Gossamer Bio, Inc. (GOSS): History, Ownership, Mission, How It Works & Makes Money

Gossamer Bio, Inc. (GOSS): History, Ownership, Mission, How It Works & Makes Money

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When you look at a clinical-stage biopharmaceutical company like Gossamer Bio, Inc. (GOSS), which is currently valued at a market capitalization of around $734.87 million as of November 2025, do you understand the true value driver behind that number? The company's focus on its lead candidate, seralutinib, for pulmonary arterial hypertension (PAH) has driven a stock price increase of 271.80% in the last year, but its third-quarter 2025 net loss of $48.2 million shows the very real cash burn of late-stage drug development. We'll defintely map out how a company with such a significant net loss can maintain a cash runway into 2027, and what the February 2026 topline data for the Phase 3 PROSERA study means for your investment thesis.

Gossamer Bio, Inc. (GOSS) History

Gossamer Bio, Inc. is a late-stage clinical biopharmaceutical company that has rapidly evolved from a well-capitalized startup into a focused player in the pulmonary hypertension space. The company's history is a classic biotech story: raise a massive war chest, in-license a promising late-stage asset, and drive it toward pivotal clinical data. Their lead asset, seralutinib, is now the central focus, which has been a major catalyst for the company's trajectory, especially in 2025.

Given Company's Founding Timeline

Year established

While Gossamer Bio, Inc. was incorporated in Delaware in 2015, the entity formally changed its name and began its operational focus in 2017.

Original location

The company is headquartered in San Diego, California, a major hub for biopharmaceutical innovation.

Founding team members

The company was founded by a team of industry veterans who previously held leadership roles at other major biopharma companies. The founding team included:

  • Sheila Gujrathi, MD
  • Faheem Hasnain
  • Bryan Giraudo

Initial capital/funding

Gossamer Bio, Inc. started with significant financial backing, securing $100 million in a Series A financing round in 2018. This was quickly followed by a substantial $230 million Series B round later that same year. This initial capital infusion was critical, allowing the company to acquire and develop a deep pipeline of assets right out of the gate.

Given Company's Evolution Milestones

Year Key Event Significance
2018 In-licensing of GB001 (seralutinib) Pivotal acquisition of a Phase 3-ready asset for pulmonary arterial hypertension (PAH), establishing the company's primary focus.
2019 Initial Public Offering (IPO) Raised $276.1 million, providing crucial capital for advancing multiple clinical development programs.
2020 GB002 (OX40 antagonist) Phase 2 Trial Initiated Advanced a novel therapy for inflammatory bowel disease (IBD), demonstrating a commitment to a broad immunology and inflammation pipeline.
2024 Global Collaboration with Chiesi Group Formed a strategic partnership to jointly develop and commercialize seralutinib, sharing development costs and commercial profits/losses in the U.S.
2025 PROSERA Phase 3 Study Enrollment Completion Screening for new patients closed, with enrollment completed in June 2025 for the pivotal PAH trial, setting up the major catalyst for February 2026.
2025 SERENATA Phase 3 Study Activation Activated the first clinical site in Q4 2025 for the global registrational trial of seralutinib in PH-ILD, expanding the addressable market.

Given Company's Transformative Moments

The most transformative moments for Gossamer Bio, Inc. all center on a single drug candidate and the capital required to push it through late-stage trials. Honestly, in biotech, you are your lead asset.

  • The Seralutinib In-Licensing: Acquiring GB001, now seralutinib, in 2018 was the single most important decision. It immediately shifted the company from a discovery-stage startup to a late-stage clinical company, giving it a clear path to market in the high-value pulmonary hypertension (PAH) space.
  • Securing the IPO Capital: The 2019 IPO and the preceding private rounds gave the company a cash runway that has been essential for weathering the long, expensive clinical development cycle. This capital allowed them to run the massive Phase 3 PROSERA study.
  • The Chiesi Collaboration: This 2024 partnership was a smart de-risking move. By splitting development costs and commercializing jointly in the U.S., Gossamer Bio, Inc. secured a strong global partner and a path to royalties in the mid to high teens outside the U.S. Plus, it helped shore up the balance sheet.

