Gossamer Bio
Clinical-stage biopharmaceutical company developing seralutinib, an inhaled PDGFRα/β, CSF1R, c-Kit kinase inhibitor, delivered via dry powder inhaler for treatment of pulmonary arterial hypertension and PH-ILD, facing major clinical and financial setbacks following Phase 3 PROSERA trial failure.
- Company typePublic
- Founded2015
- HeadquartersSan Diego, United States
- Headcount101–250
- GTM typeB2B
- OfferingHardware or Manufacturing
What Gossamer Bio does
Gossamer Bio is a clinical-stage biopharmaceutical company focused on the discovery and development of novel and differentiated therapeutic products, with its core asset seralutinib—an investigational, inhaled, small-molecule kinase inhibitor targeting PDGFRα/β, CSF1R, and c-Kit—delivered via dry powder inhaler (DPI) directly to the lungs for the treatment of pulmonary arterial hypertension (PAH) and pulmonary hypertension associated with interstitial lung disease (PH-ILD). The company's differentiated drug-device combination approach positions seralutinib as potentially the only late-stage clinical asset designed to reverse pathological vascular remodeling in PAH, rather than acting purely as a vasodilator. Gossamer Bio operates through a global collaboration with Chiesi Farmaceutici S.p.A. for ex-U.S. commercialization while leading U.S. commercialization independently. The company faces significant clinical and financial headwinds following the February 2026 failure of its Phase 3 PROSERA trial, which triggered a subsequent 48-50% workforce reduction, an 80% stock decline, and a debt restructuring that reduced outstanding convertible notes from $200M to approximately $72M.
Gossamer Bio firmographics
Firmographics- Name
- Gossamer Bio
- Legal name
- Gossamer Bio, Inc.
- Website
- https://gossamerbio.com
- Company type
- Public
- Founded year
- 2015
- Operating status
- Operating
- Headcount range
- 101–250 employees
- Short description
- Clinical-stage biopharmaceutical company developing seralutinib, an inhaled PDGFRα/β, CSF1R, c-Kit kinase inhibitor, delivered via dry powder inhaler for treatment of pulmonary arterial hypertension and PH-ILD, facing major clinical and financial setbacks following Phase 3 PROSERA trial failure.
- Ownership category
- akta.pro rank
Gossamer Bio industry classification
Industry- Product category
- Pulmonary Hypertension Therapeutics
- NAICS
- Pharmaceutical Preparation Manufacturing (325412)
- SIC
- Pharmaceutical Preparations (2834)
- akta.pro primary industry
- Pulmonary Hypertension & Rare Pulmonary Disease Therapies (HLAIAIAG)
Keywords
Where Gossamer Bio is headquartered
LocationHeadquarters
- HQ city
- San Diego
- HQ country
- United States
- HQ region
- North America
Offices2 records
Markets served
Gossamer Bio business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Technology or R&D, Personnel, Operations, Marketing or Sales, Others
Revenue model
- Collaboration revenue from Chiesi partnership: Q1 2026 revenue of $17.0 million, rising 71% year-over-year, primarily driven by collaboration revenue from the partnership with Chiesi Group including $9.3 million in cost reimbursement. Revenue stream tied to development cost-sharing under the May 2024 global collaboration and license agreement.
- Future milestone payments from Chiesi: Gossamer Bio eligible to receive up to $146 million in regulatory milestones and $180 million in sales milestones under its May 2024 collaboration with Chiesi Farmaceutici S.p.A. for seralutinib development and commercialization.
- Future US product sales (PAH and PH-ILD): Future US commercial revenue from seralutinib sales, with Gossamer Bio leading US commercialization and booking sales. Companies will evenly share commercial profits and losses in the US for both PAH and PH-ILD indications.
- Future ex-US royalty stream from Chiesi: Chiesi will have exclusive rights to commercialize seralutinib outside the US and will pay Gossamer Bio an escalating mid-to-high teens royalty on net sales in ex-US markets.
Go-to-market motion1 record
Distribution channels3 records
Marketing channels6 records
Gossamer Bio product offering
Product offeringCore offering
Gossamer Bio is developing seralutinib, an investigational, inhaled small-molecule kinase inhibitor of PDGFRα/β, CSF1R, and c-KIT, delivered via a proprietary dry powder inhaler (DPI) drug-device combination. The product is being investigated for pulmonary arterial hypertension (PAH) and pulmonary hypertension associated with interstitial lung disease (PH-ILD), with the goal of reversing pathological vascular remodeling through anti-inflammation, anti-proliferation, and anti-fibrosis mechanisms rather than acting as a vasodilator.
