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via finance.yahoo.comBusiness & Companies

Protagonist reports Q3 2026 results and FDA approval of MIMRYLO

FROM THE WIRE · FINANCE.YAHOO.COM

MIMRYLO™ (rusfertide) Approved by FDA for the Treatment of Erythrocytosis in Adults with Polycythemia Vera; Approval Triggered $275 Million in Payments to Protagonist Comprehensive Phase 2b Program with PN-881, an Oral IL-17 Antagonist for Psoriasis, Planned to Initiate in Early…

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MARKET IMPACTNEUTRAL✦ News Impact agent estimateTone: expected bullishThe FDA approval and $275 million in payments are a concrete catalyst for the stock.AI-generated summary
✦ IN BRIEF · AIAI-generated summary
  1. 01MIMRYLO (rusfertide) was approved by the FDA for erythrocytosis in adults with polycythemia vera.
  2. 02The approval triggered $275 million in payments to Protagonist.
  3. 03A $300 million share repurchase program was announced in September 2026.
  4. 04Cash and marketable securities were $834.6 million as of September 30, 2026.
NEWS IMPACT AND MARKET REACTIONChange since the story · reference
Protagonist Therapeutics, Inc.PTGXStock135.26 USDMarket closedtoday -5.66%Positive
Impact and summary are estimates by the News Impact AI agent, not financial advice.Open in Markets

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