SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C.  20549

 

FORM 10-Q

 

ý          Quarterly Report Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934

 

for the Period Ended March 31, 2003.

 

or

 

o          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 0-27436

 

Titan Pharmaceuticals, Inc.

(Exact name of registrant as specified in its charter)

 

Delaware

 

94-3171940

(State or Other Jurisdiction of
Incorporation or Organization)

 

(I.R.S. Employer
Identification No.)

 

400 Oyster Point Blvd., Suite 505, South San Francisco, California 94080

(Address of Principal Executive Offices including zip code)

 

(650) 244-4990

(Registrant’s 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 Exchange Act 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.  Yes ý  No o

 

Indicate by check mark whether the registrant is an accelerated filer (as defined on Rule 12B-2 of the Exchange Act).  Yes  o No ý

 

There were 27,642,085 shares of the Registrant’s Common Stock issued and outstanding on May 6, 2003.

 

 



 

Titan Pharmaceuticals, Inc.

Index to Form 10-Q

 

Part I.

Financial Information

 

 

 

 

 

Item 1.  Condensed Financial Statements (unaudited)

 

 

 

 

 

Condensed Consolidated Balance Sheets
March 31, 2003 and December 31, 2002

 

 

 

 

 

Condensed Consolidated Statements of Operations
Three months ended March 31, 2003 and 2002

 

 

 

 

 

Condensed Consolidated Statements of Cash Flows
Three months ended March 31, 2003 and 2002

 

 

 

 

 

Notes to Condensed Consolidated Financial Statements

 

 

 

 

 

Item 2.  Management’s Discussion and Analysis of Financial Condition and Results of Operations

 

 

 

 

Item 3.  Quantitative and Qualitative Disclosures About Market Risk

 

 

 

 

 

Item 4.  Controls and Procedures

 

 

 

 

Part II.

Other Information

 

 

 

 

 

Item 6.  Exhibits and Reports on Form 8-K

 

 

 

 

SIGNATURES

 

 

 

CERTIFICATIONS

 



 

Part I.  Financial Information

 

TITAN PHARMACEUTICALS, INC.

CONDENSED CONSOLIDATED BALANCE SHEETS

(in thousands)

 

 

 

March 31,
2003

 

December 31,
2002

 

 

 

(unaudited)

 

(Note A)

 

Assets

 

 

 

 

 

Current assets

 

 

 

 

 

Cash and cash equivalents

 

$

8,431

 

$

7,155

 

Marketable securities

 

57,649

 

66,295

 

Related party receivables

 

160

 

316

 

Prepaid expenses, receivables, and other current assets

 

1,857

 

881

 

Total current assets

 

68,097

 

74,647

 

Property and equipment, net

 

896

 

979

 

Investment in other companies

 

300

 

300

 

 

 

$

69,293

 

$

75,926

 

Liabilities and Stockholders’ Equity

 

 

 

 

 

Current liabilities

 

 

 

 

 

Accounts payable

 

$

1,897

 

$

1,901

 

Accrued clinical trials expenses

 

969

 

1,203

 

Other accrued liabilities

 

1,069

 

841

 

Total current liabilities

 

3,935

 

3,945

 

Minority interest - Series B preferred stock of Ingenex, Inc.

 

1,241

 

1,241

 

Stockholders’ equity

 

 

 

 

 

Common stock, at amounts paid in

 

191,680

 

191,680

 

Additional paid-in capital

 

9,187

 

9,161

 

Deferred compensation

 

(553

)

(621

)

Accumulated deficit

 

(136,382

)

(129,852

)

Accumulated other comprehensive income

 

185

 

372

 

Total stockholders’ equity

 

64,117

 

70,740

 

 

 

$

69,293

 

$

75,926

 

 


Note A: The balance sheet has been derived from the audited financial statements at that date but does not include all of the information and footnotes required by generally accepted accounting principles in the United States for complete financial statement presentation.

 

See Notes to Condensed Consolidated Financial Statements

 

2



 

TITAN PHARMACEUTICALS, INC.

