Second Eligard product approved

Published: 22-Aug-2002
Regulatory


The US FDA has approved Atrix Laboratories' Eligard 22.5mg (leuprolide acetate for injectable suspension), for the palliative treatment of advanced prostate cancer. This is the second Eligard product to be approved this year - Eligard 7.5mg (leuprolide acetate for injectable suspension), a once-a-month sustained release product, was approved in January.

Both products will be marketed in the US by Sanofi-Synthelabo Inc. Under the terms of the agreement, Atrix will receive royalties on sales of the Eligard products and will manufacture the products at its facility in Fort Collins, Colorado. The total worldwide market for this type of therapy is estimated at US$2.4bn (€2.5bn).

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