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
Location: Paasheuvelweg 25, Amsterdam, 1105 BP, Netherlands | Website: https://www.uniqure.com | Industry: Biotechnology | Sector: Healthcare
Market Cap
4.349B
52 Wk Range
$5.35 - $71.50
Previous Close
$70.59
Open
$69.01
Volume
309,130
Day Range
$68.01 - $69.99
Enterprise Value
3.047B
Cash
377M
Avg Qtr Burn
-43.36M
Insider Ownership
5.41%
Institutional Own.
87.96%
Qtr Updated
06/30/25
Drug Pipeline
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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 | |
NDA Submission | ||
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 Data readout |
