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   <title>Incyte to Present at Upcoming Investor Conferences</title>
   <link>http://www.streetinsider.com/Press+Releases/Incyte+to+Present+at+Upcoming+Investor+Conferences/27009041.html</link>
   <description>
&lt;p&gt;    WILMINGTON, Del.--(BUSINESS WIRE)--
Incyte (Nasdaq:INCY) announced today that it will present at the following investor conferences during the month of September:

&lt;/p&gt;&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
21st Annual Wells Fargo Healthcare Conference on Wednesday, September 9, 2026 at 11:00 a.m. EDT

&lt;/li&gt;
&lt;li&gt;
Cantor Global Healthcare Conference 2026 on Thursday, September 10, 2026 at 9:45 a.m. EDT

&lt;/li&gt;
&lt;li&gt;
Morgan Stanley 24th Annual Global Healthcare Conference on Wednesday, September 16, 2026 at 12:20 p.m. EDT

&lt;/li&gt;
&lt;/ul&gt;&lt;p&gt;
The presentations will be webcast live and can be accessed at &lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Finvestor.incyte.com%2F&amp;amp;esheet=54596718&amp;amp;newsitemid=20260901532380&amp;amp;lan=en-US&amp;amp;anchor=Investor.Incyte.com&amp;amp;index=1&amp;amp;md5=1bd58c1d33d0d013cf031b01e1dd7272&quot; shape=&quot;rect&quot;&gt;Investor.Incyte.com&lt;/a&gt; and will be available for replay for 30 days.

&lt;/p&gt;&lt;p&gt;
&lt;b&gt;About Incyte
&lt;br /&gt;&lt;/b&gt;Incyte is redefining what’s possible in biopharmaceutical innovation.</description>
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   <pubDate>Tue, 01 Sep 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">INCY</category>
   	  </item>
  <item>
   <title>Incyte to Present at Upcoming Investor Conferences</title>
   <link>http://www.streetinsider.com/Business+Wire/Incyte+to+Present+at+Upcoming+Investor+Conferences/27009041.html</link>
   <description>
&lt;p&gt;    WILMINGTON, Del.--(BUSINESS WIRE)--
Incyte (Nasdaq:INCY) announced today that it will present at the following investor conferences during the month of September:

&lt;/p&gt;&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
21st Annual Wells Fargo Healthcare Conference on Wednesday, September 9, 2026 at 11:00 a.m. EDT

&lt;/li&gt;
&lt;li&gt;
Cantor Global Healthcare Conference 2026 on Thursday, September 10, 2026 at 9:45 a.m. EDT

&lt;/li&gt;
&lt;li&gt;
Morgan Stanley 24th Annual Global Healthcare Conference on Wednesday, September 16, 2026 at 12:20 p.m. EDT

&lt;/li&gt;
&lt;/ul&gt;&lt;p&gt;
The presentations will be webcast live and can be accessed at &lt;a target=&quot;_blank&quot; rel=&quot;nofollow&quot; href=&quot;https://cts.businesswire.com/ct/CT?id=smartlink&amp;amp;url=https%3A%2F%2Finvestor.incyte.com%2F&amp;amp;esheet=54596718&amp;amp;newsitemid=20260901532380&amp;amp;lan=en-US&amp;amp;anchor=Investor.Incyte.com&amp;amp;index=1&amp;amp;md5=1bd58c1d33d0d013cf031b01e1dd7272&quot; shape=&quot;rect&quot;&gt;Investor.Incyte.com&lt;/a&gt; and will be available for replay for 30 days.

