NERLYNX
“10-K Item 1A: 'NERLYNX is the only product for which we currently receive product revenue, and we expect NERLYNX to constitute the vast majority of our product revenue for the foreseeable future.'”
Updated
The most significant concentration Puma Biotechnology discloses is NERLYNX, classified HIGH by disclosed size. Below: the full set from the latest 10-K — verbatim quotes, filing references, and a synthesis of what these exposures mean together.
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Source: Puma Biotechnology’s SEC Form 10-K filed — view the filing on SEC EDGAR ↗
Each card carries a disclosed-size chip (HIGH / MEDIUM / LOW — how large the exposure is as a share of revenue, not how dangerous it is) and a nature tag: Built-in(the company’s own model, geography, or products) or Outside party (an external customer, supplier, or distributor it relies on).
“10-K Item 1A: 'NERLYNX is the only product for which we currently receive product revenue, and we expect NERLYNX to constitute the vast majority of our product revenue for the foreseeable future.'”
Puma Biotechnology's concentration risk is singular and defining: NERLYNX is the only product for which the company currently receives product revenue, and it expects NERLYNX to constitute the vast majority of product revenue for the foreseeable future, a high-share exposure with a mixed character. Because this is flagged as mixed rather than purely structural or purely dependency-driven, it reflects both an inherent feature of a single-product commercial-stage biotech and an implicit reliance on the market's continued acceptance and prescribing of that one product. Unlike a diversified pharmaceutical company where one product's underperformance can be offset by others, Puma's near-term financial results are effectively a direct read on NERLYNX's own trajectory — whether that be pricing, competitive dynamics, or physician demand. With no other concentration points disclosed, this is the dominant, and effectively only, concentration factor for investors to weigh. Any development affecting NERLYNX specifically — competitive entry, reimbursement changes, or demand shifts — would have a disproportionate effect on the business relative to a company with multiple approved products sharing the revenue base.
For the engine’s reasoning on PBYI’s current verdict — including which dimensions drove the score — see the per-dimension breakdown.
| Symbol | Name | HIGH | MEDIUM | LOW | Total |
|---|---|---|---|---|---|
| ACAD | ACADIA Pharmaceuticals Inc. | 2 | 0 | 0 | 2 |
| ABUS | Arbutus Biopharma Corporation | 1 | 1 | 0 | 2 |
| ABSI | Absci Corporation | 1 | 0 | 0 | 1 |
| PBYI● | Puma Biotechnology Inc | 1 | 0 | 0 | 1 |
| ABCL | AbCellera Biologics Inc. | 0 | 0 | 0 | 0 |
| ACHV | Achieve Life Sciences, Inc. | 0 | 0 | 0 | 0 |
Concentration counts reflect items disclosed in each peer’s most recent 10-K; disclosed-size classification uses TrendMatrix’s internal 10-K extraction taxonomy.