Investor News

Acorda Therapeutics Reports Second Quarter 2021 Financial Results

08/05/2021
  • INBRIJA® (levodopa inhalation powder) Q2 2021 net revenue of $6.4 million; 36% increase over Q2 2020
  • AMPYRA® (dalfampridine) Extended Release Tablets, 10 mg Q2 2021 net revenue of $21.8 million
  • Agreement to commercialize INBRIJA in Spain with Esteve Pharmaceuticals
  • $69 million of convertible senior notes repaid

Acorda Therapeutics, Inc. (Nasdaq: ACOR) today reported its financial results for the second quarter 2021.

“We were pleased to see a 36% increase in INBRIJA net sales in the second quarter of 2021 over the same period in 2020. We also saw increases in total prescriptions and dispensed cartons. As Inbrija is an on-demand medication and prescription can range from one to five boxes, we believe that dispensed cartons are the best indicator of demand for the product. These are encouraging signs that the impact of the pandemic is moderating, though it is still too early to project how long it will take for prescribing patterns to return to pre-pandemic levels,” said Ron Cohen, M.D., Acorda’s President and Chief Executive Officer. “We also were delighted to enter into an agreement with Esteve to commercialize INBRIJA in Spain, providing people with Parkinson’s access to this important medication to address their OFF periods. We also are in active discussions with several parties for commercialization of INBRIJA in other territories in Europe and the rest of the world.”

Second Quarter 2021 Financial Results

For the quarter ended June 30, 2021, the Company reported INBRIJA net revenue of $6.4 million, compared to $4.7 million for the same quarter in 2020.

For the quarter ended June 30, 2021, the Company reported AMPYRA net revenue of $21.8 million compared to $26.1 million for the same quarter in 2020. In September 2018, AMPYRA lost its exclusivity and generics entered the market. Consequently, the Company expects AMPYRA revenue to continue to decline.

Research and development (R&D) expenses for the quarter ended June 30, 2021 were $2.4 million, including $0.2 million of share-based compensation compared to $5.3 million, including $0.4 million of share-based compensation for the same quarter in 2020.

Sales, general and administrative (SG&A) expenses for the quarter ended June 30, 2021 were $32.4 million, including $0.7 million of share-based compensation compared to $38.7 million, including $1.5 million of share-based compensation for the same quarter in 2020.

Change in fair value of derivative liability for the quarter ended June 30, 2021 was $(0.8) million compared to $(8.9) million for the same quarter in 2020.

Benefit from income taxes for the quarter ended June 30, 2021 was $0.5 million compared to a provision for income taxes of $0.6 million for the same quarter in 2020.

The Company reported a GAAP net loss of $22.9 million for the quarter ended June 30, 2021, or $2.29 per diluted share. GAAP net loss in the same quarter of 2020 was $17.4 million, or $2.19 per diluted share.

Non-GAAP net loss for the quarter ended June 30, 2021 was $18.7 million, or $1.87 per diluted share. Non-GAAP net loss in the same quarter of 2020 was $16.6 million, or $2.08 per diluted share. This quarterly non-GAAP net loss measure, more fully described below under “Non-GAAP Financial Measures,” excludes share-based compensation charges, non-cash interest charges on our debt, changes in the fair value of acquired contingent consideration, changes in the fair value of derivative liability related to our 2024 convertible senior secured notes, and expenses that pertain to non-routine corporate restructurings. A reconciliation of the GAAP financial results to non-GAAP financial results is included with the attached financial statements.

At June 30, 2021, the Company had cash, cash equivalents, and restricted cash of $71 million, compared to $103 million at year end 2020. Restricted cash includes $25 million in escrow related to the 6% semi-annual interest portion, payable in cash or stock, of the 2024 convertible senior secured notes. If the Company elects to pay interest due in stock, the restricted cash will be released from escrow.

Financial Guidance

  • For the full-year 2021, Acorda continues to expect AMPYRA net revenue to be $75 - $85 million, and operating expenses to be $130 - $140 million. The operating expense guidance is a non-GAAP projection that excludes restructuring costs and share-based compensation as more fully described below under “Non-GAAP Financial Measures.”
  • Due to uncertainties caused by past and potential future impacts of the COVID-19 pandemic and other factors, the Company is not providing projected peak U.S. annual net revenue of INBRIJA at this time.

Webcast

The Company will host a webcast in conjunction with its second quarter 2021 update and financial results today at 4:30 p.m. EDT.

Once you have registered, you will receive a confirmation email with webcast details. You will receive an email with the link to join the webcast 2 hours prior to the start time. The presentation will be available on the Investors section of www.acorda.com.

