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   <title>Roche wins FDA nod for HER2 companion diagnostics in GEA</title>
   <link>http://www.streetinsider.com/FDA/Roche+wins+FDA+nod+for+HER2+companion+diagnostics+in+GEA/26980827.html</link>
   <description>

&lt;p&gt;Roche (SIX: RO, ROG; OTCQX: RHHBY) has received FDA approval to expand the use of two companion diagnostic tests to identify HER2-positive metastatic gastroesophageal adenocarcinoma (GEA) patients eligible for treatment with Jazz Pharmaceuticals' ZIIHERA (zanidatamab-hrii), according to a company statement.&lt;/p&gt;

&lt;p&gt;The approved tests — the PATHWAY HER2 (4B5) Rabbit Monoclonal Primary Antibody test and the VENTANA HER2 Dual ISH DNA Probe Cocktail — are now indicated for use in patients with metastatic gastric, gastroesophageal junction, and esophageal adenocarcinoma. The approval covers identification of patients who may be eligible for two ZIIHERA-containing regimens, both of which are FDA approved for first-line treatment</description>
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   <title>Roche wins FDA nod for HER2 companion diagnostics in GEA</title>
   <link>http://www.streetinsider.com/FDA/Roche+wins+FDA+nod+for+HER2+companion+diagnostics+in+GEA/26980827.html</link>
   <description>

&lt;p&gt;Roche (SIX: RO, ROG; OTCQX: RHHBY) has received FDA approval to expand the use of two companion diagnostic tests to identify HER2-positive metastatic gastroesophageal adenocarcinoma (GEA) patients eligible for treatment with Jazz Pharmaceuticals' ZIIHERA (zanidatamab-hrii), according to a company statement.&lt;/p&gt;

&lt;p&gt;The approved tests — the PATHWAY HER2 (4B5) Rabbit Monoclonal Primary Antibody test and the VENTANA HER2 Dual ISH DNA Probe Cocktail — are now indicated for use in patients with metastatic gastric, gastroesophageal junction, and esophageal adenocarcinoma. The approval covers identification of patients who may be eligible for two ZIIHERA-containing regimens, both of which are FDA approved for first-line treatment</description>
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   <title>Roche wins FDA nod for HER2 companion diagnostics in GEA</title>
   <link>http://www.streetinsider.com/FDA/Roche+wins+FDA+nod+for+HER2+companion+diagnostics+in+GEA/26980827.html</link>
   <description>

&lt;p&gt;Roche (SIX: RO, ROG; OTCQX: RHHBY) has received FDA approval to expand the use of two companion diagnostic tests to identify HER2-positive metastatic gastroesophageal adenocarcinoma (GEA) patients eligible for treatment with Jazz Pharmaceuticals' ZIIHERA (zanidatamab-hrii), according to a company statement.&lt;/p&gt;

&lt;p&gt;The approved tests — the PATHWAY HER2 (4B5) Rabbit Monoclonal Primary Antibody test and the VENTANA HER2 Dual ISH DNA Probe Cocktail — are now indicated for use in patients with metastatic gastric, gastroesophageal junction, and esophageal adenocarcinoma. The approval covers identification of patients who may be eligible for two ZIIHERA-containing regimens, both of which are FDA approved for first-line treatment</description>
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   <title>Roche wins FDA nod for HER2 companion diagnostics in GEA</title>
   <link>http://www.streetinsider.com/FDA/Roche+wins+FDA+nod+for+HER2+companion+diagnostics+in+GEA/26980827.html</link>
   <description>

&lt;p&gt;Roche (SIX: RO, ROG; OTCQX: RHHBY) has received FDA approval to expand the use of two companion diagnostic tests to identify HER2-positive metastatic gastroesophageal adenocarcinoma (GEA) patients eligible for treatment with Jazz Pharmaceuticals' ZIIHERA (zanidatamab-hrii), according to a company statement.&lt;/p&gt;

