UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 10-Q
(Mark One)
[X] QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES
EXCHANGE ACT OF 1934
For the quarterly period ended: MARCH 31, 2003
OR
[ ] TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES
EXCHANGE ACT OF 1934
For the transition period from ____________ to ____________
Commission file number: 001-16033
ESPERION THERAPEUTICS, INC.
(Exact name of registrant as specified in its charter)
DELAWARE 38-3419139
(State of incorporation) (IRS Employer Identification No.)
3621 S. STATE STREET,
695 KMS PLACE
ANN ARBOR, MI 48108
(734) 332-0506
(Address of principal executive offices, including zip
code, and telephone number, including area code)
Indicate by check mark whether the registrant (1) has filed all reports
required to be filed by Section 13 or 15(d) of the Securities Exchange Act of
1934 during the preceding 12 months (or for such shorter period that the
registrant was required to file such reports), and (2) has been subject to such
filing requirements for the past 90 days.
[X] Yes [ ] No
Indicate by check mark whether the registrant is an accelerated filer (as
defined in Rule 12b-2 of the Exchange Act).
[X] Yes [ ] No
The number of outstanding shares of the registrant's common stock, as of May
6, 2003, was 29,456,836.
ESPERION THERAPEUTICS, INC.
FORM 10-Q
TABLE OF CONTENTS
PAGE
----
PART I - FINANCIAL INFORMATION
Item 1. Financial Statements
Condensed Consolidated Balance Sheets as of March 31, 2003 and
December 31, 2002................................................................. 3
Condensed Consolidated Statements of Operations for the Three Months Ended
March 31, 2003 and 2002, and the period from inception to March 31, 2003......... 4
Condensed Consolidated Statements of Cash Flows for the Three Months Ended
March 31, 2003 and 2002, and the period from inception to March 31, 2003......... 5
Notes to Condensed Consolidated Financial Statements................................. 6
Item 2. Management's Discussion and Analysis of Financial Condition and Results of Operations.... 9
Item 3. Quantitative and Qualitative Disclosures about Market Risk............................... 15
Item 4. Controls and Procedures.................................................................. 15
PART II -- OTHER INFORMATION
Item 1. Legal Proceedings........................................................................ 16
Item 2. Changes in Securities and Use of Proceeds................................................ 16
Item 3. Defaults Upon Senior Securities.......................................................... 16
Item 4. Submission of Matters to a Vote of Security Holders...................................... 16
Item 5. Other Information........................................................................ 16
Item 6. Exhibits and Reports on Form 8-K......................................................... 16
SIGNATURES ......................................................................................... 17
INDEX TO EXHIBITS................................................................................... 20
2
PART I -- FINANCIAL INFORMATION
ITEM 1. FINANCIAL STATEMENTS
ESPERION THERAPEUTICS, INC. AND SUBSIDIARIES
(A Company in the Development Stage)
CONDENSED CONSOLIDATED BALANCE SHEETS
MARCH 31, DECEMBER 31,
In thousands 2003 2002
---------------------------------------------------------------------------------------------
ASSETS: (UNAUDITED)
Current assets:
Cash and cash equivalents $ 31,605 $ 40,499
Short-term investments 6,253 4,354
Prepaid expenses and other 590 410
---------------------------------------------------------------------------------------------
Total current assets 38,448 45,263
---------------------------------------------------------------------------------------------
Property and equipment, net 2,710 3,001
Goodwill 3,108 3,108
Deposits and other assets 6 35
---------------------------------------------------------------------------------------------
Total assets $ 44,272 $ 51,407
=============================================================================================
LIABILITIES AND STOCKHOLDERS' EQUITY:
Current liabilities:
Current portion of long-term debt $ 1,081 $ 1,061
Accounts payable 1,878 1,687
Accrued liabilities 1,999 2,185
---------------------------------------------------------------------------------------------
Total current liabilities 4,958 4,933
---------------------------------------------------------------------------------------------
Long-term debt, less current portion 7,721 7,731
Commitments and Contingencies (Note 5)
Stockholders' equity:
Preferred stock - -
Common stock 29 29
Additional paid-in capital 133,517 133,411
Notes receivable - (3)
Accumulated deficit during the development stage (101,452) (94,046)
Deferred stock compensation (442) (589)
Accumulated other comprehensive loss (59) (59)
---------------------------------------------------------------------------------------------
Total stockholders' equity 31,593 38,743
---------------------------------------------------------------------------------------------
Total liabilities and stockholders' equity $ 44,272 $ 51,407
=============================================================================================
The accompanying notes are an integral part of these condensed
consolidated financial statements.
3
ESPERION THERAPEUTICS, INC. AND SUBSIDIARIES
(A Company in the Development Stage)
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(Unaudited)
THREE MONTHS ENDED
MARCH 31, INCEPTION TO
----------------------------- MARCH 31,
In thousands, except share and per share data 2003 2002 2003
---------------------------------------------------------------------------------------------------------------------
Operating expenses:
Research and development $ 5,460 $ 5,705 $ 81,908
General and administrative 1,629 1,645 18,745
Goodwill amortization - - 1,089
Purchased in-process research and development - - 4,000
---------------------------------------------------------------------------------------------------------------------
Total operating expenses 7,089 7,350 105,742
---------------------------------------------------------------------------------------------------------------------
Loss from operations (7,089) (7,350) (105,742)
---------------------------------------------------------------------------------------------------------------------
Other income (expense):
Interest income 149 320 7,346
Interest expense (310) (252) (2,695)
Other, net (156) (21) (361)
---------------------------------------------------------------------------------------------------------------------
Total other income (expense) (317) 47 4,290
---------------------------------------------------------------------------------------------------------------------
Net loss before income taxes (7,406) (7,303) (101,452)
Provision for income taxes - - -
---------------------------------------------------------------------------------------------------------------------
Net loss (7,406) (7,303) (101,452)
Beneficial conversion feature on preferred stock - - (22,870)
---------------------------------------------------------------------------------------------------------------------
Net loss attributable to common stockholders ($7,406) ($7,303) ($124,322)
=====================================================================================================================
Basic and diluted net loss per share ($0.25) ($0.25)
=====================================================================================================
Weighted average shares used in computing basic
and diluted net loss per share 29,395,549 29,197,523
=====================================================================================================
The accompanying notes are an integral part of these condensed
consolidated financial statements.
