Stock Events

uniQure N.V. 

€5.88
29
+€0.18+3.19% Today

Statistics

Day High
5.88
Day Low
5.88
52W High
-
52W Low
-
Volume
0
Avg. Volume
-
Mkt Cap
262.77M
P/E Ratio
-
Dividend Yield
-
Dividend
-

Upcoming

Earnings

29OctExpected
Q1 2023
Q2 2023
Q3 2023
Q4 2023
Q1 2024
Q2 2024
Next
-1.88
-0.57
0.74
2.05
Expected EPS
-0.992736
Actual EPS
N/A

People Also Follow

This list is based on the watchlists of people on Stock Events who follow UQ1.F. It's not an investment recommendation.

Competitors

This list is an analysis based on recent market events. It's not an investment recommendation.
Sangamo Therapeutics
SGMO
Mkt Cap176.57M
Sangamo Therapeutics, Inc. competes in the gene editing and therapy space, focusing on developing genomic medicines for genetic diseases, similar to uniQure's work on gene therapies.
Bluebird bio
BLUE
Mkt Cap108.22M
bluebird bio, Inc. is known for its gene therapies targeting genetic diseases and cancer, directly competing with uniQure's gene therapy products.
Biomarin Pharmaceutical
BMRN
Mkt Cap17.36B
BioMarin Pharmaceutical Inc. develops and commercializes innovative therapies for rare genetic diseases, overlapping with uniQure's target market.
Pfizer
PFE
Mkt Cap164.39B
Pfizer Inc., through its acquisition of Bamboo Therapeutics and Spark Therapeutics, has expanded into gene therapy, making it a competitor in the same field as uniQure.
Regenxbio
RGNX
Mkt Cap603.95M
REGENXBIO Inc. is a biotechnology company that develops AAV-based gene therapies for genetic and other diseases, competing in the same space as uniQure.
Sarepta Therapeutics
SRPT
Mkt Cap12.95B
Sarepta Therapeutics, Inc. specializes in the discovery and development of RNA-based and gene therapy treatments for rare diseases, making it a competitor in the gene therapy market.
Intellia Therapeutics
NTLA
Mkt Cap2.28B
Intellia Therapeutics, Inc. is involved in CRISPR/Cas9 gene editing, a next-generation technology that could compete with uniQure's gene therapy approaches.
CRISPR Therapeutics
CRSP
Mkt Cap4.06B
CRISPR Therapeutics AG focuses on the development of gene-based medicines using the CRISPR/Cas9 system, competing in the broader gene therapy and editing market alongside uniQure.

About

uniQure N.V. develops treatments for patients suffering from rare and other devastating diseases. It offers HEMGENIX that has completed Phase III HOPE-B pivotal trial for the treatment of hemophilia B. The company also develops AMT-130, a gene therapy that is in Phase I/II clinical study for the treatment of Huntington's disease. In addition, it is developing AMT-162, which is in preclinical trial for the treatment of superoxide dismutase 1- amyotrophic lateral sclerosis; AMT-260 that is in preclinical trial to treat temporal lobe epilepsy; AMT-191, which is in preclinical trial for the treatment of fabry disease; AMT-161 that is in preclinical trial to treat amyotrophic lateral sclerosis caused by mutations; AMT-240, which is in preclinical trial to for the treatment of autosomal dominant Alzheimer's disease; and AMT-210 that is in preclinical trial to treat Parkinson's disease. The company was founded in 1998 and is headquartered in Amsterdam, the Netherlands.
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CEO
Mr. Matthew Craig Kapusta
Employees
480
Country
NL
ISIN
NL0010696654
WKN
000A1XDTV

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