MacroGenics, Inc. (MGNX) Bundle
When you look at MacroGenics, Inc. (MGNX), are you seeing a clinical-stage biotech company on the brink of a breakthrough, or one navigating a difficult strategic pivot?
This is a company focused on novel antibody-based therapeutics for cancer, which, despite reporting $72.84 million in Q3 2025 revenue and securing an additional $75 million in non-dilutive partnership payments from Sanofi and Gilead, is currently valued at a modest market capitalization of around $86.6 million as of November 2025. You need to understand how their proprietary DART and Antibody-Drug Conjugate (ADC) platforms work, plus the revenue model built on massive potential milestones-like the up to $1.7 billion from Gilead Sciences, Inc. for their MGD024 program-to gauge if the risk is worth the potential reward.
MacroGenics, Inc. (MGNX) History
You're looking for the foundation of MacroGenics, Inc., and honestly, the story is one of disciplined, long-term antibody engineering that's now driving crucial pipeline decisions. The company was built on a core idea: making better antibodies to fight cancer and autoimmune diseases. It's a classic biotech trajectory, moving from foundational science to major clinical and financial pivots.
Given Company's Founding Timeline
Year established
MacroGenics, Inc. was incorporated in August 2000.
Original location
The company's original location and current corporate headquarters is in Rockville, Maryland.
Founding team members
The scientific founders who established the company's core intellectual property were Dr. Jeffrey Ravetch, Dr. LeRoy Hood, Dr. Ruedi Aebersold, and Dr. Alan Aderem.
Initial capital/funding
The initial venture-backed financing was a Series A round, which had a second tranche closing of $13.5 million on September 25, 2001. This funding was led by InterWest Partners, MPM Capital, and OrbiMed. Total funding raised by October 2004, following a $30.5 million Series B, reached $61.7 million.
Given Company's Evolution Milestones
| Year | Key Event | Significance |
|---|---|---|
| 2001 | Scott Koenig, M.D., Ph.D., appointed President and CEO | Established leadership to transition from scientific concept to therapeutic development. |
| 2013 | Initial Public Offering (IPO) | Went public on the Nasdaq Global Market (MGNX), raising capital for pipeline acceleration. |
| 2017 | Licensed ZYNYZ® (retifanlimab-dlwr) to Incyte Corporation | Secured a major collaboration, leading to $365.0 million in upfront and milestone payments through early 2025. |
| 2022 | TZIELD® (teplizumab-mzwv) approved by U.S. FDA | First-in-class approval to delay the onset of Stage 3 type 1 diabetes, a key validation of the company's early technology. |
| 2025 | Eric Risser appointed President and CEO | A major leadership transition on August 13, 2025, signaling a renewed strategic focus on capital efficiency and pipeline prioritization. |
| 2025 | Secured $70 million upfront payment for ZYNYZ® royalties | Non-dilutive financing from Sagard Healthcare Partners in June 2025, significantly bolstering the cash position to $176.5 million by June 30, 2025. |
Given Company's Transformative Moments
The most recent shifts in 2025 show a clear move toward a more focused, capital-efficient operating model, which is defintely the right call for a clinical-stage biotech.
For the third quarter ended September 30, 2025, the company reported a total revenue of $72.8 million, which included $53.0 million in collaboration revenue, largely driven by a $50.0 million milestone from the Provention (Sanofi) asset purchase agreement. This kind of non-dilutive capital is the lifeblood of a growth-stage company.
- Pipeline Consolidation: Following an evaluation of interim data from the LORIKEET study, the company decided in late 2025 to stop developing lorigerlimab in prostate cancer, but will continue the Phase 2 LINNET study for ovarian and other gynecologic cancers. This is a tough, but necessary, portfolio review decision.
- Cash Runway Extension: The combination of the $70 million Sagard royalty payment and the subsequent $75 million in partnering payments from Sanofi and Gilead in Q3/Q4 2025 extended the cash runway into late 2027. This gives them approximately two years of operational flexibility to hit key clinical readouts.
