0001193125-13-207507.txt : 20130508 0001193125-13-207507.hdr.sgml : 20130508 20130508161509 ACCESSION NUMBER: 0001193125-13-207507 CONFORMED SUBMISSION TYPE: 8-K PUBLIC DOCUMENT COUNT: 3 CONFORMED PERIOD OF REPORT: 20130508 ITEM INFORMATION: Results of Operations and Financial Condition ITEM INFORMATION: Financial Statements and Exhibits FILED AS OF DATE: 20130508 DATE AS OF CHANGE: 20130508 FILER: COMPANY DATA: COMPANY CONFORMED NAME: AVANIR PHARMACEUTICALS, INC. CENTRAL INDEX KEY: 0000858803 STANDARD INDUSTRIAL CLASSIFICATION: PHARMACEUTICAL PREPARATIONS [2834] IRS NUMBER: 330314804 STATE OF INCORPORATION: DE FISCAL YEAR END: 0930 FILING VALUES: FORM TYPE: 8-K SEC ACT: 1934 Act SEC FILE NUMBER: 001-15803 FILM NUMBER: 13824709 BUSINESS ADDRESS: STREET 1: 20 ENTERPRISE STREET 2: SUITE 200 CITY: ALISO VIEJO STATE: CA ZIP: 92656 BUSINESS PHONE: 949-389-6700 MAIL ADDRESS: STREET 1: 20 ENTERPRISE STREET 2: SUITE 200 CITY: ALISO VIEJO STATE: CA ZIP: 92656 FORMER COMPANY: FORMER CONFORMED NAME: AVANIR PHARMACEUTICALS DATE OF NAME CHANGE: 19981207 FORMER COMPANY: FORMER CONFORMED NAME: LIDAK PHARMACEUTICALS DATE OF NAME CHANGE: 19920703 8-K 1 d535538d8k.htm FORM 8-K Form 8-K

 

 

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): May 8, 2013

 

 

Avanir Pharmaceuticals, Inc.

(Exact name of registrant as specified in its charter)

 

 

 

Delaware   001-15803   33-0314804

(State or other jurisdiction

of incorporation)

 

(Commission

File Number)

 

(I.R.S. Employer

Identification No.)

20 Enterprise, Suite 200, Aliso Viejo, California   92656
(Address of principal executive offices)   (Zip Code)

Registrant’s telephone number, including area code: (949) 389-6700

Not Applicable

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:

 

¨ 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 2.02. Results of Operations and Financial Condition.

On May 8, 2013, Avanir Pharmaceuticals, Inc. (the “Company”) issued a press release announcing its financial results for the three and six months ended March 31, 2013 (the “Earnings Press Release”). A copy of the Earnings Press Release is furnished herewith as Exhibit 99.1.

The information set forth under Item 2.02 and in Exhibit 99.1 shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933, except as shall be expressly set forth by specific reference in such filing.

 

Item 9.01. Financial Statements and Exhibits.

(d) Exhibits

 

Exhibit No.

  

Description

99.1    Earnings Press Release, dated May 8, 2013

* * *

 

-2-


SIGNATURES

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: May 8, 2013     Avanir Pharmaceuticals, Inc.
    By:   /s/ Christine G. Ocampo
      Christine G. Ocampo
      Vice President, Finance

 

-3-


Exhibit Index

 

Exhibit No.

  

Description

99.1    Earnings Press Release, dated May 8, 2013

 

-4-

EX-99.1 2 d535538dex991.htm EX-99.1 EX-99.1

Exhibit 99.1

 

LOGO

AVANIR PHARMACEUTICALS REPORTS FISCAL 2013 SECOND QUARTER FINANCIAL AND BUSINESS RESULTS

ALISO VIEJO, Calif., May 8, 2013—Avanir Pharmaceuticals, Inc. (NASDAQ: AVNR) today reported financial results for the three and six months ended March 31, 2013.