4
ESPERION THERAPEUTICS, INC. AND SUBSIDIARIES
(A Company in the Development Stage)
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(Unaudited)
THREE MONTHS ENDED
MARCH 31, INCEPTION TO
------------------------ MARCH 31,
In thousands 2003 2002 2003
-----------------------------------------------------------------------------------------------------------------------
Cash flows from operating activities:
Net loss ($7,406) ($7,303) ($101,452)
Adjustments to reconcile net loss to net cash
used in operating activities:
Purchased in-process research and development - - 4,000
Depreciation and amortization 316 361 5,129
Stock-based compensation expense 147 208 3,797
Decrease in notes receivable 3 3 126
Loss on sale of property and equipment 1 1 192
Non-cash interest expense included in long-term debt 115 82 902
Changes in assets and liabilities:
Prepaid expenses and other (180) 112 (1,418)
Other assets 29 (25) 549
Accounts payable 191 44 2,147
Accrued liabilities (190) (741) 1,992
----------------------------------------------------------------------------------------------------------------------
Net cash used in operating activities (6,974) (7,258) (84,036)
----------------------------------------------------------------------------------------------------------------------
Cash flows from investing activities:
Purchases of property and equipment (25) (666) (7,528)
Acquisition of Talaria Therapeutics, Inc. - - (233)
Proceeds from sale of property and equipment - 2 32
Purchases of short-term investments (2,001) - (39,216)
Maturities of short-term investments 102 - 32,963
----------------------------------------------------------------------------------------------------------------------
Net cash used in investing activities (1,924) (664) (13,982)
----------------------------------------------------------------------------------------------------------------------
Cash flows from financing activities:
Proceeds from issuance of convertible preferred stock - - 42,200
Proceeds from the issuance of common stock 106 36 79,217
Proceeds from long-term debt - 1,834 10,171
Repayments of long-term debt (258) (325) (3,055)
----------------------------------------------------------------------------------------------------------------------
Net cash provided by (used in) financing activities (152) 1,545 128,533
----------------------------------------------------------------------------------------------------------------------
Effect of exchange rate changes on cash 156 14 1,090
----------------------------------------------------------------------------------------------------------------------
Net increase (decrease) in cash and cash equivalents (8,894) (6,363) 31,605
Cash and cash equivalents at beginning of period 40,499 70,286 -
----------------------------------------------------------------------------------------------------------------------
Cash and cash equivalents at end of period $31,605 $63,923 $ 31,605
======================================================================================================================
Supplemental disclosures of cash flow information:
Cash paid during the period for interest $ 199 $167
====================================================================================================
The accompanying notes are an integral part of these condensed
consolidated financial statements.
5
ESPERION THERAPEUTICS, INC. AND SUBSIDIARIES
NOTES TO THE CONDENSED CONSOLIDATED FINANCIAL STATEMENTS
(1) BASIS OF PRESENTATION
The accompanying unaudited condensed consolidated financial statements
include the accounts of Esperion Therapeutics, Inc. ("Esperion" or the
"Company") and its subsidiaries, and have been prepared in accordance with
accounting principles generally accepted in the United States for interim
financial information and with Article 10 of Regulation S-X. Accordingly, they
do not include all of the information and footnotes required by accounting
principles generally accepted in the United States of America for complete
financial statements. The Company believes that all adjustments, consisting of
normal recurring adjustments, considered necessary for a fair presentation, have
been included. The information included in this Form 10-Q should be read in
conjunction with Management's Discussion and Analysis of Financial Condition and
Results of Operations and the consolidated financial statements and footnotes
thereto included in the Company's Annual Report on Form 10-K for the year ended
December 31, 2002.
Operating results for the three-month periods ended March 31, 2003 and 2002
are not necessarily indicative of the results for the full year.
(2) COMPREHENSIVE LOSS
Comprehensive loss is the total of net loss and all other non-owner changes
in equity. Total comprehensive loss was $7,406,000 and $7,314,000 for the
three-month periods ended March 31, 2003 and 2002, respectively. Net loss, as
reported in the accompanying condensed consolidated statements of operations,
equaled comprehensive loss for the three-month period ended March 31, 2003. The
difference between net loss, as reported in the accompanying condensed
consolidated statements of operations, and comprehensive loss is the foreign
currency translation adjustment for the three-month period ended March 31, 2002.
(3) STOCK-BASED COMPENSATION
The Company accounts for stock-based compensation to employees using the
intrinsic value method prescribed in Accounting Principles Board Opinion No. 25,
"Accounting for Stock Issued to Employees" ("APB 25"), and related
interpretations. Accordingly, compensation cost for stock options is measured as
the excess, if any, of the fair value of the Company's common stock as of the
date of the grant over the amount the employee must pay to acquire the stock.