- New ADC Focus: Strategic priorities for 2025 and 2026 center on advancing the Antibody-Drug Conjugate (ADC) portfolio, specifically MGC026, MGC028, and MGC030, to assess clinical proof-of-concept. This is where the next leg of value creation will come from, especially with the Gilead partnership expanding to include a preclinical program leveraging the T-cell engager platform.
To be fair, the company's long-term strategy remains rooted in its proprietary platforms like Dual Activating ReTargeting (DART®) and Antibody-Drug Conjugate (ADC) technologies. You can get a deeper look at the guiding principles here: Mission Statement, Vision, & Core Values of MacroGenics, Inc. (MGNX).
MacroGenics, Inc. (MGNX) Ownership Structure
MacroGenics, Inc. (MGNX) is firmly controlled by institutional money, with over four-fifths of the company's shares held by large funds, which means their collective decisions heavily influence the stock price and strategic direction.
You need to understand who holds the power here, because in a clinical-stage biotech like this, capital allocation and pipeline focus are everything. A high institutional ownership percentage, especially one over 80%, means the major investment houses are the primary stakeholders driving governance and strategy.
Given Company's Current Status
MacroGenics is a publicly traded biopharmaceutical company, listed on the Nasdaq Global Select Market under the ticker MGNX. This public status means it must adhere to strict U.S. Securities and Exchange Commission (SEC) reporting requirements, giving you transparent, though complex, visibility into its operations and ownership, which is defintely a plus for investors.
As of November 2025, the company has a market capitalization of approximately $89.83 million, reflecting the high-risk, high-reward nature of the biotechnology sector. The company's total shares outstanding are around 63.21 million, with a public float-the shares available for trading-of about 57.97 million. For a deeper dive into the numbers, you should read Breaking Down MacroGenics, Inc. (MGNX) Financial Health: Key Insights for Investors.
Given Company's Ownership Breakdown
The ownership structure is heavily skewed toward institutional investors, a common pattern for clinical-stage biotechs where specialized funds are betting on future drug approvals. This concentration means you should pay close attention to the quarterly 13F filings, as major position changes can cause significant volatility.
Here's the quick math on who owns the company, based on data closest to the end of the 2025 fiscal year:
| Shareholder Type | Ownership, % | Notes |
|---|---|---|
| Institutional Investors | 80.43% | Includes major funds like Bellevue Asset Management AG and The Vanguard Group, Inc. |
| Public/Retail Investors | 16.32% | Calculated as the remaining float, representing individual and non-institutional holders. |
| Insiders (Management & Directors) | 3.25% | The low percentage suggests management's financial interest is primarily tied to performance-based compensation, not direct stock holdings. |
The top institutional holder, Bellevue Asset Management AG, alone holds roughly 15.68% of the outstanding shares, which is a massive stake. That's a lot of influence concentrated in a few hands.
Given Company's Leadership
The leadership team is a mix of long-time company veterans and recently appointed executives, steering the company through a critical development phase for its proprietary DART (Dual-Affinity Re-Targeting) and ADC (Antibody-Drug Conjugate) platforms.
A key change to note is the recent executive transition, which signals a strategic shift in clinical focus:
- Eric Risser: President and Chief Executive Officer (CEO), appointed in August 2025, bringing a background in business development and finance.
- James Karrels: Senior Vice President, Chief Financial Officer (CFO), and Secretary, a long-serving executive with over 25 years of finance experience in life sciences.
- Ezio Bonvini, M.D.: Senior Vice President, Research and Chief Scientific Officer (CSO), who joined in 2003, providing deep, consistent scientific leadership.
- Stephen Eck, M.D., Ph.D.: Senior Vice President, Clinical Development & Chief Medical Officer (CMO), who is departing effective December 31, 2025. This departure means clinical development oversight will be assumed on an interim basis by Frank Perabo, M.D., Ph.D., while the company searches for a permanent CMO.
This interim CMO arrangement is a near-term risk you need to monitor, as a smooth transition is vital for their ongoing clinical trials.
MacroGenics, Inc. (MGNX) Mission and Values
MacroGenics, Inc. is fundamentally driven by its mission to transform cancer treatment, focusing its entire enterprise on developing innovative, antibody-based medicines for patients with significant unmet needs. This patient-centric purpose is backed by a set of six core values, or Living Values, that dictate how the company operates, from the lab bench to the boardroom.
