Corvus Pharmaceuticals, Inc. (CRVS) Bundle
When you look at a clinical-stage biotech like Corvus Pharmaceuticals, Inc. (CRVS), are you seeing a high-risk gamble or an undervalued platform play in immunotherapy?
This company, currently trading with a market capitalization around $650 million, is pioneering a novel approach with its lead candidate, soquelitinib, an ITK inhibitor in a Phase 3 registrational trial for T-cell lymphoma and advancing to a Phase 2 trial for atopic dermatitis in early 2026. For a firm that reported a net loss of $10.2 million in the third quarter of 2025, and holds $65.7 million in cash and equivalents as of September 30, 2025, its valuation hinges entirely on the clinical success of its pipeline-so let's break down the science, the ownership structure, and the path to commercial revenue.
Corvus Pharmaceuticals, Inc. (CRVS) History
Corvus Pharmaceuticals, Inc. was founded by a team of biotech veterans who had previously developed blockbuster cancer and autoimmune disease therapies like Rituxan and Imbruvica. The company's origin story is one of applying that deep, successful experience to a new frontier: pioneering targeted immunotherapies, specifically by modulating the immune system's T cells.
You're looking for the foundational context that explains Corvus's current pipeline focus, and the short answer is that the company was built on a massive initial capital raise to fund high-risk, high-reward clinical programs, with a later strategic shift toward the versatility of its lead ITK inhibitor, soquelitinib.
Given Company's Founding Timeline
Year established
2014
Original location
Burlingame, California
Founding team members
- Richard A. Miller, M.D. (Co-founder, President, and CEO)
- Joseph J. Buggy
- Peter Thompson
Initial capital/funding
The company secured a $33.5 million Series A funding round in December 2014, led by OrbiMed Advisors, just months after its founding. This significant capital injection immediately positioned Corvus to pursue its initial immuno-oncology pipeline.
Given Company's Evolution Milestones
| Year | Key Event | Significance |
|---|---|---|
| 2015 | Completed $75 million Series B funding round. | Secured substantial capital before the IPO, bringing total pre-IPO funding to over $108.5 million. |
| 2016 | Filed for Initial Public Offering (IPO) on the NASDAQ exchange (CRVS). | Transitioned to a public company, accessing broader capital markets to fund multiple clinical-stage candidates. |
| 2022 | Initiated Phase 1b/2 trial of ciforadenant in first-line metastatic Renal Cell Cancer (RCC). | Advanced the company's adenosine A2A receptor inhibitor into a triplet combination trial for a high-unmet-need oncology indication. |
| 2023 | Confirmed Phase 3 registrational trial plan for soquelitinib in relapsed Peripheral T-Cell Lymphoma (PTCL) with the FDA. | Established a clear regulatory path for the lead asset, soquelitinib (formerly CPI-818), in a critical oncology indication. |
| 2024 | Soquelitinib granted FDA Orphan Drug Designation for T-cell lymphomas. | Provided regulatory incentives and reinforced the potential of ITK inhibition in T-cell malignancies. |
| 2025 | Reported $65.7 million in cash, cash equivalents, and marketable securities as of September 30, 2025. | Confirmed a cash runway sufficient to fund operations into the fourth quarter of 2026, de-risking near-term financing concerns. |
| 2025 | Presented interim Phase 1b/2 data for ciforadenant in RCC with an Objective Response Rate (ORR) of 46% at ESMO 2025. | Showed promising clinical activity for a secondary asset, validating the company's broader immuno-oncology platform. |
Given Company's Transformative Moments
The biggest shift for Corvus was the strategic pivot to fully embrace the potential of its ITK inhibitor, soquelitinib, moving it from a secondary program (CPI-818) to the lead asset with a dual focus on oncology and immunology.
- The ITK Inhibition Focus: The decision to pursue soquelitinib (an Interleukin-2-inducible T cell Kinase inhibitor) for both oncology (PTCL) and immunology (Atopic Dermatitis) was transformative. This dual-indication strategy broadened the addressable market and diversified clinical risk. The drug's unique mechanism-selectively modulating T cells to promote a beneficial Th1 skewing-is the core of the company's current value proposition.
- Financial Fortification in 2024/2025: The company raised approximately $30.6 million in a May 2024 registered direct offering and saw $35.7 million in cash proceeds from warrant exercises in Q2 2025. This capital infusion was critical. Here's the quick math: Q3 2025 research and development expenses were $8.5 million, so those raises were essential for maintaining the registrational Phase 3 PTCL trial and the new Phase 2 AD trial slated for early 2026.