Statement of Financial Accounting Standards No. 148, "Accounting for
Stock-Based Compensation -- Transition and Disclosure" ("SFAS No. 148") amends
Statement of Financial Accounting Standards No. 123, "Accounting for Stock-Based
Compensation" ("SFAS No. 123") to provide alternative methods of transition for
an entity that voluntarily changes to the fair value based method of accounting
for stock-based employee compensation. It also amends the disclosure provisions
of SFAS No. 123 to require prominent disclosures in both annual and interim
financial statements about the effects on reported net income of an entity's
accounting policy decisions with respect to stock-based employee compensation.
Using the intrinsic value method under APB 25, no compensation expense has
been recognized in the accompanying consolidated statements of operations for
options granted to employees at fair value. Had compensation expense been
determined based on the fair value at the date of grant consistent with SFAS No.
123, the reported net loss would have increased to the following pro forma
amounts, which may not be representative of that to be expected in future years
(in thousands, except per share data):
6
THREE MONTHS ENDED MARCH 31,
----------------------------
2003 2002
---------- ----------
Net loss, as reported................. $ (7,406) $ (7,303)
Deduct: Total stock-based employee
compensation expense determined
under fair value based method for
all awards........................... $ (764) $ (721)
Pro forma net loss.................... $ (8,170) $ (8,024)
Basic and diluted net loss per share:
As reported.......................... $ (0.25) $ (0.25)
Pro forma............................ $ (0.28) $ (0.28)
The fair value of options was estimated at the date of grant using the Black
Scholes Single Option valuation method under SFAS No. 123 with the following
assumptions as of March 31, 2003 and 2002, respectively: weighted average risk
free interest rate of 2.55% and 2.82%; dividend yield of 0%; volatility of
47.46% and 51.69%; and expected life of options of five years. The
weighted-average fair values of options granted during the three months ended
March 31, 2003 and 2002 were $3.00 and $2.99 per share, respectively. Option
valuation models require the input of highly subjective assumptions. Because
changes in subjective input assumptions can materially affect the fair value
estimate, in management's opinion, the existing model does not necessarily
provide a reliable single measure of the fair value of the Company's stock
options.
(4) BASIC AND DILUTED LOSS PER SHARE
Basic and diluted net loss per share amounts have been calculated using the
weighted average number of shares of common stock outstanding during the
respective periods. Options for the purchase of 427,457 and 367,057 shares of
common stock for the three-month periods ended March 31, 2003 and 2002,
respectively, were not included in the calculation of diluted net loss per
share, as doing so would have been anti-dilutive. The Company has entered into
certain agreements that can be settled by issuing shares of the Company's common
stock. The effect of these settlements has not been included in the calculation
of diluted loss per share as doing so would have been anti-dilutive.
(5) COMMITMENTS AND CONTINGENCIES
The Company has entered into various agreements with third parties related
to the research and development activities of its existing product candidates as
well as discovery efforts on potential new product candidates. These agreements
include costs related to manufacturing, clinical trials and toxicology or
pharmacology studies performed by third parties. The estimated remaining amount
to be incurred under these agreements totals approximately $3.7 million as of
March 31, 2003. The amount and timing of these commitments may change, as they
are largely dependent on the enrollment in and timing of the clinical trials.
The Company has entered into various license and other agreements with third
parties related to some of its products in development. The Company may be
obligated to make milestone and license maintenance payments, as defined in the
respective license and other agreements relating to the Company's proprietary
rights, up to an aggregate remaining amount of $30.2 million. Some of these
payments may be fulfilled through the issuance of the Company's common stock, at
the Company's option. Upon reaching certain milestones, the payments are charged
to research and development expenses in the accompanying consolidated statements
of operations. There were no such milestones achieved or payments made during
the first quarter of 2003. At the present time, the Company can give no
assurances that any such milestones will be achieved. In addition to the
milestone and license maintenance payments, the Company may be obligated to make
royalty payments on future sales pursuant to formulas in the agreements.
7
(6) NEW ACCOUNTING PRONOUNCEMENTS
In June 2002, the Financial Accounting Standards Board ("FASB") issued SFAS
No. 146, "Accounting for Exit or Disposal Activities." The new statement
addresses the accounting for costs associated with exit or disposal activities.
The provisions of the statement will be effective for disposal activities
initiated after December 31, 2002. The adoption of this statement did not have a
material impact on the Company's consolidated financial statements.
In November 2002, the FASB issued Interpretation No. 45, "Guarantor's
Accounting and Disclosure Requirements for Guarantees, Including Indirect
Guarantees of Indebtedness of Others." This interpretation elaborates on the
disclosures to be made by a guarantor in its interim and annual financial
statements about its obligations under certain guarantees that it has issued. It
also clarifies (for guarantees issued after January 1, 2003) that a guarantor is
required to recognize, at the inception of a guarantee, a liability for the fair
value of the obligations undertaken in issuing the guarantee. This
interpretation did not have a material impact on the Company's consolidated
financial statements.
(7) GOODWILL AND OTHER INTANGIBLE ASSETS
Under Statement of Financial Accounting Standard No. 142, "Goodwill and
Other Intangible Assets" ("SFAS No. 142"), goodwill and certain indefinite-lived
intangible assets are no longer amortized, but are reviewed at least annually
for impairment by comparing the fair value to the carrying value of net assets.
The Company has not recognized any impairment losses since its adoption of SFAS
No. 142 on January 1, 2002.