MacroGenics' Core Purpose
You're investing in a biopharmaceutical company, so you need to look past the quarterly revenue swings and see the cultural DNA that drives long-term value. For MacroGenics, that DNA is all about pioneering next-generation oncology treatments, a high-risk, high-reward endeavor that requires both scientific rigor and a clear ethical compass.
Here's the quick math on their commitment: in the third quarter of 2025 alone, MacroGenics dedicated $32.7 million to Research and Development (R&D) expenses, even as total revenue for the quarter was $72.8 million. That spending shows a defintely unwavering commitment to their core purpose, despite the Q3 2025 net income dropping to $16.8 million.
Official Mission Statement
The company's formal mission is a clear directive, guiding their strategic decisions on which programs to advance and which to divest. They are not just developing drugs; they are aiming for a transformative impact.
- Develop, manufacture, and commercialize innovative monoclonal antibody-based, life-changing medicines to transform the lives of patients with cancer.
This mission is why they continue to advance their portfolio of antibody-drug conjugates (ADCs) like MGC026 and MGC028, which are complex, targeted therapies. Breaking Down MacroGenics, Inc. (MGNX) Financial Health: Key Insights for Investors
Vision Statement
While a single, one-line vision statement can be elusive for a biotech firm, MacroGenics' actions and stated goals clearly paint a picture of their future aspiration. They aim to be a leader in a very specific, high-tech corner of oncology.
- Advance innovative oncology therapeutics with precise molecular targeting approaches, leading the future of cancer treatment.
This vision is realized through their proprietary platforms, like the DART (Dual-Affinity Re-Targeting) technology, which allows them to create bispecific antibodies-molecules that can hit two targets at once to better harness the immune system against cancer. They are pushing the boundaries of what a biologic drug (a medicine derived from a living organism) can do.
MacroGenics' Living Values
Their core values are called 'Living Values' because they are meant to be active principles, not just words on a wall. They provide the ethical and operational framework for every employee.
- Patients First: Accountability to patients to provide life-changing medicines.
- Do it Right: Adherence to the highest ethical and quality standards.
- Innovate: Developing breakthrough medicines and continuous improvement.
- Pitch In: Highly integrated and efficient collaboration across teams.
- Take Action: Proactive, empowered, and results-oriented with a sense of urgency.
- Be Inclusive: Celebrating diversity and fostering a sense of belonging.
MacroGenics Slogan/Tagline
The most concise summary of their work, often used on their corporate materials, cuts straight to their value proposition.
- Developing Breakthrough Biologics, Life-Changing Medicines.
MacroGenics, Inc. (MGNX) How It Works
MacroGenics, Inc. operates as a clinical-stage biopharmaceutical company, primarily focused on discovering and developing innovative antibody-based therapeutics to treat cancer. The company creates value by leveraging its proprietary technology platforms to engineer next-generation antibodies, then advancing these candidates through clinical trials and securing non-dilutive funding through strategic partnerships for late-stage development and commercialization.
MacroGenics' Product/Service Portfolio
The company's core value proposition revolves around its deep clinical pipeline, which is heavily weighted toward novel antibody-drug conjugates (ADCs) and bispecific antibodies. The primary revenue streams in the 2025 fiscal year come from collaboration agreements and contract manufacturing, with Q3 2025 total revenue reported at $72.8 million. The pipeline below represents the programs where MacroGenics retains significant commercial rights.
