You are currently viewing archive.bio.org. Head to our home page to check out our fresh new look!

BIO Urges Governor Deal to Sign Bill That Ensures Patient Access to Interchangeable Biologic Medicines

<div id="x_divtagdefaultwrapper">
<div dir="ltr">
<div id="x_divtagdefaultwrapper">
<p>
The Georgia Senate passed&nbsp;<a href="http://www.legis.ga.gov/Legislation/en-US/display/20152016/SB/51" target="_blank">Senate Bill 51</a>&nbsp;last week with a vote of 43-3. This action follows a unanimous vote on the same bill in the House.</p>
</div>
</div>
</div>
<p>
&nbsp;</p>

Washington, D.C. (March 30, 2015) –  The Biotechnology Industry Organization (BIO) and Georgia Bio call upon Governor Deal to sign critical legislation to create a pathway for the substitution of interchangeable biologic medicines.

The Georgia Senate passed Senate Bill 51 last week with a vote of 43-3. This action follows a unanimous vote on the same bill in the House.

The policies outlined in the bill align with BIO’s principles on biologic substitution, therefore BIO and Georgia Bio support this important legislation and encourage Governor Deal to sign the bill when it reaches his desk.

“Senate Bill 51 enjoys the support of physicians across the country, patient groups, and both innovator biologic and biosimilar manufacturing companies. This bill includes transparent communication on all biologic medicines dispensed in order to maintain a consistent and complete medical record,” said Jim Greenwood, BIO’s President and CEO. “This legislation represents a significant step forward, ensures transparency and communication between patients and their treatment teams, and is fully consistent with the BIO principles.”   

While the U.S. Food and Drug Administration (FDA) oversees approval of biologic medicines and designation of interchangeability, policies governing whether one product may be substituted in place of a doctor's prescription and whether a pharmacist must inform patients and doctors are covered by state law. Senate Bill 51 seeks to properly preserve patient access to accurate prescription information, maintains incentives for innovation and promotes a competitive market for biologic therapies. BIO will continue to advocate for full transparency in the substitution process, as patients and their physicians should have the right to know what biologic medicine the patient receives from the pharmacy.

“This legislation will benefit Georgians when the first interchangeable biologics are approved by the FDA,” said Russell Allen, President and CEO of Georgia Bio. “When they become available, these therapies will be safe, effective, and similar to innovator biologics. Furthermore, they will provide patients with more opportunities to address their unmet medical needs, particularly severely ill patients who rely on cutting-edge medical treatments.”

While the FDA recently approved the first biosimilar product for sale in the U.S, the agency continues to develop a pathway for the development and approval of safe and effective interchangeable biologic products the United States. In fact the FDA has indicated they expect to see applications for interchangeable biosimilar product approvals this year. However, there is still a major role for states to play in ensuring substitution practices remain transparent and physicians remain engaged in the process.

“Interchangeable biologics are not generics. Even slight changes to a biologic drug can change its properties entirely,” said Greenwood. “Unlike conventional generic medicines, interchangeable biologics are not the same as the drugs they seek to substitute. In fact, two biologics made using different cell lines and differing manufacturing processes will rarely, if ever, be exactly the same. Those suggesting interchangeable biologics and generics are the same are wrong.”

Patients and physicians managing chronic conditions are generally aware of which biologic treatments work best in their unique circumstances. Communicating with patients and physicians allows everyone involved the opportunity to discuss past treatment experiences so that any possible unexpected issues can be better understood and avoided.  

As the Georgia General Assembly continues to address issues related to biologic medicines, BIO and Georgia Bio encourage policy makers to continue to put patients first.

About Georgia Bio

Georgia Bio (GaBio), founded in 1989, is a non-profit, membership-based organization that promotes the interests and growth of the life sciences industry.  Members include companies, universities, research institutions, government groups and other industry associations involved in discovery and application of life sciences products and related services that improve the health and well-being of people throughout the world.