A replay of the call will be available from 7:30 p.m. EDT on May 6, 2021 until 11:59 p.m. EDT on June 3, 2021. To access the replay, please dial (800) 585-8367 (domestic) or (416) 621-4642 (international); reference code 2996776. The archived webcast will be available in the Investor Relations section of the Acorda website at www.acorda.com.

Non-GAAP Financial Measures

This press release includes financial results prepared in accordance with accounting principles generally accepted in the United States (GAAP) and also certain historical and forward-looking non-GAAP financial measures. In particular, Acorda has provided non-GAAP net loss, adjusted to exclude the items below, and has provided 2021 operating expense guidance on a non-GAAP basis. Non-GAAP financial measures are not an alternative for financial measures prepared in accordance with GAAP. However, the Company believes that the presentation of non-GAAP net loss, when viewed in conjunction with actual GAAP results, provides investors with a more meaningful understanding of our ongoing and projected operating performance because this measure excludes (i) non-cash compensation charges and benefits that are substantially dependent on changes in the market price of our common stock, (ii) non-cash interest charges related to the accounting for our convertible debt which are in excess of the actual interest expense owing on such convertible debt, as well as non-cash interest related to the Fampyra royalty monetization and acquired Biotie debt, (iii) changes in the fair value of acquired contingent consideration which do not correlate to our actual cash payment obligations in the relevant periods, (iv) asset impairment charges that are not routine to the operation of the business, (v) expenses that pertain to corporate restructurings which are not routine to the operation of the business, and (vi) changes in the fair value of derivative liability relating to the 2024 convertible senior secured notes, which is a non-cash charge and not related to the operation of the business. The Company believes its non-GAAP net loss measure helps indicate underlying trends in the Company's business and is important in comparing current results with prior period results and understanding projected operating performance. Also, management uses this non-GAAP financial measure to establish budgets and operational goals, and to manage the Company's business and to evaluate its performance.

In addition to non-GAAP net loss, we have provided 2021 operating expense guidance on a non-GAAP basis, as the guidance excludes restructuring costs and share-based compensation charges. Due to the forward looking nature of this information, the amount of compensation charges needed to reconcile this measure to the most directly comparable GAAP financial measure is dependent on future changes in the market price of our common stock and is not available at this time. Non-GAAP financial measures are not an alternative for financial measures prepared in accordance with GAAP. However, the Company believes that the presentation of this non-GAAP financial measure, when viewed in conjunction with actual GAAP results, provides investors with a more meaningful understanding of our ongoing and projected operating performance because it excludes (i) expenses that pertain to non-routine corporate restructurings, and (ii) non-cash charges that are substantially dependent on changes in the market price of our common stock. We believe this non-GAAP financial measure helps indicate underlying trends in the Company’s business and is important in comparing current results with prior period results and understanding expected operating performance. Also, management uses this non-GAAP financial measure to establish budgets and operational goals, and to manage the Company's business and to evaluate its performance.

About Acorda Therapeutics

Acorda Therapeutics develops therapies to restore function and improve the lives of people with neurological disorders. INBRIJAis approved for intermittent treatment of OFF episodes in adults with Parkinson’s disease treated with carbidopa/levodopa. INBRIJA is not to be used by patients who take or have taken a nonselective monoamine oxidase inhibitor such as phenelzine or tranylcypromine within the last two weeks. INBRIJA utilizes Acorda’s innovative ARCUS® pulmonary delivery system, a technology platform designed to deliver medication through inhalation. Acorda also markets the branded AMPYRA® (dalfampridine) Extended Release Tablets, 10 mg.

Forward-Looking Statements

This press release includes forward-looking statements. All statements, other than statements of historical facts, regarding management's expectations, beliefs, goals, plans or prospects should be considered forward-looking. These statements are subject to risks and uncertainties that could cause actual results to differ materially, including: we may not be able to successfully market AMPYRA, INBRIJA or any other products under development; the COVID-19 pandemic, including related quarantines and travel restrictions, and the potential for the illness to affect our employees or consultants or those that work for other companies we rely upon, could have a material adverse effect on our business operations or product sales; our ability to raise additional funds to finance our operations, repay outstanding indebtedness or satisfy other obligations, and our ability to control our costs or reduce planned expenditures; risks associated with the trading of our common stock and our reverse stock split; risks related to our workforce, including our ability to realize the expected benefits of our corporate restructuring; risks associated with complex, regulated manufacturing processes for pharmaceuticals, which could affect whether we have sufficient commercial supply of INBRIJA to meet market demand; our reliance on third-party manufacturers for the production of commercial supplies of AMPYRA and INBRIJA; third-party payers (including governmental agencies) may not reimburse for the use of INBRIJA at acceptable rates or at all and may impose restrictive prior authorization requirements that limit or block prescriptions; reliance on collaborators and distributors to commercialize INBRIJA and AMPYRA outside the U.S.; competition for INBRIJA and AMPYRA, including increasing competition and accompanying loss of revenues in the U.S. from generic versions of AMPYRA (dalfampridine) following our loss of patent exclusivity; the ability to realize the benefits anticipated from acquisitions, among other reasons because acquired development programs are generally subject to all the risks inherent in the drug development process and our knowledge of the risks specifically relevant to acquired programs generally improves over time; the risk of unfavorable results from future studies of INBRIJA (levodopa inhalation powder) or from other research and development programs, or any other acquired or in-licensed programs; the occurrence of adverse safety events with our products; the outcome (by judgment or settlement) and costs of legal, administrative or regulatory proceedings, investigations or inspections, including, without limitation, collective, representative or class-action litigation; failure to protect our intellectual property, to defend against the intellectual property claims of others or to obtain third-party intellectual property licenses needed for the commercialization of our products; and failure to comply with regulatory requirements could result in adverse action by regulatory agencies.