| Product/Service | Target Market | Key Features |
|---|---|---|
| Lorigerlimab | Platinum-Resistant Ovarian Cancer (PROC) and Clear Cell Gynecologic Cancer (CCGC) | DART® (Dual-Affinity Re-Targeting) bispecific antibody; simultaneously blocks PD-1 and CTLA-4 checkpoints. |
| MGC026 | Multiple Solid Tumors (e.g., B7-H3 expressing cancers) | Antibody-Drug Conjugate (ADC) with a novel, glycan-linked topoisomerase I inhibitor (TOP1i) payload; Phase 1 dose expansion initiated in Q3 2025. |
| MGC028 | Multiple Solid Tumors (e.g., GI and lung cancers) | Antibody-Drug Conjugate (ADC) targeting ADAM9, a protein overexpressed in many cancers; Phase 1 dose escalation is ongoing. |
| MGD024 | CD123+ Hematologic Malignancies | Clinical-stage bispecific DART® molecule (T-cell engager) designed to redirect T-cells to cancer cells; subject to an exclusive option agreement with Gilead. |
MacroGenics' Operational Framework
The company's operations are built on a focused, capital-efficient model that prioritizes advancing its proprietary pipeline and securing non-dilutive funding. In Q3 2025, collaboration revenue was $53.0 million, reflecting the success of this model.
Here's the quick math on their operations:
- Discovery & Engineering: Use proprietary platforms like DART® (Dual-Affinity Re-Targeting) and TRIDENT® to design multi-specific and T-cell engaging antibodies.
- Clinical Advancement: Focus resources on high-potential programs like the ADC portfolio (MGC026, MGC028) and lorigerlimab in gynecologic cancers.
- Manufacturing: Operate a contract manufacturing business, which generated $19.8 million in revenue in Q3 2025, reflecting higher third-party production.
- Strategic Partnering: Out-license or sell commercial rights to assets like ZYNYZ® and TZIELD® to large pharma partners, generating significant upfront payments and future milestones.
- Financial Management: Continually improve operational efficiency to extend the cash runway, which is currently projected into late 2027.
That strategic partnering is defintely the key to their cash flow.
MacroGenics' Strategic Advantages
MacroGenics maintains its competitive position not through product sales-as their approved products are now partnered-but through the unique quality of its antibody engineering technology and its ability to monetize its innovation early.
- Proprietary Technology Platforms: The DART® and TRIDENT® platforms allow for the precise creation of bispecific and trispecific antibodies (T-cell engagers), giving them a distinct advantage in designing complex, next-generation therapeutics.
- Non-Dilutive Capital Generation: The company has a strong track record, raising over $600 million in non-dilutive funding over the last three years through collaborations and asset monetization, which significantly de-risks their internal pipeline.
- Established Commercial Track Record: While sold, the successful FDA approval and commercialization of three originating assets-MARGENZA®, ZYNYZ®, and TZIELD®-validates their discovery and development process.
- Focused ADC Strategy: The company is now laser-focused on advancing its Antibody-Drug Conjugate (ADC) pipeline, leveraging its partnership with Synaffix for novel payload technology to compete in a rapidly growing oncology space.
For a deeper dive into the company's financial standing, see Breaking Down MacroGenics, Inc. (MGNX) Financial Health: Key Insights for Investors.
MacroGenics, Inc. (MGNX) How It Makes Money
MacroGenics, Inc. makes money primarily by licensing its proprietary antibody-based therapeutics to larger pharmaceutical partners in exchange for milestone payments and future royalties, and secondarily by utilizing its manufacturing facility to provide contract development and manufacturing services (CDMO).
MacroGenics, Inc.'s Revenue Breakdown
In the biopharmaceutical world, revenue is rarely a straight line of product sales, and MacroGenics, Inc. is a prime example of a technology-driven model. For the third quarter of 2025, the company reported total revenue of $72.8 million. This revenue is heavily weighted toward partnership income, reflecting the company's core strategy of monetizing its technology platforms like DART (Dual-Affinity Re-Targeting) and TRIDENT.
| Revenue Stream | % of Total (Q3 2025) | Growth Trend (YoY Q3) |
|---|---|---|
| Collaboration Revenue (Milestones & Royalties) | 72.8% | Decreasing |
| Contract Manufacturing Services (CDMO) | 27.2% | Increasing |
Here's the quick math: Collaboration Revenue was $53.0 million and Contract Manufacturing Revenue was $19.8 million in Q3 2025. The year-over-year comparison for Collaboration Revenue is tricky; it was lower than Q3 2024 because the prior year included a larger one-time milestone payment, but the underlying model is still the main financial engine.