&lt;/p&gt;&lt;p&gt;
&lt;b&gt;About Incyte
&lt;br /&gt;&lt;/b&gt;Incyte is redefining what’s possible in biopharmaceutical innovation.</description>
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   <pubDate>Tue, 01 Sep 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">INCY</category>
   	  </item>
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   <title>H.C. Wainwright Reiterates Buy Rating on Incyte (INCY)</title>
   <link>http://www.streetinsider.com/Analyst+Comments/H.C.+Wainwright+Reiterates+Buy+Rating+on+Incyte+%28INCY%29/27008799.html</link>
   <description>&lt;p&gt;H.C. Wainwright analyst Mitchell Kapoor reiterated a Buy rating and $150.00 price target on Incyte (NASDAQ: INCY).&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;Incyte entered a participation agreement (GENEROUS) with the Centers for Medicare and Medicaid Services (CMS) that enables participating state Medicaid programs to access Jakafi/Jakafi XR at prices aligned with a defined group of advanced industrialized nations; management places Medicaid exposure &lt;4.5%, left FY26 Jakafi/Jakafi XR guidance at $3.22-$3.27B, and does not expect a material impact on its outlook. Applying the 4.5% ceiling to guidance implies less than ~$145-147M of annual Medicaid sales subject to the agreement. Medicaid already receives statutory rebates,</description>
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   <pubDate>Tue, 01 Sep 2026 07:12:14 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">INCY</category>
   	  </item>
  <item>
   <title>BMO Capital Reiterates Market Perform Rating on Incyte (INCY)</title>
   <link>http://www.streetinsider.com/Analyst+Comments/BMO+Capital+Reiterates+Market+Perform+Rating+on+Incyte+%28INCY%29/27007628.html</link>
   <description>&lt;p&gt;BMO Capital analyst Evan David Seigerman reiterated a Market Perform rating and $130.00 price target on Incyte (NASDAQ: INCY).&lt;/p&gt;&lt;p&gt;The analyst comments &quot;Voluntary CMS agreement removes potential policy overhang for Incyte with limited anticipated impact to the Jakafi franchise. The agreement announced today will give state Medicaid programs access to Jakafi/Jakafi XR at prices aligned with industrialized nations, while exempting Incyte from certain future CMS pricing mandates (e.g., GUARD/GLOBE). In addition to some pricing protection, management expects limited financial impact to Jakafi/Jakafi XR revenues (&lt;4.5% headwind), maintaining FY26 guidance and long-term outlook. All in, we view today's agreement as an incremental</description>
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   <pubDate>Tue, 01 Sep 2026 04:02:37 -0400</pubDate>
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   <title>Knight Therapeutics Announces Supplemental Regulatory Submission for MINJUVI® (tafasitamab) in Brazil</title>
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&lt;p align=&quot;justify&quot;&gt;MONTREAL, Aug.  27, 2026  (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (&amp;quot;Knight&amp;quot;) (TSX: GUD), a pan-American (ex-US) pharmaceutical company, announced today that it has submitted a supplemental application to ANVISA, the Brazilian health regulatory agency, seeking approval for an additional indication for MINJUVI® (tafasitamab) in combination with lenalidomide added to R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; Tafa-Len-R-CHOP) as a first-line treatment for adults with previously untreated diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBL). The supplemental application for the additional indication was selected for review under Project Orbis.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;“This supplemental submission to ANVISA</description>
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   <title>Knight Therapeutics Announces Supplemental Regulatory Submission for MINJUVI® (tafasitamab) in Brazil</title>
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&lt;p align=&quot;justify&quot;&gt;MONTREAL, Aug.  27, 2026  (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (&amp;quot;Knight&amp;quot;) (TSX: GUD), a pan-American (ex-US) pharmaceutical company, announced today that it has submitted a supplemental application to ANVISA, the Brazilian health regulatory agency, seeking approval for an additional indication for MINJUVI® (tafasitamab) in combination with lenalidomide added to R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; Tafa-Len-R-CHOP) as a first-line treatment for adults with previously untreated diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBL). The supplemental application for the additional indication was selected for review under Project Orbis.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;“This supplemental submission to ANVISA</description>
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   <title>Knight Therapeutics Announces Supplemental Regulatory Submission for MINJUVI® (tafasitamab) in Brazil</title>
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&lt;p align=&quot;justify&quot;&gt;MONTREAL, Aug.  27, 2026  (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (&amp;quot;Knight&amp;quot;) (TSX: GUD), a pan-American (ex-US) pharmaceutical company, announced today that it has submitted a supplemental application to ANVISA, the Brazilian health regulatory agency, seeking approval for an additional indication for MINJUVI® (tafasitamab) in combination with lenalidomide added to R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; Tafa-Len-R-CHOP) as a first-line treatment for adults with previously untreated diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBL). The supplemental application for the additional indication was selected for review under Project Orbis.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;“This supplemental submission to ANVISA</description>
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   <title>Knight Therapeutics Announces Supplemental Regulatory Submission for MINJUVI® (tafasitamab) in Brazil</title>
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&lt;p align=&quot;justify&quot;&gt;MONTREAL, Aug.  27, 2026  (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (&amp;quot;Knight&amp;quot;) (TSX: GUD), a pan-American (ex-US) pharmaceutical company, announced today that it has submitted a supplemental application to ANVISA, the Brazilian health regulatory agency, seeking approval for an additional indication for MINJUVI® (tafasitamab) in combination with lenalidomide added to R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; Tafa-Len-R-CHOP) as a first-line treatment for adults with previously untreated diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBL). The supplemental application for the additional indication was selected for review under Project Orbis.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;“This supplemental submission to ANVISA</description>