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

(unaudited)

(in thousands, except per share amount)

 

 

 

Three Months Ended March 31,

 

 

 

2003

 

2002

 

Revenue:

 

 

 

 

 

License and contract revenue

 

$

26

 

$

2,151

 

Grant revenue

 

 

196

 

Total revenue

 

26

 

2,347

 

 

 

 

 

 

 

Operating expenses:

 

 

 

 

 

Research and development

 

5,643

 

7,486

 

General and administrative

 

1,382

 

1,210

 

Total operating expenses

 

7,025

 

8,696

 

Loss from operations

 

(6,999

)

(6,349

)

 

 

 

 

 

 

Other income (expense):

 

 

 

 

 

Interest income, net

 

472

 

1,407

 

Other expense

 

(3

)

(8

)

Other income, net

 

469

 

1,399

 

Net loss

 

$

(6,530

)

$

(4,950

)

 

 

 

 

 

 

Basic and diluted net loss per share

 

$

(0.24

)

$

(0.18

)

 

 

 

 

 

 

Weighted average shares used in computing basic and diluted net loss per share

 

27,642

 

27,642

 

 

See Notes to Condensed Consolidated Financial Statements

 

3



 

TITAN PHARMACEUTICALS, INC.

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

(unaudited)

(in thousands)

 

 

 

Three Months Ended March 31,

 

 

 

2003

 

2002

 

Cash flows from operating activities:

 

 

 

 

 

Net loss

 

$

(6,530

)

$

(4,950

)

Adjustments to reconcile net loss to net cash provided by (used in) operating activities:

 

 

 

 

 

Depreciation and amortization

 

659

 

350

 

Non-cash compensation related to stock options

 

94

 

67

 

Changes in operating assets and liabilities:

 

 

 

 

 

Prepaid expenses, receivables, and other current assets

 

(1,372

)

(945

)

Accounts payable and other accrued liabilities

 

(11

)

(292

)

Unearned contract revenue

 

 

(2,000

)

Net cash used in operating activities

 

(7,160

)

(7,770

)

 

 

 

 

 

 

Cash flows from investing activities:

 

 

 

 

 

Purchases of furniture and equipment, net

 

(23

)

(191

)

Purchases of marketable securities

 

(24,856

)

(8,623

)

Proceeds from maturities of marketable securities

 

33,315

 

8,325

 

Proceeds from sales of marketable securities

 

 

7,088

 

Net cash provided by investing activities

 

8,436

 

6,599

 

 

 

 

 

 

 

Cash flows from financing activities:

 

 

 

 

 

Issuance of common stock, net

 

 

1

 

Net cash provided by financing activities

 

 

1

 

 

 

 

 

 

 

Net decrease in cash and cash equivalents

 

1,276

 

(1,170

)

Cash and cash equivalents at beginning of period

 

7,155

 

5,772

 

Cash and cash equivalents at end of period

 

8,431

 

4,602

 

Marketable securities at end of period

 

57,649

 

91,411

 

Cash, cash equivalents and marketable securities at end of period

 

$

66,080

 

$

96,013

 

 

See Notes to Condensed Consolidated Financial Statements

 

4



 

TITAN PHARMACEUTICALS, INC.

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

(unaudited)

 

1.   Organization and Summary of Significant Accounting Policies

 

The Company

 

We are a biopharmaceutical company developing proprietary therapeutics for the treatment of central nervous system disorders, cancer, and other serious and life threatening diseases.  We operate in one business segment, the development of biopharmaceutical products.

 

Basis of Presentation

 

The accompanying unaudited condensed consolidated financial statements include the accounts of Titan and its subsidiaries after elimination of all significant intercompany accounts and transactions. Certain prior year balances have been reclassified to conform to the current year presentation.  These financial statements have been prepared in accordance with generally accepted accounting principles in the United States for interim financial information and with the instructions to Form 10-Q and Article 10 of Regulation S-X.  Accordingly, they do not include all of the information and footnotes required by generally accepted accounting principles for a complete financial statements presentation. In the opinion of management, all adjustments (consisting of normal recurring adjustments) considered necessary for a fair presentation have been included.  Operating results for the three-month period ended March 31, 2003 are not necessarily indicative of the results that may be expected for the year ending December 31, 2003.

 

The preparation of financial statements in conformity with accounting principles generally accepted in the United States requires management to make estimates and assumptions that affect the amounts reported in the financial statements and accompanying notes.  Actual results could differ from those estimates.

 

These unaudited condensed consolidated financial statements should be read in conjunction with the audited consolidated financial statements and footnotes thereto included in the Titan Pharmaceuticals, Inc. annual report on Form 10-K for the year ended December 31, 2002.

