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Gossamer Bio

Full company profile

uuid0000ew3

Namestring
Gossamer Bio
Legal namestring
Gossamer Bio, Inc.
Websiteurl
gossamerbio.com
Company typeenum
Public
Founded yearint
2015
Descriptiontext

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.

Short descriptiontext

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.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersSan Diego, United States
HQ citystring
San Diego
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
pulmonary hypertension therapeutics, inhaled kinase inhibitors, rare disease biopharmaceuticals, dry powder inhaler drugs, clinical stage drug development
Industry1 code
1Pulmonary Hypertension & Rare Pulmonary Disease Therapies
CodeHLAIAIAGPrimaryYes
NAICS code1 code
  • Pharmaceutical Preparation Manufacturing325412
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Pulmonary Hypertension Therapeutics
Social media profiles2 records
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model4 records
1Collaboration revenue from Chiesi partnership
TypeLicensing Royalties
Description

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.

businesswire.com
2Future milestone payments from Chiesi
TypeLicensing Royalties
Description

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.

gossamerbio.com
3Future US product sales (PAH and PH-ILD)
TypeSubscription Recurring
Description

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.

gossamerbio.com
4Future ex-US royalty stream from Chiesi
TypeLicensing Royalties
Description

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.

gossamerbio.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 record
1Seralutinib
Description

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.

gossamerbio.com
Core offering1 text field

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.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • Phase 3 PROSERA trial placebo-adjusted improvement of +13.3 meters in Six-Minute Walk Distance at Week 24 (p=0.0320)
+3 more records
Product overview1 text field

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.

Product and service1 record
1Seralutinib
CategoryInvestigational inhaled kinase inhibitor (pulmonary hypertension)
Description

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).

Scale indicator15 records

Each record includes

Type, Value, Description, Source

Partnership6 partners
Strategic tierFlagship - Core Strategic Partnership Defining Gossamer Bio'S Global Commercialization Path For SeralutinibTypeStrategic or Co-development PartnerAnnounced on2024-05-01
Description

In 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.

Strategic tierMinor - Patient Advocacy PartnershipTypeGTM or Marketing Partner
Description

Patient advocacy organization supporting clinical trial awareness and education for the PAH community in Europe.

Strategic tierMinor - Patient Advocacy PartnershipTypeGTM or Marketing Partner
Description

Patient advocacy organization supporting clinical trial awareness, patient education, and disease awareness for the PAH community in the US.

Strategic tierMinor - Patient Advocacy PartnershipTypeGTM or Marketing Partner
Description

Patient advocacy organization supporting clinical trial participation, patient education, and disease awareness for the PAH/PH-ILD community.

Strategic tierMinor - Patient Advocacy PartnershipTypeGTM or Marketing Partner
Description

Patient advocacy organization supporting global awareness and education for pulmonary hypertension, featured in clinical trial awareness materials.

Strategic tierMinor - Medical Research PartnershipTypeGTM or Marketing Partner
Description

Medical research organization supporting scientific conferences and education in pulmonary vascular disease.

Recent move5 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight3 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

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.

TypeDirect peer
Description

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.

TypeDirect peer
Description

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.

TypeEmerging player
Description

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.

TypeEmerging player
Description

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.

TypeEmerging player
Description

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.

TypeBroad incumbent
Description

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.

TypeBroad incumbent
Description

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.

TypeOthers
Description

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.

TypeOthers
Description

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

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat3 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles18 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries1 record

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance2 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds7 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors27 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A1 record

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Gossamer Bio

Pulmonary Hypertension Therapeuticsgossamerbio.com

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.

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

  • Pulmonary hypertension therapeutics
  • Inhaled kinase inhibitors
  • Rare disease biopharmaceuticals
  • Dry powder inhaler drugs
  • Clinical stage drug development

Where Gossamer Bio is headquartered

Location

Headquarters

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

  1. 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.
  2. 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.
  3. 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.
  4. 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 offering

