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   <title>Omeros (OMER) call put ratio 1 call to 2.4 put as share price up 4.9%</title>
   <link>http://www.streetinsider.com/Options/Omeros+%28OMER%29+call+put+ratio+1+call+to+2.4+put+as+share+price+up+4.9%25/26768039.html</link>
   <description>&lt;p&gt;Omeros (NASDAQ: OMER) 30-day option implied volatility is at 104; compared to its 52-week range of 60 to 265.  Call put ratio 1 call to 2.4 put as share price up 4.9%.&lt;/p&gt;</description>
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   <title>Form  8-K        OMEROS CORP               For: Jul 02</title>
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   <pubDate>Mon, 06 Jul 2026 08:30:00 -0400</pubDate>
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   <title>Form  8-K        OMEROS CORP               For: Jul 02</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++OMEROS+CORP+++++++++++++++For%3A+Jul+02/26733233.html</link>
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   <pubDate>Mon, 06 Jul 2026 08:30:00 -0400</pubDate>
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   <title>Omeros Corp. (OMER) PT Lowered to $33 at H.C. Wainwright</title>
   <link>http://www.streetinsider.com/Analyst+PT+Change/Omeros+Corp.+%28OMER%29+PT+Lowered+to+%2433+at+H.C.+Wainwright/26701956.html</link>
   <description>(Updated - June 29, 2026 7:07 AM EDT)

&lt;p&gt;H.C. Wainwright analyst Brandon Folkes lowered the price target on Omeros Corp. (NASDAQ: OMER) to $33.00 (from $40.00) while maintaining a Buy rating.&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;OMER’s negative CHMP opinion for YARTEMLEA is disappointing and likely creates a near-term overhang, but we do not view it as thesis-breaking. We are removing the EU opportunity from our model, lowering our exit multiple, and increasing go-forward R&amp;D spend, which takes our price target to $33 from $40; however, the EU removal itself only reduces our valuation by approximately $2/share, with the U.S. YARTEMLEA launch still representing</description>
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   <pubDate>Mon, 29 Jun 2026 07:07:29 -0400</pubDate>
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   <title>Omeros Corp. (OMER) PT Lowered to $33 at H.C. Wainwright</title>
   <link>http://www.streetinsider.com/Analyst+Comments/Omeros+Corp.+%28OMER%29+PT+Lowered+to+%2433+at+H.C.+Wainwright/26701956.html</link>
   <description>(Updated - June 29, 2026 7:07 AM EDT)

