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uniQure Announces 2023 Financial Results and Highlights Recent Company Progress ~ Presented promising clinical update from U.S. and European Phase I/II trials of AMT-130 in Huntington's disease; Up to three years of foll

Key Takeaway: uniQure N.V. reported its 2023 financial results and highlighted substantial progress in its clinical programs, including promising updates from Phase I/II trials of its gene therapy AMT-130 for Huntington's disease. The company received FDA clearance for two Investigational New Drug applications, with new trials set to begin in 2024. Despite a large net loss of $308.5 million, uniQure maintains a strong cash position of approximately $618 million, expected to support operations well into 2027. The company is focused on regulatory interactions to clarify approval pathways and advance its clinical programs efficiently.

Market Sentiment Analysis

POSITIVE FACTORS

  • Presentation of promising clinical updates from AMT-130 trials for Huntington's disease.
  • FDA clearance of IND applications and upcoming Phase I/II trials in epilepsy and Fabry disease.
  • Expected cost savings of $180 million from strategic reorganization.

CONCERNS & RISKS

  • Significant net loss of $308.5 million in 2023, nearly double the previous year's loss.
  • Drop in revenue to $15.8 million, down from $106.5 million in 2022, primarily due to the absence of milestone payments.

Full Press Release Details

2023 Financial Results
Recent Company Progress
~ Presented promising clinical update from U.S.
and European Phase I/II trials of AMT-130 in Huntington's disease; Up to three years of follow-up data to be presented in mid-2024;
Regulatory interactions and clarity on potential strategies for clinical development expected in 2024 ~
~ Announced FDA clearance of two Investigational
New Drug (IND) applications; Initiation of Phase I/II clinical trials in mesial temporal lobe epilepsy (mTLE) and Fabry disease, in addition
to SOD1-ALS, are expected in the first half of 2024 ~
~ 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 ~
Lexington, MA and Amsterdam, the Netherlands,
February 28, 2024 - uniQure N.V. (NASDAQ: QURE), a leading gene therapy company advancing transformative therapies
for patients with severe medical needs, today reported its financial results for the fourth quarter and full year 2023 and highlighted
recent progress across its business.
"We are pleased with the progress made
across the company in 2023 and are now laser-focused on execution across multiple clinical programs," stated Matt Kapusta, chief
executive officer of uniQure. "Our top priorities are to engage with regulatory authorities to clarify the approval pathway
for AMT-130 in Huntington's disease and to initiate patient enrollment across three additional clinical trials as expeditiously
"While we enter 2024 with a strong balance
sheet, we remain disciplined on the prudent and efficient allocation of our capital," he continued. "Any decision to advance
AMT-130 into late-stage development will necessitate a clear and timely approval pathway and financial feasibility, including through
a partnership which we would secure before beginning any Phase III trial."
Upcoming Investor Events
Financial Highlights
Cash position: As of December 31,
2023, the Company held cash and cash equivalents and investment securities of $617.9 million, compared to $392.8 million as of December 31,
2022. The Company entered into a royalty agreement in May 2023 and received an upfront payment of $375.0 million, and collected $100.0
million in July 2023 for a milestone due from CSL following the first sale of HEMGENIX
in the U.S. The Company expects cash, cash equivalents and investment securities will fund operations into the second quarter
Revenues: Revenue for the year ended December 31,
2023 was $15.8 million, compared to $106.5 million in the same period in 2022. Revenues in 2022
included $100.0 million of license revenue related to the U.S. first sale milestone payment of HEMGENIX
that the Company expected to receive in 2023. Revenue from contract manufacturing HEMGENIX
for CSL increased $9.1 million in 2023 compared to 2022.
Cost of contract manufacturing revenues: Cost
of contract manufacturing revenues were $13.6 million for the year ended December 31, 2023, compared to $2.1 million for the same
period in 2022. The increase relates to an increase in activities related to contract manufacturing HEMGENIX
R&D expenses: Research and development
expenses were $214.9 million for the year ended December 31, 2023, compared to $197.6 million during the same period in 2022. The