Goodwill reflects the excess of the purchase price over net assets in the
Company's September 2000 acquisition of Talaria Therapeutics, Inc. ("Talaria")
and the milestone payments made to date under the related merger agreement. The
carrying amount of goodwill is approximately $3.1 million as of March 31, 2003
and December 31, 2002. The assets acquired from Talaria relate to one of the
Company's ongoing development projects, ETC-588. This product candidate is
currently in Phase II clinical development for the treatment of cardiovascular
disease.
8
ITEM 2. MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS
OF OPERATIONS
The following discussion provides an analysis of the Company's condensed
financial condition and results of operations, and should be read in conjunction
with the Company's consolidated financial statements and the notes included in
Item 1 of this Form 10-Q.
FORWARD-LOOKING INFORMATION IS SUBJECT TO RISK AND UNCERTAINTY
The information contained in this report includes "forward-looking
statements" within the meaning of the Private Securities Litigation Reform Act
of 1995. These forward-looking statements are often identified by words such as
"hope," "may," "believe," "anticipate," "plan," "expect," "require," "intend,"
"assume" and similar expressions. We caution readers that the forward-looking
statements speak only as of the date of this filing, reflect management's
current expectations, estimations and projections and involve certain factors,
such as risks and uncertainties, that may cause our actual results, performance
or achievements to be far different from those suggested by our forward-looking
statements. These factors include, but are not limited to, risks associated
with: our ability to successfully execute our business strategies, including
entering into any strategic partnerships or other transactions; the progress and
cost of development of our product candidates; the extent and timing of market
acceptance of new products developed by us or by our competitors; dependence on
third parties to conduct clinical trials for our product candidates; the extent
and timing of regulatory approval, as desired or required, for our product
candidates; dependence on licensing arrangements and other strategic
relationships with third parties; clinical trials; manufacturing; our dependence
on patents and proprietary rights; the procurement, maintenance, enforcement and
defense of our patents and proprietary rights; competitive conditions in the
industry; business cycles affecting the markets in which any of our future
products may be sold; extraordinary events and transactions; seeking and
consummating business acquisitions, including the diversion of management
attention to the assimilation of the operations and personnel of any acquired
business; the timing and extent of our financing needs and access to funding,
including through the equity market; fluctuations in foreign exchange rates; and
economic conditions generally or in various geographic areas. All of the
foregoing factors are difficult to forecast. More detailed information about
these and other factors is set forth in our Annual Report on Form 10-K for the
year ended December 31, 2002 and other filings with the Securities and Exchange
Commission. We do not intend to update any of these factors or to publicly
announce the results of any revisions to any of these forward-looking statements
other than as required under the federal securities law.
OVERVIEW
Background
We have devoted substantially all of our resources since we began our
operations in May 1998 to the research and development of pharmaceutical product
candidates for the treatment of cardiovascular disease. We are a development
stage biopharmaceutical company and have not generated any revenues from any
source, including from product sales. We have incurred a cumulative net loss of
approximately $101.5 million from inception (May 18, 1998) through March 31,
2003. These losses have resulted principally from costs incurred in research and
development activities and general and administrative expenses. We expect to
incur significant additional operating losses for at least the next several
years, until we generate sufficient revenue to offset expenses, which will only
occur if our product candidates are approved by the FDA or we generate revenues
through licensing arrangements. Research and development costs relating to
product candidates will continue to increase. Manufacturing, sales and marketing
costs will be incurred and will increase in preparation for the intended
commercialization of our product candidates. Until we generate positive cash
flow, we will rely on financing our operations with our existing cash balance,
additional equity or debt offerings and/or payments from potential strategic
relationships that we may enter into with partners in the future.
9
RESULTS OF OPERATIONS
OPERATING EXPENSES
THREE MONTHS ENDED MARCH 31,
---------------------------------
dollars in thousands 2003 2002 % CHANGE
----------------------------------------------------------------------------
Research and development $5,460 $5,705 -4.3%
% of total 77.0% 77.6%
General and administrative $1,629 $1,645 -1.0%
% of total 23.0% 22.4%
Three Months Ended March 31, 2003 and 2002
Research and Development Expenses. Research and development expenses include
both internal and external costs related to the research and development
activities for our existing product candidates, as well as discovery efforts on
potential new product candidates. External costs include costs related to
manufacturing, process development, clinical trials, toxicology or pharmacology
studies performed by third parties, milestone payments under certain license and
other agreements and other related expenses. Internal costs include all payroll
and related costs attributable to research and development activities, as well
as an allocation of overhead expenses. Research and development expenses
decreased by 4.3% to approximately $5.5 million for the three months ended March
31, 2003 compared to approximately $5.7 million for the three months ended March
31, 2002.
This 4.3% decrease in research and development expenses is primarily
attributable to lower payroll and related internal and overhead costs
attributable to research and development activities during the first quarter of
2003 as compared to the same period last year. As of March 31, 2003 and 2002, we
had 41 and 52 employees, respectively, who were engaged in research and clinical
development. Most of this decrease in personnel resulted from actions announced
in March 2002 to curtail or significantly reduce spending on certain
pre-clinical research and other activities that lay outside of our primary areas
of focus in cardiovascular disease. The decrease in payroll and related costs
was largely offset by an increase in clinical trial costs for our three product
candidates in active clinical trials during the quarter ended March 31, 2003,
including ETC-588 (two Phase II trials), ETC-216 (Phase II trial) and ETC-642
(Phase I trial). In contrast, during the quarter ended March 31, 2002, the
Company was actively enrolling patients in two clinical trials (ETC-216 Phase II
trial and ETC-642 Phase I trial).