&lt;p&gt;The approved tests — the PATHWAY HER2 (4B5) Rabbit Monoclonal Primary Antibody test and the VENTANA HER2 Dual ISH DNA Probe Cocktail — are now indicated for use in patients with metastatic gastric, gastroesophageal junction, and esophageal adenocarcinoma. The approval covers identification of patients who may be eligible for two ZIIHERA-containing regimens, both of which are FDA approved for first-line treatment</description>
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   <title>Roche wins FDA nod for HER2 companion diagnostics in GEA</title>
   <link>http://www.streetinsider.com/FDA/Roche+wins+FDA+nod+for+HER2+companion+diagnostics+in+GEA/26980827.html</link>
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&lt;p&gt;Roche (SIX: RO, ROG; OTCQX: RHHBY) has received FDA approval to expand the use of two companion diagnostic tests to identify HER2-positive metastatic gastroesophageal adenocarcinoma (GEA) patients eligible for treatment with Jazz Pharmaceuticals' ZIIHERA (zanidatamab-hrii), according to a company statement.&lt;/p&gt;

&lt;p&gt;The approved tests — the PATHWAY HER2 (4B5) Rabbit Monoclonal Primary Antibody test and the VENTANA HER2 Dual ISH DNA Probe Cocktail — are now indicated for use in patients with metastatic gastric, gastroesophageal junction, and esophageal adenocarcinoma. The approval covers identification of patients who may be eligible for two ZIIHERA-containing regimens, both of which are FDA approved for first-line treatment</description>
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   <title>Roche wins FDA nod for HER2 companion diagnostics in GEA</title>
   <link>http://www.streetinsider.com/FDA/Roche+wins+FDA+nod+for+HER2+companion+diagnostics+in+GEA/26980827.html</link>
   <description>

&lt;p&gt;Roche (SIX: RO, ROG; OTCQX: RHHBY) has received FDA approval to expand the use of two companion diagnostic tests to identify HER2-positive metastatic gastroesophageal adenocarcinoma (GEA) patients eligible for treatment with Jazz Pharmaceuticals' ZIIHERA (zanidatamab-hrii), according to a company statement.&lt;/p&gt;

&lt;p&gt;The approved tests — the PATHWAY HER2 (4B5) Rabbit Monoclonal Primary Antibody test and the VENTANA HER2 Dual ISH DNA Probe Cocktail — are now indicated for use in patients with metastatic gastric, gastroesophageal junction, and esophageal adenocarcinoma. The approval covers identification of patients who may be eligible for two ZIIHERA-containing regimens, both of which are FDA approved for first-line treatment</description>
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   <title>Roche wins FDA nod for HER2 companion diagnostics in GEA</title>
   <link>http://www.streetinsider.com/FDA/Roche+wins+FDA+nod+for+HER2+companion+diagnostics+in+GEA/26980827.html</link>
   <description>

&lt;p&gt;Roche (SIX: RO, ROG; OTCQX: RHHBY) has received FDA approval to expand the use of two companion diagnostic tests to identify HER2-positive metastatic gastroesophageal adenocarcinoma (GEA) patients eligible for treatment with Jazz Pharmaceuticals' ZIIHERA (zanidatamab-hrii), according to a company statement.&lt;/p&gt;