&lt;p&gt;H.C. Wainwright analyst Brandon Folkes lowered the price target on Omeros Corp. (NASDAQ: OMER) to $33.00 (from $40.00) while maintaining a Buy rating.&lt;/p&gt;&lt;p&gt;The analyst commented: &quot;OMER’s negative CHMP opinion for YARTEMLEA is disappointing and likely creates a near-term overhang, but we do not view it as thesis-breaking. We are removing the EU opportunity from our model, lowering our exit multiple, and increasing go-forward R&amp;D spend, which takes our price target to $33 from $40; however, the EU removal itself only reduces our valuation by approximately $2/share, with the U.S. YARTEMLEA launch still representing</description>
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   <pubDate>Mon, 29 Jun 2026 07:07:29 -0400</pubDate>
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   <title>EMA panel issues negative opinion on Omeros narsoplimab application</title>
   <link>http://www.streetinsider.com/Corporate+News/EMA+panel+issues+negative+opinion+on+Omeros+narsoplimab+application/26695339.html</link>
   <description>&lt;p&gt;Omeros Corporation (Nasdaq: OMER) said the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has adopted a negative opinion on the company's marketing authorization application for narsoplimab in the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA).&lt;/p&gt;&lt;p&gt;The decision followed an oral explanation meeting at which Omeros presented its position alongside four international experts in hematopoietic cell transplantation. Omeros said it intends to request a re-examination of the CHMP opinion and will seek review by an Ad Hoc Expert Group, an independent panel of external scientific and clinical experts to be convened by the EMA.&lt;/p&gt;&lt;p&gt;Narsoplimab, sold under</description>
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   <pubDate>Fri, 26 Jun 2026 08:30:57 -0400</pubDate>
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   <title>EMA panel issues negative opinion on Omeros narsoplimab application</title>
   <link>http://www.streetinsider.com/FDA/EMA+panel+issues+negative+opinion+on+Omeros+narsoplimab+application/26695339.html</link>
   <description>&lt;p&gt;Omeros Corporation (Nasdaq: OMER) said the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has adopted a negative opinion on the company's marketing authorization application for narsoplimab in the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA).&lt;/p&gt;&lt;p&gt;The decision followed an oral explanation meeting at which Omeros presented its position alongside four international experts in hematopoietic cell transplantation. Omeros said it intends to request a re-examination of the CHMP opinion and will seek review by an Ad Hoc Expert Group, an independent panel of external scientific and clinical experts to be convened by the EMA.&lt;/p&gt;&lt;p&gt;Narsoplimab, sold under</description>
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   <pubDate>Fri, 26 Jun 2026 08:30:57 -0400</pubDate>
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   <title>EMA panel issues negative opinion on Omeros narsoplimab application</title>
   <link>http://www.streetinsider.com/Hot+Corp.+News/EMA+panel+issues+negative+opinion+on+Omeros+narsoplimab+application/26695339.html</link>
   <description>&lt;p&gt;Omeros Corporation (Nasdaq: OMER) said the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has adopted a negative opinion on the company's marketing authorization application for narsoplimab in the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA).&lt;/p&gt;&lt;p&gt;The decision followed an oral explanation meeting at which Omeros presented its position alongside four international experts in hematopoietic cell transplantation. Omeros said it intends to request a re-examination of the CHMP opinion and will seek review by an Ad Hoc Expert Group, an independent panel of external scientific and clinical experts to be convened by the EMA.&lt;/p&gt;&lt;p&gt;Narsoplimab, sold under</description>
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   <pubDate>Fri, 26 Jun 2026 08:30:57 -0400</pubDate>
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   <title>EMA panel issues negative opinion on Omeros narsoplimab application</title>
   <link>http://www.streetinsider.com/Hot+FDA+News/EMA+panel+issues+negative+opinion+on+Omeros+narsoplimab+application/26695339.html</link>
   <description>&lt;p&gt;Omeros Corporation (Nasdaq: OMER) said the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has adopted a negative opinion on the company's marketing authorization application for narsoplimab in the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA).&lt;/p&gt;&lt;p&gt;The decision followed an oral explanation meeting at which Omeros presented its position alongside four international experts in hematopoietic cell transplantation. Omeros said it intends to request a re-examination of the CHMP opinion and will seek review by an Ad Hoc Expert Group, an independent panel of external scientific and clinical experts to be convened by the EMA.&lt;/p&gt;&lt;p&gt;Narsoplimab, sold under</description>
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   <pubDate>Fri, 26 Jun 2026 08:30:57 -0400</pubDate>
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   <title>Omeros Corporation Announces Update on European Marketing Authorization Application for Narsoplimab in TA-TMA</title>
   <link>http://www.streetinsider.com/Press+Releases/Omeros+Corporation+Announces+Update+on+European+Marketing+Authorization+Application+for+Narsoplimab+in+TA-TMA/26695318.html</link>
   <description>
&lt;p&gt;    SEATTLE--(BUSINESS WIRE)--
&lt;b&gt;Omeros Corporation (Nasdaq: OMER) &lt;/b&gt;announced today an update on the review by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) of the company’s marketing authorization application (MAA) for narsoplimab for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA).

&lt;/p&gt;&lt;p&gt;
Following an oral explanation meeting with the CHMP held this week, at which Omeros presented its position together with four international experts in hematopoietic cell transplantation, Omeros was informed that the CHMP has adopted a negative opinion on the MAA for narsoplimab in TA-TMA.

