EX-99.1 2 a04-12091_1ex99d1.htm EX-99.1

Exhibit 99.1

 

 

FOR IMMEDIATE RELEASE

 

Contact:

Ami Knoefler

 

Senior Director

 

Corporate Communications and Investor Relations

 

510-284-6350 or 510-284-6605

 

Abgenix Announces Third Quarter 2004 Financial Results

 

FREMONT, Calif., October 26, 2004 - Abgenix, Inc. (Nasdaq:ABGX) today reported financial results for the third quarter ended September 30, 2004.

 

For the quarter ended September 30, 2004, the company reported a net loss of $42.4 million or $0.48 per share, compared to a net loss of $43.6 million or $0.50 per share for the same period in 2003.  The company ended the quarter with $230.7 million in cash, cash equivalents and marketable securities.

 

Revenues for the third quarter of 2004 were $3.4 million compared to $2.0 million for the same period in 2003.  Contract revenues for the quarter ended September 30, 2004 primarily consisted of fees under technology licensing agreements, including a milestone payment from Amgen for advancement of AMG 162, a XenoMouse®-derived antibody, into pivotal clinical trials for bone loss. The company’s revenues generally vary from quarter to quarter.

 

Operating expenses for the third quarter of 2004 were $45.4 million, compared with $45.9 million for the same period of 2003.  Expenses for both 2003 and 2004 included research and development costs to advance the company’s clinical and preclinical stage antibody product portfolio.  The majority of third quarter 2004 research and development costs related to the company’s proprietary clinical products, including its lead oncology product candidate, panitumumab, and ABX 10241, an antibody for secondary hyperparathyroidism (SHPT).  Included in both periods were manufacturing start-up costs related to operating the company’s antibody production facility.  A portion of these manufacturing costs will continue to be classified as start-up until the facility is operating closer to full utilization.  The company expects these costs to vary from quarter to quarter based on the extent of manufacturing activities for antibody product candidates, including panitumumab.

 

Net cash used in operating activities in the third quarter of 2004 was $36.5 million.  For the nine months ending September 30, 2004, net cash used in operating activities was $112.1 million.  Capital spending was $6.9 million for the nine months ended September 30.  Abgenix expects net use of cash in operations and capital expenditures to be approximately $140-145 million for the full year of 2004.

 

-more-

 



 

“We are pleased with the progress in our product portfolio beyond panitumumab, our lead antibody product, which is currently in pivotal trials as a third line monotherapy in colorectal cancer,” said Bill Ringo, president and CEO of Abgenix.  “Moving forward, we intend to build our clinical pipeline and advance our antibody ABX-PTH for secondary hyperparathyroidism, while we prudently manage our operating expenses.”

 

Third quarter 2004 and recent company highlights include:

 

                  Appointment of Ward Wolff as Chief Financial Officer and Senior Vice President of Finance, effective September 13.  Ward brings over 25 years of finance, operating and management experience to Abgenix.

 

                  Presentation of interim results from an ongoing phase 1 clinical trial of ABX 10241, an antibody that targets parathyroid hormone (PTH), at the 26th Annual Meeting of the American Society for Bone and Mineral Research. Preliminary results of the trial showed that the antibody was well tolerated with dose related suppression of PTH and serum calcium levels in hemodialysis patients with SHPT.  The company expects to launch a multiple dose phase 1 study of ABX 10241 by the first quarter of 2005.

 

                  Receipt of a milestone payment from Amgen triggered by advancement of AMG 162, a fully human antibody created using Abgenix’s proprietary XenoMouse® technology, into pivotal clinical trials for bone loss.  Under a technology licensing agreement, Abgenix is also entitled to receive additional milestones from Amgen and royalties on any future sales of AMG 162.

 

                  Completion of a 2004 goal to advance 12 targets into the company’s oncology alliance with AstraZeneca, including acceptance of four of Abgenix’s previous preclinical oncology programs.  Under the collaboration agreement, the company may also receive future payments from AstraZeneca for development activities conducted to support those programs, as the product candidates advance through development.

 

                  Three abstracts summarizing preclinical findings with panitumumab presented at 16th EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics.  The findings further characterize the antitumor effect of EGFr targeting with panitumumab.

 

2



 

Conference call information

 

Abgenix will hold a conference call today at 1:30 p.m. PT, 4:30 p.m. ET, to discuss financial results. To participate in the teleconference, please dial 800-510-9691 fifteen minutes before the conference begins. International callers should dial 617-614-3453. The pass code is 56608236. The call will also be webcast live at www.abgenix.com. A replay of the call will be available until November 9, 2004 on the company’s website or by dialing 888-286-8010. International callers should dial 617-801-6888. The replay participant code is 33544742.