 

Revenue Recognition

 

Contract revenue for research and development is recorded as earned based on the performance requirements of the contract.  Revenue associated with performance milestones, considered “at-risk” until the milestones are completed, is recognized based on the achievement of the milestones as defined in the respective agreements.  Government grants, which support our research effort in specific projects, generally provide for reimbursement of approved costs as defined in the grant documents, and revenue is recognized when associated project costs are incurred.

 

Operating Subsidiaries

 

We conduct a small portion of our operations through two subsidiaries: Ingenex, Inc. and ProNeura, Inc.  At March 31 2003, we owned 81% of Ingenex (assuming the conversion of all preferred stock to common stock) and 79% of ProNeura.

 

5



 

Recent Accounting Pronouncements

 

In January 2003, the FASB issued Interpretation No. 46 (or FIN 46), “Consolidation of Variable Interest Entities.”  FIN 46 requires a variable interest entity to be consolidated by a company if that company is subject to a majority of the risk of loss from the variable interest entity’s activities or entitled to receive a majority of the entity’s residual returns or both.  A variable interest entity is a corporation, partnership, trust, or any other legal structures used for business purposes that either (a) does not have equity investors with voting rights or (b) has equity investors that do not provide sufficient financial resources for the entity to support its activities.  A variable interest entity often holds financial assets, including loans or receivables, real estate or other property.  A variable interest entity may be essentially passive or it may engage in research and development or other activities on behalf of another company.  The consolidation requirements of FIN 46 apply immediately to variable interest entities created after January 31, 2003.  The consolidation requirements apply to older entities in the first fiscal year or interim period beginning after June 15, 2003.  The adoption of FIN 46 is not expected to have a material impact on our financial position and results of operations.

 

2.   Stock Option Plans

 

We have elected to continue to follow Accounting Principles Board Opinion No. 25 (or APB 25), “Accounting for Stock Issued to Employees,” rather than the alternative method of accounting prescribed by Statement of Financial Accounting Standards No. 123 (or SFAS 123), “Accounting for Stock-Based Compensation.”   Under APB 25, no compensation expense is recognized when the exercise price of our employee stock options equals the market price of the underlying stock on the date of grant.  The following table illustrates the effect on our net loss and net loss per share if Titan had applied the provisions of SFAS 123 to estimate and recognize compensation expense for our stock-based employee compensation.

 

 

 

Three Months Ended March 31,

 

 

 

2003

 

2002

 

Net loss, as reported

 

$

(6,530

)

$

(4,950

)

Add:  Stock-based employee compensation expense included in reported net loss

 

94

 

67

 

Deduct:  Estimated stock-based employee compensation expense determined in accordance with SFAS 123 for all stock option grants

 

(892

)

(1,973

)

Pro forma net loss

 

$

(7,328

)

$

(6,856

)

 

 

 

 

 

 

Basic and diluted net loss per share, as reported

 

$

(0.24

)

$

(0.18

)

Pro forma basic and diluted net loss per share

 

$

(0.27

)

$

(0.25

)

 

3.   Net Loss Per Share

 

We calculate net loss per share using the weighted average common shares outstanding for the period.  For periods ended March 31, 2003 and 2002, the effect of an additional 8,385,477 and 5,218,968 shares, respectively, related to our authorized and issued convertible preferred stock and options, were not included in the computation of diluted earnings per share because they are anti-dilutive.

 

6



 

4.   Comprehensive Income

 

Comprehensive income is comprised of net loss and other comprehensive income.  The only component of other comprehensive income is unrealized gains and losses on our marketable securities.  Comprehensive loss for the three months ended March 31, 2003 and 2002 were $6.7 million and $6.0 million, respectively.

 

7



 

Item 2.       Management’s Discussion and Analysis of Financial Condition and Results of Operations

 

The following discussion should be read in conjunction with the Consolidated Financial Statements and Notes thereto beginning on page F-1 in this report.

 

The following discussion contains certain forward-looking statements, within the meaning of the “safe harbor” provisions of the Private Securities Reform Act of 1995, the attainment of which involves various risks and uncertainties. Forward-looking statements may be identified by the use of forward-looking terminology such as “may,” “will,” “expect,” “believe,” “estimate,” “plan,” “anticipate,” “continue,” or similar terms, variations of those terms or the negative of those terms. Our actual results may differ materially from those described in these forward-looking statements due to, among other factors, the results of ongoing research and development activities and pre-clinical testing, the results of clinical trials and the availability of additional financing through corporate partnering arrangements or otherwise.

