UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

 

FORM 6-K

 

 

REPORT OF FOREIGN PRIVATE ISSUER

PURSUANT TO SECTION 13a-16 OR 15d-16

UNDER THE SECURITIES EXCHANGE ACT OF 1934

For the month of November, 2024

Commission File Number: 001-36815

 

 

Ascendis Pharma A/S

(Exact Name of Registrant as Specified in Its Charter)

 

 

Tuborg Boulevard 12

DK-2900 Hellerup

Denmark

(Address of principal executive offices)

 

 

Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F.

Form 20-F ☒   Form 40-F ☐

Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(1): ☐

Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(7): ☐

 

 

 


Furnished as an exhibit to this Report on Form 6-K is a press release reporting the financial results of Ascendis Pharma A/S for the fiscal quarter ended September 30, 2024.

Exhibits

 

Exhibit
No.
   Description
99.1    Press Release dated November 14, 2024.


SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

    Ascendis Pharma A/S
Date: November 14, 2024     By:   /s/ Michael Wolff Jensen
      Michael Wolff Jensen
      Executive Vice President, Chief Legal Officer

Exhibit 99.1

 

 

LOGO

PRESS RELEASE

Ascendis Pharma Reports Third Quarter 2024 Financial Results

– YORVIPATH launching in U.S. with product availability expected mid-January 2025; ex-U.S. YORVIPATH revenue of €8.5 million in Q3

– TransCon CNP NDA submission for achondroplasia planned for Q1 2025 followed by MAA submission planned for Q3 2025

– SKYTROFA Q3 revenue of €47.2 million – 60%+ year-over-year volume growth offset by current and prior period sales deductions

– Full year 2024 SKYTROFA revenue excluding sales deductions related to prior years expected to be €200 - €220 million, and full year 2024 operating expenses of approximately €600 million

– Novo Nordisk collaboration for the development of product candidates in metabolic and cardiovascular diseases, including a once-monthly GLP-1 receptor agonist, signed last week, seeking to close before the end of 2024

– Conference call today at 4:30 pm ET

COPENHAGEN, Denmark, November 14, 2024 (GLOBE NEWSWIRE) – Ascendis Pharma A/S (Nasdaq: ASND) today announced financial results for the third quarter ended September 30, 2024, and provided a business update.

“2024 has been another transformative year for Ascendis. Now, all three of our three endocrinology rare disease programs have delivered clinically differentiated pivotal data, each demonstrating potential ability to address major unmet medical needs and the potential for each to achieve blockbuster status. We are ready and very excited about launching YORVIPATH in the U.S. with product availability expected in mid-January of 2025,” said Jan Mikkelsen, Ascendis Pharma’s President and Chief Executive Officer. “In addition, our new partnership with Novo Nordisk highlights our ability to extend the success of our TransCon platform and positions Ascendis to benefit patients and capture significant value in this large, high volume therapeutic areas.”

Select Highlights & Anticipated 2024 Milestones

 

   

TransCon hGH:

(lonapegsomatropin, marketed as SKYTROFA)

 

   

SKYTROFA revenue for the third quarter of 2024 totaled €47.2 million compared to €47.0 million during the same period in 2023. Volume growth was offset by higher sales deductions and a negative adjustment to prior period sales deductions of €2.5 million.

 

   

SKYTROFA revenue for the first nine months of 2024 totaled €138.5 million, a 21% year-over-year increase compared to €114.4 million during the same period of 2023. Volume growth was partially offset by higher sales deductions. In addition, sales deductions attributable to periods prior to January 1, 2024 totaled €9.3 million.

 

Page 1 of 7


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Submitted U.S. Food & Drug Administration (FDA) supplemental Biologics License Application for TransCon hGH for the treatment of adults with growth hormone deficiency.

 

   

Topline results from Phase 2 New InsiGHTS Trial in Turner syndrome expected in the fourth quarter of 2024.

 

   

Expect to initiate a basket trial evaluating SKYTROFA in other established daily growth hormone indications in the first half of 2025.

 

   

TransCon PTH

(palopegteriparatide, marketed as YORVIPATH)

 

   

YORVIPATH launching in U.S. with our expanded U.S. field teams engaging with health care providers, our Ascendis Signature Access Program accepting prescriptions and enrolling patients starting in December in preparation for product availability in mid-January 2025

 

   

Third quarter YORVIPATH revenue outside the U.S. totaled €8.5 million, a sequential quarter-over-quarter revenue increase of more than 60%, reflecting growing physician and patient demand with now over 600 patients on treatment, partially offset by accruals reflecting the end of the free pricing period in the third quarter. Final pricing in Germany is expected to be completed next year.

 

   

TransCon CNP

(navepegritide)

 

   

Announced positive topline data from pivotal ApproaCH Trial with children with achondroplasia (ages 2-11 years) treated with once-weekly TransCon CNP.

