
Uniqure N.v (QURE) Stock
Gene therapy company targeting rare genetic disorders. Here's the price, business snapshot, and what's worth knowing about Uniqure N.v in August 2026.
uniQure NV (QURE) is a biotechnology company focused on developing and commercialising gene therapies using viral vector platforms, particularly adeno‑associated viruses (AAVs). The firm targets rare genetic disorders — including haemophilia and select neurological conditions — with the aim of delivering durable, potentially one‑time treatments rather than chronic medication. Its market capitalisation is approximately $3.89 billion, reflecting investor expectations around clinical progress and regulatory decisions. Key investor considerations include clinical trial outcomes, regulatory approvals, the complexity and cost of scaling viral‑vector manufacturing, and competition in the gene‑therapy space. Revenue today is limited and may depend on future product approvals, partnerships or licensing deals. Shares tend to be sensitive to trial readouts, filings and collaboration announcements, making them relatively volatile. This information is for educational purposes only and not personal financial advice; values can rise or fall and past performance is not a reliable guide to future results.
About This Stock
UNIQURE N.V.
QURE
Current Price
$48.68
Potential 12 Month Profit
-31.75%
Sector
Healthcare
Industry
Biotechnology & Medical Research
Ticker
QURE
Market Cap
$3.38B
Potential 12 Month Profit
-31.75%
Sector
Healthcare
Industry
Biotechnology & Medical Research
Sixth Month Growth Performance
Stock Performance Snapshot
Analyst Rating
Analysts recommend buying UNIQURE's stock, expecting it to rise to $48.17 soon.
Financial Health
UNIQURE N.V. shows strong profitability and cash flow, with significant revenue generation.
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Why You’ll Want to Watch This Stock
Gene‑therapy focus
uniQure's core expertise is in AAV‑based gene therapy, which promises durable effects; however, clinical and manufacturing hurdles mean outcomes can vary.
Rare disease market
Targeting haemophilia and other rare conditions offers high unmet need and potential value, yet commercial uptake depends on pricing, reimbursement and long‑term data.
Regulatory milestones
Trial readouts and approval decisions drive valuation swings; these catalysts can create opportunities but also pose binary risks for investors.
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