&lt;/p&gt;&lt;p&gt;
Omeros intends to request re-examination of</description>
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   <title>Omeros Corporation Announces Update on European Marketing Authorization Application for Narsoplimab in TA-TMA</title>
   <link>http://www.streetinsider.com/Press+Releases/Omeros+Corporation+Announces+Update+on+European+Marketing+Authorization+Application+for+Narsoplimab+in+TA-TMA/26695318.html</link>
   <description>
&lt;p&gt;    SEATTLE--(BUSINESS WIRE)--
&lt;b&gt;Omeros Corporation (Nasdaq: OMER) &lt;/b&gt;announced today an update on the review by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) of the company’s marketing authorization application (MAA) for narsoplimab for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA).

&lt;/p&gt;&lt;p&gt;
Following an oral explanation meeting with the CHMP held this week, at which Omeros presented its position together with four international experts in hematopoietic cell transplantation, Omeros was informed that the CHMP has adopted a negative opinion on the MAA for narsoplimab in TA-TMA.

&lt;/p&gt;&lt;p&gt;
Omeros intends to request re-examination of</description>
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   <title>Omeros Corporation Announces Update on European Marketing Authorization Application for Narsoplimab in TA-TMA</title>
   <link>http://www.streetinsider.com/Press+Releases/Omeros+Corporation+Announces+Update+on+European+Marketing+Authorization+Application+for+Narsoplimab+in+TA-TMA/26695318.html</link>
   <description>
&lt;p&gt;    SEATTLE--(BUSINESS WIRE)--
&lt;b&gt;Omeros Corporation (Nasdaq: OMER) &lt;/b&gt;announced today an update on the review by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) of the company’s marketing authorization application (MAA) for narsoplimab for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA).

&lt;/p&gt;&lt;p&gt;
Following an oral explanation meeting with the CHMP held this week, at which Omeros presented its position together with four international experts in hematopoietic cell transplantation, Omeros was informed that the CHMP has adopted a negative opinion on the MAA for narsoplimab in TA-TMA.

&lt;/p&gt;&lt;p&gt;
Omeros intends to request re-examination of</description>
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   <title>Omeros Corporation Announces Update on European Marketing Authorization Application for Narsoplimab in TA-TMA</title>
   <link>http://www.streetinsider.com/Press+Releases/Omeros+Corporation+Announces+Update+on+European+Marketing+Authorization+Application+for+Narsoplimab+in+TA-TMA/26695318.html</link>
   <description>
&lt;p&gt;    SEATTLE--(BUSINESS WIRE)--
&lt;b&gt;Omeros Corporation (Nasdaq: OMER) &lt;/b&gt;announced today an update on the review by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) of the company’s marketing authorization application (MAA) for narsoplimab for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA).

&lt;/p&gt;&lt;p&gt;
Following an oral explanation meeting with the CHMP held this week, at which Omeros presented its position together with four international experts in hematopoietic cell transplantation, Omeros was informed that the CHMP has adopted a negative opinion on the MAA for narsoplimab in TA-TMA.

&lt;/p&gt;&lt;p&gt;
Omeros intends to request re-examination of</description>
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   <title>Omeros Corporation Announces Update on European Marketing Authorization Application for Narsoplimab in TA-TMA</title>
   <link>http://www.streetinsider.com/Press+Releases/Omeros+Corporation+Announces+Update+on+European+Marketing+Authorization+Application+for+Narsoplimab+in+TA-TMA/26695318.html</link>
   <description>
&lt;p&gt;    SEATTLE--(BUSINESS WIRE)--
&lt;b&gt;Omeros Corporation (Nasdaq: OMER) &lt;/b&gt;announced today an update on the review by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) of the company’s marketing authorization application (MAA) for narsoplimab for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA).

&lt;/p&gt;&lt;p&gt;
Following an oral explanation meeting with the CHMP held this week, at which Omeros presented its position together with four international experts in hematopoietic cell transplantation, Omeros was informed that the CHMP has adopted a negative opinion on the MAA for narsoplimab in TA-TMA.

