Document


 
 

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 4, 2017
PACIRA PHARMACEUTICALS, INC.
(Exact name of registrant as specified in its charter)
Delaware
 
001-35060
 
51-0619477
(State or other jurisdiction of incorporation)
 
(Commission File Number)
 
(IRS Employer Identification No.)

5 Sylvan Way, Suite 300
Parsippany, New Jersey 07054
(Address and Zip Code of Principal Executive Offices)

(973) 254-3560
(Registrant’s Telephone Number, Including Area Code)

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:

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))

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

Emerging growth company  o

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. 


 
 





Item 2.02. Results of Operations and Financial Condition.
 
On May 4, 2017, we issued a press release announcing our results for the first quarter ended March 31, 2017. The full text of the press release issued in connection with the announcement is furnished as Exhibit 99.1 to this Current Report on Form 8-K.
 
The information in this Item 2.02 of Form 8-K and Exhibit 99.1 attached hereto 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 liabilities 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 9.01. Financial Statements and Exhibits.

Exhibit
No.
 
Description
 
 
 
99.1
 
Earnings Press Release dated May 4, 2017






SIGNATURE

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

 
 
 
PACIRA PHARMACEUTICALS, INC.
(REGISTRANT)
 
 
 
 
Dated:
May 4, 2017
By:
/s/ KRISTEN WILLIAMS
 
 
 
Kristen Williams
 
 
 
Chief Administrative Officer,
 
 
 
General Counsel and Secretary



Exhibit
https://cdn.kscope.io/6e514e2eac75b4df626d7a4f2b6e46a3-paciralogo1a05.jpg
NEWS RELEASE

FOR IMMEDIATE RELEASE


Pacira Pharmaceuticals, Inc. Reports First Quarter 2017 Financial Results

-- EXPAREL® Net Product Sales Up 6% Year-Over-Year --
-- Conference Call Today at 8:30 a.m. ET --

PARSIPPANY, N.J., May 4, 2017 - Pacira Pharmaceuticals, Inc. (NASDAQ: PCRX) today provided updates on EXPAREL® (bupivacaine liposome injectable suspension) for postsurgical pain in the United States and announced consolidated financial results for the first quarter ended March 31, 2017.

“We’re pleased with our strong first quarter highlighted by important strategic advances and solid revenue growth,” said Dave Stack, chairman and chief executive officer of Pacira. “Our newly launched partnerships with DePuy Synthes and Trinity Health center on our shared commitment to providing patients and healthcare providers with an opioid-sparing solution. We are also advancing a robust clinical program with important value-drivers on the near-term horizon, including mid-year data readouts for our two Phase 3 nerve block studies and the publication of our successful Phase 4 study in total knee arthroplasty. Finally, we significantly strengthened our balance sheet during the first quarter. We believe the foundation is in place to drive EXPAREL sales growth for the rest of 2017 and beyond.”

Recent Highlights

Positive results from Phase 4 study of EXPAREL in total knee arthroplasty (TKA). EXPAREL (bupivacaine liposome injectable suspension) achieved statistical significance for its co-primary endpoints of opioid reduction (p=0.0048) and postsurgical pain control (p=0.0381). EXPAREL also achieved statistical significance for key secondary endpoints, including time to first opioid and the percentage of patients who did not require any opioids to treat their postsurgical pain. The trial compared EXPAREL-based local analgesia infiltration to standard bupivacaine-based local analgesia infiltration, each as part of a standard multi-modal analgesic protocol.
EXPAREL focus of educational programs at American Academy of Orthopaedic Surgeons Annual Meeting. At the American Academy of Orthopaedic Surgeons Annual Meeting, Pacira and its partner DePuy Synthes, a Johnson & Johnson company, supported multiple educational programs around the impact of opioids and postsurgical pain management. The companies also hosted innovative virtual reality experiences to demonstrate EXPAREL best practice infiltration technique in total knee arthroplasty.





Pacira and DePuy Synthes entered into an agreement in January 2017 to support the promotion, education and training for EXPAREL in orthopedic procedures.
Collaboration with Trinity Health to decrease opioid use. In March 2017, Pacira and Trinity Health launched a collaboration focusing on developing standardized procedure-specific enhanced recovery and pain protocols that will include using opioid alternatives when appropriate. The two organizations will also develop educational materials and generate data to track progress.
Gross proceeds of $345 million from private offering of convertible notes. In March 2017, Pacira completed a private offering of 2.375% convertible senior notes due 2022. The Company incurred approximately $11 million in financing costs and retired approximately $118 million in principal value of its existing 3.25% convertible senior notes due 2019.
New EXPAREL patent extends exclusivity to December 2021. In March 2017, the U.S. Patent and Trademark Office issued U.S. Patent 9,585,838. The claims of the patent relate to the production of multivesicular liposomes. This is the third EXPAREL patent listed in the Food and Drug Administration Orange Book.

