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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
 
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the
Securities Exchange Act of 1934
Date of Report (Date of earliest event reported): March 1, 2010
QUESTCOR PHARMACEUTICALS, INC.
(Exact Name of Registrant as Specified in Charter)
         
California   001-14758   33-0476164
(State or Other Jurisdiction   (Commission File Number)   (I.R.S. Employer
of Incorporation)       Identification No.)
     
3260 Whipple Road, Union City, California   94587
(Address of Principal Executive Offices)   (Zip Code)
Registrant’s telephone number, including area code: (510) 400-0700
 
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):
o   Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
 
o   Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
 
o   Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
 
o   Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
 
 

 


 

Item 2.02. Results of Operations and Financial Condition.
          On March 1, 2010, Questcor Pharmaceuticals, Inc. (the “Company”) announced via press release its results for the quarter and year ended December 31, 2009. A copy of the Company’s press release is attached hereto as Exhibit 99.1.
          In accordance with General Instruction B.2. of Form 8-K, the information in Item 2.02 of this Current Report on Form 8-K, including Exhibit 99.1, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liability of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth by specific reference in such a filing.
Item 7.01 Regulation FD Disclosure.
          The information disclosed in item 2.02 is incorporated herein by this reference.
Item 9.01. Financial Statements and Exhibits.
     (c) Exhibits.
     
Exhibit No.   Description
99.1
  Questcor Pharmaceuticals, Inc. press release dated March 1, 2010.

 


 

SIGNATURE
          Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
         
Date: March 1, 2010   QUESTCOR PHARMACEUTICALS, INC.
 
 
  By:   /s/ Gary Sawka    
    Gary Sawka   
    Senior Vice President, Finance and Chief Financial Officer   
 

 


 

EXHIBIT INDEX
     
Exhibit No.   Description
99.1
  Questcor Pharmaceuticals, Inc. press release dated March 1, 2010.

 

exv99w1
Exhibit 99.1
(QUESTCOR LOGO)
QUESTCOR REPORTS SOLID FOURTH QUARTER RESULTS
-Paid commercial Acthar prescriptions for MS up 223% over prior year quarter-
- -Paid commercial IS prescriptions up 56% sequentially-
- -Received initial set of nephrotic syndrome prescriptions-
- -Fourth quarter 2009 net income per share $0.13 on $25.9 million in net sales-
- -2.5 million common shares repurchased during fourth quarter-
- -Conference call today at 5:00 PM ET-
UNION CITY, Calif. — March 1, 2010 — Questcor Pharmaceuticals, Inc. (NASDAQ: QCOR) today reported financial results for the fourth quarter and year ended December 31, 2009. The Company’s financial performance in the fourth quarter of 2009 was driven primarily by:
  a 223% increase in the number of new paid Acthar commercial prescriptions for the treatment of multiple sclerosis (MS) exacerbations versus the fourth quarter of 2008,
 
  a sequential 56% increase in new paid Acthar commercial prescriptions for the treatment of infantile spasms (IS), and
 
  lower sequential Medicaid usage.
     In addition to the financial improvement in the quarter, the Company also received an encouraging initial set of Acthar prescriptions for the treatment of nephrotic syndrome (NS). Also, during the fourth quarter, the FDA accepted for review Questcor’s supplemental New Drug Application (sNDA) filing which seeks approval for an indication for Acthar in the treatment of IS.
          Net sales totaled $25.9 million for the quarter ended December 31, 2009 compared to $13.9 million for the quarter ended September 30, 2009, and $27.0 million for the fourth quarter of 2008. Net income for the fourth quarter of 2009 was $8.4 million, or $0.13 per diluted common share compared to $1.2 million, or $0.02 per diluted common share for the third quarter of 2009, and $16.2 million, or $0.24 per diluted common share for the fourth quarter of 2008. An additional $1.2 million in sales reserves was recorded during the fourth quarter of 2009 for retroactive Tricare rebates. Significantly higher sales reserves adjustments reduced net sales and operating income for the third quarter of 2009 by $4.6 million. Tax benefits resulting from the reversal of a valuation allowance positively affected net income in the fourth quarter of 2008 by $4.4 million.

