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Gossamer Bio Inc

Gossamer Bio, Inc. is a clinical-stage biopharmaceutical company focused on developing and commercializing seralutinib for the treatment of pulmonary hypertension and pulmonary arterial hypertension in the United States. The company is developing GB002, an inhaled small molecule inhibitor of PDGFR, colony-stimulating factor 1 receptor, and c-KIT, which is in Phase 3 clinical trials for PAH. It has license agreements with Pulmokine, Inc. to develop and commercialize GB002 and related backup compounds. Formerly known as FSG Bio, Inc., the company changed its name to Gossamer Bio, Inc. in 2017, was incorporated in 2015, and is headquartered in San Diego, California.

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Biotech & Genomic Medicine▲

Gossamer Bio secures up to $250m to advance seralutinib

Gossamer Bio has announced a private placement agreement valued at up to $250m, including $150m of committed capital to support development and potential FDA approval of seralutinib for pulmonary arterial hypertension and pulmonary hypertension associated with interstitial lung disease. The financing involves an initial closing of approximately $25m through pre-funded warrants priced at $0.14 per share, a subsequent closing of $125m contingent upon FDA acceptance of a new drug application, and warrants exercisable upon FDA approval that could add up to $100m more at $0.187 per share. Key institutional investors include EcoR1 Capital and RA Capital Management, with Leerink Partners and Cantor serving as joint placement agents. Gossamer plans to submit the NDA by September 2026, and net proceeds are expected to sustain operations until 2028.
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Biotech & Genomic Medicine › Cardiovascular & Heart-Failure Therapeutics ▲Capital
GOSS · Capital · Positive Secures up to $250m financing to support seralutinib development and potential FDA approval.
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Biotech & Genomic Medicine▲impact 4

Gossamer Bio to File Seralutinib NDA in September, Forte Biosciences Acquired by argenx

Gossamer Bio plans to submit a New Drug Application for Seralutinib to treat pulmonary arterial hypertension in September 2026, while Forte Biosciences has agreed to be acquired by argenx for $77 per share in cash, representing a total equity value of roughly $2.2 billion. Gossamer also regained worldwide rights to Seralutinib from Chiesi and reported cash of approximately $57 million as of June 30, 2026. Entera Bio shares soared over 90% after announcing an oversubscribed private placement expected to generate about $275 million in gross proceeds. Omeros gained more than 15% after AstraZeneca's Ultomiris failed a Phase 3 trial for HSCT-TMA, removing a key competitive threat to Omeros's YARTEMLEA. First Tracks Biotherapeutics rose over 18%, continuing its strong performance since its April 2026 Nasdaq debut.
About megatrends
Biotech & Genomic Medicine › Autoimmune & Immunology Therapeutics ▲Competition
Biotech & Genomic Medicine › Metabolic, Diabetes & Obesity Competition
ARGX · Capital · Positive argenx is acquiring Forte Biosciences for $77 per share, expanding its pipeline.
AZN.LSE · Technology · Negative AstraZeneca's Ultomiris failed a Phase 3 trial for HSCT-TMA, a clinical setback.
ENTX · Capital · Positive Entera Bio shares soared over 90% after announcing an oversubscribed private placement expected to raise about $275 million in gross proceeds.
FBRX · Capital · Positive Forte Biosciences agreed to be acquired by argenx for $77 per share in cash, a premium to market.
GOSS · Regulation · Positive Gossamer Bio plans to file NDA for Seralutinib in September 2026, a key regulatory milestone.
OMER · Competition · Positive AstraZeneca's Ultomiris failed a Phase 3 trial, removing a key competitive threat to Omeros's YARTEMLEA.
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GOSS▲impact 4

Gossamer Bio Plans September 2026 NDA Filing for Seralutinib in PAH

Gossamer Bio announced it will submit a New Drug Application for seralutinib in pulmonary arterial hypertension in September 2026, following a productive pre-NDA meeting with the FDA. If accepted, the inhaled therapy could receive an approval decision in the third quarter of 2027. The company also reacquired worldwide rights to seralutinib from Chiesi, securing full global control and the majority of long-term economics. Gossamer reported preliminary cash and equivalents of approximately $57 million as of June 30, 2026, and completed an exchange of about $181.1 million of its 2027 Notes for new 7.50% Convertible Senior Secured First Lien Notes due 2030. Shareholders approved a convertible note exchange and a reverse stock split, strengthening the capital structure ahead of the filing. The stock rose over 41% to $0.19.
GOSS · Capital · Positive Planned NDA filing and capital restructuring (note exchange, reverse split) strengthen financial position and regulatory path.
Chiesi Group · Competition · Negative Chiesi lost worldwide rights to seralutinib, which Gossamer reacquired, reducing Chiesi's potential future revenue from the drug.
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