- Clinical Validation in 2025: The interim data showing a 64.8% mean reduction in EASI (Eczema Area and Severity Index) for the optimal soquelitinib dose in atopic dermatitis in June 2025 provided the first strong clinical validation of the drug's potential in a large-market immune disease. This data is defintely a game changer for future partnership discussions.
You can see how this all ties into the current financial outlook by Breaking Down Corvus Pharmaceuticals, Inc. (CRVS) Financial Health: Key Insights for Investors. Finance: Track the Q4 2025 capital deployment against the projected Q4 2026 cash runway to ensure the clinical milestones remain fully funded.
Corvus Pharmaceuticals, Inc. (CRVS) Ownership Structure
Corvus Pharmaceuticals, Inc. is a publicly traded, clinical-stage biopharmaceutical company, listed on the NASDAQ exchange under the ticker CRVS. The company's ownership structure is a mix, with a significant portion held by institutional funds and a near-equal stake held by individual investors, which creates a dynamic balance of influence on strategic direction.
Corvus Pharmaceuticals, Inc.'s Current Status
Corvus Pharmaceuticals, Inc. operates as a public company, meaning its shares are freely traded on the open market, specifically the NASDAQ Global Market (NasdaqGM). This public status subjects the company to rigorous reporting and transparency requirements from the U.S. Securities and Exchange Commission (SEC), which is crucial for investor confidence. Its market capitalization fluctuates, but the total shares outstanding were approximately 74.51 million as of late 2025. If you want to dive deeper into the major players, you can look at Exploring Corvus Pharmaceuticals, Inc. (CRVS) Investor Profile: Who's Buying and Why?
Corvus Pharmaceuticals, Inc.'s Ownership Breakdown
As of the 2025 fiscal year data, institutional investors hold the largest single block of shares, but the combined stake of public and individual investors is a powerful counterweight. This distribution means major strategic decisions need to consider both large fund interests and the collective voice of the retail base.
Here's the quick math on who holds the equity:
| Shareholder Type | Ownership, % | Notes |
|---|---|---|
| Institutional Investors | 41.28% | Includes major funds like OrbiMed Advisors LLC (9.59%), Point72 Asset Management, L.P. (9.43%), and BlackRock, Inc. (6.31%) as of September 2025. |
| Public Companies and Individual Investors | 35.80% | Represents the general public and retail investors; this large stake gives individual shareholders a significant collective voice. |
| Insiders | 22.92% | Comprises officers, directors, and 10%+ beneficial owners, including CEO Richard A. Miller, M.D. |
Corvus Pharmaceuticals, Inc.'s Leadership
The company is steered by a small, seasoned team with deep roots in biopharmaceutical development and oncology. This core leadership is responsible for advancing the clinical-stage pipeline, particularly the lead product candidate, soquelitinib, an investigational ITK inhibitor.
- Richard A. Miller, M.D.: President, CEO, and Co-Founder. He sets the scientific and corporate vision, holding a significant insider stake.
- Leiv Lea: Chief Financial Officer. He manages the financial strategy, a critical role for a clinical-stage company with significant R&D expenses.
- Jeffrey Arcara: Chief Business Officer. He joined in 2024 to lead corporate strategy, business development, and portfolio planning.
- David Moore: Appointed to the Board of Directors in October 2025, bringing 27 years of experience from large-cap pharma, including a key role at Novo Nordisk.
The recent addition of David Moore to the Board in October 2025 shows the company is defintely trying to bolster its commercial and strategic expertise as its pipeline matures. This move signals a near-term focus on maximizing the commercial potential of their assets.
Corvus Pharmaceuticals, Inc. (CRVS) Mission and Values
Corvus Pharmaceuticals' core purpose is to pioneer new immunotherapy treatments by targeting the immune system's control mechanisms, aiming to significantly improve life for patients battling difficult cancers and immune diseases. This mission is grounded in rigorous science and a commitment to advancing novel, precisely-designed medicines.
Corvus Pharmaceuticals' Core Purpose
As a clinical-stage biopharmaceutical company, Corvus Pharmaceuticals is not yet focused on quarterly revenue-which was $0.0 for the trailing 12 months ending June 30, 2025-but on maximizing the clinical value of its pipeline. The company's financial health is directly tied to its R&D progress, with Q3 2025 R&D expenses at $8.5 million, an increase reflecting the acceleration of clinical trials. This spending is a direct investment in their core purpose.
Official mission statement
Corvus Pharmaceuticals' mission is to pioneer the development of ITK inhibition-a new mechanism to modulate the immune system-to create novel therapies for a broad range of cancer and immune diseases. The focus is on science-driven drug development to improve patient outcomes.
