MYQORZO
“10-K Item 1: 'Our first commercial product is MYQORZO™ (aficamten)...which the FDA approved in December 2025'”
Updated
The most significant concentration Cytokinetics discloses is MYQORZO, 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: Cytokinetics’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 1: 'Our first commercial product is MYQORZO™ (aficamten)...which the FDA approved in December 2025'”
“10-K Item 1A: 'We currently rely on single source CMOs for the manufacture of any or all of MYQORZO as a finished drug product and the active pharmaceutical ingredient'”
“10-K Item 1: 'Aficamten continues to be evaluated in ACACIA-HCM, a Phase 3 clinical trial of aficamten in patients with nHCM'”
The company's concentration profile is defined by three interconnected high-share exposures that collectively reflect the typical structure of a single-asset commercial-stage biopharmaceutical company. The company's first commercial product, MYQORZO (aficamten), received FDA approval in December 2025, making it the sole source of near-term commercial revenue and the anchor of the entire business model. This product concentration is the most fundamental risk in the profile: all near-term revenues are tied to the commercial uptake of a single molecule across its approved indication. Compounding that product dependency is a manufacturing concentration. The company currently relies on single-source contract manufacturing organizations for both the finished drug product and the active pharmaceutical ingredient for MYQORZO. This is a high-share dependency by disclosed size; any disruption at a sole-source CMO — whether operational, regulatory, or contractual — could constrain supply and directly impair the commercial ramp at precisely the moment revenue visibility is being established. Layered on top is a pipeline concentration. Aficamten continues to be evaluated in the ACACIA-HCM Phase 3 clinical trial, meaning the company's medium-term growth optionality is also tied to a single molecule. The three exposures do not diversify each other — they are all aficamten-dependent in different time horizons. On balance, the profile is tightly concentrated along one asset, with manufacturing and pipeline risks amplifying the product risk rather than offsetting it.
For the engine’s reasoning on CYTK’s current verdict — including which dimensions drove the score — see the per-dimension breakdown.
| Symbol | Name | HIGH | MEDIUM | LOW | Total |
|---|---|---|---|---|---|
| CYTK● | Cytokinetics, Incorporated | 3 | 0 | 0 | 3 |
| ACAD | ACADIA Pharmaceuticals Inc. | 2 | 0 | 0 | 2 |
| ACLX | Arcellx, 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.