IDEAYA Biosciences, Inc. (IDYA) Bundle
IDEAYA Biosciences, Inc. (IDYA) is a leader in precision medicine oncology, but after reporting a Q3 2025 net income of $119.2 million, a massive turnaround from the prior quarter, do you know what strategic pivot drove that financial shift? The answer lies in their distinct focus on synthetic lethality and the $210 million upfront payment from the Servier licensing deal for darovasertib, a collaboration that immediately bolstered their financial position. With cash, cash equivalents, and marketable securities sitting at approximately $1.14 billion as of September 30, 2025, and the stock trading near its $33.64 52-week high, this is a biotech story where the balance sheet now directly fuels a deep clinical pipeline; you defintely need to understand how they plan to sustain this momentum.
IDEAYA Biosciences, Inc. (IDYA) History
IDEAYA Biosciences, Inc. is a precision medicine oncology company that has rapidly evolved by focusing on the complex but highly promising field of synthetic lethality. This strategy of targeting genetic vulnerabilities in cancer cells has de-risked their pipeline and attracted significant capital, culminating in a cash position of approximately $1.14 billion as of September 30, 2025, which funds operations into 2030.
Given Company's Founding Timeline
Year established
The company was established in 2015, with the core premise of attracting top scientific talent to pursue transformative research in oncology.
Original location
IDEAYA Biosciences began in South San Francisco, California, a central hub for biotech innovation.
Founding team members
The initial direction was set by a small, experienced group, including Yujiro S. Hata, who served as the first employee, Founder, and Chief Executive Officer. Other key figures in the early stages were Michael P. Dillon and Jeffrey L. Hager, who brought essential expertise in drug discovery and development.
Initial capital/funding
The company secured its first major institutional backing in 2016 with a Series A funding round, raising a substantial $46 million. This initial investment signaled strong early confidence from venture capital firms like 5AM Ventures and Canaan Partners in the company's synthetic lethality platform.
Given Company's Evolution Milestones
| Year | Key Event | Significance |
|---|---|---|
| 2016 | Series A Financing Secured | Raised $46 million, enabling the initial platform development and pipeline build-out. |
| 2018 | Series B Financing Completed | Secured $94 million, further capitalizing the company to advance preclinical assets toward clinical trials. |
| 2019 | Initial Public Offering (IPO) | Listed on Nasdaq (IDYA), raising approximately $57.5 million in gross proceeds and providing access to public markets for growth capital. |
| 2020 | Landmark GSK Collaboration | Established a major collaboration focused on synthetic lethality programs (MAT2A, Pol Theta, Werner Helicase), including a $100 million upfront payment from GSK. |
| 2025 (Q1) | Darovasertib FDA Breakthrough Therapy Designation | U.S. FDA granted Breakthrough Therapy Designation for darovasertib in neoadjuvant uveal melanoma (UM), accelerating its regulatory path. |
| 2025 (Q3) | Servier Exclusive License Agreement | Entered a deal for darovasertib outside the U.S., receiving $210 million upfront, extending the cash runway into 2030, and validating the lead program. |
Given Company's Transformative Moments
The company's trajectory has been defined by strategic financial moves and a relentless focus on its core scientific platform: synthetic lethality. This is where two non-essential genes, when disabled together, cause cell death-a perfect way to target cancer.
The most recent and defintely transformative moment came in the third quarter of 2025 with the Servier licensing deal for darovasertib. This single transaction provided a massive non-dilutive capital infusion of $210 million upfront, plus eligibility for up to $320 million in additional milestones.
Here's the quick math: that deal, combined with prior financings and collaborations, boosted their cash, cash equivalents, and marketable securities to approximately $1.14 billion as of September 30, 2025, which pushes their operational runway out to 2030. This is a huge de-risking event for a clinical-stage biotech.
- Strategic Pipeline Validation: The GSK and Servier partnerships validated the synthetic lethality platform and the lead candidate darovasertib, securing over $310 million in upfront payments alone from these two deals.
- Financial Strength: The company reported a significant profit for Q3 2025, with revenue of $207.83 million and earnings per share of $1.33, primarily driven by the Servier payment, materially beating analyst expectations.
- Clinical Advancement: Enrollment in the darovasertib and crizotinib registrational trial for first-line metastatic uveal melanoma (mUM) is ahead of schedule, with over 300 patients enrolled and median progression-free survival (PFS) results targeted by year-end 2025.