&lt;p&gt;The approved tests — the PATHWAY HER2 (4B5) Rabbit Monoclonal Primary Antibody test and the VENTANA HER2 Dual ISH DNA Probe Cocktail — are now indicated for use in patients with metastatic gastric, gastroesophageal junction, and esophageal adenocarcinoma. The approval covers identification of patients who may be eligible for two ZIIHERA-containing regimens, both of which are FDA approved for first-line treatment</description>
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   <title>Roche receives FDA approval for companion diagnostic tests to identify patients with HER2-positive metastatic gastroesophageal adenocarcinoma eligible for ZIIHERA</title>
   <link>http://www.streetinsider.com/Press+Releases/Roche+receives+FDA+approval+for+companion+diagnostic+tests+to+identify+patients+with+HER2-positive+metastatic+gastroesophageal+adenocarcinoma+eligible+for+ZIIHERA/26980826.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;The PATHWAY HER2 (4B5) test and VENTANA HER2 Dual ISH DNA Probe Cocktail help identify HER2-positive metastatic gastric, gastroesophageal junction and esophageal adenocarcinoma.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Differential diagnosis of these cancers, often aggressive and diagnosed at an advanced stage, is critical to improving patient outcomes.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Together, the tests enable precise assessment of HER2-positive status to help identify patients eligible for treatment with ZIIHERA.&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.az.tucson&quot; idsrc=&quot;xmltag.org&quot; &gt;TUCSON, Ariz.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 26, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Swiss:RO&quot; idsrc=&quot;xmltag.org&quot;&gt;Roche&lt;/span&gt; (SIX: RO, ROG; OTCQX: RHHBY) announced today that it has received FDA approval for expanded use of its PATHWAY&lt;sup&gt;®&lt;/sup&gt; HER2 (4B5) and VENTANA&lt;sup&gt;®&lt;/sup&gt; HER2 Dual ISH DNA</description>
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   <title>Roche receives FDA approval for companion diagnostic tests to identify patients with HER2-positive metastatic gastroesophageal adenocarcinoma eligible for ZIIHERA</title>
   <link>http://www.streetinsider.com/Press+Releases/Roche+receives+FDA+approval+for+companion+diagnostic+tests+to+identify+patients+with+HER2-positive+metastatic+gastroesophageal+adenocarcinoma+eligible+for+ZIIHERA/26980826.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;The PATHWAY HER2 (4B5) test and VENTANA HER2 Dual ISH DNA Probe Cocktail help identify HER2-positive metastatic gastric, gastroesophageal junction and esophageal adenocarcinoma.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Differential diagnosis of these cancers, often aggressive and diagnosed at an advanced stage, is critical to improving patient outcomes.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Together, the tests enable precise assessment of HER2-positive status to help identify patients eligible for treatment with ZIIHERA.&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.az.tucson&quot; idsrc=&quot;xmltag.org&quot; &gt;TUCSON, Ariz.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 26, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Swiss:RO&quot; idsrc=&quot;xmltag.org&quot;&gt;Roche&lt;/span&gt; (SIX: RO, ROG; OTCQX: RHHBY) announced today that it has received FDA approval for expanded use of its PATHWAY&lt;sup&gt;®&lt;/sup&gt; HER2 (4B5) and VENTANA&lt;sup&gt;®&lt;/sup&gt; HER2 Dual ISH DNA</description>
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   <title>Roche receives FDA approval for companion diagnostic tests to identify patients with HER2-positive metastatic gastroesophageal adenocarcinoma eligible for ZIIHERA</title>
   <link>http://www.streetinsider.com/Press+Releases/Roche+receives+FDA+approval+for+companion+diagnostic+tests+to+identify+patients+with+HER2-positive+metastatic+gastroesophageal+adenocarcinoma+eligible+for+ZIIHERA/26980826.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;The PATHWAY HER2 (4B5) test and VENTANA HER2 Dual ISH DNA Probe Cocktail help identify HER2-positive metastatic gastric, gastroesophageal junction and esophageal adenocarcinoma.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Differential diagnosis of these cancers, often aggressive and diagnosed at an advanced stage, is critical to improving patient outcomes.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Together, the tests enable precise assessment of HER2-positive status to help identify patients eligible for treatment with ZIIHERA.&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.az.tucson&quot; idsrc=&quot;xmltag.org&quot; &gt;TUCSON, Ariz.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 26, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Swiss:RO&quot; idsrc=&quot;xmltag.org&quot;&gt;Roche&lt;/span&gt; (SIX: RO, ROG; OTCQX: RHHBY) announced today that it has received FDA approval for expanded use of its PATHWAY&lt;sup&gt;®&lt;/sup&gt; HER2 (4B5) and VENTANA&lt;sup&gt;®&lt;/sup&gt; HER2 Dual ISH DNA</description>
