ALEXANDRIA, VA -- (Marketwire) -- 06/23/09 -- The Academy of Managed Care Pharmacy (AMCP) has endorsed bipartisan legislation that would create a regulatory pathway for the approval of follow-on biologics and allow competition on brand-name biologics after five years of marketing exclusivity instead of the pharmaceutical industry's preferred 14-year window.
AMCP strongly supports H.R. 1427 and S. 729, the "Promoting Innovation and Access to Live-Savings Medicine Act of 2009," the Academy said in a June 22 letter to Rep. Henry Waxman (D-Calif.), Chairman of the House Energy and Commerce Committee, and Sen. Charles Schumer (D-N.Y.). Waxman and Schumer are lead sponsors of the respective bills.
Biologics are drugs made from living cells rather than chemical compounds. Brand-name biologics hold a virtual monopoly on the market because the U.S. Food and Drug Administration (FDA) currently lacks a regulatory pathway to approve less costly versions.
"Safe alternatives to some biologics have existed for more than 20 years," Judith Cahill, executive director of AMCP, said in the letter. "In anticipation of the expiration of patents for older biologic products and the new biologic products that are expected to come to market, and in recognition of the fact that these products are often prohibitively expensive, it is imperative that Congress address this issue," she added.
According to the legislation, a five-year window of marketing exclusivity would not begin at the time of the bill's enactment, but rather from the time when the brand-name drug was first approved. In the case of some biologics that have been on the market for 20 years with no competition, drug manufacturers would be able to seek approval for their follow-on versions "right away," according to a release posted on Schumer's website.
AMCP notes that the field of biotechnology holds great promise for the development of new therapies to prevent, treat or cure disease. At the same time, biologics are consuming an ever-larger percentage of overall spending on prescription drugs, often putting them out of reach of patients, the Academy adds. AMCP supports an expedited review process by the FDA, but one that recognizes there are potentially significant differences between a follow-on biologic product and a generic chemical drug.
AMCP believes the federal government should provide incentives to encourage innovator companies to pursue the development of safe and effective biologics while encouraging competition to ensure a robust marketplace. "The approach taken in your legislation appears to be consistent in meeting these objectives," Cahill told the lawmakers in the letter.
For more information, visit AMCP at www.amcp.org. The letter is available in the Public Policy & Advocacy section under Analyses, Statements & Letters.
The Academy of Managed Care Pharmacy (AMCP) is a national professional association of pharmacists and other health care practitioners who serve society by the application of sound medication management principles and strategies to improve health care for all. The Academy's 5,700 members develop and provide a diversified range of clinical, educational and business management services and strategies on behalf of the more than 200 million Americans covered by a managed care pharmacy benefit. More news and information about AMCP can be obtained on its website, at www.amcp.org. The Academy will observe its 20th anniversary in 2009.