Tyra Biosciences, Inc. (TYRA): History, Ownership, Mission, How It Works & Makes Money

Tyra Biosciences, Inc. (TYRA): History, Ownership, Mission, How It Works & Makes Money

US | Healthcare | Biotechnology | NASDAQ

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How does a clinical-stage biotech like Tyra Biosciences, Inc. (TYRA), with a Q3 2025 net loss of $29.9 million, command a market capitalization of roughly $844 million? The answer lies in its proprietary SNÅP platform and its lead candidate, dabogratinib, an investigational precision medicine targeting Fibroblast Growth Factor Receptor (FGFR) biology for conditions like achondroplasia and bladder cancer. You need to understand the company's mission-developing next-generation therapies to overcome drug resistance-to properly value its pipeline, especially since its cash position of $274.9 million as of September 30, 2025, provides a runway through at least 2027. Let's defintely dig into how this pre-revenue company works, who owns it, and what its path to monetization truly looks like.

Tyra Biosciences, Inc. (TYRA) History

You're looking for the foundational story of Tyra Biosciences, Inc., and it's a classic biotech narrative: a focused team leveraging a novel platform to solve a major problem-acquired drug resistance in cancer. The direct takeaway is that Tyra Biosciences was founded in 2018, secured early, substantial venture capital, and has rapidly evolved from a pure oncology play to a precision medicine company with a dual focus on cancer and rare genetic disorders like achondroplasia, all powered by its proprietary SNÅP platform.

Given Company's Founding Timeline

Year established

Tyra Biosciences was officially incorporated in August 2018, setting the stage for its specialized work in precision oncology.

Original location

The company established its initial corporate office in Carlsbad, California.

Founding team members

The core founding team included Todd Harris, Ph.D., who serves as the Chief Executive Officer, and Daniel Bensen, who was a co-founder and Chief Operating Officer/Chief Scientific Officer, bringing together expertise to tackle acquired resistance in targeted therapies.

Initial capital/funding

The company's journey began with a strong financial foundation. In early 2020, Tyra Biosciences announced it had closed a $50 million Series A financing round, co-led by significant life sciences investors like Alta Partners, RA Capital Management, Boxer Capital, and Canaan Partners.

Here's the quick math on their early backing: that initial $50 million Series A, followed by a $106 million Series B, gave them a total of over $156 million in private funding before their public offering, which is defintely the fuel needed for a rapid R&D push.

Given Company's Evolution Milestones

Year Key Event Significance
2018 Company Incorporated Formal start of the business, focused on the proprietary SNÅP platform for drug discovery.
2020 Closed $50 Million Series A Financing Provided foundational capital to build the SNÅP platform and advance initial pipeline programs, including the lead candidate, Dabogratinib (formerly TYRA-300).
2021 Closed $106 Million Series B Financing Enabled significant expansion of the pipeline and accelerated the development of the lead Fibroblast Growth Factor Receptor (FGFR) inhibitor program.
Feb 2024 Announced $200 Million Private Placement (PIPE) A major capital infusion that extended the cash runway, signaling strong institutional investor confidence in the clinical data and the broader potential of the pipeline.
Q3 2025 Dosed First Patients in Phase 2 BEACH301 and SURF302 Trials Marked the transition of Dabogratinib into mid-stage trials for both pediatric achondroplasia (BEACH301) and intermediate-risk non-muscle invasive bladder cancer (SURF302).

Given Company's Transformative Moments

The company's trajectory was shaped by a few critical, high-stakes decisions that broadened their market opportunity beyond the initial oncology focus. The key was realizing the potential of their lead candidate, Dabogratinib (TYRA-300), to treat a rare genetic disorder.

  • Platform Validation with SNÅP: The early commitment to the proprietary SNÅP (Systematic Network Analysis Platform) drug discovery engine was the first transformative decision. This platform is designed to rapidly and precisely design small molecules that overcome acquired resistance, giving them a distinct competitive edge in the targeted therapy space.
  • The Dual-Indication Strategy: Moving Dabogratinib from a pure oncology candidate (for urothelial cancer) to also target achondroplasia-a skeletal dysplasia-was a massive strategic pivot. This decision, backed by positive preclinical results published in April 2025, opened up a new, high-value market in rare diseases.
  • Aggressive Clinical Execution in 2025: The financial health as of September 30, 2025, with cash, cash equivalents, and marketable securities of $274.9 million, allowed for a rapid, multi-front clinical push. This led to dosing the first patients in two pivotal Phase 2 trials (BEACH301 and SURF302) and expanding into a third indication, low-grade upper tract urothelial carcinoma (LG-UTUC), all within the third quarter of 2025. This is what you call clinical velocity.