The magnitude of our operating expenses, particularly research and
development expense, is largely dependent upon the progress, number, timing,
nature and size of clinical trials. As clinical trials continue to progress, we
anticipate that research and development costs will fluctuate as compared to
current quarter levels based on the timing and size of the trials. As our
product candidates progress through development, clinical trial costs will
continue to increase due to the need for more advanced clinical trials that
require more patients.
General and Administrative Expenses. General and administrative expenses
included the cost of salaries, employee benefits, and other costs associated
with our finance, accounting, human resources, legal, business development,
administrative and executive management functions, as well as an allocation of
overhead expenses. General and administrative expenses were approximately $1.6
million for the three months ended March 31, 2003 and March 31, 2002. General
and administrative expenses for the three months ended March 31, 2002 included
approximately $148,000 in expenses related to employee severance and benefits.
These expenses resulted from our actions to curtail or significantly reduce
spending on certain pre-clinical research and other activities that lay outside
of our primary areas of focus in cardiovascular disease. Excluding these
expenses, general and administrative expenses increased approximately $132,000,
or 8.8%, for the three months ended March 31, 2003 compared to the three months
ended March 31, 2002. This increase resulted from higher payroll and related
internal and overhead costs in support of advanced stages of research and
development for certain of our product candidates
10
as compared to the period ended March 31, 2002. As of March 31, 2003 and 2002,
we had 25 and 22 employees, respectively, who were engaged in administrative
activities.
Other Income (Expense). Other income (expense) consists of interest income,
interest expense, foreign currency transaction gain (loss), and other
non-operating income and expenses. Interest income decreased to approximately
$149,000 for the three months ended March 31, 2003 compared to approximately
$320,000 for the three months ended March 31, 2002. The decrease is primarily
attributable to lower cash levels combined with lower yields on our invested
assets in the first quarter of 2003 compared to the same period in 2002.
Interest expense for the three months ended March 31, 2003 and 2002 was
approximately $310,000 and $252,000, respectively, and represents interest
incurred on equipment financing facilities and a special project loan. The
increase in interest expense resulted from higher outstanding borrowings in the
first quarter of 2003 as compared to the same period in 2002.
During the three months ended March 31, 2003, we recorded approximately
$156,000 of foreign currency transaction losses compared to approximately
$21,000 of foreign currency transaction losses for the three months ended March
31, 2002. These transaction losses result from liabilities denominated in
foreign currencies, primarily the Swedish Kronor and the Euro. As the exchange
rate between the U.S. Dollar and these currencies fluctuates, we record a gain
(loss) on these transactions. During 2003 and 2002, the U.S. Dollar has
generally weakened against these foreign currencies, causing these unrealized
losses.
Net Loss. Our net loss was approximately $7.4 million for the three months
ended March 31, 2003 compared to approximately $7.3 million for the three months
ended March 31, 2002. The increase in net loss resulted from the increase in
foreign currency transaction losses, the increase in interest expense, and the
decrease in interest income, offset in part by the decrease in research and
development expenses and the slight decrease in general and administrative
expenses.
LIQUIDITY AND CAPITAL RESOURCES
As of March 31, 2003 and 2002, we had cash, cash equivalents and short-term
investments of approximately $37.9 million and $63.9 million, respectively. Our
investment policy emphasizes liquidity and preservation of principal over other
portfolio considerations. We select investments that maximize interest income to
the extent possible by investing cash in short-term, investment-grade,
interest-bearing securities. We believe that our current cash position will be
sufficient to fund our operations as currently planned, capital expenditures and
debt service as currently planned at least until the second half of 2004.
During the three months ended March 31, 2003 and 2002, net cash used in
operating activities was approximately $7.0 million and $7.3 million,
respectively. This cash was used to fund our net losses for the periods,
adjusted for non-cash expenses and changes in operating assets and liabilities.
Net cash used in investing activities for the three months ended March 31,
2003 and 2002 was approximately $1.9 million and $664,000, respectively. The net
cash used in investing activities for the three months ended March 31, 2003
resulted primarily from purchases of short-term investments. The net cash used
in investing activities for the three months ended March 31, 2002 resulted
primarily from the acquisition of laboratory equipment, furniture and fixtures
and office equipment.
Net cash used in financing activities was approximately $152,000 for the
three months ended March 31, 2003. The net cash used in financing activities for
the three months ended March 31, 2003 resulted primarily from repayments of
borrowings under equipment loans. The cash used was partially offset by $106,000
raised from the issuance of common stock to employees under our equity
compensation plans. Net cash proceeds from financing activities were $1.5
million for the three months ended March 31, 2002. The net cash proceeds from
financing activities for the three months ended March 31, 2002 resulted
primarily from $1.8 million of additional borrowings on a special project loan
and equipment term loans, and $36,000 raised from the issuance of common stock
to employees under our equity compensation plans. The proceeds were partially
offset by $325,000 of cash used to repay borrowings under equipment loans.
11
We frequently evaluate opportunities to sell additional equity, obtain
credit from lenders, enter into strategic relationships, or further strengthen
our financial position in other ways. The sale of additional equity, whether
publicly or privately, could result in dilution to our stockholders. In
addition, from time to time, we may consider the acquisition of or investment in
complementary businesses, products or technologies that might affect our
liquidity requirements or position or cause us to issue additional securities.
There can be no assurance that financing will be available to us in amounts or
on terms acceptable to us, if at all.
