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Dec 31, 2023

uniQure Q4 2023 Earnings Report

uniQure reported its financial results for Q4 2023 and highlighted recent progress across its business.

Key Takeaways

uniQure announced its Q4 and full year 2023 financial results. The company's cash position is expected to fund operations into the second quarter of 2027. Strategic reorganization is expected to deliver $180 million of cost savings over the next three years.

Presented promising clinical update from U.S. and European Phase I/II trials of AMT-130 in Huntington’s disease.

Announced FDA clearance of two Investigational New Drug (IND) applications.

Announced strategic reorganization to advance multiple clinical-stage programs and deliver $180 million of cost savings over the next three years.

Cash position of approximately $618 million as of December 31, 2023 expected to fund operations into the second quarter of 2027.

Total Revenue
$6.69M
Previous year: $103M
-93.5%
EPS
-$1.53
Previous year: $0.15
-1120.0%
Gross Profit
-$6.33M
Previous year: $101M
-106.2%
Cash and Equivalents
$618M
Previous year: $393M
+57.3%
Free Cash Flow
-$50.1M
Previous year: -$59.7M
-16.2%
Total Assets
$832M
Previous year: $705M
+18.0%

uniQure

uniQure

Forward Guidance

uniQure's forward-looking statements include plans to announce additional follow up data from the ongoing U.S. and European Phase I/II clinical studies of AMT-130, plans to initiate interactions with regulatory authorities regarding the further development of AMT-130, and plans to initiate patient enrollment for AMT-260, AMT-162 and AMT-191 in the first half of 2024.

Positive Outlook

  • Company’s cash runway and its ability to fund its operations into the second quarter of 2027
  • Company’s expected cost savings related to its strategic reorganization
  • Company’s plans to announce additional follow up data from the ongoing U.S. and European Phase I/II clinical studies of AMT-130
  • Company’s plans to initiate interactions with regulatory authorities regarding the further development of AMT-130 and the timing of regulatory clarity from such interactions
  • Company’s plans to initiate patient enrollment for AMT-260, AMT-162 and AMT-191 in the first half of 2024

Challenges Ahead

  • Risks associated with the clinical results and the development and timing of the Company’s programs
  • Company’s interactions with regulatory authorities, which may affect the initiation, timing and progress of clinical trials and pathways to approval
  • Company’s ability to continue to build and maintain the company infrastructure and personnel needed to achieve its goals
  • Company’s effectiveness in managing current and future clinical trials and regulatory processes
  • The impact of global economic uncertainty, rising inflation, rising interest rates or market disruptions on its business