As of Q3 2025, the company reported $180.2 million in cash, cash equivalents, and marketable securities, which management expects to fund operations into 2027. This financial stability is directly tied to those early funding decisions and the Chiesi deal. For the quarter ended September 30, 2025, the net loss was $48.2 million, showing the high cost of running these pivotal trials. This is a critical period; all eyes are on the upcoming seralutinib data. You can read more about the company's core principles here: Mission Statement, Vision, & Core Values of Gossamer Bio, Inc. (GOSS).

Gossamer Bio, Inc. (GOSS) Ownership Structure

Gossamer Bio, Inc. (GOSS) is controlled primarily by institutional investors, who collectively hold over three-quarters of the outstanding shares, while company insiders maintain a significant stake, aligning their interests with long-term performance.

Gossamer Bio, Inc.'s Current Status

Gossamer Bio, Inc. is a publicly traded, clinical-stage biopharmaceutical company. It trades on the Nasdaq Global Select Market under the ticker symbol GOSS. As of November 2025, the company's market capitalization stood at approximately $498.37 million, based on 231.46 million shares outstanding. This public status allows a diverse spectrum of investors to own a piece of the company, but it also subjects the firm to rigorous financial and regulatory scrutiny by the Securities and Exchange Commission (SEC).

Gossamer Bio, Inc.'s Ownership Breakdown

The company's ownership structure as of the 2025 fiscal year is heavily skewed toward institutional capital, which is typical for a biotech firm advancing late-stage clinical trials. This means major decisions are heavily influenced by a few large entities. Exploring Gossamer Bio, Inc. (GOSS) Investor Profile: Who's Buying and Why?

Shareholder Type Ownership, % Notes
Institutional Investors 76.37% Includes firms like BlackRock, Inc. and Vanguard Group Inc.
Company Insiders 14.90% Officers, directors, and 10%+ shareholders; includes co-founder Faheem Hasnain.
Retail Investors 8.73% Individual investors holding shares through brokerage accounts.

Here's the quick math: Institutional investors hold the majority, so their voting power defintely dictates the direction of the board and major corporate actions. For example, BlackRock, Inc. held over 13.84 million shares as of the end of Q3 2025.

Gossamer Bio, Inc.'s Leadership

The leadership team is a mix of biopharmaceutical veterans, steering the company through the high-risk, high-reward world of clinical development. Their average tenure is about 4.3 years, showing a stable, experienced management core.

  • Faheem Hasnain: Co-Founder, Chief Executive Officer, and President. He was appointed to the CEO role in November 2020.
  • Bryan Giraudo: Chief Operating Officer and Chief Financial Officer. He manages the financial strategy and operational execution, a critical role given the high cash burn of a clinical-stage company.
  • Richard Aranda, M.D.: Chief Medical Officer. He oversees the clinical development programs, including the late-stage seralutinib program.
  • Christian Waage: Executive Vice President of Technical Operations & Administration.
  • Jeff Boerneke: General Counsel & Secretary.

CEO Faheem Hasnain directly owns 2.58% of the company's shares, valued at approximately $16.17 million, which helps align his personal financial success with that of the shareholders.

Gossamer Bio, Inc. (GOSS) Mission and Values

Gossamer Bio, Inc.'s mission centers on dramatically improving the lives of patients with rare, debilitating pulmonary diseases, driven by a culture of scientific rigor and patient-centric dedication.

Gossamer Bio, Inc.'s Core Purpose

The company's cultural DNA is built around a clear, patient-focused mandate. This isn't just about developing a drug; it's about solving an urgent, unmet medical need, particularly in the pulmonary hypertension (PH) space.

Here's the quick math: Pulmonary Arterial Hypertension (PAH) is a serious, progressive disease, and Gossamer Bio is focused on potentially transforming patient care with its lead candidate, seralutinib, which is currently in a registrational Phase 3 study (PROSERA).

The core values that guide their work, especially as they manage a cash runway into 2027 with approximately $213 million in cash and marketable securities as of June 30, 2025, are:

  • Respect and humility in all interactions.
  • Transparency in science and operations.
  • Dedication and collaboration across teams.
  • A focus on fun, defintely, alongside the serious work.

Official Mission Statement

Gossamer Bio's official mission is rooted in enhancing patient outcomes for conditions where treatment options are limited or inadequate. This commitment goes beyond just the drug discovery phase.