The focus now is on translating this clinical momentum into tangible results, with interim Phase 2 data from Dabogratinib expected in 2026. For a deeper dive into the numbers underpinning this strategy, you should look at Breaking Down Tyra Biosciences, Inc. (TYRA) Financial Health: Key Insights for Investors.

Tyra Biosciences, Inc. (TYRA) Ownership Structure

Tyra Biosciences, Inc. (TYRA) is primarily controlled by institutional investors, a common structure for clinical-stage biotechnology companies, with a significant portion of the stock held by a few key venture capital and healthcare-focused funds. This concentration means strategic decisions are heavily influenced by a relatively small group of large, sophisticated financial stakeholders, but still subject to the transparency requirements of a public company.

Tyra Biosciences' Current Status

As of November 2025, Tyra Biosciences, Inc. is a publicly traded company on the NASDAQ Global Select Market under the ticker symbol TYRA. This status requires rigorous financial and operational disclosures to the Securities and Exchange Commission (SEC), providing a transparent view for all stakeholders.

The company's market capitalization was approximately $844 million as of October 31, 2025, based on roughly 53.4 million shares outstanding. This public listing was defintely crucial for raising the capital needed to advance its precision oncology pipeline, particularly its lead candidate, TYRA-300.

Tyra Biosciences' Ownership Breakdown

Institutional investors hold the majority of the company, reflecting the capital-intensive nature of drug development. Here's the quick math on the ownership distribution based on recent 2025 fiscal year filings:

Shareholder Type Ownership, % Notes
Institutional Investors 62.08% Includes major holders like Ra Capital Management, L.P. (holding approximately 22.86% of shares), Alta Partners, and Nextech Invest.
Public/Retail Investors 34.24% Shares held by individual investors and smaller entities not classified as institutional or insider.
Insiders (Executives & Directors) 3.68% Direct holdings by the leadership team and board members, aligning their interests with long-term shareholder value.

To be fair, this breakdown shows that while insiders have a smaller percentage, their interests are still aligned with shareholders, plus the institutional holders provide the deep pockets needed for a biotech firm. For a deeper dive into the company's long-term strategy, check out the Mission Statement, Vision, & Core Values of Tyra Biosciences, Inc. (TYRA).

Tyra Biosciences' Leadership

The company's strategic direction is guided by an experienced executive team and a board with deep expertise in oncology and drug commercialization, steering the development of its Structure-based Network Assessment Platform (SNAP) technology.

  • Todd Harris, Ph. D.: Chief Executive Officer (CEO) and Co-founder, leading the company since November 2018. His total yearly compensation was approximately $7.57 million, as of late 2025, with the majority tied to performance and equity.
  • Doug Warner, M.D.: Chief Medical Officer (CMO), appointed in September 2024, bringing extensive clinical development experience from his 18-year tenure at Amgen.
  • Daniel Bensen: Chief Operating Officer (COO), who recently executed sales of shares under a pre-arranged 10b5-1 trading plan in November 2025.
  • Alan Fuhrman: Chief Financial Officer (CFO), a veteran in biotech finance.
  • Robert More: Chairman of the Board, providing governance oversight.
  • Adele Gulfo: Board Member, appointed in January 2025, bringing nearly three decades of executive leadership from companies like Pfizer and AstraZeneca.

The average tenure for the management team is about 3.5 years, showing a relatively stable and experienced core leadership for a clinical-stage biotech. Finance: track all executive and institutional 13F filings weekly.

Tyra Biosciences, Inc. (TYRA) Mission and Values

Tyra Biosciences, Inc.'s core purpose is to develop next-generation precision medicines, specifically targeting Fibroblast Growth Factor Receptor (FGFR) biology, to provide improved, precise options of care for patients with diseases like skeletal dysplasia and bladder cancer. Their cultural DNA is built around a collaborative, patient-focused approach, understanding that innovative therapies require diverse minds working together.

Tyra Biosciences, Inc.'s Core Purpose

The company's operational focus is clearly on clinical execution across its portfolio of next-generation precision therapies, a strategy backed by a strong financial position. As of September 30, 2025, Tyra Biosciences, Inc. held cash, cash equivalents, and marketable securities totaling $274.9 million, giving them a runway through at least 2027.