First Quarter 2017 Financial Results

EXPAREL net product sales were $67.7 million in the first quarter of 2017, a 6% increase over the $63.8 million reported for the first quarter of 2016.

Total revenues were $69.3 million in the first quarter of 2017, a 6% increase over the $65.5 million reported for the first quarter of 2016.

Total operating expenses were $83.3 million in the first quarter of 2017, compared to $67.7 million in the first quarter of 2016.

GAAP net loss was $19.9 million, or $(0.52) per share (basic and diluted), in the first quarter of 2017, compared to a GAAP net loss of $3.9 million, or $(0.10) per share (basic and diluted), in the first quarter of 2016.

Non-GAAP net loss was $7.3 million, or $(0.19) per share (basic and diluted) in the first quarter of 2017, compared to non-GAAP net income of $5.7 million, or $0.15 per share (basic) and $0.14 per share (diluted), in the first quarter of 2016.

Pacira ended the first quarter of 2017 with cash, cash equivalents and short-term investments (“cash”) of $383.7 million.

Pacira had 38.0 million basic weighted average shares of common stock outstanding in the first quarter of 2017.

2017 Outlook

Pacira reiterated its full year 2017 financial guidance as follows:




EXPAREL net product sales of $290 million to $310 million.

Non-GAAP gross margins of approximately 70%.

Non-GAAP research and development (R&D) expense of $50 million to $60 million.

Non-GAAP selling, general and administrative (SG&A) expense of $145 million to $155 million.

Stock-based compensation of $30 million to $35 million.

See “Non-GAAP Financial Information” and “Reconciliations of GAAP to Non-GAAP 2017 Financial Guidance” below.

Today’s Conference Call and Webcast Reminder

The Pacira management team will host a conference call to discuss the company’s financial results and recent developments today, Thursday, May 4, 2017, at 8:30 a.m. ET. The call can be accessed by dialing 1-877-845-0779 (domestic) or 1-720-545-0035 (international) ten minutes prior to the start of the call and providing the Conference ID 4977296.

A replay of the call will be available approximately two hours after the completion of the call and can be accessed by dialing 1-855-859-2056 (domestic) or 1-404-537-3406 (international) and providing the Conference ID 4977296. The replay of the call will be available for two weeks from the date of the live call.

The live, listen-only webcast of the conference call can also be accessed by visiting the “Investors & Media” section of the company’s website at investor.pacira.com. A replay of the webcast will be archived on the Pacira website for two weeks following the call.

Non-GAAP Financial Information

This press release contains financial measures that do not comply with U.S. generally accepted accounting principles (GAAP), such as non-GAAP net income (loss), non-GAAP cost of goods sold, non-GAAP gross margins, non-GAAP research and development (R&D) and non-GAAP selling, general and administrative (SG&A) expenses, because such measures exclude stock-based compensation, amortization of debt discount and loss on early extinguishment of debt. These measures supplement our financial results prepared in accordance with GAAP. Pacira management uses these measures to better analyze its financial results, estimate its future cost of goods sold, gross margins, R&D and SG&A outlook for 2017 and to help make managerial decisions. In management’s opinion, these non-GAAP measures are useful to investors and other users of our financial statements by providing greater transparency into the operating performance at Pacira and the company’s future outlook. Such measures should not be deemed to be an alternative to GAAP requirements or a measure of liquidity for Pacira. Non-GAAP



measures are also unlikely to be comparable with non-GAAP disclosures released by other companies. See the tables below for a reconciliation of GAAP to non-GAAP measures, and a reconciliation of our GAAP to non-GAAP 2017 financial guidance for gross margins, R&D and SG&A.

About Pacira

Pacira Pharmaceuticals, Inc. (NASDAQ: PCRX) is a specialty pharmaceutical company focused on the clinical and commercial development of new products that meet the needs of acute care practitioners and their patients. The company’s flagship product, EXPAREL® (bupivacaine liposome injectable suspension), indicated for single-dose infiltration into the surgical site to produce postsurgical analgesia, was commercially launched in the United States in April 2012. EXPAREL and two other products have successfully utilized DepoFoam®, a unique and proprietary product delivery technology that encapsulates drugs without altering their molecular structure, and releases them over a desired period of time. Additional information about Pacira is available at www.pacira.com.

About EXPAREL®

EXPAREL (bupivacaine liposome injectable suspension) is currently indicated for single-dose infiltration into the surgical site to produce postsurgical analgesia. The product combines bupivacaine with DepoFoam®, a proven product delivery technology that delivers medication over a desired time period. EXPAREL represents the first and only multivesicular liposome local anesthetic that can be utilized in the peri- or postsurgical setting. By utilizing the DepoFoam platform, a single dose of EXPAREL delivers bupivacaine over time, providing significant reductions in cumulative pain score with up to a 45 percent decrease in opioid consumption; the clinical benefit of the opioid reduction was not demonstrated. Additional information is available at www.EXPAREL.com.

