6-K

 

 

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 March, 2021

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 Exhibit 99.1 to this Report on Form 6-K is a press release of Ascendis Pharma A/S (the “Company”) dated March 10, 2021, announcing the Company’s financial results for the year ended December 31, 2020.

Exhibits

 

Exhibit
No.

  

Description

99.1    Press Release dated March 10, 2021.


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: March 10, 2021   By:  

/s/ Michael Wolff Jensen

    Michael Wolff Jensen
    Chairman and Senior Vice President, Chief Legal Officer
EX-99.1

Exhibit 99.1

 

LOGO

Ascendis Pharma A/S Reports Full Year 2020 Financial Results

– Preparations for potential launch of first Endocrinology Rare Disease product candidate, TransCon hGH (lonapegsomatropin), continues on track –

– Oncology pipeline advancing into clinical trials beginning with TransCon TLR7/8 Agonist –

– Conference call today at 4:30 p.m. Eastern Time –

COPENHAGEN, Denmark, March 10, 2021 (GLOBE NEWSWIRE) – Ascendis Pharma A/S (Nasdaq: ASND), a biopharmaceutical company that utilizes its innovative TransCon technologies to create product candidates that address unmet medical needs, today announced financial results for the full year ended December 31, 2020.

“2020 was a year to remember for Ascendis as our global workforce delivered on time or ahead of schedule on all of our corporate milestones, advancing Vision 3x3, the company’s strategic roadmap through 2025 to build a leading biopharma company by achieving sustainable growth through multiple approaches,” said Jan Mikkelsen, Ascendis’ President and CEO. “As we look to 2021, we expect to report important clinical updates across our entire investigational product portfolio, including Endocrinology Rare Disease and Oncology, while also achieving key commercial milestones including the anticipated regulatory approval and commercial launch in the United States, and regulatory approval in Europe, of TransCon hGH for pediatric growth hormone deficiency.”

Company Highlights & Progress

 

TransCon hGH (lonapegsomatropin)

 

   

Continued to build the global commercial infrastructure in preparation for the PDUFA date of June 25, 2021, and expected subsequent commercial launch of lonapegsomatropin in the United States in the third quarter of 2021. European Commission decision is anticipated in the fourth quarter of 2021 for pediatric patients with growth hormone deficiency (GHD).

 

   

Reported two year data from the enliGHten long-term extension trial demonstrating children with GHD initially treated with lonapegsomatropin maintained an advantage in height SDS (standard deviation score) improvement.

 

   

Continued execution in the ongoing foresiGHt Trial, a global phase 3 study in adults with GHD, complete enrollment expected by late 2021 or early 2022.

 

   

Submitted Clinical Trial Notification (CTN) to initiate pediatric GHD phase 3 riGHt Trial in Japan.

 

TransCon PTH

 

   

Submitted regulatory filings in North America and Europe to initiate PaTHway, a phase 3 clinical trial evaluating the safety, tolerability and efficacy of TransCon PTH in adults with hypoparathyroidism (HP). Topline results are expected from PaTHway in the fourth quarter of 2021.

 

   

Announced six-month data from the PaTH Forward Trial open-label extension (OLE), which demonstrated TransCon PTH replaced standard of care, normalized quality of life and urinary calcium. These results will be presented in an oral presentation on March 23, 2021 at ENDO 2021.


   

As of March 10, 2021, 58 out of the 59 randomized subjects continue in the phase 2 PaTH Forward clinical trial.

 

   

On track to file CTN to initiate adult HP phase 3 trial in Japan in the second quarter of 2021.

 

TransCon CNP

 

   

Continued dose escalation in the phase 2 ACcomplisH Trial to evaluate the safety and efficacy of TransCon CNP in children ages two to ten with achondroplasia.

 

   

IND approved for the ACcomplisH China Trial, a phase 2 trial to enable dose expansion cohorts, in children ages two to ten, conducted in Greater China by Visen Pharmaceuticals (VISEN).

 

   

Clinical program update on both randomized, double-blind, placebo-controlled trials expected in the fourth quarter of 2021.

 

TransCon TLR7/8 Agonist

 

   

Filed IND application with the FDA to initiate the transcendIT-101 clinical trial.

 

   

Initial results from the first part of transcendIT-101, the monotherapy dose escalation, are expected in the fourth quarter of 2021.

 

   

Expect to initiate the second part of transcendIT-101, dose escalation of TransCon TLR7/8 Agonist in combination with a checkpoint inhibitor, in the second quarter of 2021.

 

TransCon IL-2 ß/g

 

   

New preclinical data demonstrated a single dose of TransCon IL-2 ß/g resulted in durable and robust increases in the ratios of CD8+ T cells and NK cells over Treg cells in non-human primates.

 

   

IND filing or similar planned in the third quarter of 2021.

 

Ended 2020 with cash, cash equivalents and marketable securities totaling €834.1 million.

Full Year 2020 Financial Results

For the full year 2020, Ascendis Pharma reported a net loss of €419.0 million, or €8.28 per share (basic and diluted) compared to a net loss of €218.0 million, or €4.69 per share (basic and diluted) for the same period in 2019.