 


 

          Net sales totaled $88.3 million for the year ended December 31, 2009, compared with $95.2 million for 2008. Net income for 2009 was $26.6 million, or $0.40 per diluted common share compared with net income applicable to common shareholders of $35.3 million, or $0.49 per diluted common share for 2008. The 2008 earnings were impacted by a one-time net tax benefit of $5.2 million and a deemed dividend of $5.3 million.
     “We are making excellent progress on all of Questcor’s top priorities,” said Don M. Bailey, President and CEO. “Our fourth quarter financial performance improved significantly on a sequential basis. Questcor’s sales in the MS market showed marked growth and there are preliminary indications that Acthar may also begin to be adopted in the NS market, which is much larger than either the IS or MS markets. In addition, IS prescriptions and payer mix both improved during the fourth quarter from a very weak third quarter. To date, we are seeing little or no impact on Acthar sales in the IS market from the September 2009 introduction of Sabril (vigabatrin).”
IS, MS, and NS Sales
     During the fourth quarter of 2009, Questcor shipped 1,626 vials of Acthar compared to third quarter 2009 shipments of 1,354 vials and fourth quarter 2008 shipments of 1,510 vials. Because Acthar prescriptions are filled at specialty pharmacies, the Company does not receive complete information regarding either the number of prescriptions or the number of vials by therapeutic area for all of the patients being treated with Acthar. However, Questcor is able to monitor historic trends in payer mix for new Acthar prescriptions based on data it receives from its reimbursement support center. Questcor estimates that approximately 90% of new Acthar prescriptions are processed by this support center, but that very few refill prescriptions are processed at this center. The following tables show the number of prescriptions shipped by payer category for each of three therapeutic areas for those new prescriptions processed by the Questcor support center:

 


 

Multiple Sclerosis New Prescriptions
                         
    Paid/Commercial   Medicaid   Tricare/VA
Q108
    24       5       0  
Q208
    35       1       0  
Q308
    50       5       1  
Q408
    66       3       2  
 
                       
Total 2008
    175       14       3  
 
                       
 
                       
Q109
    78       5       3  
Q209
    125       11       6  
Q309
    141       14       5  
Q409
    213       10       5  
 
                       
Total 2009
    557       40       19  
 
                       
Infantile Spasms New Prescriptions
                         
    Paid/Commercial   Medicaid   Tricare/VA
Q108
    98       38       2  
Q208
    114       47       3  
Q308
    113       67       3  
Q408
    103       56       3  
 
                       
Total 2008
    428       208       11  
 
                       
 
                       
Q109
    104       70       5  
Q209
    93       63       5  
Q309
    61       55       3  
Q409
    95       40       5  
 
                       
Total 2009
    353       228       18  
 
                       
Nephrotic Syndrome New Prescriptions
                         
    Paid/Commercial   Medicaid   Tricare/VA
Q109
    1       0       0  
Q209
    3       0       1  
Q309
    2       0       0  
Q409
    14       2       1  
 
                       
Total 2009
    20       2       2  
 
                       
 
Note: Historical trend information is not necessarily indicative of future results. The total number of vials associated with an individual prescription varies by the condition being treated and by patient.
     “As the above tables illustrate, our efforts in MS continue to show that the use of Acthar is expanding,” commented Steve Cartt, Executive Vice President. “Our initiatives to educate MS specialists about the treatment benefits of Acthar have resulted in a tripling in MS prescriptions year over year.”

 


 

     “In addition, spontaneous IS prescriptions during the fourth quarter rebounded to 140 new paid prescriptions from a low level of 119 in the third quarter,” noted Mr. Cartt. “If we are able to receive approval from the FDA to market Acthar for the treatment of IS, we may be able to expand our sales in this therapeutic area.”
     “The modest set of prescriptions for NS in the fourth quarter was an unexpected development at this stage in our efforts to generate sales in this market,” added Mr. Cartt. “NS is a devastating kidney disorder which leads to end-stage renal disease (ESRD). NS is an on-label indication for Acthar and we are working to generate more clinical data to further support the effectiveness of Acthar in the treatment of this disease.”
Sales Reserves—Medicaid, Tricare and VA Adjustments
     As required by federal regulations, the Company provides rebates to state Medicaid programs for Acthar dispensed to Medicaid patients. The Medicaid rebate portion of sales reserves for the fourth quarter of 2009 was $8.4 million or 22% of 2009 fourth quarter gross sales. While total new commercially paid Acthar prescriptions for the treatment of IS processed through the Company’s reimbursement support center increased to 95 in the fourth quarter from 61 in the third quarter, the number of Medicaid-reimbursed IS prescriptions dropped 27% sequentially.
     The Department of Defense (DOD) operates a prescription drug program through its Tricare Management Administration (Tricare). As a result of uncertainties in an on-going dispute between the pharmaceutical industry and the DOD over Tricare rebate regulations, Questcor recorded a sales reserve related to a portion of Tricare-claimed rebates during the third quarter of 2009. Due to recent developments in that dispute, Questcor recorded an additional $1.2 million in sales reserves during the fourth quarter of 2009 for the remaining potential Tricare-claimed rebates. Effective January 1, 2010, Questcor established new prices for Acthar purchased by Tricare and Veterans Administration (VA) medical centers. Additionally, Questcor has removed uncertainty regarding Tricare rebate liabilities going forward. The new agreement with Tricare does not diminish Questcor’s rights in regards to the fully reserved 2008-2009

