StockWatch
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uniQure N.V. Q2 FY26 Results

QUREQ2 FY26 Results
Filing
MetricValue ($ M)Q1 FY26Q2 FY25
Revenue5.8464.0%11.0%
Total Income5.8464.0%11.0%
Expenditure51.684.5%4.3%
PBT-79.2249.3%112.4%
Net Profit-81.0651.4%114.9%
OPM—
NPM—
EPS-1.2243.5%76.8%
View full financials

uniQure Announces Q2 2026 Financial Results and Company Update

29 Jul 2026 · 29 Jul, 4:41 pm

Summary

uniQure reported second quarter 2026 revenue of $5.8 million, up from $5.3 million in the prior year, driven by an increase in license revenue. The company also announced a significant $259 million follow-on offering, bolstering its cash position to $810.3 million as of June 30, 2026, and extending its projected cash runway into 2030. Key pipeline developments include regulatory submissions for AMT-130 for Huntington's disease on track for Q3 2026 and expected topline four-year data in September 2026. Preliminary data for AMT-260 showed promising early signals and a favorable safety profile.

Key Highlights

  1. 1

    uniQure reported revenue of $5.8 million for the second quarter of 2026, an increase from $5.3 million in the same period of 2025.

  2. 2

    The company strengthened its financial position with a $259 million follow-on offering, extending its cash runway into 2030.

  3. 3

    U.S. and U.K. regulatory submissions for AMT-130 for Huntington's disease are on track for the third quarter of 2026.

  4. 4

    Topline four-year data from the Phase I/II study of AMT-130 is expected in September 2026.

  5. 5

    Preliminary data from the first cohort of the AMT-260 Phase I/IIa trial showed early biological signals of therapeutic activity and a favorable safety profile.

  6. 6

    The net loss for the three months ending June 30, 2026, was $81.1 million, or $1.22 basic and diluted loss per ordinary share.

Management Comments

M

Matthew Kapusta

This has been a defining quarter – not just for uniQure, but for the Huntington's disease community. Following a productive Type B meeting with the FDA, we remain on track to submit our BLA for AMT-130 in the third quarter — a milestone that reflects years of rigorous science, disciplined execution, and an unwavering commitment to the patients and families living with this devastating disease. With four-year data expected in September and the U.K. regulatory activities progressing as planned, we enter the second half of 2026 with real momentum and a clear line of sight to potentially bringing this therapy to the people who need it. Beyond AMT-130, we continue to execute across our broader pipeline. With a strong balance sheet, we believe we are well-positioned for what will be a transformative period for uniQure and the patients we serve.

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