 

Spheramine®, Pivanex®, Probuphine™, CeaVac®, TriAb®, TriGem™ and CCM™ are trademarks of Titan Pharmaceuticals, Inc.

 

Overview

 

We are a biopharmaceutical company developing proprietary therapeutics for the treatment of central nervous system disorders, cancer, and other serious and life threatening diseases.  Our product development programs focus on large pharmaceutical markets with significant unmet medical needs and commercial potential.

 

Our internal resources are currently focused primarily on clinical development of the following products:

 

        Spheramine for the treatment of late stage Parkinson’s disease

        Pivanex for the treatment of non-small cell lung cancer

        Gallium maltolate for the treatment of several cancers

        Probuphine for the treatment of opiate addiction

 

We are directly developing our product candidates and also utilizing corporate partnerships, including a collaboration with Schering AG, Germany (Schering) for the development of Spheramine to treat Parkinson’s disease.  Spheramine development is primarily funded by Schering.  Iloperidone is licensed to Novartis Pharma AG (Novartis) for development and commercialization in the treatment of schizophrenia and schizoaffective disorders.  Novartis continues to evaluate the next steps for the development of iloperidone, including sublicensing the compound to another company, continuing development, or returning product rights to Titan.

 

At this time, we are not devoting any additional internal resources to the monoclonal antibodies CeaVac, TriAb, and TriGem. These treatments are currently being studied in certain cancers by national oncology cooperative groups funded by the National Cancer Institute.

 

8



 

The following table provides summary status of our products in development:

 

Product

 

Potential Indication(s)

 

Phase of Development

 

Marketing Rights

Spheramine

 

Parkinson’s Disease

 

Phase IIb

 

Schering AG

Pivanex

 

Non-small cell lung cancer

 

Phase IIb

 

Titan

Gallium Maltolate

 

Myeloma, prostate and bladder cancer, lymphoma, bone disease associated with cancer

 

Phase I/II

 

Titan

Probuphine

 

Opiate addiction

 

Phase I (to be initiated mid-2003)

 

Titan

Iloperidone

 

Schizophrenia, psychosis

 

Phase III*

 

Novartis Pharma AG

CeaVac & TriAb

 

Limited stage non-small cell lung cancer

 

Phase II (co-operative group study)*

 

Titan

CeaVac & TriAb

 

Resected Dukes D colorectal cancer

 

Phase II (co-operative group study)*

 

Titan

TriGem & TriAb

 

Small cell lung cancer

 

Phase II (co-operative group study)*

 

Titan

 


*Further development under review

 

Our products are at various stages of development and may not be successfully developed or commercialized. We do not currently have any products being commercially sold.  Our proposed products will require significant further capital expenditures, development, testing, and regulatory clearances prior to commercialization.  We may experience unanticipated problems relating to product development and cannot predict whether we will successfully develop and commercialize any products.  An estimation of product completion dates and completion costs can vary significantly for each product and are difficult to predict.  Various statutes and regulations also influence our product development progress and the success of obtaining approval is highly uncertain.  For a full discussion of risks and uncertainties in our product development, see “Risk Factors – Our products are at various stages of development and may not be successfully developed or commercialized” in our 2002 annual report on  Form 10-K.

 

Results of Operations

 

Revenues for the first quarter 2003 were approximately $26,000 compared to $2.3 million for the same quarter in 2002.  Revenue for the first quarter 2002 primarily consisted of a one-time $2.0 million milestone payment from Schering following successful completion of the Phase I/II study of Spheramine in the treatment of late-stage Parkinson’s disease, and Schering’s decision to initiate randomized clinical testing of Spheramine for the treatment of patients with late-stage Parkinson’s disease.

 

Research and development expenses for the first quarter 2003 were $5.6 million, compared to $7.5 million for the same quarter in 2002, a decrease of 25%.  This decrease resulted primarily from the completion of the Phase III clinical study of CeaVac in Dukes’ D colorectal cancer, and our planned strategic focus on the clinical development of four product programs: Spheramine, Pivanex, gallium maltolate and Probuphine.

 

General and administrative expenses for the first quarter 2003 were $1.4 million compared to $1.2 million for the same quarter in 2002.  The slight increase resulted primarily from increased insurance costs.

