Search Results for "Growth"
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Searched for Growth. Results 161 to 170 of 302 total matches.
Revumenib (Revuforj) for Acute Leukemia (online only)
The Medical Letter on Drugs and Therapeutics • Jan 06, 2025 (Issue 1719)
studies,
administration of revumenib during organogenesis was
associated with altered fetal growth ...
Revumenib (Revuforj – Syndax), an oral menin
inhibitor, has been approved by the FDA for treatment
of relapsed or refractory acute leukemia in patients
≥1 year old with a lysine methyltransferase 2A gene
(KMT2A) translocation. It is the first menin inhibitor to
be approved in the US.
Med Lett Drugs Ther. 2025 Jan 6;67(1719):e8-9 doi:10.58347/tml.2025.1719d | Show Introduction Hide Introduction
Mirdametinib (Gomekli) for Neurofibromatosis Type 1 (online only)
The Medical Letter on Drugs and Therapeutics • Apr 14, 2025 (Issue 1726)
(MAPK) pathway activation. Mirdametinib inhibits
MAPK 1 and 2, enzymes responsible for cell growth ...
Mirdametinib (Gomekli – SpringWorks Therapeutics),
an oral kinase inhibitor, has been approved by the FDA
for treatment of neurofibromatosis type 1 (NF1) in
patients ≥2 years old who have symptomatic plexiform
neurofibromas not amenable to complete resection.
Mirdametinib is the second drug to be approved for
this indication in the US and the first to be approved
for use in adults. The oral kinase inhibitor selumetinib
(Koselugo) was approved in 2020 for use in patients
2-17 years old.
Med Lett Drugs Ther. 2025 Apr 14;67(1726):e64-5 doi:10.58347/tml.2025.1726g | Show Introduction Hide Introduction
Omadacycline (Nuzyra) - A New Tetracycline Antibiotic
The Medical Letter on Drugs and Therapeutics • May 20, 2019 (Issue 1572)
with repeated short courses of
treatment), and reversible inhibition of bone growth;
omadacycline should ...
The FDA has approved omadacycline (Nuzyra – Paratek),
a semisynthetic tetracycline derivative, for once-daily
IV and oral treatment of community-acquired bacterial
pneumonia (CAP) and acute bacterial skin and skin
structure infections (ABSSSIs) in adults.
Creatine and Androstenedione--Two "Dietary Supplements"
The Medical Letter on Drugs and Therapeutics • Nov 06, 1998 (Issue 1039)
persist). In adolescents, increased blood
levels of testosterone can lead to early closing of bone growth ...
Creatine, a natural amino acid derivative, and androstenedione, a testosterone precursor, are marketed as 'dietary supplements' in health food stores and are widely believed to enhance athletic performance. Both have been in the news recently because Mark McGwire, the baseball home-run record-setter, reportedly has said he takes both. Neither has been approved for any indication by the US Food and Drug Administration (FDA).
Drug-eluting Stents
The Medical Letter on Drugs and Therapeutics • Mar 17, 2003 (Issue 1152)
(rapamycin; Rapamune), an inhibitor of cell growth with anti-inflammatory properties, is marketed ...
Most angioplasty procedures for coronary artery disease now include placement of stents, which have improved both short- and long-term success rates. The main limitation is restenosis, which occurs in about 25% of patients. Drug-eluting stents intended to reduce the incidence of restenosis have been approved for use in Europe, but not yet in the US.
Over-the-counter Omeprazole (Prilosec OTC)
The Medical Letter on Drugs and Therapeutics • Aug 04, 2003 (Issue 1162)
of proton pump inhibitors increases circulating levels of gastrin, which increases growth rates ...
The FDA recently approved the proton pump inhibitor omeprazole magnesium (Prilosec OTC) for over-the-counter use for treatment of frequent heartburn. It will be marketed in late September or early October. Five proton pump inhibitors, including omeprazole, are available by prescription in the US (Medical Letter 2001; 43:36).
Beta-Adrenergic Blockers and Breast Cancer
The Medical Letter on Drugs and Therapeutics • Jan 23, 2012 (Issue 1382)
activation had a negligible effect on primary
breast tumor growth, but increased metastasis 30-fold.2 ...
Three retrospective studies have recently reported an
association between beta-blocker use and a reduction
in breast cancer metastasis and recurrence. No
prospective, randomized trials have been published.
Axitinib (Inlyta) for Advanced Renal Cell Carcinoma
The Medical Letter on Drugs and Therapeutics • Jun 11, 2012 (Issue 1392)
angiogenesis and proliferation through
inhibition of vascular endothelial growth factor
(VEGF) or mammalian ...
Axitinib (Inlyta – Pfizer), an oral tyrosine kinase
inhibitor, has been approved by the FDA for treatment
of advanced renal cell carcinoma after failure of one
prior systemic therapy. It is the fourth oral tyrosine
kinase inhibitor to be approved for treatment of
advanced renal cell carcinoma.
Choice of Drug-Eluting Stents
The Medical Letter on Drugs and Therapeutics • Dec 24, 2012 (Issue 1406)
(rapamycin; Rapamune), an
inhibitor of cell growth with anti-inflammatory properties
first marketed ...
The use of intracoronary stents in angioplasty procedures
has improved both short- and long-term success
rates. In recent years, drug-eluting stents (DESs) have
largely replaced bare-metal stents (BMSs).
An EUA for Bamlanivimab - A Monoclonal Antibody for COVID-19
The Medical Letter on Drugs and Therapeutics • Nov 30, 2020 (Issue 1612)
19, 2020. 2. Based on CDC growth charts (https://www.cdc.gov/growthcharts/ clinical_charts.htm ...
The investigational neutralizing IgG1 monoclonal
antibody bamlanivimab (LY-CoV555; Lilly) has
been granted an FDA Emergency Use Authorization
(EUA) for treatment of recently diagnosed mild
to moderate COVID-19 in patients who are ≥12
years old, weigh at least 40 kg, and are at high
risk for progressing to severe disease and/or
hospitalization (see Table 1).