The overarching mission is:

  • Improve the lives of patients with rare diseases.
  • Unwavering commitment to supporting patient communities across the globe.

Honesty, it's a mission that requires patience and a high-risk tolerance, given the clinical-stage nature of the business.

Vision Statement

The company's long-term vision maps directly to their current development pipeline, aiming for market leadership in a critical therapeutic area. They want to be the standard of care, not just another option.

The stated goal, which functions as their near-term vision, is:

  • To be an industry leader in, and to enhance the lives of patients living with, pulmonary hypertension.

This vision is currently being executed with the Phase 3 PROSERA study for PAH and the planned Phase 3 SERANATA study for PH-ILD, with the latter activating its first sites in the fourth quarter of 2025.

Gossamer Bio, Inc. Slogan/Tagline

While a snappy, consumer-facing tagline isn't common for a late-stage biopharma focused on rare disease, Gossamer Bio uses a concise phrase on its main platform that distills its focus down to the essentials.

  • Science. Seralutinib.

This simple phrasing cuts straight to the point: their work is grounded in science, and seralutinib is the vehicle for realizing their patient-focused mission. You can find more details on their guiding principles here: Mission Statement, Vision, & Core Values of Gossamer Bio, Inc. (GOSS).

Gossamer Bio, Inc. (GOSS) How It Works

Gossamer Bio, Inc. operates as a late-stage, clinical biopharmaceutical company, creating value by advancing its lead inhaled drug candidate, seralutinib, through pivotal Phase 3 trials for rare and severe pulmonary vascular diseases. The company's primary business model is built on drug development and strategic collaboration with partners like the Chiesi Group, which helps fund the high-cost research and development (R&D) required to bring a potential first-in-class therapy to market.

This is a high-risk, high-reward model; success hinges entirely on the upcoming clinical data readouts, like the one expected in February 2026 for the PROSERA study. You can see the financial demands of this stage in the Q3 2025 financials: R&D expenses hit $45.5 million, driving a net loss of $48.2 million, even with collaboration revenue of $13.3 million. Breaking Down Gossamer Bio, Inc. (GOSS) Financial Health: Key Insights for Investors

Gossamer Bio, Inc.'s Product/Service Portfolio

The company's core focus is on building a franchise in pulmonary hypertension (PH) with its inhaled therapies, which target a multi-billion-dollar market opportunity.

Product/Service Target Market Key Features
Seralutinib (GB002) Pulmonary Arterial Hypertension (PAH) Inhaled, multi-target inhibitor (PDGFR, CSF1R, c-KIT); currently in Phase 3 PROSERA Study.
Seralutinib (GB002) Pulmonary Hypertension associated with Interstitial Lung Disease (PH-ILD) Inhaled, aims to address a critical unmet need; Phase 3 SERANATA Study initiating in Q4 2025.
Inhaled Vardenafil (RT234) Pulmonary Hypertension (PH) Inhaled Phosphodiesterase Type 5 (PDE5) Inhibitor; strategic option to acquire for pipeline expansion.

Gossamer Bio, Inc.'s Operational Framework

The operational framework is centered on managing complex, global clinical trials and leveraging a co-development partnership to mitigate financial and commercial risk.

  • Clinical Trial Execution: Manage the global Phase 3 PROSERA study (390 patients enrolled) and initiate the Phase 3 SERANATA study, ensuring regulatory compliance and data integrity.
  • Collaboration Management: Execute the global partnership with the Chiesi Group, which splits development costs for seralutinib (except for the PROSERA study, which Gossamer Bio fully funds).
  • Revenue Generation: Primarily generate revenue through collaboration payments, which include cost reimbursements from Chiesi Group. For Q3 2025, this collaboration drove $13.3 million in revenue.
  • Financial Runway: Maintain a sufficient cash position-$180.2 million as of September 30, 2025-to fund operations into 2027, ensuring the pipeline can reach key clinical catalysts without immediate dilution.
  • Commercial Planning: Transition from a purely clinical-stage company to a commercial one by preparing market access and launch strategies for seralutinib in the US, where Gossamer Bio will lead commercialization and book sales.

Gossamer Bio, Inc.'s Strategic Advantages

The company's advantages stem from its focus on a high-value, underserved market and its unique drug mechanism.