These and other risks are described in greater detail in our filings with the Securities and Exchange Commission. We may not actually achieve the goals or plans described in our forward-looking statements, and investors should not place undue reliance on these statements. Forward-looking statements made in this press release are made only as of the date hereof, and we disclaim any intent or obligation to update any forward-looking statements as a result of developments occurring after the date of this press release.

Financial Statements

Acorda Therapeutics, Inc.

Condensed Consolidated Balance Sheet Data

(in thousands)






 

 

June 30,

 

 

December 31,

 

 

2021

 

 

2020

 

 

(unaudited)

 

 

 

 

 

Assets

 

 

 

 

 

 

 

Cash and cash equivalents

$

45,714

 

 

$

71,369

 

Restricted cash - short term

 

12,883

 

 

 

12,917

 

Trade receivable, net

 

14,010

 

 

 

20,193

 

Other current assets

 

14,981

 

 

 

16,384

 

Inventories, net

 

25,355

 

 

 

28,677

 

Assets held for sale - current

 

 

 

 

71,795

 

Property and equipment, net

 

5,715

 

 

 

7,263

 

Intangible assets, net

 

351,481

 

 

 

366,981

 

Restricted cash - long term

 

12,399

 

 

 

18,609

 

Right of use assets, net

 

8,949

 

 

 

18,481

 

Other assets

 

11

 

 

 

11

 

Total assets

$

491,498

 

 

$

632,680

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Liabilities and stockholders' equity

 

 

 

 

 

 

 

Accounts payable, accrued expenses and other current liabilities

$

46,289

 

 

$

50,322

 

Current portion of lease liability

 

10,708

 

 

 

7,944

 

Current portion of royalty liability

 

9,205

 

 

 

8,731

 

Current portion of contingent consideration

 

1,454

 

 

 

1,624

 

Current portion of loans payable

 

 

 

 

68,631

 

Convertible senior notes

 

144,025

 

 

 

137,619

 

Derivative liability related to conversion option

 

613

 

 

 

1,193

 

Non-current portion of acquired contingent consideration

 

39,746

 

 

 

46,576

 

Non-current portion of lease liability

 

4,040

 

 

 

17,200

 

Non-current portion of royalty liability

 

859

 

 

 

6,526

 

Non-current portion of loans payable

 

28,302

 

 

 

28,555

 

Deferred tax liability

 

15,109

 

 

 

19,116

 

Other long-term liabilities

 

667

 

 

 

688

 

Total stockholder's equity

 

190,481

 

 

 

237,955

 

Total liabilities and stockholders' equity

$

491,498

 

 

$

632,680

 

Acorda Therapeutics, Inc.

Consolidated Statements of Operations

(in thousands, except per share amounts)

(unaudited)






 

 

Three Months Ended

 

 

Six Months Ended

 

 

June 30,

 

 

June 30,

 

 

2021

 

 

2020

 

 

2021

 

 

2020

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Revenues:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Net product revenues

$

28,199

 

 

$

30,794

 

 

$

53,446

 

 

$

55,465

 

Royalty revenues

 

3,586

 

 

 

2,824

 

 

 

7,201

 

 

 

6,251

 

Total net revenues

 

31,785

 

 

 

33,618

 

 

 

60,647

 

 

 

61,716

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Costs and expenses:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Cost of sales

 

11,324

 

 

 

6,658

 

 

 

23,285

 

 

 

10,501

 

Research and development

 

2,374

 

 

 

5,255

 

 

 

7,123

 

 

 

12,960

 

Selling, general and administrative

 

32,368

 

 

 

38,656

 

 

 

66,336

 

 

 

79,764

 

Amortization of intangible assets

 

7,691

 

 

 

7,691

 

 

 

15,382

 

 

 

15,382

 

Asset impairment

 

 

 

 

 

 

 

 

 

 

4,131

 