As of March 31, 2003, the Company had the following credit facilities and
outstanding borrowings:
- A $2.0 million credit facility with a U.S. bank that may be used to
finance purchases of equipment that is pledged as collateral: Borrowings
under this facility bear interest at the bank's prime rate (4.25% at
March 31, 2003). Borrowings outstanding under this facility as of March
31, 2003 amounted to approximately $958,000 and must be repaid by May
2006. No additional borrowings are allowed. In connection with the
agreement, the Company has to maintain a minimum tangible net worth of
$9.0 million and invest a minimum of $10.0 million with the U.S. bank.
- An additional credit facility with a U.S. lending institution to finance
purchases of equipment that is pledged as collateral: This facility
allowed for borrowings of up to $2.5 million. Approximately $1.1 million
was outstanding under this facility at a weighted average interest rate
of 12% as of March 31, 2003. Outstanding amounts under this facility
must be repaid by November 2004, and no additional borrowings are
allowed.
- A credit facility with a Swedish entity totaling 50 million Swedish
Kronor ($5.9 million as of March 31, 2003): The proceeds from this
facility may only be used to fund the development of our ETC-216 ("AIM")
product candidate. If results achieved by the AIM project show that the
product candidate is not commercially feasible, our obligation to repay
the loan plus a portion of accrued interest may be forgiven. Borrowings
under the loan facility bear interest at 17.0% of which 9.5% is payable
quarterly. The remaining 7.5% of interest together with principal is
payable in five equal annual installments starting in December 2004. The
outstanding borrowings, including accrued interest of 8.4 million
Swedish kronor ($996,000), amounted to 53.4 million Swedish Kronor ($6.3
million) as of March 31, 2003. The Company is in discussions with the
Swedish entity regarding the principal amount of 5 million Swedish
Kronor remaining under the facility, disbursement of which is related to
completion of the final milestone under the facility. The milestone may
be achieved in the future; however, the funds may be unavailable to the
Company due to the ramp down of operations in Sweden during 2002. A
condition under the credit facility is that the project be principally
carried out in Sweden.
- An agreement with a Michigan non-profit corporation whereby we can
borrow up to $447,000 for equipment purchases, pledged as collateral, at
an interest rate of 4%. As of March 31, 2003, outstanding borrowings
under this arrangement totaled $447,000 and must be repaid by November
2008. As required by the agreement, the Company will begin making
principal payments in August 2004.
We anticipate that our capital expenditures for the next twelve months will
be approximately $700,000. We expect that these expenditures will primarily
relate to lab and computer equipment.
We lease our corporate and research and development facilities under
operating leases expiring beginning December 2003 through June 2004. Total
minimum future payments under these leases through the end of 2003 are
approximately $557,000 as of March 31, 2003.
We have entered into license and other agreements with certain third parties
that require us to make payments upon achievement of the milestones set forth in
such agreements. The remaining payments that we could be obligated to make under
those agreements could over time amount to up to $30.2 million. Some of these
payments may be fulfilled through the issuance of common stock, at our option.
If we sell products using technology licensed or owned under the agreements, we
would be obligated to make royalty payments to the third parties pursuant to
formulas in the agreements. There can be no assurance that we will meet any or
all of the milestones in, or sell any products requiring royalty payments under,
our license agreements.
12
We expect our operating expenses and capital expenditures will increase in
future periods. We intend to hire additional research and development, clinical
and administrative staff. Our capital expenditure requirements will depend on
numerous factors, including the progress of our research and development
programs, the time required to file and process regulatory approval
applications, the development of commercial manufacturing capability, the
ability to obtain additional licensing arrangements, and the demand for our
product candidates, if and when approved by the FDA or other regulatory
authorities.
INCOME TAXES
As of March 31, 2003, we had operating loss carryforwards of approximately
$69.4 million. These net operating loss carryforwards expire beginning in 2013.
Additionally, utilization of net operating loss carryforwards may be limited
under Section 382 of the Internal Revenue Code. These and other deferred income
tax assets are fully reserved by a valuation allowance as the realizability of
these assets is not likely at this time.
EMPLOYEES
As of March 31, 2003, we had 66 full-time employees. Of these employees, 41
were engaged in research, pre-clinical and clinical development, regulatory
affairs and/or manufacturing activities and 25 were engaged in general and
administrative activities.
CRITICAL ACCOUNTING POLICIES
Management's discussion and analysis of the Company's financial condition
and results of operations are based upon our Consolidated Financial Statements,
which have been prepared in accordance with accounting principles generally
accepted in the United States of America. The preparation of these financial
statements requires management to make estimates and assumptions that affect the
reported amounts of assets and liabilities, the disclosure of any contingent
assets and liabilities as of the date of the financial statements and reported
amounts of revenues and expenses during the reporting period. We regularly
review our estimates and assumptions, which are based on historical experience
and on various other factors and judgments about the carrying values of assets
and liabilities that are not readily apparent from other sources. Actual results
may differ from these estimates and assumptions.
We believe that the following critical accounting policies are affected by
significant judgments and estimates used in the preparation of our consolidated
financial statements:
We review goodwill, and other intangible long-lived assets for impairment
annually or sooner if events or changes in circumstances indicate that the
carrying amount may not be recoverable. Events or changes in circumstances that
indicate the carrying amount may not be recoverable include, but are not limited
to, a significant decrease in the market value of business and asset acquired, a
significant adverse change in the extent or manner in which the business or
asset acquired is used or a significant adverse change in the business climate.