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   <title>Roche receives FDA approval for companion diagnostic tests to identify patients with HER2-positive metastatic gastroesophageal adenocarcinoma eligible for ZIIHERA</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;The PATHWAY HER2 (4B5) test and VENTANA HER2 Dual ISH DNA Probe Cocktail help identify HER2-positive metastatic gastric, gastroesophageal junction and esophageal adenocarcinoma.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Differential diagnosis of these cancers, often aggressive and diagnosed at an advanced stage, is critical to improving patient outcomes.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Together, the tests enable precise assessment of HER2-positive status to help identify patients eligible for treatment with ZIIHERA.&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.az.tucson&quot; idsrc=&quot;xmltag.org&quot; &gt;TUCSON, Ariz.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 26, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Swiss:RO&quot; idsrc=&quot;xmltag.org&quot;&gt;Roche&lt;/span&gt; (SIX: RO, ROG; OTCQX: RHHBY) announced today that it has received FDA approval for expanded use of its PATHWAY&lt;sup&gt;®&lt;/sup&gt; HER2 (4B5) and VENTANA&lt;sup&gt;®&lt;/sup&gt; HER2 Dual ISH DNA</description>
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   <title>Roche receives FDA approval for companion diagnostic tests to identify patients with HER2-positive metastatic gastroesophageal adenocarcinoma eligible for ZIIHERA</title>
   <link>http://www.streetinsider.com/Press+Releases/Roche+receives+FDA+approval+for+companion+diagnostic+tests+to+identify+patients+with+HER2-positive+metastatic+gastroesophageal+adenocarcinoma+eligible+for+ZIIHERA/26980826.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;The PATHWAY HER2 (4B5) test and VENTANA HER2 Dual ISH DNA Probe Cocktail help identify HER2-positive metastatic gastric, gastroesophageal junction and esophageal adenocarcinoma.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Differential diagnosis of these cancers, often aggressive and diagnosed at an advanced stage, is critical to improving patient outcomes.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Together, the tests enable precise assessment of HER2-positive status to help identify patients eligible for treatment with ZIIHERA.&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.az.tucson&quot; idsrc=&quot;xmltag.org&quot; &gt;TUCSON, Ariz.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 26, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Swiss:RO&quot; idsrc=&quot;xmltag.org&quot;&gt;Roche&lt;/span&gt; (SIX: RO, ROG; OTCQX: RHHBY) announced today that it has received FDA approval for expanded use of its PATHWAY&lt;sup&gt;®&lt;/sup&gt; HER2 (4B5) and VENTANA&lt;sup&gt;®&lt;/sup&gt; HER2 Dual ISH DNA</description>
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   <title>Roche receives FDA approval for companion diagnostic tests to identify patients with HER2-positive metastatic gastroesophageal adenocarcinoma eligible for ZIIHERA</title>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;The PATHWAY HER2 (4B5) test and VENTANA HER2 Dual ISH DNA Probe Cocktail help identify HER2-positive metastatic gastric, gastroesophageal junction and esophageal adenocarcinoma.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Differential diagnosis of these cancers, often aggressive and diagnosed at an advanced stage, is critical to improving patient outcomes.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Together, the tests enable precise assessment of HER2-positive status to help identify patients eligible for treatment with ZIIHERA.&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.az.tucson&quot; idsrc=&quot;xmltag.org&quot; &gt;TUCSON, Ariz.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 26, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Swiss:RO&quot; idsrc=&quot;xmltag.org&quot;&gt;Roche&lt;/span&gt; (SIX: RO, ROG; OTCQX: RHHBY) announced today that it has received FDA approval for expanded use of its PATHWAY&lt;sup&gt;®&lt;/sup&gt; HER2 (4B5) and VENTANA&lt;sup&gt;®&lt;/sup&gt; HER2 Dual ISH DNA</description>