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   <title>Knight Therapeutics Announces Supplemental Regulatory Submission for MINJUVI® (tafasitamab) in Brazil</title>
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&lt;p align=&quot;justify&quot;&gt;MONTREAL, Aug.  27, 2026  (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (&amp;quot;Knight&amp;quot;) (TSX: GUD), a pan-American (ex-US) pharmaceutical company, announced today that it has submitted a supplemental application to ANVISA, the Brazilian health regulatory agency, seeking approval for an additional indication for MINJUVI® (tafasitamab) in combination with lenalidomide added to R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; Tafa-Len-R-CHOP) as a first-line treatment for adults with previously untreated diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBL). The supplemental application for the additional indication was selected for review under Project Orbis.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;“This supplemental submission to ANVISA</description>
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   <title>Knight Therapeutics Announces Supplemental Regulatory Submission for MINJUVI® (tafasitamab) in Brazil</title>
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&lt;p align=&quot;justify&quot;&gt;MONTREAL, Aug.  27, 2026  (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (&amp;quot;Knight&amp;quot;) (TSX: GUD), a pan-American (ex-US) pharmaceutical company, announced today that it has submitted a supplemental application to ANVISA, the Brazilian health regulatory agency, seeking approval for an additional indication for MINJUVI® (tafasitamab) in combination with lenalidomide added to R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; Tafa-Len-R-CHOP) as a first-line treatment for adults with previously untreated diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBL). The supplemental application for the additional indication was selected for review under Project Orbis.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;“This supplemental submission to ANVISA</description>
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   <title>Knight Therapeutics Announces Supplemental Regulatory Submission for MINJUVI® (tafasitamab) in Brazil</title>
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&lt;p align=&quot;justify&quot;&gt;MONTREAL, Aug.  27, 2026  (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (&amp;quot;Knight&amp;quot;) (TSX: GUD), a pan-American (ex-US) pharmaceutical company, announced today that it has submitted a supplemental application to ANVISA, the Brazilian health regulatory agency, seeking approval for an additional indication for MINJUVI® (tafasitamab) in combination with lenalidomide added to R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; Tafa-Len-R-CHOP) as a first-line treatment for adults with previously untreated diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBL). The supplemental application for the additional indication was selected for review under Project Orbis.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;“This supplemental submission to ANVISA</description>
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   <title>Knight Therapeutics Announces Supplemental Regulatory Submission for MINJUVI® (tafasitamab) in Brazil</title>
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&lt;p align=&quot;justify&quot;&gt;MONTREAL, Aug.  27, 2026  (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (&amp;quot;Knight&amp;quot;) (TSX: GUD), a pan-American (ex-US) pharmaceutical company, announced today that it has submitted a supplemental application to ANVISA, the Brazilian health regulatory agency, seeking approval for an additional indication for MINJUVI® (tafasitamab) in combination with lenalidomide added to R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; Tafa-Len-R-CHOP) as a first-line treatment for adults with previously untreated diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBL). The supplemental application for the additional indication was selected for review under Project Orbis.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;“This supplemental submission to ANVISA</description>
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&lt;p align=&quot;justify&quot;&gt;MONTREAL, Aug.  27, 2026  (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (&amp;quot;Knight&amp;quot;) (TSX: GUD), a pan-American (ex-US) pharmaceutical company, announced today that it has submitted a supplemental application to ANVISA, the Brazilian health regulatory agency, seeking approval for an additional indication for MINJUVI® (tafasitamab) in combination with lenalidomide added to R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; Tafa-Len-R-CHOP) as a first-line treatment for adults with previously untreated diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBL). The supplemental application for the additional indication was selected for review under Project Orbis.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;“This supplemental submission to ANVISA</description>
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&lt;p align=&quot;justify&quot;&gt;MONTREAL, Aug.  27, 2026  (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (&amp;quot;Knight&amp;quot;) (TSX: GUD), a pan-American (ex-US) pharmaceutical company, announced today that it has submitted a supplemental application to ANVISA, the Brazilian health regulatory agency, seeking approval for an additional indication for MINJUVI® (tafasitamab) in combination with lenalidomide added to R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; Tafa-Len-R-CHOP) as a first-line treatment for adults with previously untreated diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBL). The supplemental application for the additional indication was selected for review under Project Orbis.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;“This supplemental submission to ANVISA</description>
