A.P. Pharma Announces Changes in Management
and Hires Leading Consulting Practice to Lead
FDA Review Process
May 26, 2010 06:33 AM Eastern Daylight Time
REDWOOD CITY, Calif.--(EON: Enhanced Online News)--A.P. Pharma, Inc. (Nasdaq:APPA), a specialty
pharmaceutical company, today announced that it has hired a leading consulting practice in pharmaceutical regulatory
affairs to lead the U.S. Food and Drug Administration (FDA) review process and formed a special committee of the
Board to oversee the Company’s regulatory affairs. These actions have been taken to maximize the probability of
approval by the FDA of APF530, its lead product candidate for the prevention of acute- and delayed-onset
chemotherapy-induced nausea and vomiting. APF530 is a long-acting formulation of granisetron that utilizes the
Company’s proprietary Biochronomer™ drug delivery system. In March 2010, A.P. Pharma received a Complete
Response Letter from the FDA regarding its New Drug Application submitted in May 2009. The Complete
Response Letter outlined several issues that would need to be addressed prior to FDA approval of APF530.
A.P. Pharma also announced that Ronald J. Prentki, President, Chief Executive Officer and Director, has resigned
due to differences of opinion in regulatory strategy. Mr. Prentki has agreed to assist in implementing an orderly
transition of management responsibilities. With Mr. Prentki’s resignation, the Company announced that John B.
Whelan, who has served as Vice President, Finance and Chief Financial Officer since February 2009, has been
appointed to the position of Acting Chief Executive Officer.
“In going forward, we have one goal in mind: to thoughtfully and thoroughly address FDA’s remaining concerns as
outlined in the March 2010 Complete Response Letter so that we may best facilitate the approval of our lead
product,” stated Paul Goddard, Ph.D., Chairman of the Board. “We remain fully committed to APF530, as we
believe that this product could improve the lives of many patients