Skip to Content


Treatment for Primary IGF-1 Deficiency

Tercica Announces Insmed Files Citizen Petition with the FDA to Deny Approval of Increlex NDA

BRISBANE, Calif., August 14, 2005 -- Tercica, Inc. announced today that Insmed Incorporated has filed a Citizen Petition to immediately deny approval of Tercica's NDA for Increlex. Upon inquiry, the U.S. Food & Drug Administration informed the company that the content of the Citizen Petition will be made available publicly in approximately three days.

"While we don't have access to the content of Insmed's Citizen Petition, we believe it was important to disclose this development," said John A. Scarlett, M.D., President and Chief Executive Officer of Tercica. "Tercica has received no communication from the FDA regarding how this Citizen Petition will affect the Increlex NDA, if at all."

Source: Tercica, Inc.

Posted: August 2005

Related Articles

Increlex (mecasermin) FDA Approval History