Log in
E-mail
Password
Show password
Remember
Forgot password ?
Become a member for free
Sign up
Sign up
New member
Sign up for FREE
New customer
Discover our services
Settings
Settings
Dynamic quotes 
OFFON

ASCENDIS PHARMA A/S

(ASND)
  Report
SummaryQuotesChartsNewsRatingsCalendarCompanyFinancialsConsensusRevisions 
SummaryMost relevantAll NewsAnalyst Reco.Other languagesPress ReleasesOfficial PublicationsSector newsMarketScreener Strategies

Ascendis Pharma A/S : Unaudited Condensed Consolidated Interim Statements of Profit or Loss and Comprehensive Income / (Loss) for the Three and Six Months Ended June 30 (Form 6-K)

08/27/2021 | 03:32pm EST
Unaudited Condensed Consolidated Interim Statements of Profit or Loss
and Comprehensive Income / (Loss) for the Three and Six Months Ended June 30
Three Months Ended

June 30
Six Months Ended
June 30
Notes
2021
2020
2021
2020
(EUR'000)
(EUR'000)
Consolidated Interim Statement of Profit or Loss
Revenue
5
1,022 1,436 1,767 3,661
Research and development costs
7
(83,306 ) (63,578 ) (171,455 ) (121,093 )
Selling, general and administrative expenses
7
(35,345 ) (20,805 ) (72,591 ) (38,720 )
Operating profit / (loss)
(117,629
)
(82,947
)
(242,279
)
(156,152
)
Share of profit / (loss) of associate
(4,817 ) (1,885 ) 23,289 (3,400 )
Finance income
145 86 23,268 1,996
Finance expenses
(12,141 ) (10,292 ) (1,703 ) (876 )
Profit / (loss) before tax
(134,442
)
(95,038
)
(197,425
)
(158,432
)
Tax on profit / (loss) for the period
68 106 259 183
Net profit / (loss) for the period
(134,374
)
(94,932
)
(197,166
)
(158,249
)
Attributable to owners of the Company
(134,374 ) (94,932 ) (197,166 ) (158,249 )
Basic and diluted earnings / (loss) per share
€(2.50 ) €(1.97 ) €(3.66 ) €(3.29 )
Number of shares used for calculation (basic and diluted)
(1)
53,848,166 48,207,661 53,804,300 48,096,749
(EUR'000)
(EUR'000)
Consolidated Interim Statement of Comprehensive Income
Net profit / (loss) for the period
(134,374
)
(94,932
)
(197,166
)
(158,249
)
Other comprehensive income / (loss)
Items that may be reclassified subsequently to profit or loss:
Exchange differences on translating foreign operations
77 (147 ) 1,765 (61 )
Other comprehensive income / (loss) for the period, net of tax
77
(147
)
1,765
(61
)
Total comprehensive income / (loss) for the period, net of tax
(134,297
)
(95,079
)
(195,401
)
(158,310
)
Attributable to owners of the Company
(134,297 ) (95,079 ) (195,401 ) (158,310 )
(1)
A total of 6,065,823 warrants outstanding as of June 30, 2021 can potentially dilute earnings per share in the future but have not been included in the calculation of diluted earnings per share because they are antidilutive for the periods presented. Similarly, a total of 5,788,390 warrants outstanding as of June 30, 2020 are also considered antidilutive for the periods presented and have not been included in the calculation.
