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   <title>Form  4          CORCEPT THERAPEUTICS      For: Jun 17  Filed by: MAHONEY DAVID L</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++CORCEPT+THERAPEUTICS++++++For%3A+Jun+17++Filed+by%3A+MAHONEY+DAVID+L/26666588.html</link>
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   <title>Form  4          CORCEPT THERAPEUTICS      For: Jun 17  Filed by: MAHONEY DAVID L</title>
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   <title>Form  4          CORCEPT THERAPEUTICS      For: Jun 16  Filed by: WILSON JAMES N</title>
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   <title>Form  4          CORCEPT THERAPEUTICS      For: Jun 16  Filed by: WILSON JAMES N</title>
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   <title>Form  8-K        CORCEPT THERAPEUTICS      For: Jun 17</title>
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   <title>Form  8-K        CORCEPT THERAPEUTICS      For: Jun 17</title>
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   <title>Form  4          CORCEPT THERAPEUTICS      For: Jun 15  Filed by: Mokari Atabak</title>
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   <title>Form  4          CORCEPT THERAPEUTICS      For: Jun 15  Filed by: Mokari Atabak</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++CORCEPT+THERAPEUTICS++++++For%3A+Jun+15++Filed+by%3A+Mokari+Atabak/26660384.html</link>
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   <title>Corcept resubmits NDA for relacorilant to treat Cushing's syndrome</title>
   <link>http://www.streetinsider.com/FDA/Corcept+resubmits+NDA+for+relacorilant+to+treat+Cushing%27s+syndrome/26660312.html</link>
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&lt;p&gt;Corcept Therapeutics (NASDAQ: CORT) has resubmitted its New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for relacorilant as a treatment for Cushing's syndrome, according to a company statement.&lt;/p&gt;

&lt;p&gt;The resubmission includes additional analyses of data from the original NDA, as requested by the FDA. Corcept expects the resubmission to receive a six-month review.&lt;/p&gt;

&lt;p&gt;The filing is supported by data from the pivotal GRACE trial, the double-blind, placebo-controlled Phase III GRADIENT trial, a long-term extension study, and earlier-stage development data. Corcept said the data indicate relacorilant provides improvements in the signs and symptoms of Cushing's syndrome without some of</description>
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   <title>Corcept resubmits NDA for relacorilant to treat Cushing's syndrome</title>
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&lt;p&gt;Corcept Therapeutics (NASDAQ: CORT) has resubmitted its New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for relacorilant as a treatment for Cushing's syndrome, according to a company statement.&lt;/p&gt;

&lt;p&gt;The resubmission includes additional analyses of data from the original NDA, as requested by the FDA. Corcept expects the resubmission to receive a six-month review.&lt;/p&gt;

&lt;p&gt;The filing is supported by data from the pivotal GRACE trial, the double-blind, placebo-controlled Phase III GRADIENT trial, a long-term extension study, and earlier-stage development data. Corcept said the data indicate relacorilant provides improvements in the signs and symptoms of Cushing's syndrome without some of</description>
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   <title>Corcept resubmits NDA for relacorilant to treat Cushing's syndrome</title>
   <link>http://www.streetinsider.com/FDA/Corcept+resubmits+NDA+for+relacorilant+to+treat+Cushing%27s+syndrome/26660312.html</link>
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&lt;p&gt;Corcept Therapeutics (NASDAQ: CORT) has resubmitted its New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for relacorilant as a treatment for Cushing's syndrome, according to a company statement.&lt;/p&gt;

&lt;p&gt;The resubmission includes additional analyses of data from the original NDA, as requested by the FDA. Corcept expects the resubmission to receive a six-month review.&lt;/p&gt;

&lt;p&gt;The filing is supported by data from the pivotal GRACE trial, the double-blind, placebo-controlled Phase III GRADIENT trial, a long-term extension study, and earlier-stage development data. Corcept said the data indicate relacorilant provides improvements in the signs and symptoms of Cushing's syndrome without some of</description>
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   <title>Corcept resubmits NDA for relacorilant to treat Cushing's syndrome</title>
   <link>http://www.streetinsider.com/FDA/Corcept+resubmits+NDA+for+relacorilant+to+treat+Cushing%27s+syndrome/26660312.html</link>
   <description>

&lt;p&gt;Corcept Therapeutics (NASDAQ: CORT) has resubmitted its New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for relacorilant as a treatment for Cushing's syndrome, according to a company statement.&lt;/p&gt;

&lt;p&gt;The resubmission includes additional analyses of data from the original NDA, as requested by the FDA. Corcept expects the resubmission to receive a six-month review.&lt;/p&gt;

