single approved product
“10-K Item 1A: 'we have only one product based on RNAi and our delivery technologies approved in November 2025'”
Updated
The most significant concentration Arrowhead Pharmaceuticals discloses is single approved product, 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: Arrowhead Pharmaceuticals’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: 'we have only one product based on RNAi and our delivery technologies approved in November 2025'”
“10-K Item 1A: 'must rely on third-party manufacturers to manufacture certain of our clinical supplies and our commercial products'”
The company's concentration profile is defined by two related disclosures: a high-share dependency on its sole approved product and a medium-share reliance on third-party manufacturers for both clinical and commercial supply. The company has only one product based on its RNAi and delivery technologies that received approval in November 2025, a high-share product concentration with a mixed character — structural in that the entire commercial strategy is organized around this platform and its derivatives, but dependency-like because there is no revenue diversification across multiple approved assets. A clinical safety signal, regulatory action, or competitive displacement of this single approved product would directly impair the company's financial position, as no other commercial revenue source exists to partially offset the impact. Complementing the product concentration is a medium-share manufacturing dependency: the company must rely on third-party manufacturers to produce certain clinical supplies and commercial products. The company does not own all of its own manufacturing infrastructure, which means that capacity availability, quality control, and relationship continuity with contract manufacturers are operational dependencies that sit outside the company's direct control. Taken together, the profile describes an early-commercial-stage biopharmaceutical company with one approved product that it manufactures through external partners. The approved product concentration is the most consequential exposure — it defines the entire revenue profile — while the manufacturing dependency adds an operational layer. Monitoring the commercialization trajectory of the approved product alongside contract manufacturer performance are the central watch items.
For the engine’s reasoning on ARWR’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 |
| ACLX | Arcellx, Inc. | 1 | 1 | 0 | 2 |
| ARWR● | Arrowhead Pharmaceuticals, Inc. | 1 | 1 | 0 | 2 |
| AGIO | Agios Pharmaceuticals, Inc. | 1 | 0 | 0 | 1 |
| ALMS | Alumis Inc. | 1 | 0 | 0 | 1 |
| ADMA | ADMA Biologics Inc | 0 | 1 | 0 | 1 |
Concentration counts reflect items disclosed in each peer’s most recent 10-K; disclosed-size classification uses TrendMatrix’s internal 10-K extraction taxonomy.