&lt;/p&gt;&lt;p&gt;
Omeros intends to request re-examination of</description>
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   <title>Omeros Corporation Announces Update on European Marketing Authorization Application for Narsoplimab in TA-TMA</title>
   <link>http://www.streetinsider.com/Press+Releases/Omeros+Corporation+Announces+Update+on+European+Marketing+Authorization+Application+for+Narsoplimab+in+TA-TMA/26695318.html</link>
   <description>
&lt;p&gt;    SEATTLE--(BUSINESS WIRE)--
&lt;b&gt;Omeros Corporation (Nasdaq: OMER) &lt;/b&gt;announced today an update on the review by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) of the company’s marketing authorization application (MAA) for narsoplimab for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA).

&lt;/p&gt;&lt;p&gt;
Following an oral explanation meeting with the CHMP held this week, at which Omeros presented its position together with four international experts in hematopoietic cell transplantation, Omeros was informed that the CHMP has adopted a negative opinion on the MAA for narsoplimab in TA-TMA.

&lt;/p&gt;&lt;p&gt;
Omeros intends to request re-examination of</description>
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   <title>Omeros Corporation Announces Update on European Marketing Authorization Application for Narsoplimab in TA-TMA</title>
   <link>http://www.streetinsider.com/Business+Wire/Omeros+Corporation+Announces+Update+on+European+Marketing+Authorization+Application+for+Narsoplimab+in+TA-TMA/26695318.html</link>
   <description>
&lt;p&gt;    SEATTLE--(BUSINESS WIRE)--
&lt;b&gt;Omeros Corporation (Nasdaq: OMER) &lt;/b&gt;announced today an update on the review by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) of the company’s marketing authorization application (MAA) for narsoplimab for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA).

&lt;/p&gt;&lt;p&gt;
Following an oral explanation meeting with the CHMP held this week, at which Omeros presented its position together with four international experts in hematopoietic cell transplantation, Omeros was informed that the CHMP has adopted a negative opinion on the MAA for narsoplimab in TA-TMA.

&lt;/p&gt;&lt;p&gt;
Omeros intends to request re-examination of</description>
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   <title>Omeros Corporation Announces Update on European Marketing Authorization Application for Narsoplimab in TA-TMA</title>
   <link>http://www.streetinsider.com/Business+Wire/Omeros+Corporation+Announces+Update+on+European+Marketing+Authorization+Application+for+Narsoplimab+in+TA-TMA/26695318.html</link>
   <description>
&lt;p&gt;    SEATTLE--(BUSINESS WIRE)--
&lt;b&gt;Omeros Corporation (Nasdaq: OMER) &lt;/b&gt;announced today an update on the review by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) of the company’s marketing authorization application (MAA) for narsoplimab for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA).

&lt;/p&gt;&lt;p&gt;
Following an oral explanation meeting with the CHMP held this week, at which Omeros presented its position together with four international experts in hematopoietic cell transplantation, Omeros was informed that the CHMP has adopted a negative opinion on the MAA for narsoplimab in TA-TMA.

&lt;/p&gt;&lt;p&gt;
Omeros intends to request re-examination of</description>
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   <title>Omeros Corporation Announces Update on European Marketing Authorization Application for Narsoplimab in TA-TMA</title>
   <link>http://www.streetinsider.com/Business+Wire/Omeros+Corporation+Announces+Update+on+European+Marketing+Authorization+Application+for+Narsoplimab+in+TA-TMA/26695318.html</link>
   <description>
&lt;p&gt;    SEATTLE--(BUSINESS WIRE)--
&lt;b&gt;Omeros Corporation (Nasdaq: OMER) &lt;/b&gt;announced today an update on the review by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) of the company’s marketing authorization application (MAA) for narsoplimab for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA).

&lt;/p&gt;&lt;p&gt;
Following an oral explanation meeting with the CHMP held this week, at which Omeros presented its position together with four international experts in hematopoietic cell transplantation, Omeros was informed that the CHMP has adopted a negative opinion on the MAA for narsoplimab in TA-TMA.