 

   

Plan to submit New Drug Application (NDA) to the FDA for TransCon CNP for the treatment of children with achondroplasia during the first quarter of 2025 and a Marketing Authorisation Application (MAA) for the treatment of children with achondroplasia to the European Medicines Agency during the third quarter of 2025.

 

   

Expect topline Week 26 data from COACH, the combination TransCon hGH and TransCon CNP trial of children with achondroplasia (ages 2-11 years) in the second quarter of 2025.

 

   

Oncology Programs

 

   

Presented first results from platinum-resistant ovarian cancer (PROC) cohort of the Phase 1/2 IL-Believe Trial at ESMO 2024. Initial data suggest clinical activity in heavily pre-treated PROC patients and that TransCon IL-2 ß/g in combination with chemotherapy was generally well-tolerated.

 

   

Recently, we closed enrollment to dose expansion cohorts involving TransCon TLR7/8 Agonist in the transcendIT-101 and IL Believe trials to prioritize our efforts on TransCon IL-2 ß/g.

 

Page 2 of 7


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Strategic Collaboration

 

   

In November, granted Novo Nordisk A/S an exclusive, multi-product, worldwide license to the TransCon technology platform to develop, manufacture and commercialize Novo Nordisk proprietary products in metabolic diseases and a product-by-product exclusive license in cardiovascular diseases. The lead program in the collaboration is a once-monthly GLP-1 receptor agonist product candidate that will initially target obesity and type 2 diabetes.

 

   

For the lead program, Ascendis will be eligible to receive total payments of up to $285 million in upfront, development, and regulatory milestone payments, plus sales-based milestone payments and escalating tiered, mid-single digit royalties on global net sales.

 

   

Novo Nordisk will be responsible for Ascendis’ early development costs as well as for clinical development, regulatory, commercial manufacturing, and commercialization activities.

 

   

Financial Update and Outlook Based on Current Plans

 

   

As of September 30, 2024, Ascendis Pharma had cash, cash equivalents, and marketable securities, totaling €626 million, compared to €399 million as of December 31, 2023.

 

   

Full year 2024 SKYTROFA revenue excluding sales deductions related to prior years expected to be €200 - €220 million.

 

   

Expect total operating expenses (SG&A and R&D) to be approximately €600 million for 2024.

Third Quarter 2024 Financial Results

Total revenue for the third quarter of 2024 was €57.8 million, compared to €48.0 million during the same period for 2023. The year-over-year increase in total revenue was primarily attributable to revenue contribution of €8.5 million from YORVIPATH following commercial launch in the first quarter of 2024. Non-product revenue was €2.1 million in the third quarter of 2024, compared to €1.1 million for the same period for 2023.

 

Total Revenue
(In EUR’000s)
   Three Months Ended
September 30,
     Nine Months Ended
September 30,
 
     2024      2023      2024      2023  

Revenue from external customers

           

Commercial sale of products

     55,710        46,968        153,598        114,414  

Licenses

     851        571        26,490        1,774  

Other

     1,272        495        9,637        12,828  
  

 

 

    

 

 

    

 

 

    

 

 

 

Total revenue from external customers

     57,833        48,034        189,725        129,016  
  

 

 

    

 

 

    

 

 

    

 

 

 

Research and development (R&D) costs for the third quarter of 2024 were €73.5 million, compared to €111.4 million during the same period in 2023. The decline was largely tied to lower external development costs across for TransCon hGH, TransCon PTH, and TransCon CNP as well as the Eyconis spin-off.

Selling, general, and administrative (SG&A) expenses for the third quarter of 2024 were €69.8 million, compared to €63.6 million during the same period in 2023. The increase was primarily due to higher employee costs, including the impact from commercial expansion.

Total operating expenses for the third quarter of 2024 were €143.4 million compared to €175.1 million during the same period in 2023.

 

Page 3 of 7


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Net finance income for the third quarter of 2024 was €2.9 million compared to a net finance expense of €20.4 million during the same period in 2023. The change was primarily tied the impact of currency fluctuations.

For the third quarter of 2024, Ascendis Pharma reported a net loss of €99.2 million, or €1.72 per share (basic and diluted) compared to a net loss of €162.2 million, or €2.88 per share (basic and diluted) for the same period in 2023.

As of September 30, 2024, Ascendis Pharma had cash, cash equivalents, and marketable securities totaling €625.5 million compared to €399.4 million as of December 31, 2023. As of September 30, 2024, Ascendis Pharma had 60,642,144 ordinary shares outstanding, including 881,730 ordinary shares represented by ADSs held by the company.

Conference Call and Webcast Information

Ascendis Pharma will host a conference call and webcast today at 4:30 pm Eastern Time (ET) to discuss its third quarter 2024 financial results.