Here's the quick math on their burn rate: the net loss for the third quarter of 2025 was $29.9 million, primarily driven by Research and Development (R&D) expenses of $25.5 million for clinical trials like BEACH301 and SURF302. They are defintely putting their capital to work in the clinic.

Official Mission Statement

The company's mission is fundamentally about leveraging its proprietary drug discovery engine to address significant unmet medical needs. This is what they do:

  • Develop next-generation precision medicines that target large opportunities in Fibroblast Growth Factor Receptor (FGFR) biology.
  • Apply the in-house precision medicine platform, SNÅP, to enable rapid and precise drug design.
  • Focus initial efforts on targeted oncology and genetically defined conditions.

Vision Statement

The vision is to transform how specific diseases are treated by applying a highly selective approach, moving beyond existing therapies that often have problematic off-target toxicities. The CEO's statement clearly articulates this patient-centric, transformative goal:

  • Transform the treatment of bladder cancer and skeletal dysplasia by precisely targeting FGFR3.
  • Focus remains on patients-those living with skeletal dysplasia and bladder cancer who need improved, precise options of care.
  • Build a franchise around the power of FGFR3 selectivity and sensitivity, minimizing toxicities associated with inhibiting other FGFRs.

This is a clear-eyed vision: solve a tough problem with better chemistry. Breaking Down Tyra Biosciences, Inc. (TYRA) Financial Health: Key Insights for Investors

Tyra Biosciences, Inc. Slogan/Tagline

While a single, formal slogan is not used, the company consistently employs a descriptive tagline that captures their technological edge and product focus:

  • Developing Next-Generation Precision Molecules.
  • Next-Generation Precision Medicines.

Tyra Biosciences, Inc. (TYRA) How It Works

Tyra Biosciences, Inc. is a clinical-stage biotechnology company focused on developing next-generation precision medicines that target large opportunities in Fibroblast Growth Factor Receptor (FGFR) biology. They operate by using their proprietary drug discovery platform to design highly selective, oral small molecules aimed at overcoming acquired resistance to existing therapies and treating genetically defined conditions. The company does not generate product revenue yet, reflecting its focus on advancing its pipeline through clinical trials.

Tyra Biosciences' Product/Service Portfolio

The company's value creation is centered on its pipeline of investigational drugs, with its lead candidate, dabogratinib, driving the majority of its near-term clinical milestones. This oral therapy is being developed for both oncology and a rare genetic skeletal disorder, showing the breadth of their FGFR focus.

Product/Service Target Market Key Features
Dabogratinib (formerly TYRA-300) Pediatric Achondroplasia (ACH); Intermediate-Risk Non-Muscle Invasive Bladder Cancer (IR NMIBC); Low-Grade Upper Tract Urothelial Carcinoma (LG-UTUC) Oral, investigational, FGFR3-selective inhibitor designed to avoid off-target toxicities; Phase 2 studies (BEACH301 and SURF302) are actively enrolling as of November 2025.
TYRA-430 FGF19+/FGFR4-driven cancers, including Advanced Hepatocellular Carcinoma (HCC) Oral, investigational FGFR4/3-biased inhibitor; designed to address a significant unmet need where no approved biomarker-driven, targeted therapies exist; currently in a Phase 1 study (SURF431).
TYRA-200 Advanced/Metastatic Intrahepatic Cholangiocarcinoma (ICC) and other solid tumors with activating FGFR2 gene alterations Oral, investigational FGFR1/2/3 inhibitor; potent against activating FGFR2 gene alterations and resistance mutations; currently enrolling and dosing patients in a Phase 1 study (SURF201).

Tyra Biosciences' Operational Framework

The operational framework is a lean, clinical-stage model centered on rapid, data-driven drug discovery and execution of multi-cohort clinical trials. Their entire operation is geared toward translating novel molecular insights into differentiated drug candidates.

  • Proprietary Discovery Engine: The in-house precision medicine platform, called SNÅP (Structure-based NAnoparticle Platform), is the core operational asset. It enables rapid and precise drug design.
  • Iterative Molecular Design: SNÅP uses iterative molecular 'SNÅPshots' to predict genetic alterations most likely to cause acquired resistance to existing therapies, allowing them to design next-generation inhibitors that overcome these resistance mechanisms.
  • Clinical Execution Focus: The majority of capital is deployed into Research and Development (R&D) to advance the three clinical-stage programs. R&D expenses for the third quarter of 2025 were $25.5 million, reflecting this intense focus on clinical trial progress.
  • Financial Runway Management: The company maintains a strong cash position to fund operations, reporting cash, cash equivalents, and marketable securities of $274.9 million as of September 30, 2025, which is projected to provide a runway through at least 2027.