 


 

liability. Any sales in 2010 to Tricare or the VA will represent an increase from the negligible net sales to these customers in 2009.
Regulatory Activity
     Acthar is currently approved in the U.S. for the treatment of MS exacerbations, nephrotic syndrome and many other conditions. Acthar is not approved in the U.S. for the treatment of IS, a potentially life-threatening disorder that typically begins in the first year of life. However, pursuant to guidelines published by the American Academy of Neurology and the Child Neurology Society, many child neurologists use Acthar to treat infants afflicted with IS.
     On December 23, 2009 the FDA accepted for review Questcor’s supplemental New Drug Application (sNDA) seeking approval to market Acthar for the treatment of infantile spasms. The FDA has notified Questcor that an Advisory Committee Meeting of independent experts will be held to discuss the approval and use of Acthar in infantile spasms. The FDA has also notified Questcor that it has set a PDUFA goal date of June 11, 2010, but there is no assurance that this date will not be delayed. Approval of the IS indication would allow Questcor to promote the use of Acthar in treating IS to child neurologists.
     Previously, the FDA granted Orphan Designation to Acthar for the treatment of IS. As a result of this Orphan Designation, if Questcor is successful in obtaining FDA approval for the IS indication, Questcor believes that it will also qualify for a seven-year exclusivity period during which the FDA is prohibited from approving any other adrenocorticotropic hormone (ACTH) formulation for IS unless the other formulation is demonstrated to be clinically superior to Acthar.
Cash, Accounts Receivable and Share Repurchase Program
     At February 26, 2010, Questcor’s cash, cash equivalents and short-term investments totaled approximately $81 million, and accounts receivable totaled approximately $9 million.
     During the fourth quarter, the Company repurchased 2.5 million shares of its common stock at a total cost of $9.9 million. In the last two years, Questcor has spent $67.0 million for the repurchase of 14.5 million common and preferred shares.

 


 

     As of December 31, 2009, Questcor had 61.7 million common shares outstanding, with 5.1 million shares remaining under its common share repurchase program.
Conference Call Details
The Company will host a conference call today to discuss these results at 5:00 p.m. ET. Don Bailey, President and Chief Executive Officer; Steve Cartt, Executive Vice President and Chief Business Officer; Dr. David Young, Chief Scientific Officer; Dave Medeiros, Senior Vice President, Pharmaceutical Operations; Dr. Jason Zielonka, Senior Vice President and Chief Medical Officer; and Gary Sawka, Senior Vice President, Finance and Chief Financial Officer will host the call.
To participate in the live call by telephone, please dial 877-941-2928 from the U.S. or 480-629-9724 from outside the U.S. Participants are asked to call the above numbers 5-10 minutes prior to the starting time. The call will also be webcast live at www.questcor.com. An audio replay of the call will be available for 7 days following the call. This replay can be accessed by dialing 800-406-7325 for domestic callers and 303-590-3030 for international callers, both using passcode 4221516#. An archived webcast will also be available at www.questcor.com.
About Questcor
Questcor Pharmaceuticals, Inc. is a pharmaceutical company that markets H.P. Acthar® Gel (repository corticotropin injection). H.P. Acthar Gel (“Acthar”) is an injectable drug that is approved for the treatment of certain disorders, including the treatment of exacerbations associated with multiple sclerosis (“MS”) and to induce a diuresis or a remission of proteinuria in the nephrotic syndrome without uremia of the idiopathic type or that is due to lupus erythamatosus. In addition, Acthar is not indicated for, but is used in treating patients with infantile spasms (“IS”), a rare form of refractory childhood epilepsy, and opsoclonus myoclonus syndrome, a rare autoimmune-related childhood neurological disorder. For more information, please visit www.questcor.com.
Note: Except for the historical information contained herein, this press release contains forward-looking statements that have been made pursuant to the Private Securities Litigation Reform Act of 1995. These statements relate to future events or our future financial performance. In some cases, you can identify forward-looking statements by terminology such as “may,” “will,” “if,” “should,” “forecasts,” “expects,” “plans,” “anticipates,” “believes,” “estimates,” “predicts,” “potential,” or “continue” or the negative of such terms and other comparable terminology. These statements are only predictions. Actual events or results may differ materially. Factors that could cause or contribute to such differences include, but are not limited to, the following:
    Questcor’s ability to continue to successfully implement its Acthar-centric business strategy, including its expansion in the MS marketplace;
 
