NXTCNasdaqPharmaceutical PreparationsUS GAAP · USD

NextCure, Inc.

NextCure, Inc. is a U.S.-based clinical-stage biopharmaceutical company focused on developing targeted cancer therapies, including antibody-drug conjugates. Its pipeline includes SIM0505 and LNCB74, and the company also maintains a dedicated manufacturing facility to support clinical development.

Operating profit (EBIT)-57.6m USD
+3.6 %y/y
Net income-55.8m USD
−0.3 %y/y
Free cash flow-50.1m USD
−21.3 %y/y

Fiscal year 2025 · change from previous year

Development 2020–2025

-80-60-40-2002040m USD2020: 22 m USD2020: EBIT -41 m USD20202021: 22 m USD2021: EBIT -71 m USD20212022: EBIT -76 m USD20222023: EBIT -68 m USD20232024: EBIT -60 m USD20242025: EBIT -58 m USD2025-58
RevenueOperating profit (EBIT)

Business

Share of revenue
Clinical-stage ADC programs70 %

Development of antibody-drug conjugate oncology candidates for patients with unmet need.

Licensed ADC platform technology20 %

Use of licensed ADC technology to develop additional proprietary antibody-based candidates.

Research and discovery platform10 %

Biology, biomarker, and tumor microenvironment research used to identify targets and candidates.

Customers

NextCure does not currently sell commercial products; its work is directed toward future patients with cancer, especially those who do not respond to existing therapies. In the development phase, its counterparties are research partners, contract manufacturers, clinical trial sites, regulators, and potential future healthcare providers and payors if products are approved.

Future oncology patients

Patients with cancers that do not respond to current therapies; they are the intended beneficiaries of approved products.

Clinical trial sites and investigators

Hospitals and physicians that enroll patients and administer study protocols for SIM0505, LNCB74, and other candidates.

Contract development and manufacturing organizations

Third parties that manufacture ADC intermediates and drug product or support clinical supply.

Potential future healthcare providers and payors

Oncologists, hospitals, and insurers that would influence adoption and reimbursement after approval.

Licensing and collaboration partners

Partners that may provide upfront fees, development support, or commercialization rights in selected territories.

Strategy

NextCure’s strategy is to advance SIM0505 and LNCB74 through clinical development and, if successful, toward regulatory approval and commercialization. The company also seeks external capital and potential collaborations or licensing arrangements to fund development and extend runway while preserving optionality across its pipeline.

Advance lead ADC programsShort term

Clinical progress is the main value driver for a company without commercial revenue.

Secure additional fundingShort term

Development programs require capital before any product revenue can be generated.

Preserve development optionalityMedium term

Partnerships and licensing can broaden resources and reduce single-asset dependence.

Maintain manufacturing readinessMedium term

ADC programs require reliable clinical supply and future commercial scalability.

Geography

NextCure is headquartered in the United States and conducts its core research, development, and corporate activities there. Its licensed SIM0505 rights exclude China, Hong Kong, Macau, and Taiwan, where the licensor retains rights, while manufacturing and clinical supply may also involve third-party facilities outside the U.S.

Risks

NextCure faces the typical risks of a clinical-stage biotech company: no approved products, dependence on clinical success, and ongoing need for external capital. Its pipeline also depends on third-party CROs and CDMOs, regulatory approvals, and access to specialized manufacturing capacity, which can be disrupted by operational, geopolitical, or trade-related issues.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →Clinical development failure1Financing risk2Third-party manufacturing and trial execution3Regulatory and healthcare compliance4
Impact is the risk’s severity and likelihood how probable it is over the next few years, both assessed from the company’s reports. Numbers match the list.
  1. Clinical development failureImpact: CriticalLikelihood: High

    Pipeline value depends on proving safety and efficacy in human studies.

    ExposureSIM0505LNCB74Future candidates
  2. Financing riskImpact: CriticalLikelihood: High

    The company has no product sales and must raise capital to continue operations.

    ExposureEquity dilutionDebt termsPartnership dependence
  3. Third-party manufacturing and trial executionImpact: HighLikelihood: High

    CROs and CDMOs control key steps in development and supply.

    ExposureClinical timelinesProduct supplyData quality
  4. Regulatory and healthcare complianceImpact: HighLikelihood: Medium

    Drug approval, promotion, and commercial arrangements are heavily regulated.

    ExposureFDA reviewAnti-kickbackFraud-and-abuse rules
  5. Foreign manufacturing and trade restrictionsImpact: Medium

    Some manufacturing is tied to non-U.S. facilities and counterparties.

    ExposureCMO accessSupply continuityGeopolitical disruption

Accounting

Judgemental items
Clinical trial accruals

R&D costs depend on estimated vendor work performed but not yet invoiced.

Impact: Can shift expense recognition between periods

Share-based compensation valuation

Equity awards require fair value estimates and can materially affect operating expense.

Impact: Affects G&A and R&D expense levels

Going-concern assessment

Management must evaluate whether available cash is sufficient to fund operations.

Impact: Important for liquidity disclosure and investor interpretation

No revenue recognition from product sales

The company has not commercialized products, so revenue is limited to collaboration-related items when present.

Impact: Reported results are dominated by operating expenses and financing activity

Publicly listed companies with a comparable business focus.

Last updated: 24/09/2026

NextCure, Inc. (Nasdaq) – Pharmaceutical Preparations | Financial Analysis – Clarifo