This strong financial and clinical position, with a market capitalization around $2.94 billion as of November 2025, allows them to aggressively advance their wholly-owned pipeline candidates, such as IDE397 and IDE161. Exploring IDEAYA Biosciences, Inc. (IDYA) Investor Profile: Who's Buying and Why?
IDEAYA Biosciences, Inc. (IDYA) Ownership Structure
IDEAYA Biosciences, Inc. (IDYA) is a publicly traded precision medicine oncology company, listed on the NASDAQ Global Select Market. The ownership structure is heavily weighted toward institutional investors, which is typical for a clinical-stage biotechnology firm with a market capitalization of approximately $2.94 billion as of November 2025. This high institutional control means a small group of large funds and firms holds the majority of voting power, so you should pay close attention to their quarterly 13F filings.
Given Company's Current Status
IDEAYA Biosciences is a public company trading under the ticker symbol IDYA. Its status as a NASDAQ-listed entity subjects it to rigorous financial reporting and governance standards set by the Securities and Exchange Commission (SEC). This transparency is a key benefit for investors, but it also exposes the stock to the volatility inherent in the biotechnology sector.
The company's substantial cash, cash equivalents, and marketable securities, reported at approximately $992 million as of June 30, 2025, are anticipated to fund operations into at least 2029, providing a defintely strong liquidity position for its clinical development programs.
Given Company's Ownership Breakdown
The ownership structure is dominated by institutional investors, a common feature in biotech where specialized funds provide the capital for long-term, high-risk drug development. This concentration means strategic decisions are largely influenced by a relatively small number of large financial entities, including BlackRock, Inc. and The Vanguard Group, Inc.
| Shareholder Type | Ownership, % | Notes |
|---|---|---|
| Institutional Investors | 98.29% | Includes mutual funds, pension funds, and asset managers like BlackRock and Vanguard. |
| Insiders/Individuals | 0.91% | Includes executives, directors, and other affiliated individuals. CEO Yujiro S. Hata directly owns 0.79%. |
| Public Float/Retail | 0.80% | The remaining shares available for trading by the general public and smaller investors. |
For a deeper dive into the specific funds and their investment theses, you should check out the detailed analysis: Exploring IDEAYA Biosciences, Inc. (IDYA) Investor Profile: Who's Buying and Why?
Given Company's Leadership
The company is steered by a seasoned executive team with deep expertise in oncology, drug discovery, and finance. The average tenure of the management team is relatively short at 1.9 years, which suggests a recent, strategic build-out of the executive bench to support the company's clinical pipeline advancements.
- Yujiro S. Hata: President, Chief Executive Officer, and Founder. He has led the company since its incorporation in June 2015.
- Joshua Bleharski, Ph.D.: Chief Financial Officer. He joined in May 2025 from J.P. Morgan, where he was a Managing Director and Global Co-Head of Biopharma Investment Banking.
- Michael White, Ph.D.: Chief Scientific Officer. He brings over two decades of R&D leadership experience, including prior roles at Pfizer.
- Darrin M. Beaupre, M.D., Ph.D.: Chief Medical Officer.
- Paul A. Barsanti, Ph.D.: Chief Technology Officer, Head of Drug Discovery.
- Daniel A. Simon: Chief Business Officer. He joined in August 2024 and leads business development and strategy.
The CEO's total yearly compensation was $16.93 million, with a large majority coming from bonuses and equity, aligning his incentives closely with long-term shareholder value. This is a critical point: the leadership is paid to deliver on the pipeline, not just on salary.
IDEAYA Biosciences, Inc. (IDYA) Mission and Values
IDEAYA Biosciences, Inc. (IDYA) grounds its work in a core commitment to precision oncology, aiming to deliver highly targeted therapies that fundamentally change the outlook for cancer patients. This mission is backed by a clinical-stage pipeline and a strong financial position, with approximately $1.14 billion in cash and equivalents as of September 30, 2025, which funds operations into 2030.
You're investing in more than just drug candidates; you're investing in a specific philosophy of drug development. That philosophy is about using molecular diagnostics to select the exact patient population that will benefit most, making the entire development process more efficient and ethical. Honestly, this focus is what drove their Q3 2025 collaboration revenue of $207.8 million, a clear signal of partnership validation.
Given Company's Core Purpose
The company's cultural DNA centers on an entrepreneurial spirit and a relentless pursuit of innovation, which is necessary when tackling tough targets like synthetic lethality (a strategy where inhibiting two specific genes kills a cancer cell, but inhibiting either one alone does not).
Official mission statement
The mission is a defintely clear statement of intent: to bring forth the next wave of precision oncology therapies that are more selective, more effective, and deeply personalized. This is what guides their substantial investment in research and development, which totaled $83.0 million in the third quarter of 2025 alone.
