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<bill bill-stage="Introduced-in-Senate" dms-id="A1" public-private="public" slc-id="S1-KEL23118-5FW-00-GST"><metadata xmlns:dc="http://purl.org/dc/elements/1.1/">
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<dc:title>118 S476 IS: Maintaining Investments in New Innovation Act</dc:title>
<dc:publisher>U.S. Senate</dc:publisher>
<dc:date>2023-02-16</dc:date>
<dc:format>text/xml</dc:format>
<dc:language>EN</dc:language>
<dc:rights>Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain.</dc:rights>
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<distribution-code display="yes">II</distribution-code><congress>118th CONGRESS</congress><session>1st Session</session><legis-num>S. 476</legis-num><current-chamber>IN THE SENATE OF THE UNITED STATES</current-chamber><action><action-date date="20230216">February 16, 2023</action-date><action-desc><sponsor name-id="S306">Mr. Menendez</sponsor> (for himself and <cosponsor name-id="S396">Mrs. Blackburn</cosponsor>) introduced the following bill; which was read twice and referred to the <committee-name committee-id="SSFI00">Committee on Finance</committee-name></action-desc></action><legis-type>A BILL</legis-type><official-title>To amend title XI of the Social Security Act to protect access to genetically targeted technologies.</official-title></form><legis-body><section id="S1" section-type="section-one"><enum>1.</enum><header>Short title</header><text display-inline="no-display-inline">This Act may be cited as the <quote><short-title>Maintaining Investments in New Innovation Act</short-title></quote>.</text></section><section id="idbeee0f689ccd40e49de8931369339f56"><enum>2.</enum><header>Amendment to definition of qualifying single source drug</header><text display-inline="no-display-inline">Section 1192(e) of the Social Security Act (<external-xref legal-doc="usc" parsable-cite="usc/42/1320f-1">42 U.S.C. 1320f–1(e)</external-xref>) is amended—</text><paragraph id="id4ddb2c5203bb478c80134cffe8cbc53c"><enum>(1)</enum><text>in paragraph (1)(A)(ii), by inserting <quote>(or, in the case of an advanced drug product (as defined in paragraph (4)), 11 years)</quote> after <quote>7 years</quote>; and</text></paragraph><paragraph id="idc2776102f28f463184d318e241bace7e"><enum>(2)</enum><text>by adding at the end the following new paragraph:</text><quoted-block style="OLC" display-inline="no-display-inline" id="id3512de8721544eaab8e6e8e66bd8b8df"><paragraph id="id72c2bd4208b34e558eb36378c91b8828"><enum>(4)</enum><header>Advanced drug product defined</header><text>For purposes of paragraph (1)(A)(ii), the term <term>advanced drug product</term> means a drug that incorporates or utilizes a genetically targeted technology (as defined in section 529A(c)(2) of the Federal Food, Drug, and Cosmetic Act) that may result in the modulation (including suppression, up-regulation, or activation) of the function of a gene or its associated gene product.</text></paragraph><after-quoted-block>.</after-quoted-block></quoted-block></paragraph></section></legis-body></bill> 

