Gravity Analytica

Ascendis Pharma Reports Third Quarter 2024 Financial Results

ASND 11.14.2024

SERA-AI Powered Highlights

Drug:TransCon PTH YORVIPATH

Drug:TransCon hGH SKYTROFA

Drug:TransCon CNP TransCon CNP

Diseases:achondroplasia

Date of Upcoming Event:2024-11-14

Name of Upcoming Event:unknown

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– YORVIPATH launching inU.S.with product availability expectedmid-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 Nordiskcollaboration 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 at4:30 pm ET

COPENHAGEN, Denmark,Nov. 14, 2024(GLOBE NEWSWIRE) --Ascendis Pharma A/S(Nasdaq: ASND) today announced financial results for the third quarter endedSeptember 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 theU.S.with product availability expected in mid-January of 2025,” saidJan Mikkelsen, Ascendis Pharma’s President and Chief Executive Officer. “In addition, our new partnership withNovo Nordiskhighlights 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 toJanuary 1, 2024totaled €9.3 million.
- 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 inU.S.with our expandedU.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 inmid-January 2025
- Third quarter YORVIPATH revenue outside theU.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 inGermanyis 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 theEuropean Medicines Agencyduring 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 β/γ 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 β⁄γ.
Strategic Collaboration
- In November, granted Novo Nordisk A/S an exclusive, multi-product, worldwide license to the TransCon technology platform to develop, manufacture and commercializeNovo Nordiskproprietary 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 millionin 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 ofSeptember 30, 2024,Ascendis Pharmahad cash, cash equivalents, and marketable securities, totaling €626 million, compared to €399 million as ofDecember 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 ResultsTotal 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 EndedSeptember 30,		Nine Months EndedSeptember 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.

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

Conference Call and Webcast InformationAscendis Pharmawill host a conference call and webcast today at4:30 pm Eastern Time(ET) to discuss its third quarter 2024 financial results.

Those who would like to participate may access the live webcasthere, or register in advance for the teleconferencehere. The link to the live webcast will also be available on the Investors & News section of theAscendis Pharmawebsite athttps://investors.ascendispharma.com. A replay of the webcast will be available on this section of theAscendis Pharmawebsite shortly after conclusion of the event for 30 days.

AboutAscendis Pharma A/SAscendis Pharmais 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 inCopenhagen, Denmarkand has additional facilities inEuropeandthe United States. Please visitascendispharma.comto learn more.

Forward-Looking StatementsThis 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) theU.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 theNovo Nordiskcollaboration; (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 inGermany; (xi) the timing of topline Week 26 data from COACH, the combination TransCon hGH and TransCon CNP trial of children with achondroplasia; (xii) Ascendis’ revenues from theNovo Nordiskcollaboration; (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 theU.S. Securities and Exchange Commission(SEC) onFebruary 7, 2024, and Ascendis’ other future reports filed with, or submitted to, theSEC. 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, theAscendis Pharmalogo, the company logo, TransCon, SKYTROFA^®, and YORVIPATH^®are trademarks owned by theAscendis Pharmagroup.©November 2024Ascendis 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


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 EndedSeptember 30,						Nine Months EndedSeptember 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	)

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 inApril 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

Source: Ascendis Pharma

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