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    <introducedDate>2017-06-29</introducedDate>
    <congress>115</congress>
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        <title>OPEN Act</title>
        <congress>115</congress>
        <number>1223</number>
        <type>HR</type>
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          <actionDate>2017-03-03</actionDate>
          <text>Referred to the Subcommittee on Health.</text>
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        <text>Read twice and referred to the Committee on Health, Education, Labor, and Pensions.</text>
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        <actionDate>2017-06-29</actionDate>
        <text>Introduced in Senate</text>
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        <bioguideId>H000338</bioguideId>
        <fullName>Sen. Hatch, Orrin G. [R-UT]</fullName>
        <firstName>ORRIN</firstName>
        <lastName>HATCH</lastName>
        <party>R</party>
        <state>UT</state>
        <middleName>GRANT</middleName>
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        <fullName>Sen. Menendez, Robert [D-NJ]</fullName>
        <firstName>Robert</firstName>
        <lastName>Menendez</lastName>
        <party>D</party>
        <state>NJ</state>
        <sponsorshipDate>2017-06-29</sponsorshipDate>
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        <bioguideId>S001184</bioguideId>
        <fullName>Sen. Scott, Tim [R-SC]</fullName>
        <firstName>Tim</firstName>
        <lastName>Scott</lastName>
        <party>R</party>
        <state>SC</state>
        <sponsorshipDate>2017-08-02</sponsorshipDate>
        <isOriginalCosponsor>False</isOriginalCosponsor>
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      <item>
        <bioguideId>N000032</bioguideId>
        <fullName>Sen. Nelson, Bill [D-FL]</fullName>
        <firstName>CLARENCE</firstName>
        <lastName>NELSON</lastName>
        <party>D</party>
        <state>FL</state>
        <middleName>WILLIAM</middleName>
        <sponsorshipDate>2017-08-02</sponsorshipDate>
        <isOriginalCosponsor>False</isOriginalCosponsor>
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        <fullName>Sen. Rubio, Marco [R-FL]</fullName>
        <firstName>Marco</firstName>
        <lastName>Rubio</lastName>
        <party>R</party>
        <state>FL</state>
        <sponsorshipDate>2018-01-30</sponsorshipDate>
        <isOriginalCosponsor>False</isOriginalCosponsor>
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        <bioguideId>D000607</bioguideId>
        <fullName>Sen. Donnelly, Joe [D-IN]</fullName>
        <firstName>Joe</firstName>
        <lastName>Donnelly</lastName>
        <party>D</party>
        <state>IN</state>
        <sponsorshipDate>2018-07-31</sponsorshipDate>
        <isOriginalCosponsor>False</isOriginalCosponsor>
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      <name>Health</name>
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          <name>Administrative law and regulatory procedures</name>
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        <item>
          <name>Administrative remedies</name>
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          <name>Child health</name>
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          <name>Department of Health and Human Services</name>
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          <name>Drug safety, medical device, and laboratory regulation</name>
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        <item>
          <name>Drug therapy</name>
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          <name>Food and Drug Administration (FDA)</name>
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          <name>Government information and archives</name>
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          <name>Intellectual property</name>
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          <name>Licensing and registrations</name>
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          <name>Prescription drugs</name>
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        <name>Health</name>
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      <summary>
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        <actionDate>2017-06-29</actionDate>
        <actionDesc>Introduced in Senate</actionDesc>
        <updateDate>2018-05-08T20:44:31Z</updateDate>
        <text><![CDATA[ <p><b>Orphan Products Extension Now Accelerating Cures and Treatments Act of 2017</b></p> <p>This bill amends the Federal Food, Drug, and Cosmetic Act to require the Food and Drug Administration (FDA) to extend by six months the exclusivity period for an approved drug or biological product when the product is additionally approved to prevent, diagnose, or treat a new indication that is a rare disease or condition (also known as an orphan disease). The FDA may revoke an extension if the application for the new indication contained an untrue material statement. The FDA must notify the public of products that receive this extension and patents related to those products. Products may receive only one of these extensions. This extension is in addition to other extensions. Only products approved after enactment of this bill for a new indication that is a rare disease or condition are eligible for an extension.</p> <p>For a medication to be approved as an orphan drug with seven years of marketing exclusivity when it is the same medication for the same condition as an already approved orphan drug, the sponsor of the new medication must demonstrate that the new medication is clinically superior to the approved medication.</p> The bill expands to cover brand name drugs provisions that allow generic drugs to be approved and marketed without labeling for pediatric indications when the pediatric indications are protected by patent or marketing exclusivity.]]></text>
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    </summaries>
    <title>Orphan Products Extension Now Accelerating Cures and Treatments Act of 2017</title>
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        <titleType>Display Title</titleType>
        <title>Orphan Products Extension Now Accelerating Cures and Treatments Act of 2017</title>
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        <titleType>Official Title as Introduced</titleType>
        <title>A bill to amend the Federal Food, Drug, and Cosmetic Act to authorize an extension of exclusivity periods for certain drugs that are approved for a new indication for a rare disease or condition, and for other purposes.</title>
        <billTextVersionName>Introduced in Senate</billTextVersionName>
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        <titleType>Short Titles as Introduced</titleType>
        <title>Orphan Products Extension Now Accelerating Cures and Treatments Act of 2017</title>
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        <type>Introduced in Senate</type>
        <date>2017-06-29T04:00:00Z</date>
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            <url>https://www.govinfo.gov/content/pkg/BILLS-115s1509is/xml/BILLS-115s1509is.xml</url>
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    <latestAction>
      <actionDate>2017-06-29</actionDate>
      <text>Read twice and referred to the Committee on Health, Education, Labor, and Pensions.</text>
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    <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>
    <dc:contributor>Congressional Research Service, Library of Congress</dc:contributor>
    <dc:description>This file contains bill summaries and statuses for federal legislation. A bill summary describes the most significant provisions of a piece of legislation and details the effects the legislative text may have on current law and federal programs. Bill summaries are authored by the Congressional Research Service (CRS) of the Library of Congress. As stated in Public Law 91-510 (2 USC 166 (d)(6)), one of the duties of CRS is "to prepare summaries and digests of bills and resolutions of a public general nature introduced in the Senate or House of Representatives". For more information, refer to the User Guide that accompanies this file.</dc:description>
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