FDA Approves Viracept, New Protease Inhibitor

Publication
Article
Oncology NEWS InternationalOncology NEWS International Vol 6 No 4
Volume 6
Issue 4

ROCKVILLE, Md--The FDA has given Agouron Pharmaceuticals clearance to market its protease inhibitor Viracept (nelfinavir mesylate), under the accelerated approval process. Viracept was approved in both adult and pediatric formulations, for the treatment of HIV when antiretroviral therapy is warranted.

ROCKVILLE, Md--The FDA has given Agouron Pharmaceuticals clearance tomarket its protease inhibitor Viracept (nelfinavir mesylate), under theaccelerated approval process. Viracept was approved in both adult and pediatricformulations, for the treatment of HIV when antiretroviral therapy is warranted.

The indication is based on analyses of surrogate marker changes in patientswho received Viracept in combination with nucleoside analogues or alonefor up to 24 weeks. At present, there are no results from controlled trialsevaluating the effects of Viracept on clinical progression of HIV infection,such as survival or the incidence of opportunistic infections.

Recent Videos
According to Jorge Nieva, MD, there are a multitude of things that can be explored to enhance the treatment landscape for lung cancer.
5 experts are featured in this series
2 experts are featured in this series.
5 experts are featured in this series
2 experts are featured in this series.
Taletrectinib showed improved efficacy in patients with ROS1-positive non–small cell lung cancer who were treatment-naïve.
“It’s a drug that I’m very comfortable with, and it is a drug I’ll likely use primarily in the first-line setting,” stated Jorge Nieva, MD, on taletrectinib in non–small cell lung cancer.
4 experts in this video
4 experts in this video
Those being treated for peritoneal carcinomatosis may not have to experience the complication rates or prolonged recovery associated with surgical options.
Related Content