Quarterly Financial Highlights

 

   

Total company net revenues of $17.4 million

 

   

Gross and net NUEDEXTA® sales increased to $20.8 million and $16.5 million, respectively, representing growth of 14% and 11% versus the previous quarter

 

   

Cash, cash equivalents, and restricted investments of $70.2 million as of March 31, 2013.

“Avanir achieved a major milestone with the exciting news regarding the positive CHMP opinion for NUEDEXTA in Europe. This is a significant moment in the evolution of the company towards its goal of becoming a leading mid-cap biopharmaceutical company,” said Keith A. Katkin, president and CEO of Avanir. “Additionally, we continue to execute in the U.S. as demonstrated by our commercial and clinical progress. We enter the second half of fiscal 2013 with strong momentum, a broad CNS pipeline and a continued focus on building our business.”

Fiscal 2013 Second Quarter Results

 

   

Total net revenues for the quarter ended March 31, 2013 were $17.4 million, compared with $10.0 million for the comparable quarter in fiscal 2012, representing 74% year-over-year growth. Total net revenues consist of NUEDEXTA net revenue and royalty revenue from Abreva®.

 

   

Total operating expenses, excluding cost of sales and share-based compensation were $30.1 million in the second quarter of fiscal 2013, compared with $25.3 million in the comparable period in fiscal 2012.

 

   

Cash used in operations was $9.6 million in the second quarter of fiscal 2013.

 

   

Net loss for the fiscal 2013 second quarter was $16.5 million, or $0.12 per share, compared with a net loss of $17.0 million, or $0.13 per share, for the same period in fiscal 2012.

Fiscal 2013 Six-Month Results

 

   

Total net revenues for the first six-months of fiscal 2013 totaled $34.0 million, compared with $17.2 million for the first six months of fiscal 2012.

 

   

Total operating expenses, excluding cost of sales and share-based compensation were $55.4 million in the first six-months of fiscal 2013, compared to $47.0 million in the comparable period for fiscal 2012.

 

   

Cash used in operations was $22.3 million in the first six months of fiscal 2013.

 

   

Net loss for the first six-months of fiscal 2013 was $28.6 million, or $0.21 per share, compared with a net loss of $33.0 million, or $0.25 per share for the comparable period in fiscal 2012.

NUEDEXTA Revenue

For the quarter ended March 31, 2013, the company reported NUEDEXTA gross and net revenue of $20.8 million and $16.5 million respectively. Second quarter fiscal 2013 NUEDEXTA net revenue increased 81% versus the previous year and 11% over the previous quarter.

Cash, Cash Equivalents & Marketable Securities

As of March 31, 2013 Avanir had cash, cash equivalents and restricted investments totaling $70.2 million, including cash and cash equivalents of $67.9 million.

Business Highlights

 

   

The company reported an eighth consecutive quarter of NUEDEXTA unit growth in both business channels with 13% retail and 4% institutional growth.

 

   

The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion for NUEDEXTA, recommending it be approved in two dosage strengths for the treatment of pseudobulbar affect (PBA), irrespective of neurologic cause.

 

   

The company appointed Corinne Nevinny, a seasoned life sciences executive with broad healthcare industry experience, to the company’s board of directors.

Note to Investors: As previously announced, Avanir will hold a conference call to discuss fiscal 2013 second quarter financial results today, May 8, 2013, beginning at 1:30 p.m. Pacific Time. You can listen to this call by dialing 1- 877 703 6106 for domestic callers or +1- 857 244 7305 for international callers, and entering passcode 62763985. Those interested in listening to the conference call live via the internet may do so by visiting http://ir.avanir.com.

About NUEDEXTA

NUEDEXTA is an innovative combination of two well-characterized components; dextromethorphan hydrobromide (20 mg), the ingredient active in the central nervous system, and quinidine sulfate (10 mg), a metabolic inhibitor enabling therapeutic dextromethorphan concentrations. NUEDEXTA acts on sigma-1 and NMDA receptors in the brain, although the mechanism by which NUEDEXTA exerts therapeutic effects in patients with PBA is unknown.