$17.2 million increase was primarily related to a $5.9 million net increase of external research and development expenses including a
$10.0 million payment made to Apic Bio to acquire AMT-162, an $8.8 million non-cash increase related to the fair value of contingent consideration
associated with the Company's acquisition of Corlieve Therapeutics in 2021 as well as a $1.4 million non-cash impairment loss related
to our Lexington research facility.
SG&A expenses: Selling, general and
administrative expenses were $74.6 million for the year ended December 31, 2023, compared to $55.1 million during the same period
in 2022. The $19.5 million increase was primarily related to a $9.7 million increase of professional, financial advisory and intellectual
property fees, a $3.7 million increase in information technology expenses as well as a $3.7 million increase in personnel and contractor-related
Other non-operating items, net:
Other non-operating items, net was an expense
of $23.7 million for the year ended December 31, 2023, compared to net income of $14.9 million for the same period in 2022. The $38.6
million decrease in other non-operating items, net was primarily related to a decrease in foreign currency gains, net of $24.9 million
and an increase in non-cash interest expense of $26.9 million related to the royalty agreement that the Company entered into in May 2023,
which partially was offset by an increase of $19.0 million in interest income earned on investment securities and cash on hand.
The net loss for the year ended December 31,
2023, was $308.5 million, or $6.47 basic and diluted loss per ordinary share, compared to $126.8 million net loss for the same period
in 2022, or $2.71 basic and diluted loss per ordinary share.
uniQure's mission is to reimagine the future
of medicine by delivering innovative cures that transform lives. The recent approvals of our gene therapy for hemophilia B - a
historic achievement based on more than a decade of research and clinical development - represent a major milestone in the field
of genomic medicine and ushers in a new treatment approach for patients living with hemophilia. We are now leveraging our modular and
validated technology and manufacturing platform to advance a pipeline of proprietary gene therapies for the treatment of patients
with Huntington's disease, refractory mesial temporal lobe epilepsy, amyotrophic lateral sclerosis (ALS), Fabry disease, and other severe
diseases. www.uniQure.com
uniQure Forward-Looking Statements
This press release contains forward-looking
statements. All statements other than statements of historical fact are forward-looking statements, which are often indicated by terms
such as "anticipate," "believe," "could," "establish," "estimate," "expect,"
"goal," "intend," "look forward to", "may," "plan," "potential," "predict,"
"project," "seek," "should," "will," "would" and similar expressions. Forward-looking
statements are based on management's beliefs and assumptions and on information available to management only as of the date of this press
release. Examples of these forward-looking statements include, but are not limited to, statements concerning the Company's cash
runway and its ability to fund its operations into the second quarter of 2027; the Company's expected cost savings related to its
strategic reorganization; the Company's plans to announce additional follow up data from the ongoing U.S. and European Phase I/II
clinical studies of AMT-130; the 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; and the Company's plans to initiate patient enrollment for
AMT-260, AMT-162 and AMT-191 in the first half of 2024. The Company's actual results could differ materially from those anticipated
in these forward-looking statements for many reasons. These risks and uncertainties include, among others: risks associated with
the clinical results and the development and timing of the Company's programs; the Company's interactions with regulatory
authorities, which may affect the initiation, timing and progress of clinical trials and pathways to approval; the Company's ability
to continue to build and maintain the company infrastructure and personnel needed to achieve its goals; the Company's effectiveness
in managing current and future clinical trials and regulatory processes; the continued development and acceptance of gene therapies; the
Company's ability to demonstrate the therapeutic benefits of its gene therapy candidates in clinical trials; the Company's
ability to obtain, maintain and protect intellectual property; the Company's ability to fund its operations and to raise additional