- Pursue discovery and development of targeted therapeutics for cancer.
- Improve clinical outcomes by altering the course of disease.
- Select patient populations using molecular diagnostics (biomarkers).
Vision statement
While IDEAYA Biosciences does not publish a single, one-sentence vision statement, their long-term goal is explicitly to become a global leader in precision medicine oncology. This vision is supported by their strategy to develop first-in-class or best-in-class therapeutics, particularly in the emerging area of synthetic lethality.
The vision is about market leadership driven by scientific excellence. It's a simple, but powerful, mandate. They are advancing a broad clinical pipeline, including the darovasertib program, which is targeting a median progression-free survival (PFS) readout by year-end 2025, a critical step toward potential accelerated approval.
- Become a global leader in precision medicine oncology.
- Commercialize transformative therapies for cancer.
- Integrate structural biology and bioinformatics in drug discovery.
Given Company slogan/tagline
The company consistently identifies itself with the core concept it embodies. It's a 'precision medicine oncology company committed to the discovery and development of targeted therapeutics.' This is the tagline that defines their market position and competitive edge.
Their focus on precision medicine is the whole story. You can learn more about the formal corporate objectives here: Mission Statement, Vision, & Core Values of IDEAYA Biosciences, Inc. (IDYA).
IDEAYA Biosciences, Inc. (IDYA) How It Works
IDEAYA Biosciences, Inc. operates as a precision medicine oncology company, focusing on discovering and developing targeted therapies for cancer patients selected by specific molecular diagnostics. The company creates value by advancing a deep pipeline of drug candidates, primarily based on the concept of synthetic lethality, through strategic partnerships that provide significant non-dilutive capital.
IDEAYA Biosciences, Inc.'s Product/Service Portfolio
| Product/Service | Target Market | Key Features |
|---|---|---|
| Darovasertib (PKC Inhibitor) | Uveal Melanoma (UM) and Metastatic Uveal Melanoma (MUM) patients with GNAQ/GNA11 mutations. | Potential first-in-class PKC inhibitor. Currently in a Phase 2/3 trial (OptimUM-02) in combination with crizotinib for first-line HLAA2-negative MUM, targeting median Progression-Free Survival (PFS) data by year-end 2025. |
| Synthetic Lethality Platform (IDE397, IDE275, IDE705) | Solid tumors with specific genetic alterations, such as MTAP gene deletion (approx. 15% of all solid tumors) or MSI-High. | Focuses on novel targets like MAT2A (IDE397), Werner Helicase (IDE275), and Pol Theta (IDE705). This approach exploits a tumor's specific genetic weakness to selectively kill cancer cells, a highly personalized strategy. |
IDEAYA Biosciences, Inc.'s Operational Framework
The company's operational model is built on an integrated research and development (R&D) engine that combines small-molecule drug discovery with structural biology and bioinformatics. They don't just find drugs; they find the right patients for them by validating translational biomarkers (measurable indicators of a biological state). This focused approach is designed to increase the probability of clinical success.
IDEAYA Biosciences, Inc. makes money primarily through strategic collaborations and milestone payments, not yet from commercial product sales. For example, the company reported a trailing 12-month revenue of approximately $215 million as of September 30, 2025, which was significantly boosted by a $210 million upfront payment from Servier for the exclusive ex-US rights to darovasertib. They use this non-dilutive capital to fund R&D, which totaled $83.0 million in the third quarter of 2025. Here's the quick math: a massive upfront payment covers over two quarters of R&D, extending their cash runway into 2030, which is defintely a good sign.
- Drug Discovery: Identify and validate novel synthetic lethality targets.
- Clinical Development: Advance candidates like darovasertib through registrational trials, often in combination with partners' drugs like Pfizer's crizotinib.
- Monetization: Secure large, non-dilutive payments via licensing agreements for ex-US rights or co-development deals with major pharmaceutical companies like GlaxoSmithKline (GSK).
You can see more on who is funding this model at Exploring IDEAYA Biosciences, Inc. (IDYA) Investor Profile: Who's Buying and Why?
IDEAYA Biosciences, Inc.'s Strategic Advantages
IDEAYA Biosciences, Inc.'s market success hinges on a few core, durable advantages that differentiate them in the competitive oncology space.
- Synthetic Lethality Expertise: Deep focus on synthetic lethality (SL), a precision oncology approach where inhibiting two genes simultaneously is lethal to a cancer cell, while inhibiting only one is not. This SL focus targets large, genetically-defined patient populations, such as MTAP-deleted tumors, which represent about 15% of all solid tumors.