Revenue for 2020 was €7.0 million compared to €13.4 million in 2019. The decrease was due to lower license and service revenue, partly offset by sale of clinical supply, to VISEN.

Research and development (R&D) costs for 2020 were €260.9 million compared to €191.6 million in 2019. Higher R&D costs in 2020 reflect an increase in personnel-related costs, expansion of R&D facilities and the continued progress in development of the company’s product candidates.

Selling, general and administrative expenses for 2020 were €76.7 million compared to €48.5 million in 2019. The increase is primarily due to higher personnel-related costs, higher IT costs and continued build out of the company’s commercial capabilities.

Net loss in associate was €9.5 million for 2020 compared to €8.1 million in 2019, representing the company’s share of net result from VISEN.

Net finance expenses were €79.0 million for 2020 compared to net finance income of €16.6 million in 2019, primarily reflecting negative exchange rate fluctuations compared to 2019 when the company recognized a gain.

 

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As of December 31, 2020, Ascendis Pharma had cash, cash equivalents and marketable securities totaling €834.1 million compared to €598.1 million at the beginning of the year. As of December 31, 2020, Ascendis Pharma had 53,750,386 ordinary shares outstanding.

Conference Call and Webcast information

Ascendis Pharma will host a conference call and webcast today at 4:30 p.m. Eastern Time (ET) to discuss its full year 2020 financial results. Details include:

 

Date

  

March 10, 2021

Time

  

4:30 p.m. ET / 1:30 p.m. PT

Dial In (U.S.)

   844-290-3904

Dial In (International)

   574-990-1036

Access Code

   1996657

A live webcast of the conference call will be available on the Investors and News section of the Ascendis Pharma website at www.ascendispharma.com. A webcast replay will also be available on this website shortly after conclusion of the event for 30 days.

About Ascendis Pharma’s Pipeline

Ascendis Pharma currently has three product candidates in clinical development in rare endocrine diseases and one oncology product candidate in clinical development:

 

   

TransCon hGH (lonapegsomatropin), an investigational long-acting prodrug of somatropin (human growth hormone or hGH) that releases somatropin with the identical amino acid sequence and size as daily growth hormone, is designed as a once-weekly treatment for GHD and is currently under regulatory review for pediatric GHD by the U.S. Food and Drug Administration and the European Medicines Agency.

 

   

TransCon PTH, an investigational long-acting prodrug of parathyroid hormone (PTH) in phase 3 development as a once-daily replacement therapy for adults with hypoparathyroidism (HP) designed to replace PTH at physiologic levels for 24 hours, and address both short-term symptoms and long-term complications of the disease.

 

   

TransCon CNP, an investigational long-acting prodrug of C-type natriuretic peptide (CNP) in phase 2 development as a therapy for children with achondroplasia (ACH), the most common form of dwarfism, for which there is no FDA-approved treatment. TransCon CNP is designed to provide continuous exposure of CNP at safe, therapeutic levels via a single, weekly subcutaneous dose.

 

   

TransCon TLR7/8 Agonist is an investigational long-acting prodrug of resiquimod, a small molecule agonist of Toll-like receptors (TLR) 7 and 8. Administered as an intratumoral injection, TransCon TLR7/8 Agonist is designed to provide sustained activation of intratumoral antigen presenting cells driving tumor antigen presentation and induction of immune stimulatory cytokines in the tumor.

 

   

TransCon IL-2 ß/g is an investigational long-acting prodrug of IL-2 ß/g designed for optimized IL-2Rß/g bias and potency, combined with low Cmax and long exposure.

 

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About Ascendis Pharma A/S

Ascendis Pharma is applying its innovative TransCon technologies to build a leading, fully integrated biopharmaceutical company focused on making a meaningful difference in patients’ lives. Guided by its core values of patients, science and passion, the company utilizes its TransCon technologies to create new and potentially best-in-class therapies.

Ascendis Pharma currently has a pipeline of three independent endocrinology rare disease product candidates and one oncology product candidate in clinical development. The company continues to expand into additional therapeutic areas to address unmet patient needs.

Ascendis is headquartered in Copenhagen, Denmark, with additional offices in Heidelberg and Berlin, Germany, Palo Alto and Redwood City, California, and Princeton, New Jersey.

Please visit www.ascendispharma.com (for global information) or www.ascendispharma.us (for U.S. information.)