2
Unaudited Condensed Consolidated Interim Statements of Financial Position
Notes
June 30,
2021
December 31,
2020
(EUR'000)
Assets
Non-current
assets
Intangible assets
5,495 5,717
Property, plant and equipment
123,924 108,112
Investment in associate
45,783 9,176
Deposits
1,702 1,375
Marketable securities
8
90,693 115,280
267,597
239,660
Current assets
Trade receivables
394 387
Other receivables
11,398 6,957
Prepayments
21,826 13,994
Marketable securities
8
166,094 134,278
Cash and cash equivalents
384,539 584,517
584,251
740,133
Total assets
851,848
979,793
Equity and liabilities
Equity
Share capital
9
7,237 7,217
Distributable equity
680,250 831,494
687,487
838,711
Non-current
liabilities
Lease liabilities
10
94,059 85,116
Other payables
- 3,162
94,059
88,278
Current liabilities
Lease liabilities
10
6,950 6,859
Contract liabilities
145 363
Trade payables and accrued expenses
44,207 21,897
Other payables
18,623 23,384
Income taxes payable
377 301
70,302
52,804
Total liabilities
164,361
141,082
Total equity and liabilities
851,848
979,793
3
Unaudited Condensed Consolidated Interim Statements of Changes in Equity
Distributable Equity
Share
Capital
Share
Premium
Foreign
Currency
Translation
Reserve
Share-based
Payment
Reserve
Accumulated
Deficit
Total
(EUR'000)
Equity at January 1, 2021
7,217
1,728,747
(76
)
133,101
(1,030,278
)
838,711
Loss for the period
- - - - (197,166 )
(197,166
)
Other comprehensive income / (loss), net of tax
- - 1,765 - -
1,765
Total comprehensive income / (loss)
-
-
1,765
-
(197,166
)
(195,401
)
Transactions with Owners
Share-based payment (Note 7)
-
-
-
39,396 -
39,396
Capital increase
20 4,761 - - -
4,781
Equity at June 30, 2021
7,237
1,733,508
1,689
172,497
(1,227,444
)
687,487
Distributable Equity
Share
Capital
Share
Premium
Foreign
Currency
Translation
Reserve
Share-based
Payment
Reserve
Accumulated
Deficit
Total
(EUR'000)
Equity at January 1, 2020
6,443
1,122,097
(34
)
79,931
(611,323
)
597,114
Loss for the period
- - - - (158,249 )
(158,249
)
Other comprehensive income / (loss), net of tax
- - (61 ) - -
(61
)
Total comprehensive income / (loss)
- -
(61
)
-
(158,249
)
(158,310
)
Transactions with Owners
Share-based payment (Note 7)
- - - 28,364 -
28,364
Capital increase
48 9,928 - - -
9,976
Equity at June 30, 2020
6,491
1,132,025
(95
)
108,295
(769,572
)
477,144
4
Unaudited Condensed Consolidated Interim Cash Flow Statements for the
Six Months Ended June 30
Six Months Ended
June 30,
2021
2020
(EUR'000)
Operating activities
Net profit / (loss) for the period
(197,166
)
(158,249
)
Reversal of finance income
(23,268 ) (1,996 )
Reversal of finance expenses
1,703 876
Reversal of tax charge
(259 ) (183 )
Adjustments for
non-cash
items:
Reversal of
non-cash
consideration relating to revenue
(1,155 ) (2,215 )
Reversal of share of profit / (loss) of associate
(23,289 ) 3,400
Share-based payment
39,396 28,364
Depreciation
7,112 4,192
Amortization
222 -
Changes in working capital:
Receivables
(4,035 ) (944 )
Prepayments
(7,832 ) (5,385 )
Contract liabilities (deferred income)
(218 ) (858 )
Trade payables and other payables
10,902 8,008
Cash flows generated from / (used in) operations
(197,887
)
(124,990
)
Finance income received
1,915 1,776
Finance expenses paid
(699 ) (798 )
Income taxes re
c
eived / (paid)
(149 ) 615
Cash flows from / (used in) operating activities
(196,820
)
(123,397
)
Investing activities
Investment in associate
(10,187 ) -
Acquisition of property, plant and equipment
(7,607 ) (10,725 )
Development expenditures (software)
(530 ) (311 )
Purchase of marketable securities
(76,358 ) (233,446 )
Settlement of marketable securities
75,600 -
Cash flows from / (used in) investing activities
(19,082
)
(244,482
)
Financing activities
Payment of principal portion of lease liabilities
(3,371 ) (2,306 )
Proceeds from exercise of warrants
4,782 9,976
Cash flows from / (used in) financing activities
1,411
7,670
Increase / (decrease) in cash and cash equivalents
(214,491
)
(360,209
)
Cash and cash equivalents at January 1
584,517 598,106
Effect of exchange rate changes on balances held in foreign currencies
14,513 2,708
Cash and cash equivalents at June 30
384,539
240,605
Cash and cash equivalents include:
Bank deposits
383,073 183,153
