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Disclaimer: The content on this page is for informational and educational purposes only and does not constitute investment advice, a recommendation, or an offer to buy or sell any security. Past performance does not guarantee future results. Consult a licensed financial advisor before making any investment decisions.
Quarterly filings sourced directly from SEC EDGAR. Real-time earnings actuals are in the Earnings panel above.
| Date | Open | Close | Δ | Vol |
|---|---|---|---|---|
| 05-11 | $7.21 | $7.00 | -2.91% | 0.6M |
| 05-12 | $7.01 | $6.96 | -0.71% | 0.6M |
| 05-13 | $6.95 | $7.25 | +4.32% | 0.5M |
| 05-14 | $7.28 | $7.11 | -2.34% | 0.5M |
| 05-15 | $6.98 | $6.69 | -4.15% | 0.4M |
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| Metric | Q3 2021 2021-09-30 |
|---|---|
Revenue | $7.80M |
Operating Income | $-57.49M |
Net Income | $-57.36M |
EPS (Diluted) | $-1.71 |
Total Assets | $255.55M |
Total Liabilities | $24.94M |
Cash & Equivalents | $65.47M |
Free Cash Flow OCF − CapEx | $-57.81M |
Shares Outstanding | 40.53M |
These are published opinions from external sell-side analysts — not Stonvex recommendations. Ratings may change without notice, may conflict with each other, and may be wrong. Not investment advice.
Consensus aggregated from publicly disclosed sell-side analyst ratings. Stonvex is not a registered investment advisor and does not endorse any of the ratings shown. Past analyst ratings do not predict future price movements.
Fulcrum Therapeutics Inc is a clinical-stage biopharmaceutical company focused on developing small molecules for genetically defined rare diseases. Its product candidate, Pociredir, is an oral small molecule designed to induce fetal hemoglobin (HbF) and is in clinical development for sickle cell disease (SCD). The company completed dosing in the Phase 1b PIONEER trial evaluating pociredir in adults with SCD and reported clinical data showing clinically relevant HbF induction and improvements in markers of hemolysis and anemia. The company has also generated a pipeline of clinical-stage and pre-clinical programs targeting the root causes of rare genetic diseases.