Here's the quick math: The Q3 2025 net loss was $29.9 million, so the cash burn rate is manageable against the current cash balance. You can learn more about their long-term goals here: Mission Statement, Vision, & Core Values of Tyra Biosciences, Inc. (TYRA).

Tyra Biosciences' Strategic Advantages

Tyra Biosciences' market success hinges on its ability to develop best-in-class molecules that address the limitations of existing Fibroblast Growth Factor Receptor (FGFR) inhibitors. Their advantages are rooted in precision and selectivity.

  • Resistance-Busting Design: Dabogratinib is specifically designed to remain active even in the presence of treatment-emergent resistance mutations, such as the V555 gatekeeper mutation, which can limit the effectiveness of other FGFR inhibitors.
  • Superior Selectivity: The lead candidate, dabogratinib, is a selective FGFR3 inhibitor. This selectivity is key, as it aims to avoid the off-target side effects-like hyperphosphatemia, a common issue-associated with inhibiting other FGFR isoforms (FGFR1, FGFR2, and FGFR4).
  • First-in-Class Potential: Dabogratinib is positioned as a potential first-in-class selective FGFR3 inhibitor, and it is the only oral therapy currently in clinical development for intermediate-risk non-muscle invasive bladder cancer (IR NMIBC).
  • Dual-Market Strategy: By targeting both oncology (bladder cancer) and a rare genetic disease (achondroplasia) with the same lead candidate, the company diversifies its clinical opportunities and potential market reach. Achondroplasia, for instance, is caused by a mutation in the FGFR3 gene in over 99% of cases, making it a highly precise target.

The defintely clear action here is that their entire valuation is tied to the clinical data readouts for dabogratinib in 2026.

Tyra Biosciences, Inc. (TYRA) How It Makes Money

Tyra Biosciences, Inc. is a clinical-stage biotechnology company, so it does not currently generate revenue from the sale of commercial products; its financial engine is fueled by capital raised through equity financing and interest income on its substantial cash reserves to fund its drug development pipeline.

Tyra Biosciences, Inc.'s Revenue Breakdown

As a pre-commercial entity, Tyra Biosciences' business model is focused on research and clinical development, not product sales. For the 2025 fiscal year through the third quarter (Q3 2025), the company reported $0.0 million in product revenue. This is normal for a biotech company with its lead candidate, dabogratinib, still in Phase 2 clinical trials.

Revenue Stream % of Total Growth Trend
Product Sales (Dabogratinib, etc.) 0% Stable (at zero)
Collaboration/Licensing Revenue <1% Stable/N/A
Interest and Investment Income >99% Increasing (Based on cash reserves)

The vast majority of the company's reported income comes from interest earned on its cash, cash equivalents, and marketable securities, which totaled $274.9 million as of September 30, 2025. This is a crucial metric for a development-stage company, as it shows the runway for funding operations without having to raise more capital immediately.

Business Economics

The core economic driver for Tyra Biosciences is the potential future value of its proprietary drug candidates, particularly its lead asset, dabogratinib (formerly TYRA-300), an oral investigational Fibroblast Growth Factor Receptor 3 (FGFR3)-selective inhibitor. The economics are not based on current sales, but on successfully navigating the costly and lengthy clinical trial process (Investigational New Drug (IND) through Phase 3 and regulatory approval).

  • Value Creation: The company's value is tied to clinical milestones, like the interim Phase 2 results for dabogratinib in pediatric achondroplasia (BEACH301) and non-muscle invasive bladder cancer (SURF302), both expected in 2026.
  • Cost Structure: The business is entirely expense-driven, with Research and Development (R&D) being the dominant cost. Here's the quick math: R&D expenses for Q3 2025 were $25.5 million, far exceeding the General and Administrative (G&A) expenses of $7.5 million for the same period.
  • Pricing Strategy (Future): If approved, the drugs would enter specialty markets (precision oncology and rare diseases like achondroplasia), allowing for premium pricing, which is standard for novel therapies addressing unmet medical needs.
  • Platform Leverage: The proprietary SNÅP platform (Selective Next-generation Kinase Inhibitor Platform) is designed to generate multiple differentiated drug candidates (like TYRA-430 and TYRA-200) efficiently. This internal capability helps lower the long-term cost of drug discovery.

The company's model is a classic biotech bet: invest heavily now for a massive payoff later. You can get a better sense of the institutional confidence in this model by Exploring Tyra Biosciences, Inc. (TYRA) Investor Profile: Who's Buying and Why?