Business Economics
The economic engine for MacroGenics, Inc. is a hybrid model designed to fund high-risk, high-reward research and development (R&D) through non-dilutive capital. You're essentially investing in a technology incubator that occasionally spins off major cash events.
- Collaboration Pricing: The company's core pricing strategy involves a multi-tiered payment structure for its licensed assets, such as the deal for MGA012 (retifanlimab) with Incyte. This includes a large upfront payment, a series of development and regulatory milestone payments (which can total hundreds of millions of dollars), and tiered sales royalties ranging from 15% to 24% on future net sales. This structure de-risks the pipeline for MacroGenics, Inc.
- CDMO Margin: The contract manufacturing business leverages the company's commercial-scale cGMP facility in Rockville, Maryland. This acts as a strategic cost-offset. For Q3 2025, the Contract Manufacturing Revenue of $19.8 million substantially exceeded the Cost of Manufacturing Services of $11.6 million, indicating a healthy gross margin on this service line. This is a smart use of excess capacity.
- R&D Fuel: Milestone payments directly fuel the internal pipeline, which includes Antibody-Drug Conjugates (ADCs) like MGC026 and MGC028. This is the lifeblood of a biotech. The sale of MARGENZA rights to TerSera Therapeutics, LLC in November 2024 for an upfront payment plus potential sales milestones, and the subsequent cessation of commercialization activities, streamlined the cost structure by reducing selling, general, and administrative (SG&A) expenses.
The business model is built on trading future commercial upside (product sales) for immediate, non-dilutive cash (upfront and milestone payments) to fund the next generation of drug candidates. You can read more about the company's strategic focus in their Mission Statement, Vision, & Core Values of MacroGenics, Inc. (MGNX).
MacroGenics, Inc.'s Financial Performance
Looking at the near-term financials through Q3 2025, the company has made significant moves to improve its balance sheet and extend its operational runway, even as R&D remains the largest expense category.
- Q3 2025 Profitability: MacroGenics, Inc. reported a Net Income of $16.8 million for the quarter ended September 30, 2025, and Earnings Per Share (EPS) of $0.27. This is a notable surprise, beating analyst expectations for a loss.
- Cash Position and Runway: As of September 30, 2025, the company held $146.4 million in cash, cash equivalents, and marketable securities. Importantly, this figure does not include the expected $75.0 million in partnering payments from Sanofi and Gilead Sciences, Inc. anticipated by year-end 2025. This capital, plus anticipated cost savings, is expected to support the company's cash runway into late 2027. That's a defintely solid buffer.
- Expense Management: Research and Development (R&D) expenses were $32.7 million in Q3 2025, down from $40.5 million in the same period a year prior, reflecting a sharp focus on pipeline prioritization and cost discipline. Selling, General, and Administrative (SG&A) expenses also dropped to $9.9 million in Q3 2025, largely due to the exit from commercialization activities for MARGENZA.
The key action for you here is to track the timing and size of those future milestone payments, as they are the primary non-dilutive funding mechanism for the company's long-term value creation.
MacroGenics, Inc. (MGNX) Market Position & Future Outlook
MacroGenics is positioned as a high-risk, high-reward biopharmaceutical company, pivoting from earlier clinical setbacks to focus its $146.4 million cash reserve as of September 30, 2025, on its next-generation oncology pipeline. The company's future trajectory hinges on successful clinical data from its Antibody-Drug Conjugate (ADC) and bispecific platforms, particularly as it has extended its cash runway into late 2027 through strategic non-dilutive financing.
You need to see this company not as a commercial entity today, but as a pure-play R&D engine; its estimated 2025 annual revenue of $127.625 million is dwarfed by its projected net loss of -$75.886 million, making pipeline execution the singular driver of value.
Competitive Landscape
MacroGenics operates in the highly competitive immuno-oncology and targeted therapy space, competing directly with established giants in the development of bispecific antibodies and ADCs. To be fair, MacroGenics' market share is negligible compared to commercial-stage biopharma, but its competition is defined by platform technology, not commercial sales volume.