&lt;p&gt;The filing is supported by data from the pivotal GRACE trial, the double-blind, placebo-controlled Phase III GRADIENT trial, a long-term extension study, and earlier-stage development data. Corcept said the data indicate relacorilant provides improvements in the signs and symptoms of Cushing's syndrome without some of</description>
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   <title>Corcept resubmits NDA for relacorilant to treat Cushing's syndrome</title>
   <link>http://www.streetinsider.com/FDA/Corcept+resubmits+NDA+for+relacorilant+to+treat+Cushing%27s+syndrome/26660312.html</link>
   <description>

&lt;p&gt;Corcept Therapeutics (NASDAQ: CORT) has resubmitted its New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for relacorilant as a treatment for Cushing's syndrome, according to a company statement.&lt;/p&gt;

&lt;p&gt;The resubmission includes additional analyses of data from the original NDA, as requested by the FDA. Corcept expects the resubmission to receive a six-month review.&lt;/p&gt;

&lt;p&gt;The filing is supported by data from the pivotal GRACE trial, the double-blind, placebo-controlled Phase III GRADIENT trial, a long-term extension study, and earlier-stage development data. Corcept said the data indicate relacorilant provides improvements in the signs and symptoms of Cushing's syndrome without some of</description>
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   <title>Corcept resubmits NDA for relacorilant to treat Cushing's syndrome</title>
   <link>http://www.streetinsider.com/FDA/Corcept+resubmits+NDA+for+relacorilant+to+treat+Cushing%27s+syndrome/26660312.html</link>
   <description>

&lt;p&gt;Corcept Therapeutics (NASDAQ: CORT) has resubmitted its New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for relacorilant as a treatment for Cushing's syndrome, according to a company statement.&lt;/p&gt;

&lt;p&gt;The resubmission includes additional analyses of data from the original NDA, as requested by the FDA. Corcept expects the resubmission to receive a six-month review.&lt;/p&gt;

&lt;p&gt;The filing is supported by data from the pivotal GRACE trial, the double-blind, placebo-controlled Phase III GRADIENT trial, a long-term extension study, and earlier-stage development data. Corcept said the data indicate relacorilant provides improvements in the signs and symptoms of Cushing's syndrome without some of</description>
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   <title>Corcept resubmits NDA for relacorilant to treat Cushing's syndrome</title>
   <link>http://www.streetinsider.com/FDA/Corcept+resubmits+NDA+for+relacorilant+to+treat+Cushing%27s+syndrome/26660312.html</link>
   <description>

&lt;p&gt;Corcept Therapeutics (NASDAQ: CORT) has resubmitted its New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for relacorilant as a treatment for Cushing's syndrome, according to a company statement.&lt;/p&gt;

&lt;p&gt;The resubmission includes additional analyses of data from the original NDA, as requested by the FDA. Corcept expects the resubmission to receive a six-month review.&lt;/p&gt;

&lt;p&gt;The filing is supported by data from the pivotal GRACE trial, the double-blind, placebo-controlled Phase III GRADIENT trial, a long-term extension study, and earlier-stage development data. Corcept said the data indicate relacorilant provides improvements in the signs and symptoms of Cushing's syndrome without some of</description>
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   <title>Corcept resubmits NDA for relacorilant to treat Cushing's syndrome</title>
   <link>http://www.streetinsider.com/FDA/Corcept+resubmits+NDA+for+relacorilant+to+treat+Cushing%27s+syndrome/26660312.html</link>
   <description>

&lt;p&gt;Corcept Therapeutics (NASDAQ: CORT) has resubmitted its New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for relacorilant as a treatment for Cushing's syndrome, according to a company statement.&lt;/p&gt;

&lt;p&gt;The resubmission includes additional analyses of data from the original NDA, as requested by the FDA. Corcept expects the resubmission to receive a six-month review.&lt;/p&gt;

&lt;p&gt;The filing is supported by data from the pivotal GRACE trial, the double-blind, placebo-controlled Phase III GRADIENT trial, a long-term extension study, and earlier-stage development data. Corcept said the data indicate relacorilant provides improvements in the signs and symptoms of Cushing's syndrome without some of</description>
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   <title>Corcept Resubmits New Drug Application for Relacorilant as a Treatment for Patients with Cushing’s Syndrome</title>
   <link>http://www.streetinsider.com/Press+Releases/Corcept+Resubmits+New+Drug+Application+for+Relacorilant+as+a+Treatment+for+Patients+with+Cushing%E2%80%99s+Syndrome/26660308.html</link>
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&lt;p&gt;    REDWOOD CITY, Calif.--(BUSINESS WIRE)--&lt;/p&gt;
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