Macrogenics (MGNX) risk factors, FY2024 10-K

Macrogenics's FY2024 10-K, filed Mar 20, 2025, lists 43 risk factors in 7 groups. There is no earlier 10-K to compare against, so the most company-specific risks are listed below.

Risk factors listed
437 groups
Section length
25k wordsItem 1A

Macrogenics's biggest risks in the FY2024 10-K

  • MacroGenics faces significant ongoing financial losses with an accumulated deficit of approximately $1.2 billion and a critical need for substantial additional funding.
  • The company relies heavily on clinical trials for multiple product candidates and key development and commercialization collaborations.
  • Operations are subject to extensive regulatory oversight, intellectual property challenges, and strict healthcare laws.

The risks most specific to Macrogenics

  • Risks Related to Our Financial Position and Need for Additional Capital

    We will require substantial additional funding, which may not be available to us on acceptable terms, or at all, and, if not available, may require us to delay, scale back, or cease our product development programs or operations

    We will require substantial additional funding to discover, develop, and commercialize pharmaceutical products and conduct necessary nonclinical studies and clinical trials.

  • Risks Related to Our Financial Position and Need for Additional Capital

    We have incurred significant losses since inception and anticipate that we will continue to incur losses for the foreseeable future. We may never achieve or sustain profitability

    We have incurred significant losses since inception, resulting in an accumulated deficit of approximately $1.2 billion as of December 31, 2024.

  • Risks Related to Our Business and the Development and Commercialization of Our Product Candidates

    If clinical trials for our product candidates are prolonged, delayed or stopped, for any reason, we may be unable to obtain regulatory approval and commercialize our product candidates on a timely basis, which would require us to incur additional costs and delay our receipt of any product revenue

    Clinical trials for molecules including lorigerlimab, retifanlimab, vobra duo, MGD024, MGC026, and MGC028 may be prolonged, delayed, or stopped.

  • Risks Related to Our Business and the Development and Commercialization of Our Product Candidates

    Certain of our antibody-drug conjugate, or ADC, product candidates incorporate technology developed by our collaboration partners. To date, no ADC product candidates incorporating any such technology have been approved by the FDA

    Certain ADC product candidates incorporate partner technology, such as seco-DUBA from Byondis and Hydraspace, GlycoConnect, and toxSYN from Synaffix, which have no FDA approvals to date.

  • Risks Related to Our Business and the Development and Commercialization of Our Product Candidates

    Our manufacturing facilities are subject to significant government regulations and approvals, which are often costly and could result in adverse consequences to our business if we fail to comply with the regulations or maintain the approvals

    Our manufacturing facilities must comply with FDA cGMP requirements and maintain quality control and quality assurance standards.

  • Risks Related to Our Dependence on Third Parties

    Our existing therapeutic collaborations are important to our business, and future collaborations may also be important to us. If we are unable to maintain any of these collaborations, or if these collaborations are not successful, our business could be adversely affected

    We depend heavily on existing and future therapeutic collaborations with companies like Gilead Sciences and Incyte due to limited internal sales and marketing capabilities.

  • Risks Related to Employee Matters and Human Capital Management

    We may need to grow or contract our organization, and we may experience difficulties in managing this growth or contraction, which could disrupt our operations

    As of December 31, 2024, we had 341 full-time employees and may experience difficulties managing organizational growth or contraction.

All 43 risk factors

Headings as the filing states them, in filing order.

Other

  1. 01Summary of Risk Factors Affecting Our Business

Risks Related to Our Financial Position and Need for Additional Capital

  1. 02We will require substantial additional funding, which may not be available to us on acceptable terms, or at all, and, if not available, may require us to delay, scale back, or cease our product development programs or operations
  2. 03We have incurred significant losses since inception and anticipate that we will continue to incur losses for the foreseeable future. We may never achieve or sustain profitability
  3. 04Raising additional capital may cause dilution to our stockholders, restrict our operations or require us to relinquish substantial rights
  4. 05Our ability to use our net operating loss carryforwards and other tax attributes may be limited

Risks Related to Our Business and the Development and Commercialization of Our Product Candidates

  1. 06If clinical trials for our product candidates are prolonged, delayed or stopped, for any reason, we may be unable to obtain regulatory approval and commercialize our product candidates on a timely basis, which would require us to incur additional costs and delay our receipt of any product revenue
  2. 07Certain of our antibody-drug conjugate, or ADC, product candidates incorporate technology developed by our collaboration partners. To date, no ADC product candidates incorporating any such technology have been approved by the FDA
  3. 08Our product candidates, if approved, may fail to achieve or maintain market acceptance by physicians, patients, third-party payors and others in the medical community necessary for commercial success
  4. 09Our product candidates may have undesirable side effects, including fatalities. These side effects may delay or prevent further clinical development or marketing approval, or, if approval is received, require them to be taken off the market, require them to include safety warnings or otherwise limit their sales
  5. 10Our manufacturing facilities are subject to significant government regulations and approvals, which are often costly and could result in adverse consequences to our business if we fail to comply with the regulations or maintain the approvals
  6. 11We face significant competition and if our competitors continue to develop and market products that are more effective, safer or less expensive than our product candidates, our current or future commercial opportunities may be negatively impacted
  7. 12Public health crises such as pandemics or similar outbreaks may have a significant negative impact on our clinical trials, nonclinical studies, development, manufacturing and commercialization of our product candidates and other aspects of our business, staff, and operations
  8. 13Actual or anticipated changes to the laws and regulations governing the health care system may have a negative impact on cost and access to health insurance coverage and reimbursement of healthcare items and services
  9. 14Reimbursement decisions by third-party payors may have an adverse effect on pricing and market acceptance. If there is not sufficient reimbursement for our products, it is less likely that our products will be widely used
  10. 15If any product liability lawsuits are successfully brought against us or any of our collaborators, we may incur substantial liabilities and may be required to limit commercialization of our products or product candidates
  11. 16We and/or our collaboration partners may never obtain approval or commercialize our products outside of the United States, which would limit our ability to realize their full market potential
  12. 17Changes in U.S. tax law may have a material adverse effect on our business, financial condition and results of operations, and changes in international trade relations may have a material adverse effect on the commercialization of some or all of our product candidates

