Table 1 for adults and Table 2
for children.
Med Lett Drugs Ther. 2023 Apr 17;65(1674):57-62 doi:10.58347/tml.2023.1674a | Show Introduction Hide Introduction