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   <title>Roche receives FDA approval for companion diagnostic tests to identify patients with HER2-positive metastatic gastroesophageal adenocarcinoma eligible for ZIIHERA</title>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;The PATHWAY HER2 (4B5) test and VENTANA HER2 Dual ISH DNA Probe Cocktail help identify HER2-positive metastatic gastric, gastroesophageal junction and esophageal adenocarcinoma.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Differential diagnosis of these cancers, often aggressive and diagnosed at an advanced stage, is critical to improving patient outcomes.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Together, the tests enable precise assessment of HER2-positive status to help identify patients eligible for treatment with ZIIHERA.&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.az.tucson&quot; idsrc=&quot;xmltag.org&quot; &gt;TUCSON, Ariz.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 26, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Swiss:RO&quot; idsrc=&quot;xmltag.org&quot;&gt;Roche&lt;/span&gt; (SIX: RO, ROG; OTCQX: RHHBY) announced today that it has received FDA approval for expanded use of its PATHWAY&lt;sup&gt;®&lt;/sup&gt; HER2 (4B5) and VENTANA&lt;sup&gt;®&lt;/sup&gt; HER2 Dual ISH DNA</description>
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   <title>Roche receives FDA approval for companion diagnostic tests to identify patients with HER2-positive metastatic gastroesophageal adenocarcinoma eligible for ZIIHERA</title>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;The PATHWAY HER2 (4B5) test and VENTANA HER2 Dual ISH DNA Probe Cocktail help identify HER2-positive metastatic gastric, gastroesophageal junction and esophageal adenocarcinoma.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Differential diagnosis of these cancers, often aggressive and diagnosed at an advanced stage, is critical to improving patient outcomes.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Together, the tests enable precise assessment of HER2-positive status to help identify patients eligible for treatment with ZIIHERA.&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.az.tucson&quot; idsrc=&quot;xmltag.org&quot; &gt;TUCSON, Ariz.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 26, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Swiss:RO&quot; idsrc=&quot;xmltag.org&quot;&gt;Roche&lt;/span&gt; (SIX: RO, ROG; OTCQX: RHHBY) announced today that it has received FDA approval for expanded use of its PATHWAY&lt;sup&gt;®&lt;/sup&gt; HER2 (4B5) and VENTANA&lt;sup&gt;®&lt;/sup&gt; HER2 Dual ISH DNA</description>
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   <title>Roche receives FDA approval for companion diagnostic tests to identify patients with HER2-positive metastatic gastroesophageal adenocarcinoma eligible for ZIIHERA</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;The PATHWAY HER2 (4B5) test and VENTANA HER2 Dual ISH DNA Probe Cocktail help identify HER2-positive metastatic gastric, gastroesophageal junction and esophageal adenocarcinoma.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Differential diagnosis of these cancers, often aggressive and diagnosed at an advanced stage, is critical to improving patient outcomes.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Together, the tests enable precise assessment of HER2-positive status to help identify patients eligible for treatment with ZIIHERA.&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.az.tucson&quot; idsrc=&quot;xmltag.org&quot; &gt;TUCSON, Ariz.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 26, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Swiss:RO&quot; idsrc=&quot;xmltag.org&quot;&gt;Roche&lt;/span&gt; (SIX: RO, ROG; OTCQX: RHHBY) announced today that it has received FDA approval for expanded use of its PATHWAY&lt;sup&gt;®&lt;/sup&gt; HER2 (4B5) and VENTANA&lt;sup&gt;®&lt;/sup&gt; HER2 Dual ISH DNA</description>
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   <title>Roche receives FDA approval for companion diagnostic tests to identify patients with HER2-positive metastatic gastroesophageal adenocarcinoma eligible for ZIIHERA</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;The PATHWAY HER2 (4B5) test and VENTANA HER2 Dual ISH DNA Probe Cocktail help identify HER2-positive metastatic gastric, gastroesophageal junction and esophageal adenocarcinoma.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Differential diagnosis of these cancers, often aggressive and diagnosed at an advanced stage, is critical to improving patient outcomes.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Together, the tests enable precise assessment of HER2-positive status to help identify patients eligible for treatment with ZIIHERA.&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.az.tucson&quot; idsrc=&quot;xmltag.org&quot; &gt;TUCSON, Ariz.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 26, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Swiss:RO&quot; idsrc=&quot;xmltag.org&quot;&gt;Roche&lt;/span&gt; (SIX: RO, ROG; OTCQX: RHHBY) announced today that it has received FDA approval for expanded use of its PATHWAY&lt;sup&gt;®&lt;/sup&gt; HER2 (4B5) and VENTANA&lt;sup&gt;®&lt;/sup&gt; HER2 Dual ISH DNA</description>