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&lt;p align=&quot;justify&quot;&gt;MONTREAL, Aug.  27, 2026  (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (&amp;quot;Knight&amp;quot;) (TSX: GUD), a pan-American (ex-US) pharmaceutical company, announced today that it has submitted a supplemental application to ANVISA, the Brazilian health regulatory agency, seeking approval for an additional indication for MINJUVI® (tafasitamab) in combination with lenalidomide added to R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; Tafa-Len-R-CHOP) as a first-line treatment for adults with previously untreated diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBL). The supplemental application for the additional indication was selected for review under Project Orbis.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;“This supplemental submission to ANVISA</description>
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&lt;p align=&quot;justify&quot;&gt;MONTREAL, Aug.  27, 2026  (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (&amp;quot;Knight&amp;quot;) (TSX: GUD), a pan-American (ex-US) pharmaceutical company, announced today that it has submitted a supplemental application to ANVISA, the Brazilian health regulatory agency, seeking approval for an additional indication for MINJUVI® (tafasitamab) in combination with lenalidomide added to R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; Tafa-Len-R-CHOP) as a first-line treatment for adults with previously untreated diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBL). The supplemental application for the additional indication was selected for review under Project Orbis.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;“This supplemental submission to ANVISA</description>
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&lt;p align=&quot;justify&quot;&gt;MONTREAL, Aug.  27, 2026  (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (&amp;quot;Knight&amp;quot;) (TSX: GUD), a pan-American (ex-US) pharmaceutical company, announced today that it has submitted a supplemental application to ANVISA, the Brazilian health regulatory agency, seeking approval for an additional indication for MINJUVI® (tafasitamab) in combination with lenalidomide added to R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; Tafa-Len-R-CHOP) as a first-line treatment for adults with previously untreated diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBL). The supplemental application for the additional indication was selected for review under Project Orbis.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;“This supplemental submission to ANVISA</description>
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&lt;p align=&quot;justify&quot;&gt;MONTREAL, Aug.  27, 2026  (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (&amp;quot;Knight&amp;quot;) (TSX: GUD), a pan-American (ex-US) pharmaceutical company, announced today that it has submitted a supplemental application to ANVISA, the Brazilian health regulatory agency, seeking approval for an additional indication for MINJUVI® (tafasitamab) in combination with lenalidomide added to R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; Tafa-Len-R-CHOP) as a first-line treatment for adults with previously untreated diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBL). The supplemental application for the additional indication was selected for review under Project Orbis.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;“This supplemental submission to ANVISA</description>
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&lt;p align=&quot;justify&quot;&gt;MONTREAL, Aug.  27, 2026  (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (&amp;quot;Knight&amp;quot;) (TSX: GUD), a pan-American (ex-US) pharmaceutical company, announced today that it has submitted a supplemental application to ANVISA, the Brazilian health regulatory agency, seeking approval for an additional indication for MINJUVI® (tafasitamab) in combination with lenalidomide added to R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; Tafa-Len-R-CHOP) as a first-line treatment for adults with previously untreated diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBL). The supplemental application for the additional indication was selected for review under Project Orbis.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;“This supplemental submission to ANVISA</description>
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&lt;p align=&quot;justify&quot;&gt;MONTREAL, Aug.  27, 2026  (GLOBE NEWSWIRE) -- Knight Therapeutics Inc. (&amp;quot;Knight&amp;quot;) (TSX: GUD), a pan-American (ex-US) pharmaceutical company, announced today that it has submitted a supplemental application to ANVISA, the Brazilian health regulatory agency, seeking approval for an additional indication for MINJUVI® (tafasitamab) in combination with lenalidomide added to R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone; Tafa-Len-R-CHOP) as a first-line treatment for adults with previously untreated diffuse large B-cell lymphoma (DLBCL) or high-grade B-cell lymphoma (HGBL). The supplemental application for the additional indication was selected for review under Project Orbis.&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;“This supplemental submission to ANVISA</description>
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   <description>&lt;p&gt;H.C. Wainwright analyst Mitchell Kapoor reiterated a Buy rating and $150.00 price target on Incyte (NASDAQ: INCY).&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;Yesterday, the FDA approved Revolution Medicines’ RASONQUE (daraxonrasib) 300 mg QD for metastatic pancreatic adenocarcinoma (PDAC) after at least one prior systemic therapy, or when multi-agent systemic therapy is unsuitable, without requiring an RAS genotype, based on the previously disclosed 13.2-month vs. 6.7-month median OS result from RASolute 302. Daraxonrasib’s approval raises the bar for success for '734 because broad RAS inhibition has now delivered an approved survival benefit without genotype selection and showed an OS HR of 0.38 in Revolution’s</description>
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   <description>&lt;p&gt;TD Cowen analyst Tara Bancroft assumes coverage on Incyte (NASDAQ: INCY) with a Buy rating and a price target of $138.00.&lt;/p&gt;
&lt;p&gt;For an analyst ratings summary and ratings history on Incyte &lt;a href=&quot;http://www.streetinsider.com/rating_history.php?q=INCY&quot;&gt;click here&lt;/a&gt;. For more ratings news on Incyte &lt;a href=&quot;http://www.streetinsider.com/stock_lookup_news.php?q=INCY&amp;amp;type=analyst&quot;&gt;click here&lt;/a&gt;.&lt;/p&gt;
&lt;p&gt;Shares of Incyte closed at $127.81 yesterday.&lt;/p&gt;</description>
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