Clinical development failure
The company has no approved products and relies on obicetrapib's trial results.
- Scope
- BROADWAY and TANDEM programs
- Materiality
- high
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.
−1 001,9 %
−905,7 %
−50,6 %
7.88
7.88
| % | |
|---|---|
| Clinical-stage drug candidates | 0% Development-stage cardiovascular therapies, primarily obicetrapib and related formulations. |
| Licensed intellectual property | 70% License rights granted to Menarini for commercialization in defined territories. |
| Product supply | 30% Sale of obicetrapib tablets and active pharmaceutical ingredients to Menarini. |
The company’s primary commercial counterparty is Menarini, which holds rights to commercialize obicetrapib in most...
Buys license rights and product supply for commercialization in most European territories.
Prescribe obicetrapib if approved for patients needing additional LDL-C lowering.
End users targeted for oral therapy after standard lipid-lowering treatment.
May handle distribution and fulfillment outside the U.S. or in selected regions.
Potential collaborators for Japan, China, and other non-core markets.
NewAmsterdam Pharma is incorporated in the Netherlands, with a registered office in Naarden and a U.S...
The company’s strategy is to advance obicetrapib through late-stage development, seek regulatory approval, and build...
Approval is required before the company can generate meaningful product sales.
The company intends to sell in the U.S. itself and needs sales and distribution infrastructure.
Partnering can extend reach while limiting the need to build local infrastructure everywhere.
Additional candidates can diversify the company beyond a single lead asset.
The company depends heavily on successful development and approval of a single lead asset, so clinical, regulatory, and...
The company has no approved products and relies on obicetrapib's trial results.
Revenue depends on obtaining marketing authorization before commercialization.
The company has limited internal sales and marketing infrastructure.
Menarini is the key European commercialization counterparty and supply customer.
Future value depends on protecting obicetrapib from generic or legal challenges.
The company expects continued losses and may need external capital.
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: 29/04/2026