Important Safety Information

EXPAREL is contraindicated in obstetrical paracervical block anesthesia. EXPAREL has not been studied for use in patients younger than 18 years of age. Non-bupivacaine-based local anesthetics, including lidocaine, may cause an immediate release of bupivacaine from EXPAREL if administered together locally. The administration of EXPAREL may follow the administration of lidocaine after a delay of 20 minutes or more. Other formulations of bupivacaine should not be administered within 96 hours following administration of EXPAREL. Monitoring of cardiovascular and neurological status, as well as vital signs should be performed during and after injection of EXPAREL as with other local anesthetic products. Because amide-type local anesthetics, such as bupivacaine, are metabolized by the liver, EXPAREL should be used cautiously in patients with hepatic disease. Patients with severe hepatic disease, because of their inability to metabolize local anesthetics normally, are at a greater risk of developing toxic plasma concentrations. In clinical trials, the most common adverse reactions (incidence greater-than or equal to 10%) following EXPAREL administration were nausea, constipation, and vomiting.




Please see the full Prescribing Information for more details available at http://www.exparel.com/pdf/EXPAREL_Prescribing_Information.pdf.

Forward Looking Statements

Any statements in this press release about our future expectations, plans, outlook and prospects, and other statements containing the words “believes,” “anticipates,” “plans,” “estimates,” “expects,” “intends,” “may” and similar expressions, constitute forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. Actual results may differ materially from those indicated by such forward-looking statements as a result of various important factors, including risks relating to: the success of our sales and manufacturing efforts in support of the commercialization of EXPAREL; the rate and degree of market acceptance of EXPAREL and our other products; the size and growth of the potential markets for EXPAREL and our ability to serve those markets; our plans to expand the use of EXPAREL to additional indications and opportunities, and the timing and success of any related clinical trials; the related timing and success of United States Food and Drug Administration supplemental New Drug Applications; the outcome of the U.S. Department of Justice inquiry; our plans to evaluate, develop and pursue additional DepoFoam-based product candidates; clinical trials in support of an existing or potential DepoFoam-based product; our plans to continue to manufacture and provide support services for our commercial partners who have licensed DepoCyt(e); our commercialization and marketing capabilities; our and Patheon UK Limited’s ability to successfully and timely construct dedicated EXPAREL manufacturing suites; and other factors discussed in the “Risk Factors” of our most recent Annual Report on Form 10-K for the fiscal year ended December 31, 2016 and in other filings that we periodically make with the SEC. In addition, the forward-looking statements included in this press release represent our views as of the date of this press release. Important factors could cause our actual results to differ materially from those indicated or implied by forward-looking statements, and as such we anticipate that subsequent events and developments will cause our views to change. However, while we may elect to update these forward-looking statements at some point in the future, we specifically disclaim any obligation to do so. These forward-looking statements should not be relied upon as representing our views as of any date subsequent to the date of this press release.



Investor Contact:
Susan Mesco, (973) 451-4030
susan.mesco@pacira.com
    
Media Contact:
Coyne Public Relations
Alyssa Schneider, (973) 588-2270
aschneider@coynepr.com
 


(Tables to Follow)



Pacira Pharmaceuticals, Inc.
Condensed Consolidated Balance Sheets
(in thousands)
(unaudited)
 
March 31,
2017
 
December 31,
2016
ASSETS
 

 
 

Current assets:
 

 
 

     Cash, cash equivalents and short-term investments
$
383,699

 
$
172,597

     Accounts receivable, net
27,702

 
29,937

     Inventories, net
30,311

 
31,278

     Prepaid expenses and other current assets
6,252

 
9,277

          Total current assets
447,964

 
243,089

Fixed assets, net
102,571

 
101,016

Goodwill
48,829

 
46,737

Other assets
598

 
624

          Total assets
$
599,962

 
$
391,466

 
 
 
 
LIABILITIES AND STOCKHOLDERS’ EQUITY
 

 
 

Current liabilities:
 

 
 

     Accounts payable
$
9,373

 
$
7,511

     Accrued expenses
34,900

 
36,666

     Convertible senior notes (1)
759

 

     Current portion of deferred revenue
520

 
595

     Income taxes payable
96

 
66

          Total current liabilities
45,648

 
44,838

Deferred revenue
7,357

 
7,487

Other liabilities
10,332

 
11,427

Convertible senior notes (2)
265,992

 
108,738

Total stockholders’ equity
270,633

 
218,976

          Total liabilities and stockholders’ equity
$
599,962

 
$
391,466

 
(1) $759 thousand relates to our 3.25% convertible senior notes due 2019. These notes are classified as current at March 31, 2017 because the note holders can convert any time during the quarter ended June 30, 2017. These convertible senior notes were classified as non-current at December 31, 2016.