- De-Risked Pipeline Funding: Strategic partnerships with GlaxoSmithKline (GSK) for Werner Helicase and Pol Theta programs, and the Servier deal for darovasertib, validate their science and provide a clear path to commercialization outside the US, while substantially reducing IDEAYA's financial burden.
- Translational Biomarker Capabilities: Strong internal capabilities in identifying and validating biomarkers ensure their drug candidates are precisely matched to the patients most likely to respond, increasing clinical trial efficiency and potential efficacy.
- Near-Term Data Catalysts: The darovasertib program is a near-term value driver, with median PFS data from the Phase 2/3 trial expected by year-end 2025. Positive data could enable a potential accelerated approval filing, moving the company closer to its first commercial product.
IDEAYA Biosciences, Inc. (IDYA) How It Makes Money
IDEAYA Biosciences, Inc. (IDYA) is a clinical-stage precision medicine oncology company, meaning it does not sell commercial products yet. Instead, the company makes money almost entirely through strategic collaboration and licensing agreements with large pharmaceutical partners, securing upfront payments, milestone payments tied to development progress, and reimbursement for its research and development (R&D) services.
For the nine months ended September 30, 2025, this model generated $207.83 million in total revenue, a figure defintely dominated by a major licensing deal. This cash flow funds the massive R&D costs necessary to advance its pipeline of targeted cancer therapies.
IDEAYA Biosciences, Inc.'s Revenue Breakdown
For a company like IDEAYA, revenue is not a steady stream; it's a series of large, lumpy payments triggered by clinical and regulatory milestones. The third quarter of 2025 was transformative due to the Servier agreement.
| Revenue Stream | % of Total (9M FY2025) | Growth Trend |
|---|---|---|
| Collaboration & Licensing Revenue | ~100% | Increasing |
| Product Sales | 0% | Stable (Pre-commercial) |
The $207.8 million in collaboration revenue reported for Q3 2025 represents virtually all of the company's revenue for the first nine months of the fiscal year. This massive spike was driven primarily by a $210 million upfront payment from Servier for the exclusive license of darovasertib outside the U.S.. This type of revenue is recognized over time, not all at once, which is why the reported revenue figure is slightly different from the cash received. The rest of the collaboration revenue comes from R&D service reimbursements, which is the remaining balance of $143.1 million in performance obligations as of September 30, 2025.
Business Economics
IDEAYA's economic engine is built on the high-risk, high-reward model typical of a clinical-stage biotech, specifically focusing on synthetic lethality (a concept where two non-lethal gene defects become lethal when combined). The core value proposition is the intellectual property (IP) around its drug candidates like darovasertib, IDE397, and IDE849.
- Pricing Strategy: The 'price' of their assets is realized through the terms of their licensing deals, which include large upfront payments (like the $210 million from Servier), development and regulatory milestones (up to $320 million potential from Servier), and future double-digit royalties on net sales if the drug is approved.
- Cost Structure: The business is defined by its substantial R&D spend. In Q3 2025, R&D expenses totaled $83.0 million, significantly higher than the $16.4 million spent on General and Administrative (G&A) expenses. You have to spend big to get a drug through the pipeline.
- De-Risking through Partnerships: Collaborations with companies like Servier and Gilead Sciences are crucial. They validate the science, provide non-dilutive capital (cash that doesn't come from selling more stock), and share the escalating cost of late-stage clinical trials.
The company's primary economic goal right now is to hit those clinical milestones to unlock the next tranche of milestone payments, thus sustaining the R&D burn rate without needing to raise more capital frequently. This is the Exploring IDEAYA Biosciences, Inc. (IDYA) Investor Profile: Who's Buying and Why? question everyone is asking.
IDEAYA Biosciences, Inc.'s Financial Performance
The recent financial results show a strong inflection point, moving from a net loss to a significant net income, which is a rare event for a company at this stage. This is a snapshot of the business health as of September 30, 2025.
- Cash Position: The company's cash, cash equivalents, and marketable securities stood at approximately $1.14 billion as of September 30, 2025. This is a massive war chest.
- Cash Runway: Management projects this cash balance will fund planned operations into 2030. Here's the quick math: with a Q3 2025 R&D spend of $83.0 million, that $1.14 billion buys a lot of time.