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) Ascendis’ expectations regarding Ascendis’ strategic roadmap through 2025 to build a leading biopharma company by achieving sustainable growth, (ii) Ascendis’ expectations regarding potential commercial launch of lonapegsomatropin, (iii) Ascendis’ 2020 corporate goals and Vision 3x3, (iv) Ascendis’ PDUFA date for its Biologics License Application for lonapegsomatropin, (v) Ascendis’ ability to apply its platform technology to build a leading, fully integrated biopharma company, (vi) Ascendis’ product pipeline and expansion into additional therapeutic areas and (vii) Ascendis’ expectations regarding its ability to utilize 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: unforeseen safety or efficacy results in its oncology programs, lonapegsomatropin, TransCon PTH and TransCon CNP or other development programs; unforeseen expenses related to the development and potential commercialization of its oncology programs, lonapegsomatropin, TransCon PTH and TransCon CNP or other development programs, selling, general and administrative expenses, other research and development expenses and Ascendis’ business generally; delays in the development of its oncology programs, lonapegsomatropin, TransCon PTH and TransCon CNP or other development programs related to manufacturing, regulatory requirements, speed of patient recruitment or other unforeseen delays; dependence on third party manufacturers to supply study drug for planned clinical studies; Ascendis’ ability to obtain additional funding, if needed, to support its business activities and the effects on its business of the worldwide COVID-19 pandemic. 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’ prospectus supplement filed on July 9, 2020 and Ascendis’ current and future reports filed with, or submitted to, the U.S. Securities and Exchange Commission (SEC), including its Annual Report on Form 20-F filed with the SEC on April 3, 2020. Forward-looking statements do not reflect the potential impact of any future in-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.

 

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Ascendis, Ascendis Pharma, the Ascendis Pharma logo, the company logo and TransCon are trademarks owned by the Ascendis Pharma Group. © March 2021 Ascendis Pharma A/S.

 

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FINANCIAL TABLES FOLLOW

Ascendis Pharma A/S

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

(In EUR’000s, except share and per share data)

 

     Year ended December 31,  
     2020     2019  

Revenue

     6,953       13,375  

Research and development costs

     (260,904     (191,621

Selling, general and administrative expenses

     (76,669     (48,473
  

 

 

   

 

 

 

Operating profit / (loss)

     (330,620     (226,719

Share of profit / (loss) of associate

     (9,524     (8,113

Finance income

     1,812       17,803  

Finance expenses

     (80,842     (1,221
  

 

 

   

 

 

 

Profit / (loss) before tax

     (419,174     (218,250

Tax on profit / (loss) for the year

     219       234  
  

 

 

   

 

 

 

Net profit / (loss) for the year

     (418,955     (218,016
  

 

 

   

 

 

 

Attributable to owners of the Company

     (418,955     (218,016
  

 

 

   

 

 

 

Basic and diluted earnings / (loss) per share

   (8.28   (4.69

Number of shares used for calculation (basic and diluted)

     50,616,528       46,506,862  
  

 

 

   

 

 

 

Net profit / (loss) for the year

     (418,955     (218,016

Other comprehensive income / (loss)

    

Items that may be reclassified subsequently to profit or loss:

    

Exchange differences on translating foreign operations

     (42     (37
  

 

 

   

 

 

 

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

     (42     (37
  

 

 

   

 

 

 

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

     (418,997     (218,053
  

 

 

   

 

 

 

Attributable to owners of the Company

     (418,997     (218,053
  

 

 

   

 

 

 

 

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Ascendis Pharma A/S

Consolidated Statements of Financial Position

(In EUR’000s)

 

     December 31,      December 31,  
   2020      2019  

Assets

     

Non-current assets

     

Intangible assets

     5,717        3,495  

Property, plant and equipment

     108,112        45,069  

Investment in associate

     9,176        15,538  

Other receivables

     1,375        1,463  

Marketable securities

     115,280        —    
  

 

 

    

 

 

 
     239,660        65,565  
  

 

 

    

 

 

 

Current assets

     

Trade receivables

     387        804  

Other receivables

     6,957        4,609  

Prepayments

     13,994        7,648  

Marketable securities

     134,278        —    

Cash and cash equivalents

     584,517        598,106  
  

 

 

    

 

 

 
     740,133        611,167  
  

 

 

    

 

 

 

Total assets

     979,793        676,732  
  

 

 

    

 

 

 

Equity and liabilities

     

Equity

     

Share capital

     7,217        6,443  

Distributable equity

     831,494        590,671  
  

 

 

    

 

 

 

Total equity

     838,711        597,114  
  

 

 

    

 

 

 

Non-current liabilities

     

Lease liabilities

     85,116        30,720  

Other liabilities

     3,162        908  
  

 

 

    

 

 

 
     88,278        31,628  
  

 

 

    

 

 

 

Current liabilities

     

Lease liabilities

     6,859        5,899  

Contract liabilities

     363        858  

Trade payables and accrued expenses

     21,897        27,765  

Other liabilities

     23,384        13,349  

Income taxes payable

     301        119  
  

 

 

    

 

 

 
     52,804        47,990  
  

 

 

    

 

 

 

Total liabilities

     141,082        79,618  
  

 

 

    

 

 

 

Total equity and liabilities

     979,793        676,732  
  

 

 

    

 

 

 

 

Investor contacts:

       

Media contact:

Tim Lee       Ron Rogers
Ascendis Pharma       Ascendis Pharma
(650) 374-6343       (650) 507-5208

 

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tle@ascendispharma.com                                                                      rrs@ascendispharma.com

Patti Bank    

Westwicke Partners                

(415) 513-1284                

patti.bank@westwicke.com

ir@ascendispharma.com                

 

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