(2) At March 31, 2017, $266.0 million relates to our 2.375% convertible senior notes due 2022 that are not currently convertible. $108.7 million at December 31, 2016 relates to our 3.25% convertible senior notes due 2019 that are now current liabilities as explained in footnote 1 above.




Pacira Pharmaceuticals, Inc.
Consolidated Statements of Operations
(in thousands, except per share amounts)
(unaudited)
 
Three Months Ended
 
March 31,
 
2017
 
2016
 Net product sales:
 
 
 
      EXPAREL
$
67,701

 
$
63,752

      DepoCyt(e) and other product sales
724

 
750

 Total net product sales
68,425

 
64,502

 Collaborative licensing and milestone revenue
206

 
356

 Royalty revenue
652

 
616

      Total revenues
69,283

 
65,474

 
 
 
 
Operating expenses:
 

 
 

     Cost of goods sold
24,581

 
20,278

     Research and development
16,632

 
9,493

     Selling, general and administrative
42,120

 
37,957

          Total operating expenses
83,333

 
67,728

Loss from operations
(14,050
)
 
(2,254
)
 
 
 
 
Other (expense) income:
 

 
 

     Interest income
514

 
252

     Interest expense
(2,589
)
 
(1,868
)
     Loss on early extinguishment of debt (1)
(3,721
)
 

     Other, net
10

 
48

          Total other expense, net
(5,786
)
 
(1,568
)
Loss before income taxes
(19,836
)
 
(3,822
)
     Income tax expense
(30
)
 
(32
)
Net loss
$
(19,866
)
 
$
(3,854
)
 
 
 
 
Net loss per share:
 

 
 

     Basic and diluted net loss per common share
$
(0.52
)
 
$
(0.10
)
Weighted average common shares outstanding:
 

 
 

     Basic and diluted
37,998

 
37,020

 
(1) Amount relates to the loss on early extinguishment from our repurchase of $117.7 million of principal amount of our 3.25% convertible senior notes due 2019.



Pacira Pharmaceuticals, Inc.
Reconciliation of GAAP to Non-GAAP Financial Information
(in thousands, except per share amounts)
(unaudited)
 
Three Months Ended
 
March 31,
 
2017
 
2016
 
 
 
 
GAAP net loss
$
(19,866
)
 
$
(3,854
)
 
 
 
 
Non-GAAP adjustments:
 
 
 
     Stock-based compensation
7,400

 
8,490

     Loss on early extinguishment of debt
3,721

 

     Amortization of debt discount
1,411

 
1,022

          Total Non-GAAP adjustments
12,532

 
9,512

 
 
 
 
Non-GAAP net income (loss)
$
(7,334
)
 
$
5,658

 
 
 
 
GAAP basic and diluted net loss per common share
$
(0.52
)
 
$
(0.10
)
 
 
 
 
Non-GAAP basic net income (loss) per common share
$
(0.19
)
 
$
0.15

Non-GAAP diluted net income (loss) per common share
$
(0.19
)
 
$
0.14

 
 
 
 
Weighted average common shares outstanding - basic
37,998

 
37,020

Weighted average common shares outstanding - diluted
37,998

 
41,144

 
 
 
 
Cost of goods sold reconciliation:
 
 
 
GAAP cost of goods sold
$
24,581

 
$
20,278

     Stock-based compensation
(1,375
)
 
(1,549
)
Non-GAAP cost of goods sold
$
23,206

 
$
18,729

 
 
 
 
Research and development reconciliation:
 
 
 
GAAP research and development
$
16,632

 
$
9,493

     Stock-based compensation
(658
)
 
(893
)
Non-GAAP research and development
$
15,974

 
$
8,600

 
 
 
 
Selling, general and administrative reconciliation:
 
 
 
GAAP selling, general and administrative
$
42,120

 
$
37,957

     Stock-based compensation
(5,367
)
 
(6,048
)
Non-GAAP selling, general and administrative
$
36,753

 
$
31,909




Pacira Pharmaceuticals, Inc.
Reconciliation of GAAP to Non-GAAP 2017 Financial Guidance
(dollars in millions)
GAAP to Non-GAAP Guidance
 
GAAP
 
Stock-Based Compensation
 
Non-GAAP
EXPAREL net product sales
 
$290 to $310
 
 
Gross margin
 
Approx. 68%
 
Approx. 2%
 
Approx. 70%
Research and development expense
 
$52 to $64
 
$2 to $4
 
$50 to $60
Selling, general and administrative expense
 
$167 to $180
 
$22 to $25
 
$145 to $155
Stock-based compensation
 
$30 to $35