&lt;/p&gt;&lt;p&gt;
Omeros intends to request re-examination of</description>
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   <title>Omeros Corporation Announces Update on European Marketing Authorization Application for Narsoplimab in TA-TMA</title>
   <link>http://www.streetinsider.com/Business+Wire/Omeros+Corporation+Announces+Update+on+European+Marketing+Authorization+Application+for+Narsoplimab+in+TA-TMA/26695318.html</link>
   <description>
&lt;p&gt;    SEATTLE--(BUSINESS WIRE)--
&lt;b&gt;Omeros Corporation (Nasdaq: OMER) &lt;/b&gt;announced today an update on the review by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) of the company’s marketing authorization application (MAA) for narsoplimab for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA).

&lt;/p&gt;&lt;p&gt;
Following an oral explanation meeting with the CHMP held this week, at which Omeros presented its position together with four international experts in hematopoietic cell transplantation, Omeros was informed that the CHMP has adopted a negative opinion on the MAA for narsoplimab in TA-TMA.

&lt;/p&gt;&lt;p&gt;
Omeros intends to request re-examination of</description>
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   <title>Omeros Corporation Announces Update on European Marketing Authorization Application for Narsoplimab in TA-TMA</title>
   <link>http://www.streetinsider.com/Business+Wire/Omeros+Corporation+Announces+Update+on+European+Marketing+Authorization+Application+for+Narsoplimab+in+TA-TMA/26695318.html</link>
   <description>
&lt;p&gt;    SEATTLE--(BUSINESS WIRE)--
&lt;b&gt;Omeros Corporation (Nasdaq: OMER) &lt;/b&gt;announced today an update on the review by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) of the company’s marketing authorization application (MAA) for narsoplimab for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA).

&lt;/p&gt;&lt;p&gt;
Following an oral explanation meeting with the CHMP held this week, at which Omeros presented its position together with four international experts in hematopoietic cell transplantation, Omeros was informed that the CHMP has adopted a negative opinion on the MAA for narsoplimab in TA-TMA.

&lt;/p&gt;&lt;p&gt;
Omeros intends to request re-examination of</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Omeros+Corporation+Announces+Update+on+European+Marketing+Authorization+Application+for+Narsoplimab+in+TA-TMA/26695318.html</guid>
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   <title>Omeros Corporation Announces Update on European Marketing Authorization Application for Narsoplimab in TA-TMA</title>
   <link>http://www.streetinsider.com/Business+Wire/Omeros+Corporation+Announces+Update+on+European+Marketing+Authorization+Application+for+Narsoplimab+in+TA-TMA/26695318.html</link>
   <description>
&lt;p&gt;    SEATTLE--(BUSINESS WIRE)--
&lt;b&gt;Omeros Corporation (Nasdaq: OMER) &lt;/b&gt;announced today an update on the review by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) of the company’s marketing authorization application (MAA) for narsoplimab for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA).

&lt;/p&gt;&lt;p&gt;
Following an oral explanation meeting with the CHMP held this week, at which Omeros presented its position together with four international experts in hematopoietic cell transplantation, Omeros was informed that the CHMP has adopted a negative opinion on the MAA for narsoplimab in TA-TMA.