If such events or changes in circumstances are present, the fair value of a
reporting unit is compared with its carrying amount, including goodwill. If the
fair value of a reporting unit exceeds its carrying amount, goodwill of the
reporting unit is not considered impaired. If the carrying amount of a reporting
unit exceeds its fair value, the amount of impairment will be measured in
accordance with the guidance of SFAS 142. All of our goodwill was assigned to a
single reporting unit, which is our sole operating segment.
We record estimated expenses under the contracts with third parties on a
percentage of completion basis. These contracts cover ongoing clinical trials,
manufacturing and supply agreements, and third party toxicology or pharmacology
studies. These contracts generally have terms ranging from a couple of months to
approximately two years. The expenses are recorded as the work under the
contract is completed and we may record an accrued liability or prepaid expense
on its Consolidated Balance Sheet, depending on the payment terms under each
contract. As of March 31, 2003, we had total potential obligations of
approximately $10.3 million under contracts accounted for on the percentage of
completion basis. We estimate that approximately $6.6 million of the contract
obligations had been
13
incurred through March 31, 2003 and approximately $940,000 is included in
accrued liabilities in the accompanying balance sheet for expenses under
contracts on a percentage of completion basis.
NEW ACCOUNTING PRONOUNCEMENTS
In June 2002, the Financial Accounting Standards Board ("FASB") issued SFAS
No. 146, "Accounting for Exit or Disposal Activities." The new statement
addresses the accounting for costs associated with exit or disposal activities.
The provisions of the statement will be effective for disposal activities
initiated after December 31, 2002. The adoption of this statement did not have a
material impact on our consolidated financial statements.
In November 2002, the FASB issued Interpretation No. 45, "Guarantor's
Accounting and Disclosure Requirements for Guarantees, Including Indirect
Guarantees of Indebtedness of Others." This interpretation elaborates on the
disclosures to be made by a guarantor in its interim and annual financial
statements about its obligations under certain guarantees that it has issued. It
also clarifies (for guarantees issued after January 1, 2003) that a guarantor is
required to recognize, at the inception of a guarantee, a liability for the fair
value of the obligations undertaken in issuing the guarantee. This
interpretation did not have a material impact on our consolidated financial
statements.
14
ITEM 3. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
Our exposure to market risk for changes in interest rates relates primarily
to the increase or decrease in the amount of interest income that we can earn on
our investment portfolio and on the increase or decrease in the amount of
interest expense that we must pay with respect to our various outstanding debt
instruments. Under our current policies, we do not use interest rate derivative
instruments to manage our exposure to interest rate changes. We ensure the
safety and preservation of our invested funds by limiting default risks, market
risk and reinvestment risk. We mitigate default risk by investing in investment
grade securities and limiting our exposure to any one security. A hypothetical
100 basis point adverse move in interest rates along the entire interest rate
yield curve would not materially affect the fair value of our interest sensitive
financial instruments at March 31, 2003. Declines in interest rates reduce our
interest income as described on page 11 in Management's Discussion and Analysis,
under the subcaption "Three Months Ended March 31, 2003 and 2002, Other Income
(Expense)", while increases in interest rates increase our interest expense.
The functional currency for our foreign operation is the Swedish Kronor. As
such, changes in exchange rates between the Swedish Kronor and the U.S. Dollar
could adversely affect our future net income (loss). Given the level of activity
we currently have with our foreign operations, we consider this exposure to be
minimal. A 10% change in exchange rates would not have a significant impact on
our future net income (loss). Additionally, at March 31, 2003, we had
approximately $6.3 million in inter-company advances denominated in Swedish
Kronor for which changes in the exchange rate will result in foreign currency
transaction gains or losses that are charged to Other income (expense) in the
accompanying Statements of Operations.
ITEM 4. CONTROLS AND PROCEDURES
An evaluation of the effectiveness of the design and operation of our
disclosure controls and procedures as of May 13, 2003 was carried out by the
Company under the supervision and with the participation of our Chief Executive
Officer and Chief Financial Officer. Based on that evaluation, our Chief
Executive Officer and Chief Financial Officer, concluded that our disclosure
controls and procedures have been designed and are being operated in a manner
that provides reasonable assurance that the information required to be disclosed
by the Company in reports filed under the Exchange Act is recorded, processed,
summarized and reported within the time periods specified in the SEC's rules and
forms. A controls system, no matter how well designed and operated, cannot
provide absolute assurance that the objectives of the controls system are met,
and no evaluation of controls can provide absolute assurance that all control
issues and instances of fraud, if any, within a company have been detected.
Subsequent to the date of the most recent evaluation of our internal controls,
there were no significant changes in our internal controls or in other factors
that could significantly affect the internal controls, including any corrective
actions with regard to significant deficiencies and material weaknesses.
15
PART II - OTHER INFORMATION
ITEM 1. LEGAL PROCEEDINGS
Not applicable.
ITEM 2. CHANGES IN SECURITIES AND USE OF PROCEEDS
Not applicable.
ITEM 3. DEFAULTS UPON SENIOR SECURITIES
Not applicable.
ITEM 4. SUBMISSION OF MATTERS TO A VOTE OF SECURITY HOLDERS
Not applicable.
ITEM 5. OTHER INFORMATION
Not applicable.
ITEM 6. EXHIBITS AND REPORTS ON FORM 8-K
(a) EXHIBITS
NUMBER EXHIBIT
--------------- ----------------------------------------------------------------
10.54 Third Amendment to Commercial Sublease Agreement between
Southwest Michigan Innovation Center, Inc. (formerly known as
SWMF Holdings Corporation) and Esperion Therapeutics, Inc. dated
March 3, 2003.
99.1 Certification pursuant to 18 U.S.C. Section 1350, as adopted
pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.