Product overview
Gossamer Bio is a clinical-stage biopharmaceutical company with a single-asset focused portfolio built around its investigational drug product seralutinib. The company's offering is not a multi-product platform but rather a focused clinical-stage pipeline anchored on one inhaled small-molecule inhibitor (PDGFRα/β, CSF1R, c-KIT) targeting pulmonary hypertension. The named products and clinical programs within this portfolio are: seralutinib (the core investigational drug product, delivered via dry powder inhaler); the Phase 3 PROSERA Study in pulmonary arterial hypertension (PAH); the Phase 3 SERANATA Study in pulmonary hypertension associated with interstitial lung disease (PH-ILD); the completed Phase 2 TORREY Study in PAH; and the open-label extension studies (PROSERA-EXT and PAH OLE) providing long-term safety and efficacy follow-up. These products/programs are all variations or stages of development of the same underlying asset (seralutinib) and together constitute the entirety of Gossamer Bio's product portfolio.
Differentiator
Problem solved
Functional benefit
Brands
- Seralutinib: Investigational inhaled small molecule inhibitor of PDGFRα/β, CSF1R, and c-KIT, delivered via dry powder inhaler for PAH and PH-ILD. Previously known as GB002.
Products and services
- Seralutinib Seralutinib is an investigational, inhaled, small-molecule inhibitor of platelet-derived growth factor receptor (PDGFRα/β), colony-stimulating factor 1 receptor (CSF1R), and mast/stem cell growth factor receptor kit (c-KIT), intentionally designed to target mechanisms underlying pulmonary hypertension and delivered via dry powder inhaler for the potential treatment of pulmonary arterial hypertension (PAH) and pulmonary hypertension associated with interstitial lung disease (PH-ILD).
Quantifiable outcome
- Phase 3 PROSERA trial placebo-adjusted improvement of +13.3 meters in Six-Minute Walk Distance at Week 24 (p=0.0320)
- +3 more outcomes
Companies that use Gossamer Bio
Customer profileNamed customers1 record
Segments3 records
Ideal customer profiles3 records
Gossamer Bio technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature3 records
Gossamer Bio partnerships and signals
Strategic signalPartnerships
Six partnerships are on record, tiered flagship - core strategic partnership defining gossamer bio's global commercialization path for seralutinib, minor - patient advocacy partnership and minor - medical research partnership.
- Chiesi Farmaceutici S.p.A.flagship - core strategic partnership defining gossamer bio's global commercialization path for seralutinibIn May 2024, Gossamer Bio and Chiesi Farmaceutici entered into a global collaboration and license agreement to develop and commercialize seralutinib. Under the agreement: Gossamer leads global development of seralutinib in PAH and PH-ILD; companies evenly split development costs (except PROSERA Study which Gossamer funds alone); in US, companies evenly share commercial profits and losses with Gossamer leading commercialization and booking sales; Chiesi leads US commercialization in additional indications; Chiesi has exclusive ex-US commercialization rights paying escalating mid-to-high teens royalty on net sales; Gossamer eligible for up to $146M in regulatory milestones and $180M in sales milestones.
- PHA Europeminor - patient advocacy partnershipPatient advocacy organization supporting clinical trial awareness and education for the PAH community in Europe.
- Pulmonary Hypertension Association (PHA)minor - patient advocacy partnershipPatient advocacy organization supporting clinical trial awareness, patient education, and disease awareness for the PAH community in the US.
- Team PHenomenal Hopeminor - patient advocacy partnershipPatient advocacy organization supporting clinical trial participation, patient education, and disease awareness for the PAH/PH-ILD community.
- phaware globalminor - patient advocacy partnershipPatient advocacy organization supporting global awareness and education for pulmonary hypertension, featured in clinical trial awareness materials.
- Pulmonary Vascular Research Institute (PVRI)minor - medical research partnershipMedical research organization supporting scientific conferences and education in pulmonary vascular disease.
Scale indicators15 records
Recent moves5 records
Expansion highlights3 records
Gossamer Bio competitors and assessment
Company assessmentDirect peers
- United Therapeutics Corporation: United Therapeutics is a direct competitor in PAH with Tyvaso DPI and Remodulin (inhaled and infused treprostinil), and is the current standard-of-care inhaled therapy in PAH — directly comparable to Gossamer Bio's seralutinib DPI product. Gossamer SVP Rob Roscigno is a former principal developer of Remodulin at United Therapeutics.
- Liquidia Corporation: Liquidia is a direct PAH competitor with YUTREPIA (inhaled treprostinil) and is a near-term rival in the inhaled PAH space; Gossamer's SVP Rob Roscigno previously led the LIQ861 program at Liquidia, making the overlap on assets, modality (inhaled DPI), and talent highly comparable.
- Acceleron Pharma (Merck): Acceleron's WINREVAIR (sotatercept), now marketed by Merck following an $11B+ acquisition, is a recently approved PAH therapy targeting a distinct mechanism, and is a direct competitive threat to seralutinib in the same patient population; Gossamer director John Quisel led the sotatercept re-acquisition effort at Acceleron.