Here's the quick math on scale: MacroGenics' November 2025 market capitalization of approximately $88.56 million is a fraction of its competitors, but its core value lies in its proprietary technology platforms that others seek to license.
| Company | Market Share, % (Based on Combined 2025 Revenue Estimate) | Key Advantage |
|---|---|---|
| MacroGenics, Inc. | 0.32% | Proprietary DART®/TRIDENT® Bispecific and Trispecific Platforms; Novel ADC Payloads. |
| Amgen, Inc. | 90.66% | Commercial-stage BiTE® (Bispecific T-cell Engager) platform; Massive scale; 2025 Revenue Outlook of $35.8 billion to $36.6 billion. |
| Genmab A/S | 9.01% | Proprietary DuoBody® and HexaBody® platforms; Multiple commercialized products; 2025 Revenue Outlook of $3.5 billion to $3.7 billion. |
Opportunities & Challenges
The company's strategy is clear: double down on high-potential assets and monetize non-core programs to fund the next wave of innovation. This is a defintely smart move in the capital-constrained biotech environment.
| Opportunities | Risks |
|---|---|
| Positive Phase 2 data from the LINNET trial (lorigerlimab in platinum-resistant ovarian cancer). | High clinical risk following the discontinuation of the LORIKEET prostate cancer trial in November 2025. |
| Advancing the B7-H3 TOP1 ADC (MGC026) into Phase 1 expansion cohorts in late 2025. | Ongoing negative earnings per share (EPS) forecasts, indicating continued cash burn. |
| Monetizing platform assets through new, non-dilutive partnerships, such as the $75 million secured from Sanofi and Gilead in Q4 2025. | Reliance on milestone payments from partners (like Incyte for Zynyz and Sanofi for TZIELD) for a significant portion of future revenue. |
Industry Position
MacroGenics is a technology-driven player, not a commercial powerhouse. Its industry standing is built on its proprietary platforms, which are key to developing next-generation antibody-based therapeutics.
- Platform Differentiation: The DART® (Dual-Affinity Re-Targeting) and TRIDENT® platforms allow for the creation of bispecific and trispecific antibodies, respectively, which is a critical differentiator in the T-cell engager market.
- ADC Focus: The company is a key innovator in the crowded Antibody-Drug Conjugate (ADC) space, leveraging novel Topoisomerase I inhibitor (TOP1i) payloads in its MGC026, MGC028, and MGC030 programs.
- Strategic Partnerships: Its ability to attract major partners like Gilead Sciences, Sanofi, and Incyte validates its technology, with potential future milestone payments totaling over $1.7 billion.
- Financial Resilience: The Q3 2025 net income of $16.8 million, largely driven by partnership revenue, demonstrates financial agility in a challenging development-stage environment.
To understand the full scope of the company's foundational principles, you should review the Mission Statement, Vision, & Core Values of MacroGenics, Inc. (MGNX).

MacroGenics, Inc. (MGNX) DCF Excel Template
5-Year Financial Model
40+ Charts & Metrics
DCF & Multiple Valuation
Free Email Support
Disclaimer
All information, articles, and product details provided on this website are for general informational and educational purposes only. We do not claim any ownership over, nor do we intend to infringe upon, any trademarks, copyrights, logos, brand names, or other intellectual property mentioned or depicted on this site. Such intellectual property remains the property of its respective owners, and any references here are made solely for identification or informational purposes, without implying any affiliation, endorsement, or partnership.
We make no representations or warranties, express or implied, regarding the accuracy, completeness, or suitability of any content or products presented. Nothing on this website should be construed as legal, tax, investment, financial, medical, or other professional advice. In addition, no part of this site—including articles or product references—constitutes a solicitation, recommendation, endorsement, advertisement, or offer to buy or sell any securities, franchises, or other financial instruments, particularly in jurisdictions where such activity would be unlawful.
All content is of a general nature and may not address the specific circumstances of any individual or entity. It is not a substitute for professional advice or services. Any actions you take based on the information provided here are strictly at your own risk. You accept full responsibility for any decisions or outcomes arising from your use of this website and agree to release us from any liability in connection with your use of, or reliance upon, the content or products found herein.