Risks Related to Our Dependence on Third Parties

  1. 18Our existing therapeutic collaborations are important to our business, and future collaborations may also be important to us. If we are unable to maintain any of these collaborations, or if these collaborations are not successful, our business could be adversely affected
  2. 19Failure to successfully develop and commercialize companion diagnostics with third party contractors for use with our product candidates could harm our ability to commercialize our product candidates
  3. 20Independent clinical investigators and CROs that we engage to conduct our clinical trials may not devote sufficient time or attention to our clinical trials or be able to repeat their past success
  4. 21Commercialization collaborations will be important to our business. If we are unable to maintain commercialization collaborations, or if commercialization collaborations are not successful, our business could be adversely affected
  5. 22All of the risks relating to commercialization, and health care legal compliance described in this Annual Report on Form 10-K also apply to the commercialization activities of our collaborators
  6. 23acquired or integrated entities, and it may be difficult to integrate companies into our information technology environment and security program

Risks Related to Our Intellectual Property

  1. 24Our success depends significantly on our ability to operate without infringing the valid patents and other proprietary rights of third parties
  2. 25Our success will depend in part on our ability to operate without infringing the proprietary rights of third parties. Third parties may have or obtain patents or proprietary rights that could limit our ability to make, use, sell, offer for sale or import our future approved products or impair our competitive position
  3. 26If we are unable to obtain and enforce patent protection for our products and our product candidates and related technology, our business could be materially harmed
  4. 27We may become involved in lawsuits to protect or enforce our patents, which could be expensive, time consuming and unsuccessful
  5. 28If we fail to comply with our obligations under our intellectual property licenses with third parties, we could lose license rights that are important to our business
  6. 29If we are unable to protect the confidentiality of our proprietary information, the value of our technology and products could be adversely affected
  7. 30Obtaining and maintaining our patent protection depends on compliance with various procedural, documentary, fee payment and other requirements imposed by governmental patent agencies, and our patent protection could be reduced or eliminated for non-compliance with these requirements
  8. 31If we do not obtain protection under the Hatch-Waxman Amendments and similar foreign legislation for extending the term of patents covering each of our product candidates, our business may be materially harmed

Risks Related to Legal Compliance Matters

  1. 32If we do not comply with laws regulating the protection of the environment and health and human safety, our business could be adversely affected
  2. 33We and our collaborators are subject to various healthcare laws, and our failure, or the failure of our collaborators, to comply with those laws could result in significant penalties and adversely affect our business, operations and financial condition
  3. 34representatives, as well as to prohibit pharmacies and other healthcare entities from providing certain physician prescribing data to pharmaceutical companies for use in sales and marketing, and to prohibit certain other sales and marketing practices
  4. 35In addition, our operations and those of our collaborators may be subject to analogous foreign health care laws in the jurisdictions in which we operate
  5. 36Governments have passed and are likely to pass additional laws regulating generative AI. Any use of this technology could result in additional compliance costs, regulatory investigations and actions, and lawsuits
  6. 37Our employees may engage in misconduct or other improper activities, including noncompliance with regulatory standards and requirements and insider trading

Risks Related to Employee Matters and Human Capital Management

  1. 38Our future success depends on our ability to attract or retain key executives and to attract, retain and motivate qualified personnel
  2. 39We may undertake internal restructuring activities, including associated workforce reductions, that could result in disruptions to our business or otherwise materially harm our results of operations or financial condition
  3. 40We may need to grow or contract our organization, and we may experience difficulties in managing this growth or contraction, which could disrupt our operations
  4. 41weaknesses in our infrastructure, give rise to operational errors, loss of business opportunities, loss of employees and reduced productivity among remaining employees

Risks Related to Our Common Stock

  1. 42We have been and may in the future be subject to securities litigation, which is expensive and could divert management attention and adversely impact our business
  2. 43Provisions of our charter, bylaws, third-party agreements and Delaware law may make an acquisition of us or a change in our management more difficult

Other Macrogenics 10-Ks

  • FY2025 10-K risk factors
    45 risks6 new4 dropped12 reworded

    MacroGenics faces a partial clinical hold on the LINNET study after Grade 5 and other severe adverse events. The company relies on third parties for companion diagnostics and CDMO services at its Rockville facility. Employee headcount dropped from 341 to 293 full-time workers.

    Filed Mar 09, 2026

About this page

The headings are the filing's own. The one-line readings and the overview are automated and can be wrong: read Item 1A of the 10-K for the exact wording.