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   <title>Roche receives FDA approval for companion diagnostic tests to identify patients with HER2-positive metastatic gastroesophageal adenocarcinoma eligible for ZIIHERA</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;The PATHWAY HER2 (4B5) test and VENTANA HER2 Dual ISH DNA Probe Cocktail help identify HER2-positive metastatic gastric, gastroesophageal junction and esophageal adenocarcinoma.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Differential diagnosis of these cancers, often aggressive and diagnosed at an advanced stage, is critical to improving patient outcomes.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Together, the tests enable precise assessment of HER2-positive status to help identify patients eligible for treatment with ZIIHERA.&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.az.tucson&quot; idsrc=&quot;xmltag.org&quot; &gt;TUCSON, Ariz.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 26, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Swiss:RO&quot; idsrc=&quot;xmltag.org&quot;&gt;Roche&lt;/span&gt; (SIX: RO, ROG; OTCQX: RHHBY) announced today that it has received FDA approval for expanded use of its PATHWAY&lt;sup&gt;®&lt;/sup&gt; HER2 (4B5) and VENTANA&lt;sup&gt;®&lt;/sup&gt; HER2 Dual ISH DNA</description>
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   <title>Roche receives FDA approval for companion diagnostic tests to identify patients with HER2-positive metastatic gastroesophageal adenocarcinoma eligible for ZIIHERA</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;The PATHWAY HER2 (4B5) test and VENTANA HER2 Dual ISH DNA Probe Cocktail help identify HER2-positive metastatic gastric, gastroesophageal junction and esophageal adenocarcinoma.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Differential diagnosis of these cancers, often aggressive and diagnosed at an advanced stage, is critical to improving patient outcomes.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Together, the tests enable precise assessment of HER2-positive status to help identify patients eligible for treatment with ZIIHERA.&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.az.tucson&quot; idsrc=&quot;xmltag.org&quot; &gt;TUCSON, Ariz.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 26, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Swiss:RO&quot; idsrc=&quot;xmltag.org&quot;&gt;Roche&lt;/span&gt; (SIX: RO, ROG; OTCQX: RHHBY) announced today that it has received FDA approval for expanded use of its PATHWAY&lt;sup&gt;®&lt;/sup&gt; HER2 (4B5) and VENTANA&lt;sup&gt;®&lt;/sup&gt; HER2 Dual ISH DNA</description>
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   <title>Roche receives FDA approval for companion diagnostic tests to identify patients with HER2-positive metastatic gastroesophageal adenocarcinoma eligible for ZIIHERA</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;The PATHWAY HER2 (4B5) test and VENTANA HER2 Dual ISH DNA Probe Cocktail help identify HER2-positive metastatic gastric, gastroesophageal junction and esophageal adenocarcinoma.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Differential diagnosis of these cancers, often aggressive and diagnosed at an advanced stage, is critical to improving patient outcomes.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Together, the tests enable precise assessment of HER2-positive status to help identify patients eligible for treatment with ZIIHERA.&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.az.tucson&quot; idsrc=&quot;xmltag.org&quot; &gt;TUCSON, Ariz.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 26, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Swiss:RO&quot; idsrc=&quot;xmltag.org&quot;&gt;Roche&lt;/span&gt; (SIX: RO, ROG; OTCQX: RHHBY) announced today that it has received FDA approval for expanded use of its PATHWAY&lt;sup&gt;®&lt;/sup&gt; HER2 (4B5) and VENTANA&lt;sup&gt;®&lt;/sup&gt; HER2 Dual ISH DNA</description>
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   <title>Roche receives FDA approval for companion diagnostic tests to identify patients with HER2-positive metastatic gastroesophageal adenocarcinoma eligible for ZIIHERA</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;The PATHWAY HER2 (4B5) test and VENTANA HER2 Dual ISH DNA Probe Cocktail help identify HER2-positive metastatic gastric, gastroesophageal junction and esophageal adenocarcinoma.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Differential diagnosis of these cancers, often aggressive and diagnosed at an advanced stage, is critical to improving patient outcomes.&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;Together, the tests enable precise assessment of HER2-positive status to help identify patients eligible for treatment with ZIIHERA.&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.az.tucson&quot; idsrc=&quot;xmltag.org&quot; &gt;TUCSON, Ariz.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 26, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Swiss:RO&quot; idsrc=&quot;xmltag.org&quot;&gt;Roche&lt;/span&gt; (SIX: RO, ROG; OTCQX: RHHBY) announced today that it has received FDA approval for expanded use of its PATHWAY&lt;sup&gt;®&lt;/sup&gt; HER2 (4B5) and VENTANA&lt;sup&gt;®&lt;/sup&gt; HER2 Dual ISH DNA</description>