  • First-in-Class Potential: Seralutinib is an inhaled, multi-target inhibitor, offering a novel mechanism of action in the PH treatment landscape, potentially addressing the underlying disease pathology beyond current vasodilators.
  • Market Focus: Targeting Pulmonary Hypertension, a rare disease market with high unmet need and potential for Orphan Drug designation, which provides market exclusivity and faster regulatory pathways.
  • Strategic Partnership: The collaboration with Chiesi Group provides a global commercial footprint and non-dilutive funding, reducing the burden of international development and commercialization.
  • Inhaled Delivery: The inhaled route of administration delivers the drug directly to the lungs, potentially maximizing efficacy and minimizing systemic side effects, a key differentiator for patients with severe lung conditions.
  • Pipeline Expansion: The option to acquire inhaled vardenafil provides a complementary, late-stage asset, positioning Gossamer Bio to build a broader PH-focused product portfolio.

Gossamer Bio, Inc. (GOSS) How It Makes Money

Gossamer Bio, Inc. is a clinical-stage biopharmaceutical company, meaning it does not yet sell an approved drug; instead, it generates revenue almost entirely through strategic partnerships, specifically by receiving payments for development services and cost reimbursements from its collaboration with the Chiesi Group.

The company's financial engine is built on advancing its lead product candidate, seralutinib, through late-stage clinical trials for pulmonary arterial hypertension (PAH) and pulmonary hypertension associated with interstitial lung disease (PH-ILD), with collaboration payments funding the significant research and development (R&D) costs.

Gossamer Bio's Revenue Breakdown

As of the third quarter of 2025 (Q3 2025), Gossamer Bio's total revenue of $13.3 million was derived exclusively from its collaboration with the Chiesi Group. This structure is typical for a biotech company in the clinical phase, where partnership funding replaces product sales as the primary income source.

Revenue Stream % of Total (Q3 2025) Growth Trend
Collaboration Cost Reimbursement (Chiesi) 69.2% Increasing
Other Collaboration Revenue (Chiesi) 30.8% Increasing

The total collaboration revenue of $13.3 million in Q3 2025 represents a strong increase from the $9.5 million reported in the same period a year prior. This growth is driven by the acceleration of clinical activities, particularly the Phase 3 PROSERA Study for seralutinib, which triggers higher cost reimbursements from the partner.

Business Economics

The economics of Gossamer Bio are centered on a risk-sharing, high-potential-reward model through its global collaboration agreement with the Chiesi Group for seralutinib.

  • Primary Asset: Seralutinib, an inhaled PDGFR, CSF1R, and c-KIT inhibitor, is the company's core value driver, targeting the multi-billion-dollar pulmonary hypertension market.
  • Partnership Structure: The Chiesi deal is crucial. Gossamer Bio and Chiesi Group are jointly developing seralutinib. They will evenly share commercial profits and losses in the U.S. for PAH and PH-ILD, which is a significant future revenue stream.
  • Funding Mechanism: Current revenue is essentially a funding mechanism. Chiesi pays Gossamer for R&D services and reimburses a portion of the development costs, which is why $9.2 million of the Q3 2025 revenue was cost reimbursement.
  • Future Upside: The real financial payoff will come upon regulatory approval. Gossamer Bio is eligible to receive up to $146 million in regulatory milestones and up to $180 million in sales milestones from Chiesi, plus escalating mid-to-high teens royalties on ex-U.S. net sales. That's the big money.

The entire business model hinges on positive top-line data from the PROSERA Phase 3 study, which is expected in February 2026.

Gossamer Bio's Financial Performance

As a late-stage clinical company, Gossamer Bio's financial performance is characterized by significant investment in R&D, resulting in a net loss despite the collaboration revenue.

  • Net Loss: For the third quarter ended September 30, 2025, the net loss was $48.2 million, or $0.21 basic net loss per share. This is a widening from the $30.8 million net loss in Q3 2024, reflecting the increased costs of running large-scale Phase 3 trials.
  • R&D Expense: R&D expenses are the largest cost center, totaling $45.5 million in Q3 2025, up from $34.9 million in the prior year period. This jump shows the heavy financial commitment to completing the seralutinib trials, which is defintely where the focus should be.
  • Cash Position: The company reported a strong cash position, with cash, cash equivalents, and marketable securities totaling $180.2 million as of September 30, 2025. This capital is projected to fund operations into 2027, providing a solid runway past the key seralutinib data readouts.
  • Trailing Twelve-Month (TTM) Revenue: As of September 30, 2025, the TTM revenue was $44.1 million, demonstrating the consistent, though non-product-based, financial inflow from the partnership.