NUEDEXTA Important Safety Information

NUEDEXTA is indicated for the treatment of pseudobulbar affect (PBA). PBA occurs secondary to a variety of otherwise unrelated neurological conditions, and is characterized by involuntary, sudden, and frequent episodes of laughing and/or crying. PBA episodes typically occur out of proportion or incongruent to the underlying emotional state.


Studies to support the effectiveness of NUEDEXTA were performed in patients with amyotrophic lateral sclerosis (ALS) and multiple sclerosis (MS). NUEDEXTA has not been shown to be safe and effective in other types of emotional liability that can commonly occur, for example, in Alzheimer’s disease and other dementias.

NUEDEXTA and certain other medicines can interact, causing serious side effects. If you take certain drugs or have certain heart problems, NUEDEXTA may not be right for you.

NUEDEXTA causes dose-dependent QTc prolongation. When initiating NUEDEXTA in patients at risk for QT prolongation and torsades de pointes, electrocardiographic (ECG) evaluation should be conducted at baseline and 3-4 hours after the first dose.

The most common adverse reactions are diarrhea, dizziness, cough, vomiting, asthenia, peripheral edema, urinary tract infection, influenza, increased gamma-glutamyltransferase, and flatulence. NUEDEXTA may cause dizziness.

These are not all the risks from use of NUEDEXTA. Please refer to full Prescribing Information at www.NUEDEXTA.com.

About Avanir Pharmaceuticals, Inc.

Avanir Pharmaceuticals, Inc. is a biopharmaceutical company focused on bringing innovative medicines to patients with central nervous system disorders of high unmet medical need. As part of our commitment, we have extensively invested in our pipeline and are dedicated to advancing medicines that can substantially improve the lives of patients and their loved ones. For more information about Avanir, please visit www.avanir.com.

AVANIR® and NUEDEXTA® are trademarks or registered trademarks of Avanir Pharmaceuticals, Inc. in the United States and other countries.

©2013 Avanir Pharmaceuticals, Inc. All Rights Reserved.

Forward Looking Statements

Except for the historical information contained herein, the matters set forth in this press release, including statements regarding Avanir’s plans, potential opportunities, financial or other expectations, projections, goals objectives, milestones, strategies, market growth, timelines, legal matters, product pipeline, clinical studies, product development and the potential benefits of its commercialized products and products under development are forward-looking statements within the meaning of the “safe harbor” provisions of the Private Securities Litigation Reform Act of 1995. These forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially, including the risks and uncertainties associated with Avanir’s operating performance and financial position, the market demand for and acceptance of Avanir’s products domestically and internationally, research, development and commercialization of new products domestically and internationally, obtaining additional indications, obtaining and maintaining regulatory approvals domestically and internationally, and other risks detailed from time to time in the Company’s most recent Annual Report on Form 10-K and other documents subsequently filed with or furnished to the Securities and Exchange Commission. These forward-looking statements are based on current information that may change and you are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this press release. All forward-looking statements are qualified in their entirety by this cautionary statement, and the Company undertakes no obligation to revise or update any forward-looking statement to reflect events or circumstances after the issuance of this press release.

Avanir Investor & Media Contact

Ian Clements, PhD

ir@avanir.com

+1 (949) 389-6700


AVANIR PHARMACEUTICALS, INC.

