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Gossamer Bio Announces Third Quarter 2026 Financial Results and Provides Business Update

  • Gossamer Bio submitted a New Drug Application for seralutinib to treat pulmonary arterial hypertension to the U.S. FDA in September 2026.
  • A structured private placement secured $25 million upfront with up to $125 million additional committed capital pending FDA acceptance of the NDA.
  • The company completed a 1-for-80 reverse stock split in September 2026 to regain Nasdaq compliance.
  • Gossamer reacquired worldwide rights to seralutinib from Chiesi in July 2026, receiving a $5 million payment while retaining royalty obligations.
  • Cash, cash equivalents, Marketable securities totaled $51.2 million as of September 30, 2026.
  • Revenue from contracts with collaborators reached $38.4 million for the quarter, driven by the termination of the Chiesi collaboration.
  • Research development expenses decreased to $18.8 million for the quarter due to reduced clinical trial costs.
  • The company reported a net loss of $48.1 million, or $7.36 per share, for the three months ended September 30, 2026.
  • Management aims to support FDA review prepare for a potential seralutinib commercial launch in 2027.