- Pioneer ITK inhibition: Establish a new therapeutic class by selectively inhibiting ITK (Inducible T-cell Kinase).
- Improve patient lives: Develop cleverly-designed medicines for the most difficult-to-treat cancers and immune disorders.
- Drive clinical progress: Advance the lead candidate, soquelitinib, through late-stage trials, including a Phase 3 registrational trial for relapsed/refractory peripheral T cell lymphoma (PTCL).
Vision statement
The company's vision extends beyond current trials to establishing selective blockade of ITK as a fundamental new therapeutic approach for autoimmune inflammatory diseases, essentially rebalancing cellular immunity. This is a defintely ambitious goal for a company that had cash, cash equivalents, and marketable securities totaling $65.7 million as of September 30, 2025.
- New therapeutic approach: Establish ITK inhibition as a standard mechanism of action for a wide range of immune diseases.
- Broaden impact: Move beyond oncology to address significant inflammatory conditions like atopic dermatitis, with a Phase 2 trial for soquelitinib on track for early Q1 2026.
- Long-term runway: Maintain a strong financial position, with cash expected to fund operations into the fourth quarter of 2026, supporting continuous pipeline advancement.
To be fair, the market is watching their clinical milestones closely. You can read more about the institutional interest here: Exploring Corvus Pharmaceuticals, Inc. (CRVS) Investor Profile: Who's Buying and Why?
Corvus Pharmaceuticals slogan/tagline
Corvus Pharmaceuticals uses a concise phrase that encapsulates their scientific focus and potential impact, clearly stating their unique value proposition in the crowded biotech space.
- Pioneering ITK inhibition.
- Power to Control the Immune System.
Corvus Pharmaceuticals, Inc. (CRVS) How It Works
Corvus Pharmaceuticals, Inc. operates as a clinical-stage biopharmaceutical company, meaning it focuses entirely on the research and development of novel drug candidates rather than selling approved products for revenue. The company's core work is pioneering a new class of oral immunotherapy drugs that modulate the immune system by selectively targeting a protein called ITK (Itk Tyrosine Kinase).
This approach aims to rebalance a patient's T-cells-the immune system's workhorses-to better fight cancer and correct the underlying causes of autoimmune diseases. The value creation is entirely tied to the successful progression of its lead candidate, soquelitinib, through rigorous and expensive clinical trials, with the goal of securing regulatory approval and commercialization.
Corvus Pharmaceuticals' Product/Service Portfolio
| Product/Service | Target Market | Key Features |
|---|---|---|
| Soquelitinib (Investigational Drug) | Relapsed/Refractory Peripheral T-cell Lymphoma (PTCL) | Selective, oral, small molecule inhibitor of ITK. Currently in a registrational Phase 3 clinical trial (targeting approximately 150 patients). Modulates T-cell differentiation to enhance anti-tumor immunity. |
| Soquelitinib (Investigational Drug) | Moderate-to-Severe Atopic Dermatitis (AD) | Oral, once or twice-daily dosing. Phase 1 data showed a mean reduction in Eczema Area and Severity Index (EASI) of 64.8% in the highest dose cohort (200 mg BID) after 28 days. Aims to suppress Th2 and Th17 T helper cells implicated in allergic/autoimmune conditions. |
| Mupadolimab (Investigational Drug) | Non-Small Cell Lung Cancer (NSCLC) and other Oncology Indications (Greater China) | Humanized monoclonal antibody directed against CD73. Licensed to Angel Pharmaceuticals for development and commercialization in Greater China. Proposed dual mechanism: activates B cells and inhibits immunosuppressive adenosine in the tumor microenvironment. |
Corvus Pharmaceuticals' Operational Framework
The company's operational framework is lean, centered on clinical-stage development and strategic partnerships to manage risk and expand its reach. It's a classic biotech model: high research and development (R&D) spend, zero product revenue, and a limited cash runway. Here's the quick math:
- R&D Focus: R&D expenses for the third quarter of 2025 were $8.5 million, primarily driven by higher clinical trial and manufacturing costs for soquelitinib.
- Financial Runway: As of September 30, 2025, Corvus had cash, cash equivalents, and marketable securities of $65.7 million, which they expect to fund operations into the fourth quarter of 2026.
- Strategic De-risking: A key operational component is the partnership with Angel Pharmaceuticals, which holds the rights to develop and commercialize Corvus' three clinical-stage candidates-soquelitinib, ciforadenant, and mupadolimab-in greater China. Corvus maintains a significant equity stake of 49.7% in Angel Pharmaceuticals. This defintely helps fund development outside the US.
