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. Show more
Paasheuvelweg 25, Amsterdam, 1105 BP, Netherlands
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Market Cap
1.524B
52 Wk Range
$7.76 - $71.50
Previous Close
$24.46
Open
$23.85
Volume
1,531,529
Day Range
$23.34 - $24.76
Enterprise Value
3.047B
Cash
694.2M
Avg Qtr Burn
-16.4M
Insider Ownership
5.50%
Institutional Own.
-
Qtr Updated
09/30/25
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| Drug & Indication | Stage & Event | Catalyst Date |
|---|---|---|
HEMGENIX® (etranacogene dezaparvovec-drlb) (AMT-061) Details Hemophilia, Rare diseases, Rare genetic disease | Approved Quarterly sales | |
AMT-130 Details Huntington's disease | BLA FDA meeting | |
AMT-260 Details Mesial temporal lobe epilepsy (MTLE) | Phase 1/2 Data readout | |
AMT-162 Details Amyotrophic lateral sclerosis | Phase 1/2 Data readout | |
AMT-191 Details Fabry disease | Phase 1/2 Update |