 

9



 

Other income, net of amortization and other expenses, for the first quarter 2003 was $0.5 million compared to $1.4 million in the first quarter 2002.  The decrease, primarily in interest income, was a result of lower interest rates and a lower balance of cash and marketable securities.

 

Our net loss for the first quarter 2003 was $6.5 million, or $0.24 per share, compared to $5.0 million, or $0.18 per share, for the same quarter in 2002.

 

Liquidity and Capital Resources

 

We have funded our operations since inception through our initial public offering and private placements of our securities, as well as proceeds from warrant and option exercises, corporate licensing and collaborative agreements, and government sponsored research grants.  At March 31, 2003, we had $66.1 million of cash, cash equivalents, and marketable securities.

 

Our operating activities used $7.2 million and $7.8 million of cash in the first quarter 2003 and 2002, respectively.  Uses of cash in operating activities were primarily to fund product development programs and administrative expenses.  We have entered into various agreements with research institutions, universities, and other entities for the performance of research and development activities and for the acquisition of licenses related to those activities.  The aggregate commitments we have under these agreements, including minimum license payments, for the next 12 months is approximately $0.9 million.  Certain of the licenses require us to pay royalties on future product sales, if any.  In addition, in order to maintain license and other rights while products are under development, we must comply with customary licensee obligations, including the payment of patent related costs and diligent efforts in product development.

 

We expect to continue to incur substantial additional operating losses from costs related to continuation and expansion of product and technology development, clinical trials, and administrative activities.  We believe that we currently have sufficient working capital to sustain our planned operations through 2005.

 

Item 3.       Quantitative and Qualitative Disclosures About Market Risk

 

Our market risk disclosures set forth in our Form 10-K for the period ended December 31, 2002, have not changed significantly.

 

Item 4.       Controls and Procedures

 

Based on the evaluation by Titan under the supervision and with the participation of our management, including our Chief Executive Officer and Chief Financial Officer, of the effectiveness of the design and operation of Titan’s disclosure controls and procedures pursuant to Rule 13a-14 of the Securities and Exchange Act of 1934, as amended (the Exchange Act), as of a date within 90 days of the filing date of this quarterly report, our Chief Executive Officer and Chief Financial Officer have concluded that the disclosure controls and procedures are effective in ensuring that information required to be disclosed by Titan in the reports we file or submit under the Exchange Act is recorded, processed, summarized and reported within the time period specified by the Securities and Exchange Commission’s rules and forms.

 

Subsequent to the date of their evaluation, there were no significant changes in Titan’s internal controls or in other factors that could significantly affect these controls nor were any corrective actions required with regard to significant deficiencies and material weaknesses.

 

10



 

PART II

 

Item 6.       Exhibits and Reports on Form 8-K

 

(b)                                 Exhibits

 

99.0                           Section 906 Certifications

 

(c)                                  Reports on Form 8-K

 

There were no current reports on Form 8-K filed for the quarter ended March 31, 2003.

 

11



 

SIGNATURES

 

In accordance with the requirements of the Exchange Act, the registrant caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

 

 

TITAN PHARMACEUTICALS, INC.

 

 

 

 

 

 

May 15, 2003

By:

/s/ Louis R. Bucalo

 

 

 

Louis R. Bucalo, M.D.

 

 

Chairman, President and Chief Executive Officer

 

 

 

 

 

 

May 15, 2003

By:

/s/ Robert E. Farrell

 

 

 

Robert E. Farrell

 

 

Executive Vice President and Chief Financial Officer

 

12



 

CERTIFICATIONS

 

I, Louis R. Bucalo, M.D., Chairman, President and Chief Executive Officer of Titan Pharmaceuticals, Inc., certify that:

 

1.               I have reviewed this quarterly report on Form 10-Q of Titan Pharmaceuticals, 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:

 

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.

 

Date: May 15, 2003

 

/s/ Louis R. Bucalo

 

 

 

Louis R. Bucalo, M.D.

 

 

Chairman, President and Chief Executive Officer

 

13



 

I, Robert E. Farrell, J.D., Executive Vice President and Chief Financial Officer of Titan Pharmaceuticals, Inc., certify that:

 

1.               I have reviewed this quarterly report on Form 10-Q of Titan Pharmaceuticals, 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:

 

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.

 

Date: May 15, 2003

 

/s/ Robert E. Farrell

 

 

 

Robert E. Farrell, J.D.

 

 

Executive Vice President and Chief Financial Officer

 

14