    FDA approval of and the market introduction of competitive products and our inability to market Acthar in IS prior to approval of IS as a labeled indication;
 
    Questcor’s ability to operate within an industry that is highly regulated at both the Federal and state level;
 
    Regulatory changes or actions including Federal or State health care reform initiatives;
 
    Questcor’s ability to accurately forecast the demand for its products;
 
    The gross margin achieved from the sale of its products;
 
    Questcor’s ability to estimate the quantity of Acthar used by government entities and Medicaid-eligible patients;
 
    That the actual amount of rebates and chargebacks related to the use of Acthar by government entities, including the Department of Defense Tricare network, and Medicaid-eligible patients may differ materially from Questcor’s estimates;
 
    Questcor’s expenses and other cash needs for upcoming periods;
 
    The inventories carried by Questcor’s distributors, specialty pharmacies and hospitals;
 
    Volatility in Questcor’s monthly and quarterly Acthar shipments and end-user demand;

 


 

    Questcor’s ability to obtain finished goods from its sole source contract manufacturers on a timely basis if at all;
 
    Questcor’s ability to attract and retain key management personnel;
 
    Research and development risks, including risks associated with Questcor’s sNDA for IS and its preliminary work in the area of nephrotic syndrome;
 
    Uncertainties regarding Questcor’s intellectual property;
 
    The uncertainty of receiving required regulatory approvals in a timely way, or at all; and,
 
    Questcor’s ability to identify product acquisition candidates and consummate transactions on terms acceptable to the Company.
 
    Other risks discussed in Questcor’s annual report on Form 10-K for the year ended December 31, 2008 and other documents filed with the Securities and Exchange Commission.
The risk factors and other information contained in these documents should be considered in evaluating Questcor’s prospects and future financial performance.
Questcor undertakes no obligation to publicly release the result of any revisions to these forward-looking statements, which may be made to reflect events or circumstances after the date hereof or to reflect the occurrence of unanticipated events.
For more information, please visit www.questcor.com or www.acthar.com.
CONTACT:
         
Questcor
  Investors   Media
Don Bailey
  EVC Group   EVC Group
dbailey@Questcor.com
  Barbara Domingo, 415-896-6820   Chris Gale, 646-201-5431
510-400-0776
  Douglas Sherk, 415-896-6820    

 


 

Questcor Pharmaceuticals, Inc.
Consolidated Statements of Income
(In thousands, except per share amounts)
                                 
    Three Months Ended     Years Ended  
    December 31,     December 31,  
    2009     2008     2009     2008  
Net sales
  $ 25,905     $ 27,018     $ 88,320     $ 95,248  
Cost of sales (exclusive of amortization of purchased technology)
    1,898       1,858       7,017       7,304  
 
                       
Gross profit
    24,007       25,160       81,303       87,944  
Gross margin
    93 %     93 %     92 %     92 %
Operating expenses:
                               
Selling, general and administrative
    7,841       5,075       29,950       19,247  
Research and development
    2,662       2,511       9,653       10,614  
Depreciation and amortization
    121       124       480       503  
 
                       
Total operating expenses
    10,624       7,710       40,083       30,364  
 
                       
Income from operations
    13,383       17,450       41,220       57,580  
Other income:
                               
Interest and other income, net
    101       247       686       1,075  
Gain on sale of product rights
          75       225       75  
 
                       
Total other income
    101       322       911       1,150  
 
                       
Income before income taxes
    13,484       17,772       42,131       58,730  
Income tax expense
    5,063       1,530       15,502       18,198  
 
                       
Net income
    8,421       16,242       26,629       40,532  
Deemed dividend on Series A preferred stock
                      5,267  
 
                       
Net income applicable to common shareholders
  $ 8,421     $ 16,242     $ 26,629     $ 35,265  
 
                       
Net income per share applicable to common shareholders:
                               
Basic
  $ 0.13     $ 0.25     $ 0.41     $ 0.52  
 
                       
Diluted
  $ 0.13     $ 0.24     $ 0.40     $ 0.49  
 
                       
Shares used in computing net income per share applicable to common shareholders:
                               
Basic
    63,086       65,135       64,196       67,761  
 
                       
Diluted
    64,783       68,345       66,257       71,350  
 
                       

