Form 8-K

 

 

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, DC 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 28, 2012

 

 

MAP PHARMACEUTICALS, INC.

(Exact Name of Registrant as Specified in its Charter)

 

 

 

Delaware   001-33719   20-0507047

(State or Other Jurisdiction

of Incorporation)

 

(Commission

File Number)

 

(IRS Employer

Identification No.)

 

2400 Bayshore Parkway, Suite 200, Mountain View, CA   94043
(Address of Principal Executive Offices)   (Zip Code)

Registrant’s telephone number, including area code: (650) 386-3100

(Former Name or Former Address, if Changed Since Last Report.)

 

 

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):

 

¨ Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

 

¨ Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

 

¨ Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

 

¨ Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

 

 

 


Item 4.02 Non-Reliance on Previously Issued Financial Statements or a Related Audit Report or Completed Interim Review.

On March 28, 2012, the Audit Committee of the Board of Directors of MAP Pharmaceuticals, Inc. (the “Company”) determined, following a review by the Securities and Exchange Commission (“SEC”) of the Company’s Annual Report on Form 10-K for the year ended December 31, 2010 and Quarterly Report on Form 10-Q for the quarterly period ended March 31, 2011 (the “Staff Review”), that the Company will restate its unaudited financial results for the quarters ended March 31, 2011, June 30, 2011 and September 30, 2011. The audited financial statements for the year ended December 31, 2010 are unaffected. The Company’s Quarterly Reports on Form 10-Q for the quarters ended March 31, 2011, June 30, 2011 and September 30, 2011 and all related earnings releases and similar communications relating to those unaudited financial periods should no longer be relied upon.

The restatement relates to correcting the accounting treatment for the nonrefundable $60.0 million upfront cash payment received by the Company in February 2011 (the “Upfront Payment”) for a license (the “License”) granted by the Company pursuant to a Collaboration Agreement with Allergan, Inc. and Allergan USA, Inc. (“Collaboration Agreement” and “Allergan,” respectively). The restatement relates to the timing of revenue recognition for the Upfront Payment and not the total amount of revenue ultimately to be recorded by the Company, and will have no impact on the Company’s previously reported cash position, total assets or operating expenses. For the three quarters ended March 31, 2011, June 30, 2011 and September 30, 2011, unaudited reported revenue will be adjusted as follows:

 

     Quarterly Collaboration Revenue (unaudited)  
(in thousands)    Previously reported      Adjustments     As restated  

Quarter ended March 31, 2011

   $ 34,162       $ (33,604   $ 558   

Quarter ended June 30, 2011

   $ 3,513       $ (2,676   $ 837   

Quarter ended September 30, 2011

   $ 23,861       $ (3,024   $ 20,837   

In accordance with Accounting Standards Update 2009-13, Revenue Arrangements with Multiple Deliverables which was adopted by the Company effective January 1, 2011, and under the criteria set forth in Accounting Standards Codification (“ASC”) 605-25, the Company, based on an analysis of the facts, including consultation with its independent registered public accountants, originally determined that the License and other deliverables provided to Allergan under the Collaboration Agreement had standalone value for accounting purposes. As a result, the Company recognized as collaboration revenue $34.2 million of the nonrefundable $60.0 million upfront payment received from Allergan which primarily represented the allocated fair value of the License in the quarter ended March 31, 2011. The remaining $25.8 million was recorded as deferred revenue and would be amortized as collaboration revenue over the estimated obligation periods for the remaining deliverables. For the quarters ended June 30, 2011 and September 30, 2011, the Company recognized $3.5 million and $3.8 million, respectively, relating to the Upfront Payment.

Based on (i) the Staff Review and (ii) subsequent communications between the staff of the SEC, the Company and its independent registered public accountants relating to the Staff Review, the Company has determined the License does not have standalone value because Allergan is unable to use the License for its intended purpose without the performance of other deliverables by the Company over the term of the Collaboration Agreement. The Company believes that, since the License does not have standalone value, revenue received for the License must be recognized with these remaining deliverables. Accordingly, the Company will treat the deliverables as a single unit of accounting to be deferred and amortized on a straight-line basis over the term of the Collaboration Agreement.

For the nine months ended September 30, 2011, the Company expects that the effect of the restatement on the Company’s unaudited condensed consolidated financial statements will be as follows:

 

     Nine Months Ended September 30, 2011 (unaudited)  
(in thousands)    Previously reported      Adjustments     As restated  

Collaboration revenue

   $ 61,536       $ (39,304   $ 22,232   

Research and development

     25,552         —          25,552   

Sales, general and administrative

     15,529         —          15,529   

Total operating expenses

     41,081         —          41,081   

Net income (loss)

   $ 20,185       $ (39,304   $ (19,119

Net income (loss) per share attributed to common stockholders:

  

Basic

   $ 0.67       $ (1.30   $ (0.63

Diluted

   $ 0.64       $ (1.27   $ (0.63


The Company expects that, as an effect of the restatement, previously recorded items in the Company’s unaudited quarterly consolidated balance sheet as of September 30, 2011, will be as follows:

 

     As of September 30, 2011 (unaudited)  
(in thousands)    Previously reported     Adjustments     As restated  

Cash and cash equivalents

   $ 111,844      $ —        $ 111,844   

Total assets

     118,881        —          118,881   

Current portion of deferred revenue

     11,748        (8,399     3,349   

Total current liabilities

     22,053        (8,399     13,654   

Deferred revenue, less current portion

     6,715        47,703        54,418   

Total liabilities

     28,768        39,304        68,072   

Accumulated deficit

     (219,379     (39,304     (258,683

Total liabilities and stockholders’ equity

   $ 118,881      $ —        $ 118,881   

The Company’s management assessed the effectiveness of its internal control over financial reporting and disclosure controls and procedures. Based on its assessment, management determined there was a material weakness in its internal control over the evaluation of, and accounting for, complex multiple element revenue arrangements. The Company’s Audit Committee has discussed the matters pertaining to the restatement as disclosed in this Current Report on Form 8-K with the Company’s independent registered public accountants.


SIGNATURE

Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the Registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

Date: March 29, 2012

 

MAP PHARMACEUTICALS, INC.
By:  

/s/ Charlene A. Friedman

Name:   Charlene A. Friedman
Title:   Senior Vice President, General Counsel and Secretary