Tyra Biosciences, Inc.'s Financial Performance

Tyra Biosciences' financial performance for the 2025 fiscal year reflects its status as a high-burn, high-potential clinical-stage company. The key metrics show operational expansion and deep investment into the pipeline.

  • Cash Position: The company ended Q3 2025 with a strong cash, cash equivalents, and marketable securities balance of $274.9 million. This cash runway is projected to fund operations through at least 2027.
  • Net Loss: The Trailing Twelve Months (TTM) net loss ending Q3 2025 was approximately $111.2 million. The net loss for Q3 2025 alone was $29.9 million, up from $24.0 million in Q3 2024, showing the increased investment in clinical trials.
  • R&D Investment: R&D expenses are the primary cash defintely sink. TTM R&D expenses ending Q3 2025 were approximately $96.9 million, reflecting the acceleration of its Phase 2 studies for dabogratinib.
  • Net Loss Per Share (EPS): The net loss per share for Q3 2025 was ($0.50). This loss is expected to continue or even increase as the company advances its costly late-stage clinical trials.

Tyra Biosciences, Inc. (TYRA) Market Position & Future Outlook

Tyra Biosciences, Inc. is positioned as a high-risk, high-reward clinical-stage oncology company, leveraging its proprietary SNÅP platform to develop next-generation precision medicines targeting Fibroblast Growth Factor Receptor (FGFR) biology. The near-term outlook is entirely dependent on clinical milestones, with interim Phase 2 data for its lead candidate, dabogratinib, expected in 2026, which will be the defintely most critical catalyst.

Competitive Landscape

In the precision oncology space, Tyra Biosciences competes not just with other FGFR inhibitors but also with companies developing targeted therapies for molecularly defined solid tumors and genetically defined conditions. Since Tyra Biosciences is pre-revenue, its market share is currently zero, but its competitive edge rests on the highly selective nature of its lead asset, dabogratinib, designed to overcome common resistance mutations.

Company Market Share, % Key Advantage
Tyra Biosciences 0% First-in-class, highly selective FGFR3 inhibitor (dabogratinib) via SNÅP platform.
Day One Biopharmaceuticals, Inc. <0.1% (Targeted Niche) Commercial-stage asset (OJEMDA) for pediatric low-grade glioma; established revenue base.
IDEAYA Biosciences 0% Deep pipeline focused on Synthetic Lethality (e.g., PARG, Werner Helicase) with major pharma partnerships.

Opportunities & Challenges

The company's focus on both oncology and achondroplasia (a skeletal dysplasia) provides two distinct, high-value opportunities, but this diversification also stretches development resources. The financial runway is strong, but the binary nature of clinical trial results remains the primary risk factor.

Opportunities Risks
Dabogratinib's potential as a first-in-class, selective FGFR3 inhibitor for achondroplasia (BEACH301) and urothelial carcinoma (SURF302/303). Binary risk of Phase 2 clinical trial failure; interim results for dabogratinib are not expected until 2026.
Robust cash position of $274.9 million (Q3 2025) provides an operational runway through at least 2027, reducing near-term dilution risk. Significant cash burn with a Q3 2025 net loss of $29.9 million, requiring continued capital raises without product revenue.
Expanding the pipeline with next-generation candidates like TYRA-430 (FGFR4/3) and TYRA-200 (FGFR1/2/3) addresses a broader range of FGFR-driven cancers. Intense competition from larger pharmaceutical companies with approved pan-FGFR inhibitors and established oncology market presence.

Industry Position

Tyra Biosciences is a specialized player in the biotechnology industry, not a market share leader, but a technology innovator. Its position is defined by its platform technology, SNÅP, which is designed to preemptively address acquired resistance-a major challenge in targeted oncology. The company's current market capitalization of approximately $844 million (as of October 2025) places it among mid-cap clinical biotechs, a valuation that reflects the high potential of its pipeline.

Analysts show confidence, with a consensus rating of Moderate Buy and an average 12-month price target of $32.00, suggesting a potential upside of over 50% from recent trading levels, contingent on positive clinical data. The company's strategic focus and long-term goals are detailed further in their Mission Statement, Vision, & Core Values of Tyra Biosciences, Inc. (TYRA).

  • Maintain a cash runway into 2027, minimizing financing pressure during key clinical readouts.
  • Prioritize dabogratinib's Phase 2 data in achondroplasia and bladder cancer for 2026.
  • Leverage the SNÅP platform to identify new targets beyond current pipeline assets.

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