ERAS-0015 and ERAS-4001 Phase 1 programs
“10-K Item 1A: 'AURORAS-1 and BOREALIS-1 Phase 1 trials for ERAS-0015 and ERAS-4001 ... all of our other programs are still in the preclinical or discovery stage'”
Updated
The most significant concentration Erasca discloses is ERAS-0015 and ERAS-4001 Phase 1 programs, 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: Erasca’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: 'AURORAS-1 and BOREALIS-1 Phase 1 trials for ERAS-0015 and ERAS-4001 ... all of our other programs are still in the preclinical or discovery stage'”
“10-K Item 1: 'ERAS-0015, which we license from Guangzhou Joyo Pharmatech Co., Ltd. (Joyo)'”
The company's concentration profile is defined by two interconnected exposures that together characterize a clinical-stage single-program biotech. The first is pipeline concentration: the AURORAS-1 and BOREALIS-1 Phase 1 trials for ERAS-0015 and ERAS-4001 are the lead clinical programs, with all other programs still in preclinical or discovery stages — a high-share structural exposure. The company's near-term value creation is substantially dependent on advancing these two programs, and any clinical setback, regulatory hold, or failure to demonstrate proof-of-concept in the Phase 1 studies would have a large impact on the enterprise. The second exposure is a supplier dependency: ERAS-0015 is licensed from Guangzhou Joyo Pharmatech Co., Ltd. — a medium-share dependency that adds a licensing and supply-chain dimension to the lead program. The dependency character means that the relationship with Joyo governs the company's ability to develop and eventually commercialize one of its two lead clinical-stage assets, introducing counterparty risk at the development level. The two exposures compound each other: the most advanced programs define the entirety of near-term clinical value, and one of those programs is contingent on a single external licensor. There is no commercial revenue, geographic diversification, or customer base to offset these concentrations. On balance, the profile is that of a concentrated early-clinical biotech where pipeline execution and the Joyo licensing relationship are the primary variables governing the investment outcome.
For the engine’s reasoning on ERAS’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 |
| ERAS● | Erasca, 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.