Change in fair value of derivative liability

 

(805

)

 

 

(8,928

)

 

 

(580

)

 

 

(35,456

)

Change in fair value of acquired

contingent consideration

 

(5,478

)

 

 

(6,164

)

 

 

(6,429

)

 

 

(9,847

)

Total operating expenses

 

47,474

 

 

 

43,168

 

 

 

105,117

 

 

 

77,435

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Operating loss

$

(15,689

)

 

$

(9,550

)

 

$

(44,470

)

 

$

(15,719

)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Other expense, (net)

 

(7,706

)

 

 

(7,300

)

 

 

(15,528

)

 

 

(14,601

)

Loss before income taxes

 

(23,395

)

 

 

(16,850

)

 

 

(59,998

)

 

 

(30,320

)

(Provision for) benefit from income taxes

 

531

 

 

 

(571

)

 

 

3,683

 

 

 

6,427

 

Net loss

$

(22,864

)

 

$

(17,421

)

 

$

(56,315

)

 

$

(23,893

)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Net loss per common share - basic

$

(2.29

)

 

$

(2.19

)

 

$

(5.79

)

 

$

(3.00

)

Net loss per common share - diluted

$

(2.29

)

 

$

(2.19

)

 

$

(5.79

)

 

$

(3.00

)

Weighted average common shares - basic

 

9,992

 

 

 

7,960

 

 

 

9,733

 

 

 

7,960

 

Weighted average common shares - diluted

 

9,992

 

 

 

7,960

 

 

 

9,733

 

 

 

7,960

 

Acorda Therapeutics, Inc.

Non-GAAP Net Loss and Net Loss per Common Share Reconciliation

(in thousands, except per share amounts)

(unaudited)






 

 

Three Months Ended

 

 

Six Months Ended

 

 

June 30,

 

 

June 30,

 

 

2021

 

 

2020

 

 

2021

 

 

2020

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

GAAP net loss

$

(22,864

)

 

$

(17,421

)

 

$

(56,315

)

 

$

(23,893

)

Pro forma adjustments:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Non-cash interest expense (1)

 

4,304

 

 

 

4,052

 

 

 

8,575

 

 

 

8,107

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Change in fair value of acquired

contingent consideration (2)

 

(5,478

)

 

 

(6,164

)

 

 

(6,429

)

 

 

(9,847

)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Restructuring costs (3)

 

27

 

 

 

 

 

 

2,151

 

 

 

343

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Asset impairment charge (4)

 

 

 

 

 

 

 

 

 

 

4,131

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Gain on change in fair value of derivative liability (5)

 

(805

)

 

 

(8,928

)

 

 

(580

)

 

 

(35,456

)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Share-based compensation expenses

included in Cost of Sales

 

9

 

 

 

86

 

 

 

16

 

 

 

167

 

Share-based compensation expenses

included in R&D

 

208

 

 

 

448

 

 

 

374

 

 

 

864

 

Share-based compensation expenses

included in SG&A

 

737

 

 

 

1,522

 

 

 

1,271

 

 

 

3,001

 

Total share-based compensation expenses

 

954

 

 

 

2,056

 

 

 

1,661

 

 

 

4,032

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Total pro forma adjustments

 

(998

)

 

 

(8,984

)

 

 

5,378

 

 

 

(28,690

)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Income tax effect of reconciling items

above (6)

 

(5,167

)

 

 

(9,835

)

 

 

(8,900

)

 

 

(11,655

)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Non-GAAP net loss

$

(18,694

)

 

$

(16,570

)

 

$

(42,037

)

 

$

(40,928

)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Net loss per common share - basic

$

(1.87

)

 

$

(2.08

)

 

$

(4.32

)

 

$

(5.14

)

Net loss per common share - diluted

$

(1.87

)

 

$

(2.08

)

 

$

(4.32

)

 

$

(5.14

)

Weighted average common shares - basic

 

9,992

 

 

 

7,960

 

 

 

9,733

 

 

 

7,960

 

Weighted average common shares - diluted

 

9,992

 

 

 

7,960

 

 

 

9,733

 

 

 

7,960

 

(1) Non-cash interest expense related to convertible senior notes, Biotie non-convertible and R&D loans and Fampyra royalty monetization.

(2) Changes in fair value of acquired contingent consideration related to the Civitas acquisition.

(3) Costs associated with non-routine corporate restructurings.

(4) Asset Impairment charge related to the 2020 impairment of BTT1023 acquired in the Biotie acquisition.

(5) Reduction in the fair value of the derivative liability related to the 2024 convertible senior secured notes.

(6) Represents the tax effect of the non-GAAP adjustments.

 

Tierney Saccavino
(914) 326-5104
tsaccavino@acorda.com

Source: Acorda Therapeutics, Inc.

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