PRNewsWire
02 Jul 2026, 00:11 UTC · 2h ago
NewsImpactScreener rates every claim in this story for market impact and maps it to the tickers most exposed.
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2 claims · each scored for market impact
The EMA's Committee for Medicinal Products for Human Use (CHMP) issued a negative opinion on the marketing authorization application for narsoplimab in the treatment of TA-TMA. — Regulatory rejection of a primary drug candidate typically leads to significant valuation loss and removes a key revenue catalyst.
-0.90Pomerantz LLP has launched an investigation into whether Omeros Corporation and its officers engaged in securities fraud or unlawful business practices. — The threat of class-action litigation introduces legal risk and potential financial liabilities for the company.
-0.40Which stocks this story touches
The company received a negative opinion from the EMA for a drug application and is now facing a securities fraud investigation.
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The company is the subject of an investigation by Pomerantz Law Firm on behalf of investors.
The company is the subject of an investigation by Pomerantz Law Firm on behalf of investors.
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