- Net Income/Loss: For the third quarter of 2025, IDEAYA reported a net income of $119.2 million, a substantial turnaround from prior quarters. However, the net loss for the first nine months of 2025 was still $30.43 million, showing the underlying cost of operations before the Q3 licensing boost.
- Earnings Per Share (EPS): Q3 2025 EPS was $1.35, significantly beating analyst consensus. What this estimate hides is that future quarters will likely revert to a net loss until the next major milestone payment hits.
IDEAYA Biosciences, Inc. (IDYA) Market Position & Future Outlook
IDEAYA Biosciences, Inc. is positioned as a high-growth, clinical-stage oncology player, leveraging its synthetic lethality platform to target genetically defined patient populations. The company's future outlook hinges on its lead asset, darovasertib, which is on the cusp of registrational data, and its strong balance sheet, which was significantly bolstered by a $210 million upfront payment from its Servier partnership in late 2025. Your investment thesis here is simple: it's a pipeline story with a long cash runway.
Competitive Landscape
In the precision oncology space, IDEAYA Biosciences, Inc. competes not on current commercial market share-since it is a pre-commercial company with negligible revenue outside of collaborations-but on the novelty and depth of its pipeline. Its primary focus on synthetic lethality (a therapeutic strategy where a combination of two deficiencies leads to cell death) provides a distinct advantage over competitors focused on more traditional targets. The company's market capitalization stands at approximately $2.82 billion as of November 2025, placing it in the mid-cap biotech range, but still significantly smaller than some peers.
| Company | Market Share, % | Key Advantage |
|---|---|---|
| IDEAYA Biosciences, Inc. | <1% | Synthetic Lethality Platform & PKC Inhibition (Darovasertib) |
| Cytokinetics | <1% | Precision Cardiac Mechanics; Aficamten (near-term PDUFA) |
| Nuvalent | <1% | Targeted Kinase Inhibitors; Brain-Penetrant NSCLC Focus |
Opportunities & Challenges
The near-term trajectory for IDEAYA Biosciences, Inc. is driven by clinical catalysts, which offer both the biggest opportunities and the most acute risks. The recent Servier deal for ex-US rights to darovasertib provides a massive financial cushion, extending the cash runway into 2030. This is defintely a key differentiator in the capital-intensive biotech world.
| Opportunities | Risks |
|---|---|
| Potential accelerated approval filing for Darovasertib/crizotinib in 1L mUM based on median PFS data (expected YE 2025/1Q 2026). | Failure of Darovasertib/crizotinib Phase 2/3 trial to meet primary endpoints (PFS or OS) in metastatic uveal melanoma (mUM). |
| Deep pipeline expansion with three new IND filings targeted in 2025 (PRMT5, B7H3/PTK7 ADC, KAT6/7), creating multiple shots on goal. | Intense competition in the broader oncology and ADC (Antibody-Drug Conjugate) space, particularly for DLL3 and other synthetic lethality targets. |
| Strong cash position of approximately $1.14 billion (as of Sept 30, 2025) funds operations well into 2030, reducing near-term financing risk. | Reliance on partnerships (GSK, Pfizer, Servier) for combination therapies and ex-US commercialization, which introduces partner-dependent execution risk. |
Industry Position
IDEAYA Biosciences, Inc. occupies a specialized, high-potential niche within oncology, focusing on synthetic lethality (SL). This is a precision medicine approach that exploits a tumor's specific genetic weakness. The company's competitive standing is best assessed by its pipeline maturity and strategic partnerships, not its current revenue, which for Q3 2025 was primarily collaboration revenue of $207.8 million. Here's the quick math: that Q3 revenue beat expectations, largely due to the Servier upfront payment, which is a one-time boost.
- SL Leadership: The company is a leader in advancing first-in-class SL programs, including Werner Helicase (WRN), Poly (ADP-ribose) glycohydrolase (PARG), and Pol Theta, which are all being developed in collaboration with GlaxoSmithKline (GSK).
- Key Catalyst: The most significant near-term value driver is the Darovasertib program, which received U.S. FDA Breakthrough Therapy Designation in neoadjuvant uveal melanoma (UM), signaling regulatory confidence in the early data.
- Financial Strength: With a cash position of approximately $1.14 billion as of September 30, 2025, the company has the financial independence to execute its clinical trials without immediate capital constraints, providing a significant advantage over many smaller biotechs.
For a deeper dive into the company's foundational principles, you should review its Mission Statement, Vision, & Core Values of IDEAYA Biosciences, Inc. (IDYA).
Your next step should be to monitor the Darovasertib median Progression-Free Survival (PFS) data readout closely; that's the inflection point.

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