 

About Abgenix

 

Abgenix is a biopharmaceutical company focused on the discovery, development and manufacturing of human therapeutic antibodies. The company’s antibody development platform includes a leading technology and state-of-the-art manufacturing capabilities that enable the rapid generation, selection and production of high affinity, fully human antibody product candidates to a variety of disease targets. Abgenix leverages its leadership position in human antibody technology to build a diversified product portfolio through the establishment of collaborations with multiple pharmaceutical and biotechnology companies. For more information on Abgenix, visit the company’s website at www.abgenix.com.

 

This press release contains forward-looking statements about Abgenix’s technologies, product development activities, collaborative arrangements, process science and manufacturing activities, projected financial and operating results, achievement of financial goals and achievement of milestone payments or other revenues. Such statements are subject to a number of uncertainties that could cause actual results to differ materially from the statements made, including risks associated with the success of clinical trials, the progress of research and product development programs, product manufacturing and utilization of manufacturing capacity, regulatory approval processes, competitive products and services, capital requirements and the extent and breadth of Abgenix’s patent portfolio. Please see Abgenix’s public filings with the Securities and Exchange Commission for information about risks that may affect Abgenix.

 

###

 

3



 

CONSOLIDATED STATEMENT OF OPERATIONS DATA

 

 

 

Three Months Ended
September 30,

 

Nine Months Ended
September 30,

 

(in thousands except per share data)

 

2004

 

2003

 

2004

 

2003

 

 

 

(unaudited)

 

(unaudited)

 

 

 

 

 

 

 

 

 

 

 

Revenues:

 

 

 

 

 

 

 

 

 

Contract revenue

 

$

3,434

 

$

1,957

 

$

10,513

 

$

10,463

 

Contract manufacturing revenue

 

 

 

1,325

 

 

Total revenues

 

3,434

 

1,957

 

11,838

 

10,463

 

 

 

 

 

 

 

 

 

 

 

Operating expenses:

 

 

 

 

 

 

 

 

 

Cost of goods manufactured

 

 

 

1,857

 

 

Research and development

 

29,978

 

26,008

 

94,583

 

66,500

 

Manufacturing start-up costs

 

6,351

 

10,282

 

16,487

 

63,127

 

General and administrative

 

7,673

 

7,828

 

21,038

 

21,182

 

Amortization of intangible assets

 

1,441

 

1,792

 

5,024

 

5,398

 

Impairment of intangible assets

 

 

 

17,241

 

1,443

 

Total operating expenses

 

45,443

 

45,910

 

156,230

 

157,650

 

 

 

 

 

 

 

 

 

 

 

Loss from operations

 

(42,009

)

(43,953

)

(144,392

)

(147,187

)

 

 

 

 

 

 

 

 

 

 

Other income (expense):

 

 

 

 

 

 

 

 

 

Interest and other income

 

1,347

 

2,036

 

4,831

 

8,010

 

Interest expense

 

(1,758

)

(1,652

)

(5,048

)

(4,133

)

Total other income (expense)

 

(411

)

384

 

(217

)

3,877

 

 

 

 

 

 

 

 

 

 

 

Loss before income tax expense

 

(42,420

)

(43,569

)

(144,609

)

(143,310

)

 

 

 

 

 

 

 

 

 

 

Foreign income tax expense

 

 

 

 

84

 

 

 

 

 

 

 

 

 

 

 

Net loss

 

$

(42,420

)

$

(43,569

)

$

(144,609

)

$

(143,394

)

Basic and diluted net loss per share

 

$

(0.48

)

$

(0.50

)

$

(1.63

)

$

(1.63

)

Shares used in computing basic and diluted net loss per share

 

88,845

 

87,962

 

88,609

 

87,865

 

 

CONSOLIDATED BALANCE SHEET DATA

 

(in thousands)

 

September 30,
2004

 

December 31,
2003

 

 

 

(unaudited)

 

*

 

 

 

 

 

 

 

Cash, cash equivalents and marketable securities

 

$

230,668

 

$

347,763

 

Other current assets

 

13,785

 

17,816

 

Total current assets

 

244,453

 

365,579

 

Property and equipment, net

 

229,914

 

246,277

 

Long-term investments

 

16,524

 

20,695

 

Intangible assets, net

 

96,231

 

118,496

 

Deposits & other assets

 

28,268

 

29,146

 

Total assets

 

$

615,390

 

$

780,193

 

Deferred revenue

 

$

7,662

 

$

10,919

 

Other current liabilities

 

28,318

 

50,368

 

Total current liabilities

 

35,980

 

61,287

 

Convertible subordinated notes

 

249,876

 

200,000

 

Deferred rent

 

7,203

 

6,153

 

Other long-term liabilities

 

6,370

 

 

Redeemable convertible preferred stock

 

49,869

 

99,737

 

Stockholders’ equity

 

266,092

 

413,016

 

Total liabilities and stockholders’ equity

 

$

615,390

 

$

780,193

 

 


* Derived from the December 31, 2003 audited financial statements.

 

Note: Certain amounts have been reclassified to conform to the current year presentation.