CONDENSED CONSOLIDATED BALANCE SHEETS

 

     March 31      September 30,  
     2013      2012  
     (unaudited)      (audited)  

ASSETS

  

Current assets:

     

Cash and cash equivalents

   $ 67,859,426       $ 69,778,406   

Restricted cash and cash equivalents

     654,624         652,913   

Trade receivables, net

     9,679,775         7,231,759   

Inventories, net

     428,969         415,475   

Prepaid expenses and other current assets

     2,570,074         2,434,590   

Restricted short-term investment

     —            401,550   
  

 

 

    

 

 

 

Total current assets

     81,192,868         80,914,693   

Restricted long-term investments

     1,303,938         1,302,136   

Property and equipment, net

     1,680,317         1,808,594   

Non-current inventories, net

     908,366         908,364   

Other assets

     625,196         1,078,009   
  

 

 

    

 

 

 

TOTAL ASSETS

   $ 85,710,685       $ 86,011,796   
  

 

 

    

 

 

 

LIABILITIES AND STOCKHOLDERS’ EQUITY

  

Current liabilities:

     

Accounts payable, accrued expenses and other liabilities

   $ 20,734,658       $ 15,598,666   

Current portion of note payable

     7,812,014         2,162,263   

Current portion of deferred royalty revenues

     2,557,464         2,557,464   
  

 

 

    

 

 

 

Total current liabilities

     31,104,136         20,318,393   

Accrued expenses and other liabilities, net of current portion

     1,073,265         666,179   

Note Payable

     21,325,055         26,698,263   

Deferred royalty revenues, net of current portion

     117,022         1,491,854   
  

 

 

    

 

 

 

Total liabilities

     53,619,478         49,174,689   
  

 

 

    

 

 

 

Total stockholders’ equity

     32,091,207         36,837,107   
  

 

 

    

 

 

 

TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY

   $ 85,710,685       $ 86,011,796   
  

 

 

    

 

 

 


AVANIR PHARMACEUTICALS, INC.

CONDENSED STATEMENT OF OPERATIONS

 

     Three Months Ended March 31,     Six Months Ended March 31,  
     2013     2012     2013     2012  

REVENUES

        

Net product sales

   $ 16,535,059      $ 9,141,873        31,414,321        14,630,636   

Revenues from royalties

     899,129        898,515        2,525,139        2,574,635   

Revenue from research grant services

     —           —           15,000        —      
  

 

 

   

 

 

   

 

 

   

 

 

 

Total revenues

     17,434,188        10,040,388        33,954,460        17,205,271   
  

 

 

   

 

 

   

 

 

   

 

 

 

OPERATING EXPENSES

        

Cost of product sales

     933,426        534,345        1,771,555        844,148   

Cost of research grant services

     69,090        —           78,488        —      

Research and development

     8,874,298        6,395,155        15,522,389        10,139,670   

Selling and marketing

     16,061,408        14,814,013        29,583,827        28,596,850   

General and administrative

     6,978,684        5,346,991        13,517,087        10,639,173   
  

 

 

   

 

 

   

 

 

   

 

 

 

Total operating expenses

     32,916,906        27,090,504        60,473,346        50,219,841   
  

 

 

   

 

 

   

 

 

   

 

 

 

Loss from operations

     (15,482,718     (17,050,116     (26,518,886     (33,014,570

OTHER INCOME (EXPENSE)

        

Interest income

     15,065        7,882        34,396        22,173   

Interest expense

     (1,059,245     —           (2,118,490     —      

Other, net

     197        75        197        4,081   
  

 

 

   

 

 

   

 

 

   

 

 

 

Loss before provision for income taxes

     (16,526,701     (17,042,159     (28,602,783     (32,988,316

Provision for income taxes

        
  

 

 

   

 

 

   

 

 

   

 

 

 

Net loss and comprehensive loss

   $ (16,526,701   $ (17,042,159   $ (28,602,783   $ (32,988,316
  

 

 

   

 

 

   

 

 

   

 

 

 

Basic and diluted net loss per share

   $ (0.12   $ (0.13   $ (0.21   $ (0.25
  

 

 

   

 

 

   

 

 

   

 

 

 

Basic and diluted weighted average number of common shares outstanding

     139,173,746        133,463,300        137,959,958        130,683,671   
  

 

 

   

 

 

   

 

 

   

 

 

 
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