Core 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 profile

Named customers1 record

Segments3 records

Ideal customer profiles3 records

Gossamer Bio technology and API

Technology

Technology 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 signal

Partnerships

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 seralutinibStrategic or Co-development Partner · 1 May 2024In 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 partnershipGTM or Marketing PartnerPatient advocacy organization supporting clinical trial awareness and education for the PAH community in Europe.
  • Pulmonary Hypertension Association (PHA)minor - patient advocacy partnershipGTM or Marketing PartnerPatient advocacy organization supporting clinical trial awareness, patient education, and disease awareness for the PAH community in the US.
  • Team PHenomenal Hopeminor - patient advocacy partnershipGTM or Marketing PartnerPatient advocacy organization supporting clinical trial participation, patient education, and disease awareness for the PAH/PH-ILD community.
  • phaware globalminor - patient advocacy partnershipGTM or Marketing PartnerPatient advocacy organization supporting global awareness and education for pulmonary hypertension, featured in clinical trial awareness materials.
  • Pulmonary Vascular Research Institute (PVRI)minor - medical research partnershipGTM or Marketing PartnerMedical 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 assessment

Direct 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 presence

Gossamer Bio compliance and trust

Trust signal

Compliance2 records

Gossamer Bio financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Gossamer Bio leadership team

Management profile

Number of profiles

Profiles18 records

Gossamer Bio subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

Gossamer Bio funding detail

Funding detail

Funding 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 investment

M&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.

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Defense World396,727 Shares of Gossamer Bio, Inc. $GOSS Acquired by Bank of America Corp DEBank of America Corp DE acquired a new position in Gossamer Bio, purchasing 396,727 shares valued at about $65,000 in Q2. Analysts have an average "Hold" rating with a consensus target price of $256.00, and the stock's 52-week range is $9.10 to $309.60.MarketBeat396,727 Shares of Gossamer Bio, Inc. $GOSS Acquired by Bank of America Corp DEBank of America Corp DE acquired 396,727 shares of Gossamer Bio in Q2, valued at about $65,000, giving it a 0.17% stake. Analysts have a consensus 'Hold' rating with a $256 target, and institutional ownership stands at 81.23%.Ticker ReportGossamer Bio, Inc. (NASDAQ:GOSS) Short Interest UpdateGossamer Bio's short interest fell 98.9% to 948,623 shares as of September 15th. Analysts rate the stock a Hold with a consensus price target of $256.00. The company's lead product is seralutinib, an inhaled tyrosine kinase inhibitor for pulmonary hypertension.Markets DailyGossamer Bio, Inc. (NASDAQ:GOSS) Stock Has Consensus Target Price of $256.00 According to BrokeragesGossamer Bio's stock has a consensus 'Hold' rating with a $256 average price target from nine analysts. The company submitted an FDA NDA for seralutinib, its lead candidate for pulmonary arterial hypertension, though the stock fell after the filing. Institutional investors hold 81.23% of shares.BioSpaceGossamer Bio Submits New Drug Application to U.S. FDA for Seralutinib for the Treatment of Pulmonary Arterial HypertensionGossamer Bio submitted its first New Drug Application to the FDA for seralutinib to treat pulmonary arterial hypertension, supported by the Phase 3 PROSERA study and Phase 2 TORREY study. The FDA will review the application, with an acceptability decision expected later this year.Seeking AlphaGossamer Bio submits NDA for seralutinib for pulmonary arterial hypertensionGossamer Bio submitted an NDA to the US FDA for seralutinib to treat pulmonary arterial hypertension. The application is supported by data from the phase 3 PROSERA study, phase 2 TORREY study, and supportive analyses.Business Wire BlogGossamer Bio Submits New Drug Application to U.S. FDA for Seralutinib for the Treatment of Pulmonary Arterial HypertensionGossamer Bio submitted its first New Drug Application to the FDA for seralutinib to treat pulmonary arterial hypertension, supported by the Phase 3 PROSERA study and Phase 2 TORREY study. The FDA will review the application, with an acceptability decision expected later this year.The future of tradingGossamer Bio director Gregory Austin Ciongoli files initial beneficial ownership statementGossamer Bio director Gregory Austin Ciongoli filed an initial Form 3 disclosing a pre-funded warrant for 250 shares of Series A-1 preferred stock. The filing was published via EDGAR on September 22, 2026.Markets DailyGossamer Bio (NASDAQ:GOSS) Lowered to “Sell” Rating by Wall Street ZenWall Street Zen lowered Gossamer Bio from a hold to a sell rating. The stock has an average analyst rating of Hold with a consensus target price of $256.00. Institutional investors own 81.23% of the stock.BioSpaceGossamer Bio Appoints Greg Ciongoli to Board of DirectorsGossamer Bio appointed Greg Ciongoli to its board of directors, effective September 16, 2026, with a seat on the Audit Committee. Ciongoli, founder of Adiumentum Capital Management, will support advancing seralutinib toward potential FDA approval for pulmonary hypertension.