The financial health of a company like this isn't about current profit, but about maintaining the cash runway to hit the clinical milestones that will unlock future product revenue. You can dive deeper into the sustainability of this model here: Breaking Down Gossamer Bio, Inc. (GOSS) Financial Health: Key Insights for Investors

Gossamer Bio, Inc. (GOSS) Market Position & Future Outlook

Gossamer Bio, Inc. is a high-stakes, late-stage clinical biopharmaceutical company whose near-term trajectory is a binary bet on its lead asset, seralutinib. The company currently holds a pre-commercial market position in the Pulmonary Arterial Hypertension (PAH) space, but a positive readout from its Phase 3 PROSERA study, expected in February 2026, could transform its market capitalization of approximately $0.70 Billion USD as of November 2025 into a multi-billion dollar valuation, positioning it as a major competitor in the specialized pulmonary hypertension market.

Competitive Landscape

The PAH market is dominated by established players with multi-billion dollar franchises, but Gossamer Bio aims to disrupt this landscape with a first-in-class inhaled therapy. Your analysis must consider that the current leaders have a significant head start and a deep portfolio of approved drugs; Gossamer Bio's market share is currently 0%, but its potential is in carving out a niche with a novel mechanism of action and delivery system.

Company Market Share, % (Estimated PAH) Key Advantage
Gossamer Bio 0% (Pre-commercial) First-in-class inhaled tyrosine kinase inhibitor (TKI) for PAH/PH-ILD.
Johnson & Johnson (Actelion) ~40% Established, broad portfolio of oral therapies (Opsumit, Uptravi); dominant market position.
United Therapeutics ~26% Leadership in prostacyclin analogs; innovative inhaled delivery (Tyvaso DPI) with 9M 2025 Tyvaso sales of $1.41 billion.

Opportunities & Challenges

The company's strategy is clear: secure approval for seralutinib in PAH, then expand into the highly underserved Pulmonary Hypertension associated with Interstitial Lung Disease (PH-ILD) market. This is a classic biotech risk/reward profile. You can see how the Q3 2025 net loss of $48.2 million reflects the investment in these pivotal trials. Here's the quick map of the near-term landscape.

Opportunities Risks
First-in-class inhaled TKI (seralutinib) could become a backbone therapy for PAH. Binary event risk: Negative Phase 3 PROSERA data (expected Feb 2026) would be catastrophic.
PH-ILD market entry with Phase 3 SERANATA (Q4 2025 start) targets a high unmet need. Competition from Merck's Winrevair (sotatercept), a new, approved, first-in-class biologic with 9M 2025 sales of $976 million.
Global commercialization partnership with Chiesi Group reduces launch execution risk. High cash burn rate: Cash, cash equivalents, and marketable securities of $180.2 million (as of Sept 30, 2025) funds operations only into 2027.

Industry Position

Gossamer Bio is positioned as a high-potential, late-stage challenger in the pulmonary hypertension therapeutic area. The global PAH market is valued at over $8.11 billion in 2025, with growth driven by new disease-modifying agents like Merck's Winrevair. This new competition is defintely a challenge, but it also validates the market's appetite for novel mechanisms beyond the traditional vasodilators.

  • Challenger Status: The company is a clinical-stage entity with a market cap of $0.70 Billion USD, dwarfed by multi-billion dollar competitors, making it a pure-play investment on seralutinib success.
  • Inhaled Advantage: Seralutinib's inhaled delivery is a key differentiator, potentially offering better tolerability and targeted delivery compared to systemic oral or injectable therapies, which could capture share from United Therapeutics' inhaled franchise.
  • Pipeline Focus: By focusing solely on seralutinib for PAH and PH-ILD, the company has a clear, singular path to commercialization. This concentration minimizes R&D sprawl but maximizes the risk associated with a single drug's clinical outcome.

To fully grasp the capital structure supporting this high-risk strategy, you should review Breaking Down Gossamer Bio, Inc. (GOSS) Financial Health: Key Insights for Investors.

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