&lt;/p&gt;&lt;p&gt;
Omeros intends to request re-examination of</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/Omeros+Corporation+Announces+Update+on+European+Marketing+Authorization+Application+for+Narsoplimab+in+TA-TMA/26695318.html</guid>
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   <title>Omeros stock tumbles after EU panel rejects Yartemlea</title>
   <link>http://www.streetinsider.com/Investing/Omeros+stock+tumbles+after+EU+panel+rejects+Yartemlea/26694953.html</link>
   <description>&lt;p&gt;Investing.com -- Omeros Corporation (NASDAQ:OMER) fell 14% Friday morning after the European Medicines Agency's Committee for Medicinal Products for Human Use adopted a negative opinion for Yartemlea.&lt;/p&gt;&lt;p&gt;The CHMP recommended against approval of Yartemlea (narsoplimab) for the treatment of adults and children from two years of age with haematopoietic stem cell transplant-associated thrombotic microangiopathy. Thrombotic microangiopathy is a serious and potentially life-threatening complication following HSCT, a procedure where the patient's bone marrow is replaced by stem cells from a donor to form new bone marrow that produces healthy cells.&lt;/p&gt;&lt;p&gt;The committee also adopted negative opinions for two other medicines: Tacquell (autologous melanoma-derived</description>
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   <pubDate>Fri, 26 Jun 2026 07:13:04 -0400</pubDate>
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   <title>Omeros stock tumbles after EU panel rejects Yartemlea</title>
   <link>http://www.streetinsider.com/FDA/Omeros+stock+tumbles+after+EU+panel+rejects+Yartemlea/26694953.html</link>
   <description>&lt;p&gt;Investing.com -- Omeros Corporation (NASDAQ:OMER) fell 14% Friday morning after the European Medicines Agency's Committee for Medicinal Products for Human Use adopted a negative opinion for Yartemlea.&lt;/p&gt;&lt;p&gt;The CHMP recommended against approval of Yartemlea (narsoplimab) for the treatment of adults and children from two years of age with haematopoietic stem cell transplant-associated thrombotic microangiopathy. Thrombotic microangiopathy is a serious and potentially life-threatening complication following HSCT, a procedure where the patient's bone marrow is replaced by stem cells from a donor to form new bone marrow that produces healthy cells.&lt;/p&gt;&lt;p&gt;The committee also adopted negative opinions for two other medicines: Tacquell (autologous melanoma-derived</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/Omeros+stock+tumbles+after+EU+panel+rejects+Yartemlea/26694953.html</guid>
   <pubDate>Fri, 26 Jun 2026 07:13:04 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">OMER</category>
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   <title>Omeros stock tumbles after EU panel rejects Yartemlea</title>
   <link>http://www.streetinsider.com/Trader+Talk/Omeros+stock+tumbles+after+EU+panel+rejects+Yartemlea/26694953.html</link>
   <description>&lt;p&gt;Investing.com -- Omeros Corporation (NASDAQ:OMER) fell 14% Friday morning after the European Medicines Agency's Committee for Medicinal Products for Human Use adopted a negative opinion for Yartemlea.&lt;/p&gt;&lt;p&gt;The CHMP recommended against approval of Yartemlea (narsoplimab) for the treatment of adults and children from two years of age with haematopoietic stem cell transplant-associated thrombotic microangiopathy. Thrombotic microangiopathy is a serious and potentially life-threatening complication following HSCT, a procedure where the patient's bone marrow is replaced by stem cells from a donor to form new bone marrow that produces healthy cells.&lt;/p&gt;&lt;p&gt;The committee also adopted negative opinions for two other medicines: Tacquell (autologous melanoma-derived</description>
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   <pubDate>Fri, 26 Jun 2026 07:13:04 -0400</pubDate>
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   <title>Omeros stock tumbles after EU panel rejects Yartemlea</title>
   <link>http://www.streetinsider.com/Hot+FDA+News/Omeros+stock+tumbles+after+EU+panel+rejects+Yartemlea/26694953.html</link>
   <description>&lt;p&gt;Investing.com -- Omeros Corporation (NASDAQ:OMER) fell 14% Friday morning after the European Medicines Agency's Committee for Medicinal Products for Human Use adopted a negative opinion for Yartemlea.&lt;/p&gt;&lt;p&gt;The CHMP recommended against approval of Yartemlea (narsoplimab) for the treatment of adults and children from two years of age with haematopoietic stem cell transplant-associated thrombotic microangiopathy. Thrombotic microangiopathy is a serious and potentially life-threatening complication following HSCT, a procedure where the patient's bone marrow is replaced by stem cells from a donor to form new bone marrow that produces healthy cells.&lt;/p&gt;&lt;p&gt;The committee also adopted negative opinions for two other medicines: Tacquell (autologous melanoma-derived</description>
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