 


 

Questcor Pharmaceuticals, Inc.
Consolidated Balance Sheets
(In thousands, except share amounts)
                 
    December 31,  
    2009     2008  
ASSETS
               
Current assets:
               
Cash and cash equivalents
  $ 45,829     $ 13,282  
Short-term investments
    29,878       42,169  
 
           
Total cash, cash equivalents and short-term investments
    75,707       55,451  
Accounts receivable, net of allowance for doubtful accounts of $77 and $62 at December 31, 2009 and 2008, respectively
    14,833       10,418  
Inventories, net
    3,378       2,459  
Prepaid income taxes
          3,316  
Prepaid expenses and other current assets
    1,162       1,101  
Deferred tax assets
    8,180       6,252  
 
           
Total current assets
    103,260       78,997  
Property and equipment, net
    407       450  
Purchased technology, net
    3,372       3,669  
Goodwill
    299       299  
Deposits and other assets
    710       710  
Deferred tax assets
    3,392       5,021  
 
           
Total assets
  $ 111,440     $ 89,146  
 
           
LIABILITIES AND SHAREHOLDERS’ EQUITY
               
Current liabilities:
               
Accounts payable
  $ 12,921     $ 4,302  
Accrued compensation
    2,140       1,896  
Sales-related reserves
    14,922       11,825  
Income taxes payable
    477        
Other accrued liabilities
    1,751       1,702  
 
           
Total current liabilities
    32,211       19,725  
Lease termination and deferred rent liabilities and other non-current liabilities
    1,226       1,529  
 
           
Total liabilities
    33,437       21,254  
 
           
Shareholders’ equity:
               
Preferred stock, no par value, 7,500,000 shares authorized; none outstanding
           
Common stock, no par value, 105,000,000 shares authorized; 61,726,609 and 65,970,653 shares issued and outstanding at December 31, 2009 and 2008, respectively
    67,793       84,028  
Retained earnings (accumulated deficit)
    10,224       (16,405 )
Accumulated other comprehensive income (loss)
    (14 )     269  
 
           
Total shareholders’ equity
    78,003       67,892  
 
           
Total liabilities and shareholders’ equity
  $ 111,440     $ 89,146  
 
           

 


 

Questcor Pharmaceuticals, Inc.
Consolidated Statements of Cash Flows
(In thousands)
                 
    Years Ended  
    December 31,  
    2009     2008  
OPERATING ACTIVITIES
               
Net income
  $ 26,629     $ 40,532  
Adjustments to reconcile net income to net cash provided by operating activities:
               
Share-based compensation expense
    3,066       4,119  
Deferred income taxes
    (290 )     4,649  
Amortization of investments
    181       (456 )
Depreciation and amortization
    480       503  
Gain on sale of product rights
    (225 )     (75 )
Income tax benefit realized from share-based compensation plans
    783       4,932  
Excess tax benefit from share-based compensation plans
    (743 )     (4,841 )
Changes in operating assets and liabilities:
               
Accounts receivable
    (4,415 )     13,221  
Inventories
    (919 )     (94 )
Prepaid income taxes
    3,316       (3,316 )
Prepaid expenses and other current assets
    (61 )     (323 )
Accounts payable
    8,619       2,525  
Accrued compensation
    244       (49 )
Sales-related reserves
    3,097       3,649  
Income taxes payable
    477       (1,330 )
Other accrued liabilities
    49       210  
Other non-current liabilities
    (303 )     (347 )
 
           
Net cash flows provided by operating activities
    39,985       63,509  
 
           
INVESTING ACTIVITIES
               
Purchase of property and equipment
    (140 )     (133 )
Purchase of short-term investments
    (61,557 )     (69,613 )
Proceeds from the sale and maturities of short-term investments
    73,375       42,388  
Net proceeds from sale of product rights
    225       75  
Changes in deposits and other assets
          34  
 
           
Net cash flows provided by (used in) investing activities
    11,903       (27,249 )
 
           
FINANCING ACTIVITIES
               
Issuance of common stock, net
    1,002       2,161  
Repurchase of common stock
    (21,086 )     (35,571 )
Repurchase of Series A preferred stock
          (10,348 )
Excess tax benefit from share-based compensation plans
    743       4,841  
 
           
Net cash flows used in financing activities
    (19,341 )     (38,917 )
 
           
Increase (decrease) in cash and cash equivalents
    32,547       (2,657 )
Cash and cash equivalents at beginning of year
    13,282       15,939  
 
           
Cash and cash equivalents at end of year
  $ 45,829     $ 13,282