Emerging players
- Aerovate Therapeutics: Aerovate is an emerging PAH-focused company developing inhaled imatinib for pulmonary arterial hypertension, sharing the same targeted-DPI-for-PAH model as seralutinib and competing for similar specialist physician adoption, albeit with a kinase-inhibitor mechanism aimed at a different pathway.
- Insmed Incorporated: Insmed is a commercial-stage inhaled therapeutics company with ARIKAYCE for nontuberculous mycobacterial lung disease, sharing the rare-disease inhaled-pulmonary delivery model with seralutinib and demonstrating the commercial viability of inhaled specialty lung disease drugs.
- MannKind Corporation: MannKind is a specialty pulmonary and endocrine company built around dry powder inhaler drug-device platforms (Afrezza, Tyvaso DPI collaboration with United Therapeutics), and is a technology-platform comparable to seralutinib's DPI delivery approach.
Broad incumbents
- Actelion / Janssen Pharmaceuticals (J&J): Actelion (acquired by J&J for $30B) is the historical market leader in PAH with OPSUMIT, UPTRAVI, and Tracleer; several Gossamer executives (Bob Smith, Jeanine Anthony) are former Actelion PAH launch leaders, making J&J the dominant incumbent comparable for understanding seralutinib's competitive context.
- Bayer Pharmaceuticals (Adempas / riociguat): Bayer markets Adempas (riociguat) in PAH/PH-ILD, making it a broad incumbent in the same indication space as seralutinib and a reference for specialty distribution and PH-accredited center engagement.
Others
- Disc Medicine: Disc Medicine is a clinical-stage hematology and rare-disease company whose CEO (John Quisel) is a Gossamer board member, providing a comparable reference point for a small-cap rare-disease biopharma pursuing an NDA path with limited commercial infrastructure.
- Pulmokine Inc. Pulmokine is a private company with a secondary-market economic interest in seralutinib (acquired by XOMA Royalty for $20M); it serves as an adjacent ecosystem reference to Gossamer Bio's seralutinib program and a small-cap comparable in the inhaled PAH development space.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat3 records
Key risks6 records
Key highlights7 records
Customer concentration
Gossamer Bio social profiles
Digital presenceGossamer Bio compliance and trust
Trust signalCompliance2 records
Gossamer Bio financial estimates
Financial estimateRevenue estimate
Valuation estimate
Gossamer Bio leadership team
Management profileNumber of profiles
Profiles18 records
Gossamer Bio subsidiaries and ownership
Company hierarchySubsidiaries1 record
Gossamer Bio funding detail
Funding detailFunding overview
Funding rounds7 records
Investors27 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Gossamer Bio M&A and investment
M&A and investmentM&A1 record
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Gossamer Bio
What does Gossamer Bio do?
Gossamer Bio is developing seralutinib, an investigational, inhaled small-molecule kinase inhibitor of PDGFRα/β, CSF1R, and c-KIT, delivered via a proprietary dry powder inhaler (DPI) drug-device combination. The product is being investigated for pulmonary arterial hypertension (PAH) and pulmonary hypertension associated with interstitial lung disease (PH-ILD), with the goal of reversing pathological vascular remodeling through anti-inflammation, anti-proliferation, and anti-fibrosis mechanisms rather than acting as a vasodilator.
Is Gossamer Bio a public or private company?
Gossamer Bio is a public company. It is classified as public and is currently operating.
When was Gossamer Bio founded?
Gossamer Bio was founded in 2015. It employs 101 to 250 people.
Where is Gossamer Bio based?
Gossamer Bio is headquartered in San Diego, United States, in the North America region.
How does Gossamer Bio make money?
Four revenue lines are on record. Collaboration revenue from Chiesi partnership is the primary driver. The others are future milestone payments from Chiesi, future US product sales (PAH and PH-ILD) and future ex-US royalty stream from Chiesi.
Who are Gossamer Bio's main competitors?
Direct peers on record are United Therapeutics Corporation, Liquidia Corporation and Acceleron Pharma (Merck). Emerging players are Aerovate Therapeutics, Insmed Incorporated and MannKind Corporation. Broad incumbents are Actelion / Janssen Pharmaceuticals (J&J) and Bayer Pharmaceuticals (Adempas / riociguat). Others are Disc Medicine and Pulmokine Inc..
Does Gossamer Bio have an API?
No public API is recorded for Gossamer Bio.
What industry is Gossamer Bio in?
Gossamer Bio's product category is Pulmonary Hypertension Therapeutics. Its primary akta.pro industry code is HLAIAIAG, Pulmonary Hypertension & Rare Pulmonary Disease Therapies. Its NAICS code is 325412 and its SIC code is 2834.