Short-term marketable securities
1,466 57,452
Cash and cash equivalents at June 30
384,539
240,605
5
Notes to the Unaudited Condensed Consolidated Interim Financial Statements
Note 1-General Information
Ascendis Pharma A/S, together with its subsidiaries, is a biopharmaceutical company applying its innovative TransCon technologies to build a leading, fully integrated biopharmaceutical company. Ascendis Pharma A/S was incorporated in 2006 and is headquartered in Hellerup, Denmark. Unless the context otherwise requires, references to the 'Company,' 'we,' 'us' and 'our' refer to Ascendis Pharma A/S and its subsidiaries.
The address of the Company's registered office is Tuborg Boulevard 12,
DK-2900,
Hellerup, Denmark.
On February 2, 2015, the Company completed an initial public offering which resulted in the listing of American Depositary Shares, or ADSs, representing the Company's ordinary shares, under the symbol 'ASND' in the United States on The Nasdaq Global Select Market.
The Company's Board of Directors approved these unaudited condensed consolidated interim financial statements on August 25, 2021.
Note 2-Summary of Significant Accounting Policies
Basis of Preparation
The unaudited condensed consolidated interim financial statements of the Company are prepared in accordance with International Accounting Standard 34, 'Interim Financial Reporting.' Certain information and disclosures normally included in the annual consolidated financial statements prepared in accordance with International Financial Reporting Standards ('IFRS') have been condensed or omitted. Accordingly, these unaudited condensed consolidated interim financial statements should be read in conjunction with the Company's audited annual consolidated financial statements for the year ended December 31, 2020 and accompanying notes, which have been prepared in accordance with IFRS as issued by the International Accounting Standards Board, and as adopted by the European Union.
The accounting policies applied are consistent with those of the previous financial year. A description of our accounting policies is provided in the
Accounting Policies section of the audited consolidated financial statements as of and for the year ended December 31, 2020.
The preparation of financial statements in conformity with IFRS requires the use of certain significant accounting estimates and requires management to exercise its judgement in the process of applying the Company's accounting policies. The areas involving a higher degree of judgement or complexity, or areas where assumptions and estimates are significant to the unaudited condensed consolidated interim financial statements are disclosed in Note 3.
New and Amended IFRS Standards Adopted by the Company
Several new amendments and interpretations became applicable for the current reporting period, but do not have an impact on the accounting policies applied by the Company.
6
Notes to the Unaudited Condensed Consolidated Interim Financial Statements
Note 3-Critical Accounting Judgements and Key Sources of Estimation Uncertainty
In the application of the Company's accounting policies, management is required to make judgements, estimates and assumptions about the carrying amount of assets and liabilities that are not readily apparent from other sources. Judgements and estimates applied are based on historical experience and other factors that are relevant, and which are available at the reporting date. Uncertainty concerning judgements and estimates could result in outcomes, that require a material adjustment to assets and liabilities in future periods.
Estimates and underlying assumptions are reviewed on an ongoing basis. Revisions to accounting estimates are recognized in the period in which the estimate is revised if the revision affects only that period, or in the period of the revision and future periods if the revision affects both current and future periods. While the application of significant accounting estimates is subject to material estimation uncertainties, management's ongoing revisions of significant accounting estimates have not revealed any material impact in the consolidated interim statements of profit or loss for any of the periods presented.
