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NAMS

NEWAMSTERDAM PHARMA CO N.V.

Biopharma developer (SEC filing verified)·Phase 3·Naarden, Netherlands·CEO: Dr. Michael Harvey Davidson FACC, Facp., M.D.
OncologyCardiovascularMetabolic

NAMS evidence brief

What we can confirm

BioSniper Score:
5.4 / 10
Market Cap:
$2.66B
Lead Asset:
obicetrapib (Phase 3)

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $2.66B · Lead Asset: obicetrapib (Phase 3)
BioSniper AIPage evidence connected

Prepared research question

What matters most for NAMS—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · NAMS

NEWAMSTERDAM PHARMA CO N.V. (NAMS) is a late-stage biopharmaceutical company developing oral, non-statin medicines, primarily obicetrapib, for cardiovascular disease and exploring its potential in Alzheimer's disease and diabetes.

Key risk: No approved products

5.4/10

BioSniper Score

Based on 4 of 6 signals

Market Cap

$2.66B

Cash Runway

—

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 1 pipeline candidate · 8 clinical trials for NEWAMSTERDAM PHARMA CO N.V..

AI OverviewAI overview is shown in English only.

NEWAMSTERDAM PHARMA CO N.V. (NAMS) is a late-stage biopharmaceutical company developing oral, non-statin medicines, primarily obicetrapib, for cardiovascular disease and exploring its potential in Alzheimer's disease and diabetes.

  • Cash & equivalents of $424.2M as of 2026-06-30 [sec].
  • Total revenue of $3.7M and net income of -$64.1M as of 2026-06-30 [sec].
  • Shareholders' equity of $631.4M as of 2026-06-30 [sec].
  • Phase 3 PREVAIL trial expected to complete by end of 2027 if interim analysis continues [sec_mda · as of 2026-08-05].
  • Enrollment completed in March 2026 for Phase 3 REMBRANDT trial (323 patients) [sec_mda · as of 2026-08-05].

What works

  • Strong cash position of $424.2M as of 2026-06-30 provides runway for ongoing trials [sec].
  • Multiple Phase 3 trials (PREVAIL, REMBRANDT, RUBENS) are underway, indicating a robust late-stage pipeline [sec_mda · as of 2026-08-05].
  • Exploration of obicetrapib in Alzheimer's disease and diabetes could open additional large markets [sec_mda · as of 2026-08-05].

What to weigh

  • Net income of -$64.1M as of 2026-06-30 reflects ongoing operating losses with no approved product revenue [sec].
  • Total revenue of only $3.7M as of 2026-06-30 indicates minimal commercial activity [sec].
  • PREVAIL trial may be stopped early for efficacy or futility, creating binary outcome risk [sec_mda · as of 2026-08-05].

From the filings

Quoted directly from source documents.

  • PREVAIL trial completion timeline

    “If the interim analysis results in the trial continuing, we expect to complete PREVAIL by the end of 2027.”

    SEC MD&A · August 5, 2026

  • REMBRANDT trial enrollment

    “In March 2026, we completed enrollment of 323 patients in REMBRANDT”

    SEC MD&A · August 5, 2026

Catalyst timeline

  • 2021-12-15 · Phase3_Start: A Placebo-Controlled, Double-Blind, Randomized Phase 3 Study to Evaluate the Effect of 10mg Obicetrapib in Participants With HeFH and/or ASCVD Who Are Not Adequately Controlled by Their Lipid Modifying Therapies — Initiation of a key Phase 3 trial for obicetrapib in cardiovascular disease.
  • 2022-07-25 · Phase3_Start: A Placebo-Controlled, Double-Blind, Randomized, Phase 3 Study to Evaluate the Effect of 10 mg Obicetrapib in Participants With a History of HeFH Who Are Not Adequately Controlled by Their Lipid Modifying Therapies — Second Phase 3 trial for obicetrapib in patients with familial hypercholesterolemia.
  • 2023-11-11 · Phase1_Start: A Study to Evaluate the Effect of Daily Doses of Obicetrapib Tablets on the Pharmacokinetics of Atorvastatin Calcium Tablets or Rosuvastatin Calcium Tablets in Healthy Adult Subjects — Phase 1 drug-drug interaction study with statins.
  • 2024-03-01 · Phase3_Start: A Placeb — Initiation of another Phase 3 trial (details truncated in source).
Risks & what to watch (3)›

Key risks

  • No approved products — Company has no approved products; all revenue is minimal ($3.7M as of 2026-06-30) [sec].
  • PREVAIL interim analysis risk — PREVAIL trial may be stopped early for efficacy or futility, creating binary outcome risk [sec_mda · as of 2026-08-05].
  • Operating losses — Net loss of -$64.1M as of 2026-06-30 indicates ongoing cash burn [sec].

What to watch

  • PREVAIL interim analysis results and potential early stop [sec_mda · as of 2026-08-05].
  • Initiation of new Alzheimer's disease clinical trial for obicetrapib expected in 2026 [sec_mda · as of 2026-08-05].
  • Completion of REMBRANDT and RUBENS Phase 3 trials [sec_mda · as of 2026-08-05].
  • Presentations at ESC Congress 2026 (August 2026) [news · published 2026-08-26].

Sources: Catalysts · News · SEC filings · SEC MD&A · Generated October 12, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 4 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health9.8

D/E 0.12 · 0% dilution

Pipeline Maturity8.5

Lead: Phase 3

Pipeline Breadth3.3

1 candidate

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider Signal0.1

0 buys · 7 sells (180d)

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

168

Total value held

$3.83B

Showing top 10 of 168 institutional holders of NEWAMSTERDAM PHARMA CO N.V.. Open the full 13F history after sign-in.

Short Interest

as of Apr 19, 2026
% of float
8.3%
Days to cover
8.6
Shares short
8,047,048
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

NAMS short interest

Governance

Frequently asked questions

What is the AI investment thesis for NEWAMSTERDAM PHARMA CO N.V.?

NEWAMSTERDAM PHARMA CO N.V. (NAMS) is a late-stage biopharmaceutical company developing oral, non-statin medicines, primarily obicetrapib, for cardiovascular disease and exploring its potential in Alzheimer's disease and diabetes.

What is NEWAMSTERDAM PHARMA CO N.V.'s lead drug candidate?

NEWAMSTERDAM PHARMA CO N.V.'s most advanced tracked candidate is obicetrapib (Phase 3) for Dyslipidemias; Healthy Volunteers; Antioxidant Absorption.

Who is the CEO of NEWAMSTERDAM PHARMA CO N.V.?

Dr. Michael Harvey Davidson FACC, Facp., M.D. is the chief executive officer of NEWAMSTERDAM PHARMA CO N.V. (NAMS).

Where is NEWAMSTERDAM PHARMA CO N.V. headquartered?

NEWAMSTERDAM PHARMA CO N.V. (NAMS) is headquartered in Naarden, Netherlands.

What therapeutic areas does NEWAMSTERDAM PHARMA CO N.V. focus on?

NEWAMSTERDAM PHARMA CO N.V. develops therapies across Oncology, Cardiovascular, Metabolic.

923 companies304,846 SEC filings22,720 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.