- Revenue Generation: Since there are no approved products, the company's 'revenue' is non-existent, and its Q3 2025 net loss was $10.2 million. Any income, like the Q1 2025 net income of $15.2 million, is typically a non-cash gain from warrant liability changes or cash from financing activities like the $35.7 million from warrant exercises in Q2 2025.
You can learn more about the company's guiding principles here: Mission Statement, Vision, & Core Values of Corvus Pharmaceuticals, Inc. (CRVS).
Corvus Pharmaceuticals' Strategic Advantages
Corvus's market success hinges on its scientific edge and the versatility of its lead drug, which gives it multiple shots on goal across different therapeutic areas.
- Novel Mechanism of Action (MOA): The company is a pioneer in ITK inhibition, a novel approach to T-cell modulation. This MOA aims to overcome resistance to current immunotherapies by precisely controlling the immune system's balance, which is a significant unmet medical need in both cancer and autoimmune diseases.
- Pipeline Versatility: Soquelitinib is a single drug being advanced in a registrational Phase 3 trial for a rare cancer (PTCL) and a Phase 2 trial for a large market autoimmune disease (Atopic Dermatitis). This dual-indication strategy diversifies clinical risk and expands market potential beyond oncology.
- Strong Asian Partnership: The equity-based collaboration with Angel Pharmaceuticals provides non-dilutive capital for US operations and accelerates the clinical development of its pipeline in the large and growing Greater China market. This partnership validates the platform and spreads the cost of global development.
Corvus Pharmaceuticals, Inc. (CRVS) How It Makes Money
As a clinical-stage biopharmaceutical company, Corvus Pharmaceuticals, Inc. currently generates essentially no product sales revenue; its financial engine is fueled by non-recurring collaboration agreements, licensing fees, and grant funding, all of which are highly volatile and dependent on pipeline progress. The company's primary focus is on advancing its lead product candidate, soquelitinib, through costly clinical trials, meaning its financial health is measured by its cash runway, not sales. Breaking Down Corvus Pharmaceuticals, Inc. (CRVS) Financial Health: Key Insights for Investors
Corvus Pharmaceuticals' Revenue Breakdown
The company's revenue streams are not from commercial product sales but from strategic funding sources typical of a pre-commercial biotech. For the trailing twelve months ended September 30, 2025, Corvus Pharmaceuticals reported $0.00 in revenue, which is a key indicator of its clinical-stage status.
| Revenue Stream | % of Total | Growth Trend |
|---|---|---|
| Collaboration/Licensing Revenue | 100% | Decreasing (Currently $0.00) |
| Grant/Other Income | 0% | Stable (Currently $0.00) |
The revenue line is currently empty, but historically, the 'Collaboration/Licensing Revenue' stream is where any non-grant income lands, such as funding from its partner, Angel Pharmaceuticals, for the Greater China rights to its drug candidates. This is a binary business model: either a partnership pays a milestone, or revenue is zero. Right now, it's zero.
Business Economics
The economics of Corvus Pharmaceuticals are pure research and development (R&D) leverage, meaning the company's value hinges on the successful progression of its drug pipeline, not on current profitability. You're investing in future cash flows from potential blockbusters, not today's sales. The primary economic mechanism is the Intellectual Property (IP) Value Creation through clinical trial success.
- Pricing Strategy: Not applicable yet, but the target market for its lead candidate, soquelitinib (an ITK inhibitor for atopic dermatitis and T cell lymphomas), suggests a future specialty drug pricing model, likely in the high-cost, high-margin biopharma range, given the unmet medical need.
- Cost Structure: Dominated by R&D expenses, which are the cost of creating the future revenue. For the third quarter of 2025, R&D expenses were $8.5 million, a significant increase from $5.2 million in the same period a year prior, reflecting the accelerated pace of clinical trials, particularly for soquelitinib.
- Capital Infusion: The company relies on equity financing and strategic partnerships to fund its burn rate. For example, in May 2025, the exercise of common stock warrants brought in approximately $31.3 million in cash proceeds, a crucial lifeline.
Corvus Pharmaceuticals' Financial Performance
The financial performance of a clinical-stage biotech is best viewed through its burn rate and cash position, which determines its lifespan. Corvus is making progress in controlling its losses, but it is still fundamentally a cash-consuming operation.
- Net Loss: For the third quarter ended September 30, 2025, the company reported a net loss of $10.2 million. This is a substantial narrowing from the $40.2 million net loss reported in Q3 2024, though that prior-year figure included a large non-cash loss related to warrant liability.
- Cash Position and Runway: As of September 30, 2025, Corvus Pharmaceuticals held cash, cash equivalents, and marketable securities totaling $65.7 million. This capital is projected to fund its current operations and clinical programs into the fourth quarter of 2026. That's a defintely clear runway, which is the most important metric right now.