99.2 Certification pursuant to 18 U.S.C. Section 1350, as adopted
pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.
(b) REPORTS ON FORM 8-K
Not applicable.
16
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 thereunto duly authorized.
Dated: May 14, 2003 ESPERION THERAPEUTICS, INC.
(Registrant)
By: /s/ Roger S. Newton
---------------------------------------
Roger S. Newton
President and Chief Executive Officer
(Principal Executive Officer)
By: /s/ Timothy M. Mayleben
---------------------------------------
Timothy M. Mayleben
Chief Operating Officer
and Chief Financial Officer
(Principal Financial Officer)
17
CERTIFICATIONS
I, Roger S. Newton, certify that:
1. I have reviewed this quarterly report on Form 10-Q of Esperion Therapeutics,
Inc.;
2. Based on my knowledge, this quarterly report does not contain any untrue
statement of a material fact or omit to state a material fact necessary to make
the statements made, in light of the circumstances under which such statements
were made, not misleading with respect to the period covered by this quarterly
report;
3. Based on my knowledge, the financial statements, and other financial
information included in this quarterly report, fairly present in all material
respects the financial condition, results of operations and cash flows of the
registrant as of, and for, the periods presented in this quarterly report;
4. The registrant's other certifying officers and I are responsible for
establishing and maintaining disclosure controls and procedures (as defined in
Exchange Act Rules 13a-14 and 15d-14) for the registrant and we have:
a) designed such disclosure controls and procedures to ensure that
material information relating to the registrant, including its
consolidated subsidiaries, is made known to us by others within those
entities, particularly during the period in which this quarterly report
is being prepared;
b) evaluated the effectiveness of the registrant's disclosure controls
and procedures as of a date within 90 days prior to the filing date of
this quarterly report (the "Evaluation Date"); and
c) presented in this quarterly report our conclusions about the
effectiveness of the disclosure controls and procedures based on our
evaluation as of the Evaluation Date;
5. The registrant's other certifying officers and I have disclosed, based on our
most recent evaluation, to the registrant's auditors and the audit committee of
registrant's board of directors (or persons performing the equivalent function):
a) all significant deficiencies in the design or operation of internal
controls which could adversely affect the registrant's ability to
record, process, summarize and report financial data and have
identified for the registrant's auditors any material weaknesses in
internal controls; and
b) any fraud, whether or not material, that involves management or
other employees who have a significant role in the registrant's
internal controls; and
6. The registrant's other certifying officers and I have indicated in this
quarterly report whether or not there were significant changes in internal
controls or in other factors that could significantly affect internal controls
subsequent to the date of our most recent evaluation, including any corrective
actions with regard to significant deficiencies and material weaknesses.
/s/ Roger S. Newton
--------------------------------
Roger S. Newton
Chief Executive Officer
Date: May 14, 2003
18
I, Timothy M. Mayleben, certify that:
1. I have reviewed this quarterly report on Form 10-Q of Esperion Therapeutics,
Inc.;
2. Based on my knowledge, this quarterly report does not contain any untrue
statement of a material fact or omit to state a material fact necessary to make
the statements made, in light of the circumstances under which such statements
were made, not misleading with respect to the period covered by this quarterly
report;
3. Based on my knowledge, the financial statements, and other financial
information included in this quarterly report, fairly present in all material
respects the financial condition, results of operations and cash flows of the
registrant as of, and for, the periods presented in this quarterly report;
4. The registrant's other certifying officers and I are responsible for
establishing and maintaining disclosure controls and procedures (as defined in
Exchange Act Rules 13a-14 and 15d-14) for the registrant and we have:
a) designed such disclosure controls and procedures to ensure that
material information relating to the registrant, including its
consolidated subsidiaries, is made known to us by others within those
entities, particularly during the period in which this quarterly report
is being prepared;
b) evaluated the effectiveness of the registrant's disclosure controls
and procedures as of a date within 90 days prior to the filing date of
this quarterly report (the "Evaluation Date"); and
c) presented in this quarterly report our conclusions about the
effectiveness of the disclosure controls and procedures based on our
evaluation as of the Evaluation Date;
5. The registrant's other certifying officers and I have disclosed, based on our
most recent evaluation, to the registrant's auditors and the audit committee of
registrant's board of directors (or persons performing the equivalent function):
a) all significant deficiencies in the design or operation of internal
controls which could adversely affect the registrant's ability to
record, process, summarize and report financial data and have
identified for the registrant's auditors any material weaknesses in
internal controls; and
b) any fraud, whether or not material, that involves management or
other employees who have a significant role in the registrant's
internal controls; and
6. The registrant's other certifying officers and I have indicated in this
quarterly report whether or not there were significant changes in internal
controls or in other factors that could significantly affect internal controls
subsequent to the date of our most recent evaluation, including any corrective
actions with regard to significant deficiencies and material weaknesses.
/s/ Timothy M. Mayleben
---------------------------
Timothy M. Mayleben
Chief Financial Officer
Date: May 14, 2003
19
INDEX TO EXHIBITS
NUMBER EXHIBIT
-------------- -----------------------------------------------------------------
10.54 Third Amendment to Commercial Sublease Agreement between
Southwest Michigan Innovation Center, Inc. (formerly known as
SWMF Holdings Corporation) and Esperion Therapeutics, Inc. dated
March 3, 2003.
99.1 Certification pursuant to 18 U.S.C. Section 1350, as adopted
pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.
99.2 Certification pursuant to 18 U.S.C. Section 1350, as adopted
pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.
20