Case Study

Genentech’s dilemma: Avastin vs. Lucentis

3 pages
October 2008
Reference: IMD-3-2004

On October 19, 2007, Herb Kohl, the chairman of the US Senate’s Special Committee on Aging, asked Genentech to clarify its decision to limit the availability of its product Avastin in favor of its more expensive drug Lucentis, both applied in the treatment of wet age-related macular degeneration. In 2007 age-related macular degeneration (AMD) was the leading cause of severe vision loss in people over the age of 65 in the Western world. In the US, more than 1.6 million people had one or both eyes affected by the advanced stage of AMD, another 7 million were estimated to be “at risk” and more than 230,000 people were deemed to be legally blind due to it. The direct cost of illness associated with AMD was estimated to be above $10 billion annually. Wet AMD (wAMD) accounted for 10% to 15% of the cases.

Keywords
Off-label Drug Use, Biopharmaceutical
Settings
United States of America
Novartis, Health Care, Biopharmaceuticals
2007
Type
Published Sources
Copyright
© 2008
Available Languages
English
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