The unaudited condensed consolidated interim financial statements do not include all disclosures for significant accounting judgements, estimates and assumptions, that are required in the annual consolidated financial statements, and therefore, should be read in conjunction with the Company's audited consolidated financial statements as of and for the year ended December 31, 2020.
Significant judgements made in the process of applying our accounting policies and that have the most significant effect on the amounts recognized in the unaudited condensed consolidated interim financial statements relate to revenue recognition, share-based payment, internally generated intangible assets related to drug development, classification of collaboration agreements and recognition principles related to
pre-launch
inventories. For the six months ended June 30, 2021, the Company has for the first time, in connection with determining the grant date fair value of warrants and accordingly, warrant compensation costs, applied its own share price as input for expected volatility. Details are provided in section 'Warrant Compensation Costs'. Until December 31, 2020, the expected volatility was calculated using a simple average of daily historical data of comparable publicly traded companies, as the Company did not have sufficient data for the volatility of the Company's own share price.
The key sources of estimation uncertainty that have a significant risk of causing a material adjustment to the carrying amount of assets and liabilities within the next financial year, primarily relate to recognition and measurement of accruals and prepayments for manufacturing and clinical trial activities.
Other than as set out below, there have been no other changes to the application of significant accounting judg
e
ments, or estimation uncertainties regarding accounting estimates compared to December 31, 2020.
Warrant Compensation Costs
IFRS 2, 'Share-Based Payment' requires an entity to reflect in its consolidated statement of profit or loss and financial position, the effects of share-based payment transactions. Warrant compensation costs are recognized over the vesting period as research and development costs or selling, general and administrative expenses, as appropriate, based on management's best estimate of the number of warrants that will ultimately vest, which is subject to uncertainty.
Warrant compensation costs are measured according to the grant date fair values of the warrants granted. Estimating fair values requires the Company to apply generally accepted valuation models and apply these models consistently according to the terms and conditions of the specific warrant program. Under all warrant programs, the Black-Scholes option-pricing model has been applied to determine the fair value of warrants granted. Subjective judgements and assumptions, which are subject to estimation uncertainties, need to be exercised in determining the appropriate input to the valuation model. These inputs include expected volatility of the Company's share price for a historic period equaling the expected lifetime of the warrants, reflecting the assumption that the historical volatility over a period similar to the life of the warrants is indicative of future trends. For the six months ended June 30, 2021, the expected volatility has been calculated using the Company's own share price.
7
Notes to the Unaudited Condensed Consolidated Interim Financial Statements
Note 4-Significant Events in the Reporting Period
Impact from
COVID-19
pandemic
A novel strain of coronavirus,
('COVID-19')
was reported to have surfaced in Wuhan, China, in December 2019. Since then, COVID-19 has spread around the world into a pandemic, including into countries where we are operating, where we have planned or have ongoing clinical trials, and where we rely on third-parties to manufacture preclinical and clinical supplies, as well as commercial supply.
We monitor these risks closely, and work with relevant stakeholders to avoid disruptions, and to develop and establish working measures. However, while
COVID-19
continues to impact global societies, the uncertainty related to the duration and direction of the pandemic makes the future impact from
COVID-19,
including the magnitude of any impact on our operational results, highly uncertain and unpredictable. At the reporting date,
COVID-19
did not have a direct impact on the
consolidated
interim financial statements
.
VISEN Pharmaceuticals Investment
On January 8, 2021, the Company entered into an equity investment of $12.5 million in its associate, VISEN Pharmaceuticals, or VISEN, as part of VISEN's $150 million Series B financing. Following VISEN's Series B financing, the Company retains approximately 44% of VISEN's issued and outstanding shares. As a result, the Company has recognized a
non-cash
gain in the first quarter of 2021 of €42.3 million, which is presented as part of 'Share of profit / (loss) of associate' in the consolidated interim statement of profit or loss. The Series B financing has not changed the Company's accounting treatment of VISEN.