capital as needed; and the impact of global economic uncertainty, rising inflation, rising interest rates or market disruptions on its
business. These risks and uncertainties are more fully described under the heading "Risk Factors" in the Company's periodic
filings with the U.S. Securities & Exchange Commission ("SEC"), including its Annual Report on Form 10-K filed
February 28, 2024 and in other filings that the Company makes with the SEC from time to time. Given these risks, uncertainties and
other factors, you should not place undue reliance on these forward-looking statements, and the Company assumes no obligation to update
these forward-looking statements, even if new information becomes available in the future.
FOR INVESTORS: FOR MEDIA:
Maria E. Cantor Chiara Russo Tom Malone
Direct: 339-970-7536 Direct: 617-306-9137 Direct: 339-970-7558
Mobile: 617-680-9452 Mobile: 617-306-9137 Mobile:339-223-8541
m.cantor@uniQure.com c.russo@uniQure.com t.malone@uniQure.com
UNAUDITED CONSOLIDATED BALANCE SHEETS
December 31, December 31,
2023 2022
(in thousands, except share and per share amounts)
Current assets
Cash and cash equivalents $ 241,360 $ 228,012
Current investment securities 376,532 124,831
Accounts receivable and contract asset 4,193 102,376
Inventories, net 12,024 6,924
Prepaid expenses 15,089 11,817
Other current assets and receivables 2,655 2,814
Total current assets 651,853 476,774
Non-current assets
Property, plant and equipment, net 46,548 50,532
Non-current investment securities - 39,984
Operating lease right-of-use assets 28,789 32,726
Intangible assets, net 60,481 58,778
Goodwill 26,379 25,581
Deferred tax assets, net 12,276 14,528
Other non-current assets 5,363 6,061
Total non-current assets 179,836 228,190
Total assets $ 831,689 $ 704,964
Current liabilities
Accounts payable $ 6,586 $ 10,984
Accrued expenses and other current liabilities $ 30,534 $ 30,571
Current portion of contingent consideration 28,211 25,982
Current portion of operating lease liabilities 8,344 8,382
Total current liabilities 73,675 75,919
Non-current liabilities
Long-term debt 101,749 102,791
Liability from royalty financing agreement 394,241 -
Operating lease liabilities, net of current portion 28,316 31,719
Contingent consideration, net of current portion 14,795 9,334
Deferred tax liability, net 7,543 8,257
Other non-current liabilities 3,700 935
Total non-current liabilities 550,344 153,036
Total liabilities 624,019 228,955
Shareholders' equity
Total shareholders' equity 207,670 476,009
Total liabilities and shareholders' equity $ 831,689 $ 704,964
UNAUDITED CONSOLIDATED STATEMENTS OF OPERATIONS
Years ended December 31,
2023 2022 2021
(in thousands, except share and per share amounts)
License revenues $ 2,758 $ 100,000 $ 517,400
Contract manfuacturing revenues 10,835 1,717 -
Collaboration revenues 2,250 4,766 6,602
Total revenues 15,843 106,483 524,002
Operating expenses:
Cost of license revenues (65 ) (1,254 ) (24,976 )
Cost of contract manufacturing revenues (13,563 ) (2,089 ) -
Research and development expenses (214,864 ) (197,591 ) (143,548 )
Selling, general and administrative expenses (74,591 ) (55,059 ) (56,290 )
Total operating expenses (303,083 ) (255,993 ) (224,814 )
Other income 6,059 7,171 12,306
Other expense (1,690 ) (820 ) (876 )
(Loss) / income from operations (282,871 ) (143,159 ) 310,618
Non-operating items, net (23,686 ) 14,900 22,188
(Loss) / income before income tax (expense) / benefit $ (306,557 ) $ (128,259 ) $ 332,806
Income tax (expense) / benefit (1,921 ) 1,470 (3,217 )
Net (loss) / income $ (308,478 ) $ (126,789 ) $ 329,589
Earnings per ordinary share - basic
Basic net (loss) / income per ordinary share $ (6.47 ) $ (2.71 ) $ 7.17
Earnings per ordinary share - diluted
Diluted net (loss) / income per ordinary share $ (6.47 ) $ (2.71 ) $ 7.04
Weighted average shares - basic 47,670,986 46,735,045 45,986,467
Weighted average shares - diluted 47,670,986 46,735,045 46,840,972

Frequently Asked Questions

What clinical trials is uniQure focusing on in 2024?

uniQure plans to initiate Phase I/II trials for mTLE, Fabry disease, and SOD1-ALS in 2024.

What is the financial outlook for uniQure through 2027?

As of December 31, 2023, uniQure's cash will fund operations into the second quarter of 2027.

What were uniQure's revenues in 2023?

uniQure's revenues for 2023 were $15.8 million, down from $106.5 million in 2022.

How much did uniQure lose in 2023?

uniQure reported a net loss of $308.5 million for the year ended December 31, 2023.

What are uniQure's plans for AMT-130?

uniQure aims to clarify the approval pathway for AMT-130 and engage regulators in 2024.

Last updated: Feb 28, 2024