Those who would like to participate may access the live webcast here, or register in advance for the teleconference here. The link to the live webcast will also be available on the Investors & News section of the Ascendis Pharma website at https://investors.ascendispharma.com. A replay of the webcast will be available on this section of the Ascendis Pharma website shortly after conclusion of the event for 30 days.

About Ascendis Pharma A/S

Ascendis Pharma is applying its innovative TransCon technology platform to build a leading, fully integrated biopharma company focused on making a meaningful difference in patients’ lives. Guided by its core values of Patients, Science, and Passion, Ascendis uses its TransCon technologies to create new and potentially best-in-class therapies. Ascendis is headquartered in Copenhagen, Denmark and has additional facilities in Europe and the United States. Please visit ascendispharma.com to learn more.

Forward-Looking Statements

This press release contains forward-looking statements that involve substantial risks and uncertainties. All statements, other than statements of historical facts, included in this press release regarding Ascendis’ future operations, plans and objectives of management are forward-looking statements. Examples of such statements include, but are not limited to, statements relating to (i) the U.S. launch of YORVIPATH; (ii) the timing of NDA and MAA submissions for TransCon CNP; (iii) projections for full year 2024 SKYTROFA revenue and operating expenses; (iv) the closing of the Novo Nordisk collaboration; (v) the ability of Ascendis’ three endocrinology rare disease programs to address major unmet medical needs and achieve blockbuster status; (vi) Ascendis’ ability to extend the success of its TransCon platform and capture significant value in the areas of metabolic and cardiovascular disease; (vii) the timing of topline results from Phase 2 New InsiGHTS Trial in Turner syndrome; (viii) the initiation of a basket trial evaluating SKYTROFA in other daily growth hormone indications; (ix) the timing by which the Ascendis Signature Access Program will begin accepting prescriptions and enrolling patients; (x) the timing of final YORVIPATH pricing in Germany; (xi) the timing of topline Week 26 data from COACH, the combination TransCon hGH and TransCon CNP trial of children with achondroplasia; (xii) Ascendis’

 

Page 4 of 7


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revenues from the Novo Nordisk collaboration; (xiii) Novo Nordisk’s responsibilities under the collaboration; (xiv) Ascendis’ ability to apply its TransCon technology platform to build a leading, fully integrated biopharma company, and (xv) Ascendis’ use of its TransCon technologies to create new and potentially best-in-class therapies. Ascendis may not actually achieve the plans, carry out the intentions or meet the expectations or projections disclosed in the forward-looking statements and you should not place undue reliance on these forward-looking statements. Actual results or events could differ materially from the plans, intentions, expectations and projections disclosed in the forward-looking statements. Various important factors could cause actual results or events to differ materially from the forward-looking statements that Ascendis makes, including the following: dependence on third party manufacturers, distributors and service providers for Ascendis’ products and product candidates; unforeseen safety or efficacy results in Ascendis’ development programs or on-market products; unforeseen expenses related to commercialization of any approved Ascendis products; unforeseen expenses related to Ascendis’ development programs; unforeseen selling, general and administrative expenses, other research and development expenses and Ascendis’ business generally; delays in the development of its programs related to manufacturing, regulatory requirements, speed of patient recruitment or other unforeseen delays; Ascendis’ ability to obtain additional funding, if needed, to support its business activities; the impact of international economic, political, legal, compliance, social and business factors. For a further description of the risks and uncertainties that could cause actual results to differ from those expressed in these forward-looking statements, as well as risks relating to Ascendis’ business in general, see Ascendis’ Annual Report on Form 20-F filed with the U.S. Securities and Exchange Commission (SEC) on February 7, 2024, and Ascendis’ other future reports filed with, or submitted to, the SEC. Forward-looking statements do not reflect the potential impact of any future licensing, collaborations, acquisitions, mergers, dispositions, joint ventures, or investments that Ascendis may enter into or make. Ascendis does not assume any obligation to update any forward-looking statements, except as required by law.

Ascendis, Ascendis Pharma, the Ascendis Pharma logo, the company logo, TransCon, SKYTROFA®, and YORVIPATH® are trademarks owned by the Ascendis Pharma group. ©

November 2024 Ascendis Pharma A/S.

