Home・Aandelen Lijst・uniQure NV

uniQure NV

Open

48.87 0.23

Buy Sell

Overzicht

Wijziging aandelenprijs

24u

Huidig

Min

46.88

Max

49.58

Belangrijke statistieken
By Trading Economics
Inkomsten	-28M -81M
Verkoop	2.3M 5.8M
EPS	-1.22
Winstmarge	-1,387.759
Werknemers	221
EBITDA	-34M -70M

Aanbevelingen
By TipRanks
Aanbevelingen	Strong Buy
12 Maanden Prognose	+34.6% upside

Dividenden
By Acuity
Volgende Winsten	9 nov 2026

Marktinformatie
By TradingEconomics
Marktkapitalisatie	700M 3.3B
Vorige openingsprijs	48.64
Vorige sluitingsprijs	48.87

uniQure NV Grafiek

Eerdere prestaties zijn geen betrouwbare indicator voor toekomstige resultaten.

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Peer Vergelijking

Prijswijziging

uniQure NV Prognose

Koersdoel

By TipRanks

34.6% opwaarts potentieel

12 Maanden Prognose

Gemiddelde 65.63 USD 34.6%

Hoogste 80 USD

Laagste 46 USD

Gebaseerd op 10 Wall Street-analisten die 12-maands prijsdoelen bieden voor uniQure NV - Dist. in de afgelopen 3 maanden.

Beoordelingsconsensus

By TipRanks

Strong Buy

10 ratings

Buy

Hold

Sell

Gebaseerd op 10 analisten die aandelenratings hebben gegeven aan uniQure NV - Dist in de afgelopen 3 maanden.

Financieel

Verkoop- en administratiekosten

Bedrijfskosten

Winst voor belastingen

Verkoop

Kosten van verkopen

Brutowinst op verkopen

Rente-uitgaven op schulden

EBITDA

Operationele winst

Over uniQure NV

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.