- Market Valuation: As of early November 2025, the company's market capitalization stood at approximately $571 million, with about 74.7 million shares outstanding. This market value is a direct reflection of investor confidence in the future commercial potential of its pipeline, especially soquelitinib's Phase 3 trial in peripheral T cell lymphoma (PTCL) and Phase 2 trial in atopic dermatitis.
Here's the quick math: with a cash balance of $65.7 million and a quarterly net loss of $10.2 million, the company has a solid, but not infinite, buffer to reach critical clinical milestones. Finance: continuously model the cash burn rate against the soquelitinib Phase 3 enrollment timeline.
Corvus Pharmaceuticals, Inc. (CRVS) Market Position & Future Outlook
Corvus Pharmaceuticals is positioned as a high-risk, high-reward clinical-stage biotech, with its future trajectory tied almost entirely to the success of its lead asset, soquelitinib (an Interleukin-2-inducible T cell kinase, or ITK, inhibitor). The company's strategy is to validate ITK inhibition as a novel mechanism of action (MOA) across two major therapeutic areas: the large Atopic Dermatitis (AD) market and the niche Peripheral T cell Lymphoma (PTCL) oncology market.
As of November 2025, the company has a cash runway extending into the fourth quarter of 2026, supported by a cash, cash equivalents, and marketable securities balance of $65.7 million as of September 30, 2025. This runway is defintely critical to fund the ongoing Phase 3 PTCL trial and the planned Phase 2 AD trial, which are the primary value drivers. If you want a deeper dive on the numbers, check out Breaking Down Corvus Pharmaceuticals, Inc. (CRVS) Financial Health: Key Insights for Investors.
Competitive Landscape
In the Atopic Dermatitis space, Corvus Pharmaceuticals is a pre-commercial challenger entering a market dominated by established biologics and newer oral small molecules. Soquelitinib's core competitive advantage is its novel MOA, which aims to modulate T-cell function without the broad immunosuppression risks associated with some existing treatments.
| Company | Market Share, % | Key Advantage |
|---|---|---|
| Corvus Pharmaceuticals, Inc. | 0% | Novel selective ITK inhibitor (T-cell modulation). |
| Sanofi / Regeneron (Dupixent) | ~73% of Dupixent's 2024 revenue in AD | Entrenched market leader; first-in-class biologic; broad label. |
| Incyte (Opzelura) | N/A (Topical JAK inhibitor) | First-in-class topical JAK inhibitor; projected 2025 US net revenue up to $670 million. |
Opportunities & Challenges
The company's dual focus on a large inflammatory disease market (AD) and a rare oncology indication (PTCL) creates a balanced, though highly concentrated, pipeline risk profile. The next 12 months are packed with critical data readouts that will determine the stock's trajectory.
| Opportunities | Risks |
|---|---|
| Large Atopic Dermatitis Market: Global AD market expected to approach $30 billion by 2030. | Clinical Trial Failure: Any negative data from the Phase 3 PTCL or Phase 2 AD trials. |
| Novel Mechanism of Action (ITK Inhibition): Potential for a differentiated safety/efficacy profile in AD. | Competition: Facing entrenched biologics like Dupixent and oral JAK inhibitors with widespread adoption. |
| Near-Term Data Catalysts: Phase 1 AD extension data in January 2026; Phase 3 PTCL trial enrollment advancing. | Funding and Dilution: Cash runway into Q4 2026; high R&D expense (Q3 2025: $8.5 million) necessitates future capital raise. |
Industry Position
Corvus Pharmaceuticals is a small-cap biotech with an approximate market capitalization of just over $560 million as of November 2025, placing it firmly in the clinical-stage, high-beta category.
- Niche Oncology Focus: The Phase 3 trial for soquelitinib in relapsed/refractory PTCL targets a rare, high-unmet-need population, offering a potential path to an Orphan Drug designation and premium pricing, but it is a small patient pool.
- High-Value Pivot: The pivot to Atopic Dermatitis is the primary growth driver; positive Phase 1 data showed a 64.8% mean reduction in EASI scores for the 200 mg BID dose, significantly better than the 34.4% for placebo, suggesting a strong efficacy signal.
- Financial Headwinds: The net loss for Q3 2025 was $10.2 million, underscoring the high cash burn typical of a late-stage clinical company. This burn rate means the company will definitely need to secure additional financing before commercialization.
The market's perception is that the soquelitinib platform is a promising asset, but its valuation is a speculative bet on the successful execution of multiple, costly clinical trials over the next two years.

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