Erasca/$ERAS

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About Erasca

Erasca Inc is a clinical-stage precision oncology company singularly focused on discovering, developing, and commercializing therapies for patients with RAS/MAPK pathway-driven cancers. Its focused RAS/MAPK pathway pipeline comprises modality-agnostic programs aligned with three therapeutic strategies of: targeting key upstream and downstream signaling nodes in the RAS/MAPK pathway; targeting RAS directly; and targeting escape routes that emerge in response to treatment. Its pipeline includes two clinical-stage programs (ERAS-0015, a pan-RAS molecular glue; and ERAS-4001, a pan-KRAS inhibitor), and ERAS-12, a discovery-stage program.
Ticker
$ERAS
Sector
Health
Primary listing
NASDAQ
Employees
103

Erasca Metrics

BasicAdvanced
$5.4B
-
-$0.97
0.65
-

What the Analysts think about Erasca

Analyst ratings (Buy, Hold, Sell) for Erasca stock.
Analyst projections of the future price of Erasca stock.

Bulls say / Bears say

ERAS-0015 produced a 57% eight-week overall response rate in seven patients with second-line-or-later KRAS G12X pancreatic cancer at the recommended dose. All responding patients remained on treatment at the data cut-off, with no dose-limiting toxicities or treatment-related discontinuations reported. (GlobeNewswire)
The FDA granted Fast Track designation to ERAS-0015 for metastatic pancreatic adenocarcinoma. This gives Erasca more structured interaction with regulators as it prepares a planned Phase 3 pancreatic trial and further lung-cancer studies. (BioSpace)
Erasca strengthened its funding position with a July offering that generated about $632.5 million gross, while management said the post-offering cash position should fund its key milestones. That reduces near-term financing pressure as the company advances ERAS-0015 and prepares ERAS-4001 data. (BioSpace, BioSpace)
The headline 57% eight-week response rate is preliminary, includes unconfirmed responses and came from only seven patients at the recommended dose. The trial is still Phase 1, so durability and performance in larger, controlled studies remain unproven. (GlobeNewswire, BioSpace)
Erasca stopped developing naporafenib and terminated its Novartis licence, leaving the investment case more concentrated in ERAS-0015, ERAS-4001 and the early ERAS-12 programme. That narrows diversification and makes a setback in the lead RAS programmes more damaging. (StockTitan)
The July offering raised $632.5 million gross by selling 36.1 million new shares, diluting existing holders. Erasca has no product revenue and says it may need further equity, debt or other funding before any product can generate meaningful sales. (BioSpace, StockTitan)
Data summarised monthly by Lightyear AI. Last updated on 17 Sept 2026.

Erasca Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

Erasca Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise
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