 

Investor Contacts:    Media Contact:   
Scott Smith    Melinda Baker   
Ascendis Pharma    Ascendis Pharma   
ir@ascendispharma.com    +1 (650) 709-8875   
   media@ascendispharma.com   

Patti Bank

ICR Healthcare

+1 (415) 513-1284

patti.bank@icrhealthcare.com

 

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FINANCIAL TABLES FOLLOW

Ascendis Pharma A/S

Consolidated Statements of Profit or (Loss) and Comprehensive Income / (Loss)

 

(In EUR’000s, except share and per share data)    Three Months Ended
September 30,
    Nine Months Ended
September 30,
 
     2024     2023     2024     2023  

Consolidated Statement of Profit or (Loss)

        

Revenue

     57,833       48,034       189,725       129,016  

Cost of sales

     11,201       7,388       30,235       24,938  
  

 

 

   

 

 

   

 

 

   

 

 

 

Gross profit

     46,632       40,646       159,490       104,078  

Research and development costs

     73,544       111,439       227,708       322,573  

Selling, general and administrative expenses

     69,831       63,614       210,928       200,435  
  

 

 

   

 

 

   

 

 

   

 

 

 

Operating profit/(loss)

     (96,743     (134,407     (279,146     (418,930

Share of profit/(loss) of associate

     (4,367     (6,794     (15,485     (15,471

Finance income

     28,279       4,142       29,262       76,985  

Finance expenses

     25,347       24,519       70,488       35,640  
  

 

 

   

 

 

   

 

 

   

 

 

 

Profit/(loss) before tax

     (98,178     (161,578     (335,857     (393,056

Income taxes/(expenses)

     (1,020     (645     (3,758     (1,513
  

 

 

   

 

 

   

 

 

   

 

 

 

Net profit/(loss) for the period

     (99,198     (162,223     (339,615     (394,569
  

 

 

   

 

 

   

 

 

   

 

 

 

Attributable to owners of the Company

     (99,198     (162,223     (339,615     (394,569
  

 

 

   

 

 

   

 

 

   

 

 

 

Basic and diluted earnings/(loss) per share

   (1.72   (2.88   (5.93   (7.02

Number of shares used for calculation (basic and diluted)

     57,535,349       56,272,698       57,255,764       56,194,956  
  

 

 

   

 

 

   

 

 

   

 

 

 

Consolidated Statement of Comprehensive Income or (Loss)

        

Net profit/(loss) for the period

     (99,198     (162,223     (339,615     (394,569

Items that may be reclassified subsequently to profit or (loss):

        

Exchange differences on translating foreign operations

     154       571       232       (1,232
  

 

 

   

 

 

   

 

 

   

 

 

 

Other comprehensive income/(loss) for the period, net of tax

     154       571       232       (1,232
  

 

 

   

 

 

   

 

 

   

 

 

 

Total comprehensive income/(loss) for the period, net of tax

     (99,044     (161,652     (339,383     (395,801
  

 

 

   

 

 

   

 

 

   

 

 

 

Attributable to owners of the Company

     (99,044     (161,652     (339,383     (395,801
  

 

 

   

 

 

   

 

 

   

 

 

 

 

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Ascendis Pharma A/S

Consolidated Statements of Financial Position

 

(In EUR’000s)    September 30,
2024
    December 31,
2023
 

Assets

    

Non-current assets

    

Intangible assets

     4,106       4,419  

Property, plant and equipment

     97,522       110,634  

Investment in associates

     16,213       5,686  

Other receivables

     2,202       2,127  
  

 

 

   

 

 

 
     120,043       122,866  
  

 

 

   

 

 

 

Current assets

    

Inventories

     265,433       208,931  

Trade receivables

     33,098       35,874  

Income tax receivables

     1,995       802  

Other receivables

     15,259       19,097  

Prepayments

     32,440       38,578  

Marketable securities

     —        7,275  

Cash and cash equivalents

     625,515       392,164  
  

 

 

   

 

 

 
     973,740       702,721  
  

 

 

   

 

 

 

Total assets

     1,093,783       825,587  
  

 

 

   

 

 

 

Equity and liabilities

    

Equity

    

Share capital

     8,143       7,749  

Distributable equity

     (105,463     (153,446
  

 

 

   

 

 

 

Total equity

     (97,320     (145,697
  

 

 

   

 

 

 

Non-current liabilities

    

Borrowings

     338,930       222,996  

Contract liabilities

     5,000       5,949  

Deferred tax liabilities

     8,716       5,830  
  

 

 

   

 

 

 
     352,646       234,775  
  

 

 

   

 

 

 

Current liabilities

    

Convertible notes, matures in April 2028

    

Borrowings

     422,064       407,095  

Derivative liabilities

     168,346       143,296  
  

 

 

   

 

 

 
     590,410       550,391  

Other current liabilities

    

Borrowings

     27,668       14,174  

Contract liabilities

     1,586       1,184  

Trade payables and accrued expenses

     75,268       94,566  

Other liabilities

     42,241       41,176  

Income tax payables

     1,016       2,299  

Provisions

     100,268       32,719  
  

 

 

   

 

 

 
     248,047       186,118  
  

 

 

   

 

 

 
     838,457       736,509  
  

 

 

   

 

 

 

Total liabilities

     1,191,103       971,284  
  

 

 

   

 

 

 

Total equity and liabilities

     1,093,783       825,587  
  

 

 

   

 

 

 

 

Page 7 of 7


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