Note 5-Revenue
The Company's revenue is primarily generated from three license agreements, which were entered into in 2018. The licenses grant VISEN exclusive rights to develop and commercialize TransCon hGH, TransCon PTH and TransCon CNP in Greater China. As consideration for the granting of such rights, the Company has received
up-front,
non-refundable,
non-cash
consideration of $40.0 million in the form of 50% ownership in VISEN. At the reporting date, the Company retains approximately 44% of VISEN's issued and outstanding shares.
Consideration received is recognized partly as license revenue, and partly as rendering of services over time. In addition to granting exclusive rights, the Company will provide clinical trial supply and development services to VISEN.
Three Months Ended
June 30,
Six Months Ended
June 30,
2021
2020
2021
2020
(EUR'000)
(EUR'000)
Revenue from external customers
Revenue from the rendering of services (recognized over time)
226 779 395 2,091
Sale of clinical supply (recognized at a point in time)
217 - 217 246
'Right-to-use'
licenses (recognized at a point in time)
579 657 1,155 1,324
Total revenue
(1)
1,022
1,436
1,767
3,661
Attributable to
VISEN Pharmaceuticals
913 1,436 1,550 3,661
Other collaboration partners
109 - 217 -
Total revenue
1,022
1,436
1,767
3,661
Revenue by geographical location
North America
688 657 1,373 1,324
China
334 779 394 2,337
Total revenue
1,022
1,436
1,767
3,661
(1)
For the three months ended June 30, 2021 and 2020, and for the six months ended June 30, 2021 and 2020, 'Total revenue' includes recognition of previously deferred revenue/internal profit from associate of €579 thousand and €1,013 thousand, and of €1,155 thousand and €2,215 thousand, respectively.
Note 6-Segment Information
The Company is managed and operated as one business unit. No separate business areas or separate business units have been identified in relation to product candidates or geographical markets. Accordingly, no additional information on business segments or geographical areas is disclosed.
8
Notes to the Unaudited Condensed Consolidated Interim Financial Statements
Note 7-Warrants and Share-based Payment
Share-based
Payment
Ascendis Pharma A/S has established warrant programs and equity-settled share-based payment transactions, as an incentive for all its employees, members of its Board of Directors and select external consultants.
Warrants are granted by the Company's Board of Directors in accordance with authorizations given to it by the shareholders of the Company. As of June 30, 2021, 11,023,308 warrants have been granted, of which 19,580 warrants have been cancelled, 4,327,249 warrants have been exercised, 2,168 warrants have expired without being exercised, and 608,488 warrants have been forfeited. As of June 30, 2021, the Company's Board of Directors was authorized to grant up to 2,603,979 additional warrants to employees, board members and select consultants without preemptive subscription rights for the shareholders of the Company. Each warrant carries the right to subscribe for one ordinary share of a nominal value of DKK 1. The exercise price is fixed at the fair market value of the Company's ordinary shares at the time of grant as determined by the Company's Board of Directors. The exercise prices of outstanding warrants under the Company's warrant programs range from €6.48 to €145.5 depending on the grant dates. Vested warrants may be exercised in two or four annual exercise periods. Apart from exercise prices and exercise periods, the programs are similar.
Warrant Activity
The following table specifies the warrant activity during the six months ended June 30, 2021:
Total

Warrants
Weighted Average
Exercise Price
EUR
Outstanding at January 1, 2021
6,148,004
69.97
Granted during the period
158,590 120.15
Exercised during the period
(150,604 ) 33.51
Forfeited during the period
(90,167 ) 121.80
Outstanding at June 30, 2021
6,065,823
71.04
Vested at June 30, 2021
3,565,573
46.23
Warrant Compensation Costs
Warrant compensation costs are determined with a basis in the grant date fair value of the warrants granted and recognized over the vesting period as research and development costs or as selling, general and administrative expenses. For the three months ended June
30
, 2021 and 2020, and for the six months ended June 30, 2021 and 2020, warrant compensation costs recognized in the consolidated interim statement of profit or loss was €16,320 thousand and €13,415 thousand, and €39,396 thousand and €28,364 thousand, respectively.
