NAMSWNasdaqPharmaceutical PreparationsUS GAAP · USD

NewAmsterdam Pharma Co N.V.

NewAmsterdam Pharma Co N.V. is a clinical-stage biopharmaceutical company focused on developing oral therapies for cardiovascular disease, centered on obicetrapib and related formulations. The company is organized under Dutch law with operations and commercial planning tied to the United States and partnered European markets.

Revenue22.5m USD
−50.6 %y/y
Operating profit (EBIT)-226m USD
−28.0 %y/y
EBIT margin-1,002.9%
−616.0 ppy/y
Net income-204m USD
+15.6 %y/y
Free cash flow-148m USD
+6.8 %y/y

Fiscal year 2025 · change from previous year

Development 2020–2025

-300-200-1000100200m USD20202021: EBIT -35 m USD20212022: 103 m USD2022: EBIT -3.6 m USD20222023: 14 m USD2023: EBIT -183 m USD20232024: 46 m USD2024: EBIT -176 m USD20242025: 23 m USD2025: EBIT -226 m USD202523-226
RevenueOperating profit (EBIT)

Business

Share of revenue
Clinical-stage drug candidates0 %

Development-stage cardiovascular therapies, primarily obicetrapib and related formulations.

Licensed intellectual property70 %

License rights granted to Menarini for commercialization in defined territories.

Product supply30 %

Sale of obicetrapib tablets and active pharmaceutical ingredients to Menarini.

Customers

The company’s primary commercial counterparty is Menarini, which holds rights to commercialize obicetrapib in most European countries if approved. In the United States, the intended end customers are patients with high cardiovascular risk and residual elevated LDL-C, reached through physicians and specialty channels after regulatory approval.

Menarini

Buys license rights and product supply for commercialization in most European territories.

Cardiovascular physicians

Prescribe obicetrapib if approved for patients needing additional LDL-C lowering.

Patients with residual LDL-C elevation

End users targeted for oral therapy after standard lipid-lowering treatment.

Specialty pharmacies and distributors

May handle distribution and fulfillment outside the U.S. or in selected regions.

Future licensing partners

Potential collaborators for Japan, China, and other non-core markets.

Strategy

The company’s strategy is to advance obicetrapib through late-stage development, seek regulatory approval, and build commercialization capabilities in the United States. Outside the U.S., it relies on partnering, with Menarini serving as the key European commercialization partner and additional collaborations considered for other regions.

Complete development and regulatory path for obicetrapibShort term

Approval is required before the company can generate meaningful product sales.

Build U.S. commercialization capabilityShort term

The company intends to sell in the U.S. itself and needs sales and distribution infrastructure.

Expand through partnerships outside core marketsMedium term

Partnering can extend reach while limiting the need to build local infrastructure everywhere.

Broaden pipeline through licensing or acquisitionMedium term

Additional candidates can diversify the company beyond a single lead asset.

Geography

NewAmsterdam Pharma is incorporated in the Netherlands, with a registered office in Naarden and a U.S. agent subsidiary in Florida. Commercial rights for obicetrapib cover the majority of European countries through Menarini, while the company plans to pursue U.S. commercialization itself and evaluate partners for Japan, China, and other jurisdictions.

Risks

The company depends heavily on successful development and approval of a single lead asset, so clinical, regulatory, and commercialization setbacks could materially impair value. As a clinical-stage business with limited operating history, it also faces financing, execution, intellectual property, and partner-dependence risks typical of drug developers.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →Clinical development failure1Regulatory approval delay or denial2Partner concentration3Intellectual property and patent risk4Financing and dilution risk5Commercial execution risk6
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: Medium

    The company has no approved products and relies on obicetrapib's trial results.

    Exposure: BROADWAY and TANDEM programs

  2. Regulatory approval delay or denialImpact: HighLikelihood: Medium

    Revenue depends on obtaining marketing authorization before commercialization.

    Exposure: FDA and ex-U.S. regulators

  3. Partner concentrationImpact: HighLikelihood: Medium

    Menarini is the key European commercialization counterparty and supply customer.

    Exposure: License and supply agreements

  4. Intellectual property and patent riskImpact: HighLikelihood: Medium

    Future value depends on protecting obicetrapib from generic or legal challenges.

    ExposurePatent termANDA riskForeign patent filings
  5. Financing and dilution riskImpact: HighLikelihood: Medium

    The company expects continued losses and may need external capital.

    ExposureEquityDebtConvertibleOr collaboration funding
  6. Commercial execution riskImpact: HighLikelihood: Low

    The company has limited internal sales and marketing infrastructure.

    Exposure: U.S. launch and partner-managed territories

Accounting

Judgemental items
License and collaboration revenue recognition

Upfront fees and ongoing obligations are allocated between license and R&D services.

Impact: Affects timing of revenue recognition and deferred revenue balances

Variable consideration in supply agreement

Menarini supply pricing includes a markup on actual costs and estimate updates.

Impact: Can cause quarter-to-quarter revenue variability

Milestone and development contributions

Recognition depends on whether future payments are considered highly probable.

Impact: Can shift revenue between periods

Clinical trial accruals and estimates

R&D costs rely on estimates for CROs, sites, and investigator services.

Impact: Affects operating expense timing and comparability

Publicly listed companies with a comparable business focus.

Last updated: 24/09/2026