| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
| Gross Profit | -832.00K | 0.00 | -3.73M | -2.64M | -829.00K | 0.00 |
| EBITDA | -125.90M | -153.28M | -121.31M | -240.16M | -121.94M | -36.97M |
| Net Income | -127.69M | -161.65M | -125.04M | -242.81M | -122.76M | -101.66M |
Balance Sheet | ||||||
| Total Assets | 420.40M | 502.53M | 395.30M | 514.91M | 501.42M | 124.83M |
| Cash, Cash Equivalents and Short-Term Investments | 288.40M | 298.31M | 312.35M | 435.62M | 414.48M | 118.70M |
| Total Debt | 48.29M | 51.89M | 55.86M | 55.10M | 18.79M | 2.99M |
| Total Liabilities | 72.52M | 79.03M | 78.61M | 103.06M | 44.89M | 17.40M |
| Stockholders Equity | 347.89M | 423.50M | 316.69M | 411.85M | 456.53M | 107.42M |
Cash Flow | ||||||
| Free Cash Flow | -98.43M | -131.98M | -102.99M | -119.81M | -98.48M | -71.38M |
| Operating Cash Flow | -98.31M | -109.42M | -101.22M | -103.26M | -79.60M | -32.69M |
| Investing Cash Flow | 98.33M | -156.62M | -91.22M | -71.08M | -64.59M | -71.20M |
| Financing Cash Flow | 1.32M | 240.70M | 1.29M | 98.08M | 439.40M | 139.99M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
61 Neutral | $783.54M | -15.19 | ― | ― | ― | ― | |
56 Neutral | $2.13B | -14.98 | -59.22% | ― | ― | 17.23% | |
56 Neutral | $917.60M | ― | -26.64% | ― | ― | -103.95% | |
52 Neutral | $2.73B | -21.34 | -32.00% | ― | ― | 45.66% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
46 Neutral | $207.14M | -2.96 | -27.43% | ― | -41.53% | -11.32% |
On January 12, 2026, Erasca updated its corporate presentation and announced clinical progress across its RAS-targeting franchise, highlighting that dose escalation in the Phase 1 AURORAS-1 trial of ERAS-0015 has been advancing faster than anticipated, with ongoing confirmed and unconfirmed partial responses seen at low doses across multiple tumor types and RAS mutations, alongside favorable safety, tolerability, and linear pharmacokinetics observed as of a January 7, 2026 data cutoff. The company also reported that dose escalation for its pan-KRAS inhibitor ERAS-4001 in the Phase 1 BOREALIS-1 trial is proceeding as expected and laid out a detailed development timeline, with initial Phase 1 monotherapy data for ERAS-0015 expected in the first half of 2026, initial monotherapy data for ERAS-4001 in the second half of 2026, and subsequent expansion and combination cohort readouts slated into 2027, while shifting to use its website rather than regulatory filings as the primary channel for future corporate presentation updates, a move that underscores its growing clinical momentum and investor outreach efforts around its core RAS/MAPK-focused strategy.
The most recent analyst rating on (ERAS) stock is a Hold with a $6.00 price target. To see the full list of analyst forecasts on Erasca stock, see the ERAS Stock Forecast page.