9
Notes to the Unaudited Condensed Consolidated Interim Financial Statements
Note 8-Marketable Securities
Marketable securities are measured at amortized cost, and fair values are determined based on quoted market prices (Level 1 in the fair value hierarchy).
The composition of the portfolio is specified in the following table
.
June 30, 2021
December 31, 2020
Carrying amount
Fair value
Carrying amount
Fair value
(EUR'000)
Marketable securities
U.S. Treasury bills
- - 46,243 46,245
U.S. Government bonds
85,049 85,049 62,088 62,101
Commercial papers
8,832 8,833 10,583 10,581
Corporate bonds
144,830 144,734 121,282 121,234
Agency bonds
18,076 18,077 9,362 9,369
Total marketable securities
256,787
256,693
249,558
249,530
Classified based on maturity profiles
Non-current
assets
90,693 90,623 115,280 115,277
Current assets
166,094 166,070 134,278 134,253
Total marketable securities
256,787
256,693
249,558
249,530
Specified by rate structure
Fixed rate
231,342 231,249 175,757 175,732
Floating rate
16,613 16,611 16,975 16,972
Zero-coupon
8,832 8,833 56,826 56,826
Total marketable securities
256,787
256,693
249,558
249,530
Specified by investment grade credit rating
Prime
6,398 6,398 7,716 7,714
High grade
127,690 127,678 142,339 142,352
Upper medium grade
119,785 119,706 99,503 99,464
Lower medium grade
2,914 2,911 - -
Total marketable securities
256,787
256,693
249,558
249,530
The Company's marketable securities are all denominated in U.S. Dollars. At June 30, 2021, the portfolio has a weighted average duration of 6.6 and 17.5 months, for current and
non-current
positions, respectively. The entire portfolio has a weighted average duration of 10.4 months.
All marketable securities have investment grade ratings, and accordingly, the risk from probability of default is low. The risk of expected credit loss over marketable securities has been considered, including the hypothetical impact arising from the probability of default which is considered in conjunction with the expected loss given default from securities with similar credit ratings and attributes. This assessment did not reveal a material expected credit loss, and accordingly, no provision for expected credit loss has been recognized.
10
Notes to the Unaudited Condensed Consolidated Interim Financial Statements
Note 9-Share Capital
The share capital of Ascendis Pharma A/S consists of 53,900,990 outstanding shares at a nominal value of DKK 1, all in the same share class.
Note 10 -Lease Liabilities
The Company primarily leases office and laboratory facilities. Lease arrangements contain a range of different terms and conditions and are typically entered into for fixed periods. Generally, the lease terms are determined according to the
non-cancellable
period and are between twoand twelve years. In addition, in order to improve flexibility to the Company's operations, lease terms may provide the Company with options to extend the lease or to terminate the lease within the enforceable lease term. In the Company's current lease portfolio, extension and termination options range between twoto ten years, in addition to the
non-cancellable
period.
Maturity analysis for lease liabilities recognized in the consolidated statements of financial position at June 30, 2021 is specified below.
