Could $1 Stock Be Sitting on a Billion-Dollar Discovery?
This $1 stock has already made its mark with a listing on the prestigious NYSE. Now, it's sitting on prime land in one of America's richest gold districts, with the potential for a billion-dollar discovery. For savvy investors, this may be a $1 "Golden Ticket" to massive returns.
Financials
| Curr Year EPS Estimate | -2.75 |
| Next Quarter EPS Estimate | -0.71 |
| Profit Margin | -1387.98% |
| Operating Margin | -1,255.40 |
| Return on Assets | -0.15 |
| Return on Equity | -4.27 |
| Revenue | 14.3M |
| Earnings Per Share | -3.71 |
| Revenue Per Share | 0.28 |
| Gross Profit | -121,873,000 |
| Quarterly Revenue Growth | -0.53 |
General
| Name | uniQure N.V |
| Ticker | QURE |
| Exchange | NASDAQ |
| Sector | Healthcare |
| Industry | Biotechnology |
| Currency | USD |
| Country | USA |
| Fiscal Year End | December |
| Full Time Employees | 209 |
About uniQure N.V
uniQure N.V. develops treatments for patients suffering from rare and other devastating diseases in the United States. The company offers HEMGENIX that allows people living with hemophilia B to produce factor IX, which can lower the risk of bleeding. Its lead product candidate is AMT-130, a gene therapy candidate, which is in Phase I/II clinical study for the treatment of Huntington's disease. The company also develops AMT-260, which is in Phase I/IIa clinical trial for the treatment of mesial temporal lobe epilepsy; AMT-162, which is in Phase I/IIa clinical trial to treat superoxide dismutase enzyme-amyotrophic lateral sclerosis; and AMT-191, an investigational gene therapy candidate which is in phase I/IIa clinical trial for the treatment of fabry disease. It has a licensing agreement with Apic Bio to develop, manufacture, and commercialize intrathecally administered investigational gene therapy for ALS caused by mutations in SOD-1; and development and commercial supply agreement with CLS Bhering. uniQure N.V. was founded in 1998 and is headquartered in Amsterdam, the Netherlands.
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