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   <pubDate>Wed, 26 Aug 2026 14:52:00 -0400</pubDate>
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   <title>Azenta names board member as interim CEO after Marotta resigns</title>
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   <description>&lt;p&gt;Azenta, Inc. (Nasdaq: AZTA) announced that John Marotta has resigned as president, CEO, and director, and that board member Dr. Martin Madaus has been appointed interim president and CEO, according to a company press release dated Aug. 24, 2026.&lt;/p&gt;&lt;p&gt;Dr. Madaus has served on the Azenta board since 2024 and is a Senior Operating Executive at the Carlyle Group Inc. (Nasdaq: CG). He has previously held CEO roles at Millipore Corporation, Ortho-Clinical Diagnostics, and Roche Diagnostics North America.&lt;/p&gt;&lt;p&gt;The company said it has retained search firm Heidrick &amp; Struggles to conduct a permanent CEO search.&lt;/p&gt;&lt;p&gt;Azenta reaffirmed its previously issued fourth quarter fiscal</description>
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   <pubDate>Mon, 24 Aug 2026 08:01:03 -0400</pubDate>
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   <title>Azenta names board member as interim CEO after Marotta resigns</title>
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   <description>&lt;p&gt;Azenta, Inc. (Nasdaq: AZTA) announced that John Marotta has resigned as president, CEO, and director, and that board member Dr. Martin Madaus has been appointed interim president and CEO, according to a company press release dated Aug. 24, 2026.&lt;/p&gt;&lt;p&gt;Dr. Madaus has served on the Azenta board since 2024 and is a Senior Operating Executive at the Carlyle Group Inc. (Nasdaq: CG). He has previously held CEO roles at Millipore Corporation, Ortho-Clinical Diagnostics, and Roche Diagnostics North America.&lt;/p&gt;&lt;p&gt;The company said it has retained search firm Heidrick &amp; Struggles to conduct a permanent CEO search.&lt;/p&gt;&lt;p&gt;Azenta reaffirmed its previously issued fourth quarter fiscal</description>
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   <title>Azenta names board member as interim CEO after Marotta resigns</title>
   <link>http://www.streetinsider.com/Corporate+News/Azenta+names+board+member+as+interim+CEO+after+Marotta+resigns/26964448.html</link>
   <description>&lt;p&gt;Azenta, Inc. (Nasdaq: AZTA) announced that John Marotta has resigned as president, CEO, and director, and that board member Dr. Martin Madaus has been appointed interim president and CEO, according to a company press release dated Aug. 24, 2026.&lt;/p&gt;&lt;p&gt;Dr. Madaus has served on the Azenta board since 2024 and is a Senior Operating Executive at the Carlyle Group Inc. (Nasdaq: CG). He has previously held CEO roles at Millipore Corporation, Ortho-Clinical Diagnostics, and Roche Diagnostics North America.&lt;/p&gt;&lt;p&gt;The company said it has retained search firm Heidrick &amp; Struggles to conduct a permanent CEO search.&lt;/p&gt;&lt;p&gt;Azenta reaffirmed its previously issued fourth quarter fiscal</description>
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   <title>Azenta names board member as interim CEO after Marotta resigns</title>
   <link>http://www.streetinsider.com/Corporate+News/Azenta+names+board+member+as+interim+CEO+after+Marotta+resigns/26964448.html</link>
   <description>&lt;p&gt;Azenta, Inc. (Nasdaq: AZTA) announced that John Marotta has resigned as president, CEO, and director, and that board member Dr. Martin Madaus has been appointed interim president and CEO, according to a company press release dated Aug. 24, 2026.&lt;/p&gt;&lt;p&gt;Dr. Madaus has served on the Azenta board since 2024 and is a Senior Operating Executive at the Carlyle Group Inc. (Nasdaq: CG). He has previously held CEO roles at Millipore Corporation, Ortho-Clinical Diagnostics, and Roche Diagnostics North America.&lt;/p&gt;&lt;p&gt;The company said it has retained search firm Heidrick &amp; Struggles to conduct a permanent CEO search.&lt;/p&gt;&lt;p&gt;Azenta reaffirmed its previously issued fourth quarter fiscal</description>
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