1-5 years
>5 years
Total
contractual
cash-flows
Carrying
amount
(EUR'000)
June 30, 2021
Lease liabilities
7,051 45,162 71,397 123,610 101,009
Total lease liabilities
7,051
45,162
71,397
123,610
101,009
Note 11-Subsequent Events
O
n August 25, 2021, the Company announced that the U.S. Food and Drug Administration, or FDA, has approved SKYTROFA (lonapegsomatropin-tcgd) for the treatment of pediatric patients one year and older who weigh at least 11.5 kg (25.4 lb) and have growth failure due to inadequate secretion of endogenous growth hormone (GH). In order to accommodate market demands, the Company has initiated manufacturing of inventories prior to obtaining marketing approval, or pre-launch inventories, for SKYTROFA. However, since pre-launch inventories are not realizable prior to obtaining marketing approval, pre-launch inventories are immediately written down to zero through research and development costs. As a result of the marketing approval received on August 25, 2021, the Company will reverse prior periods' write-downs of pre-launch inventories through research and development costs, at the lower of cost and net-realizable value. Subsequent to the reporting date, reversal of prior periods' write-downs is expected to have a positive impact on research and development costs of approximately €
50
million.
No other events have occurred after the reporting date that would influence the evaluation of these unaudited condensed consolidated interim financial statements.
11

Disclaimer

Ascendis Pharma A/S published this content on 27 August 2021 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 27 August 2021 19:31:28 UTC.


ę Publicnow 2021
All news about ASCENDIS PHARMA A/S
11/18Ascendis Pharma A/S Announces Top-Line Results from Week 84 of Its Phase 2 PaTH Forwar..
GL
11/18Ascendis Pharma A/S Announces Top-Line Results from Week 84 of Its Phase 2 PaTH Forward..
CI
11/18Ascendis Pharma A/S Elects Rafa?le Tordjman as A Class II Director
CI
11/17Ascendis Pharma A/S to Participate in the Evercore ISI 4th Annual HealthCONx Conference
AQ
11/16European ADRs Mixed in Tuesday Morning Trading
MT
11/15SVB Leerink Adjusts Ascendis Pharma's Price Target to $190 from $182, Keeps Outperform ..
MT
11/15Ascendis Pharma A/S - Share Repurchase Program Update
AQ
11/12Ascendis Pharma Says EMA Panel Issues Positive Opinion Backing Approval of Growth Hormo..
MT
11/12Ascendis Pharma A/S Receives Positive CHMP Opinion for TransCon™ hGH for Patients..
GL
11/12Ascendis Pharma A/S Receives Positive CHMP Opinion for TransCon? hGH for Patients with ..
CI
More news
Analyst Recommendations on ASCENDIS PHARMA A/S
More recommendations
Financials
Sales 2021 7,69 M 8,71 M 8,71 M
Net income 2021 -401 M -454 M -454 M
Net cash 2021 677 M 766 M 766 M
P/E ratio 2021 -17,0x
Yield 2021 -
Capitalization 6 866 M 7 772 M 7 770 M
EV / Sales 2021 804x
EV / Sales 2022 90,4x
Nbr of Employees 482
Free-Float 10,5%
Chart ASCENDIS PHARMA A/S
Duration : Period :
Ascendis Pharma A/S Technical Analysis Chart | MarketScreener
Full-screen chart
Technical analysis trends ASCENDIS PHARMA A/S
Short TermMid-TermLong Term
TrendsBearishNeutralBullish
Income Statement Evolution
Consensus
Sell
Buy
Mean consensus BUY
Number of Analysts 12
Last Close Price 125,12 €
Average target price 171,04 €
Spread / Average Target 36,7%
EPS Revisions
Managers and Directors
Jan M°ller Mikkelsen President, CEO & Executive Director
Scott Thomas Smith Chief Financial Officer & Senior Vice President
Albert Cha Chairman
Birgitte Volck SVP, Head-Clinical Development & Medical Affairs
Kennett Sprog°e Senior Vice President, Head-Innovation & Research
Sector and Competitors
1st jan.Capi. (M$)
ASCENDIS PHARMA A/S-17.84%7 772
GILEAD SCIENCES, INC.18.31%86 465
BIONTECH SE331.48%84 953
WUXI APPTEC CO., LTD.30.33%66 734
REGENERON PHARMACEUTICALS31.76%66 553
VERTEX PHARMACEUTICALS-20.90%47 530