Search Results for "Macular Degeneration"
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Searched for Macular Degeneration. Results 21 to 24 of 24 total matches.
A Progestin Implant (Implanon) for Long-Term Contraception
The Medical Letter on Drugs and Therapeutics • Oct 09, 2006 (Issue 1245)
in The Medical Letter –
Antiviral Drugs for Influenza
Ranibizumab (Lucentis) for Macular Degeneration ...
Implanon (Organon), an implantable contraceptive containing the progestin etonogestrel, has been approved by the FDA. Two other implantable contraceptives, Norplant and Jadelle, which both contain levonorgestrel, are FDA-approved but not marketed in the US.
Bevacizumab (Avastin) for Metastatic Breast Cancer
The Medical Letter on Drugs and Therapeutics • Jun 02, 2008 (Issue 1287)
macular degeneration,
2
it has now also been
approved by the FDA for use in combination with paclitaxel ...
Bevacizumab (Avastin - Genentech) is a recombinant humanized monoclonal antibody that binds to vascular endothelial growth factor and prevents it from binding to receptors on endothelial cells, inhibiting formation of new blood vessels. Previously approved by the FDA for use in combination regimens for first-line treatment of metastatic colon cancer and metastatic non-small cell lung cancer, and used off-label for treatment of agerelated macular degeneration, it has now also been approved by the FDA for use in combination with paclitaxel (Taxol, and others) for first-line treatment of...
Revakinagene Taroretcel (Encelto) – A Gene Therapy for Idiopathic Macular Telangiectasia (online only)
The Medical Letter on Drugs and Therapeutics • Apr 28, 2025 (Issue 1727)
Revakinagene Taroretcel (Encelto) – A Gene Therapy for Idiopathic Macular Telangiectasia (online ...
Revakinagene taroretcel-lwey (Encelto – Neurotech),
an intravitreal allogeneic cell-based gene therapy, has
been approved by the FDA for treatment of idiopathic
macular telangiectasia type 2 in adults. It is the first
treatment to be approved in the US for this indication.
Med Lett Drugs Ther. 2025 Apr 28;67(1727):e74 doi:10.58347/tml.2025.1727f | Show Introduction Hide Introduction
Voretigene Neparvovec-rzyl (Luxturna) for Inherited Retinal Dystrophy
The Medical Letter on Drugs and Therapeutics • Mar 26, 2018 (Issue 1543)
to reduced or absent
enzyme activity, blocking the visual cycle and leading
to degeneration of retinal ...
The FDA has approved voretigene neparvovec-rzyl
intraocular suspension (Luxturna – Spark), an
adeno-associated virus vector-based gene therapy,
for treatment of confirmed biallelic RPE65 mutation-associated
retinal dystrophy in patients who have viable
retinal cells. It is the first gene replacement therapy
approved in the US that targets a disease caused by
mutations in a specific gene and the first pharmacologic
treatment to be approved for this disorder.