BioTime Announces Fourth Quarter and Fiscal Year End 2012 Financial Results and Recent Corporate Acc

Updated

BioTime Announces Fourth Quarter and Fiscal Year End 2012 Financial Results and Recent Corporate Accomplishments

ALAMEDA, Calif.--(BUSINESS WIRE)-- BioTime, Inc. (NYSE MKT: BTX), today reported financial results for the fourth quarter and year ended December 31, 2012 and highlighted its fourth quarter and recent corporate accomplishments.

Fourth Quarter and Recent Highlighted Corporate Accomplishments

  • Entered into a definitive agreement with Geron Corporation in which BioTime's subsidiary BioTime Acquisition Corporation (BAC) will acquire the patents and patent applications, biological materials, and other assets related to Geron's human embryonic stem (hES) cell programs, including Geron's Phase I clinical trial of oligodendrocyte progenitor cells in patients with acute spinal cord injury, as well as its Phase I/II clinical trial of its autologous cellular immunotherapy program in patients with acute myelogenous leukemia.

  • Expanded the HyStem® field-of-use license from the University of Utah to an exclusive worldwide license for all human medical applications.

  • Submitted protocol to European regulatory authorities for initiation of human clinical trials of Renevia™ as a medical device for the delivery of adipose stem cells for reconstructive surgery.

  • Updated plans for OncoCyte's initiation of a clinical study using PanC-Dx™ for breast cancer screening in 2013.

  • Launched LifeMap BioReagents™ portal, Malacards database, and LifeMap Discovery™ database though LifeMap Sciences.

  • Raised cash proceeds of $14.7 million over the past five months through the sale of BioTime common shares, including $1.4 million in the fourth quarter of 2012, $13.3 million in the first quarter of 2013 to date, and will raise an additional $3 million through an amended agreement with an investor which is expected to close on April 10, 2013.


"We have positioned 2013 to be a very pivotal year in the development of our product opportunities as BioTime begins human clinical trials for Renevia™, OncoCyte initiates its PanC-Dx™ clinical study, LifeMap Sciences expands its revenue generating product offerings, and we move to close our transaction with BAC and Geron," said Michael D. West, Ph.D., BioTime's President and Chief Executive Officer. "The proceeds from our recent equity financings will support the funding of our operations and cash commitment to BAC through this year."

Financial Results

Revenue

For the quarter ended December 31, 2012, on a consolidated basis, total revenue was $1.2 million, down $0.5 million from $1.7 million for the same period one year ago. The decrease in fourth quarter revenue is primarily attributable to lower grant revenue related to the completion of BioTime's research grant from the California Institute for Regenerative Medicine (CIRM), and a decrease in the sale of research products, partially offset by subscription and advertising revenues from LifeMap Sciences' online database GeneCards®, which LifeMap Sciences began marketing in May of 2012.

For the full year 2012, total revenue, on a consolidated basis, was $3.9 million, down $0.5 million from $4.4 million in 2011. The decrease in annual revenue is primarily due to the same factors that contributed to the decline in fourth quarter revenues. License revenue included subscription and advertising revenues from LifeMap Sciences' online database GeneCards®, and accounted for approximately $0.8 million in new revenue beginning at the end of the second quarter of 2012.

Expenses

Total expenses for the three months ended December 31, 2012 were $8.1 million, compared to expenses of $7.1 million for the same period of 2011. Fourth quarter operating expenses increased 14% from 2011 due to an increase in staffing, and the expansion of research and development efforts, including additional expenses in the Renevia™clinical development program and PanC-Dx™ cancer diagnostic development program, and one-time transaction legal expenses related to Geron's stem cell assets contribution agreement.

Total expenses for the full year ended December 31, 2012 were $28.5 million, compared to $23.0 million for the full year ended December 31, 2011. The increase in expenses is primarily related to an increase in staffing, the expansion of research and development efforts, and transaction legal expenses.

Net Loss

Net loss attributable to BioTime for the three months ended December 31, 2012 was $6.0 million or $0.12 per share, compared to a net loss of $5.4 million or $0.11 per share for the same period in 2011. Net loss attributable to BioTime for the full year ended December 31, 2012 was $21.4 million or $0.44 per share, compared to a net loss of $16.5 million or $0.35 per share for the full year ended December 31, 2011. Net losses attributable to BioTime include losses from BioTime majority owned subsidiaries based upon BioTime's percentage ownership of those subsidiaries.

Cash Flow

Net cash used in operating activities in the fourth quarter of 2012 was $5.0 million compared to $3.8 million in the fourth quarter of 2011. For the full year ended December 31, 2012, net cash used in operating activities was $19.7 million, compared to $13.6 million for the same period in 2011. The increased use of cash in 2012 reflects the hiring of additional staff and the increased cost of research and development programs in BioTime subsidiaries, including programs expanded through business acquisitions, and specific transaction related legal and administrative expenses..

Balance Sheet and Subsequent Financing Events

Cash and cash equivalents, on a consolidated basis, totaled $4.3 million as of December 31, 2012, compared with $22.2 million as of December 31, 2011.

During the fourth quarter of 2012, BioTime raised gross proceeds of $1.1 million from the sale of 314,386 BioTime common shares at an average price of $3.60 per share, and thus far during 2013, BioTime has raised gross proceeds of $9.7 million from the sale of 2,191,175 BioTime common shares at a weighted average price of $4.43 per share, in at-the-market transactions. Additionally, certain BioTime majority-owned subsidiaries hold BioTime common shares which may be sold in at-the-market or similar transactions. During the fourth quarter of 2012, BioTime subsidiaries raised gross proceeds of $0.3 million, and since January 1, 2013, subsidiaries of BioTime have raised gross proceeds of $1.6 million from the sale of BioTime common shares in at-the-market transactions. Cantor Fitzgerald & Co. acted as sales agent for BioTime and BioTime's subsidiaries in these transactions.

In January 2013, we entered into a stock and warrant purchase agreement with Romulus Films Ltd. to provide BioTime with $5 million in equity financing. Under the terms of the agreement, Romulus committed to invest $5 million in BioTime by purchasing an aggregate of 1,350,000 BioTime common shares at a purchase price of approximately $3.70 per share and warrants to purchase 650,000 additional BioTime common shares with an exercise price of $5.00 per share and a term expiring in January 2016. The first tranche of $2 million was funded in January 2013 and the second investment tranche of $3 million will be funded on April 10, 2013. This $5 million investment will be used to fund BioTime's $5 million cash contribution to BAC.

About BioTime, Inc.

BioTime, headquartered in Alameda, California, is a biotechnology company focused on regenerative medicine and blood plasma volume expanders. Its broad platform of stem cell technologies is enhanced through subsidiaries focused on specific fields of application. BioTime develops and markets research products in the fields of stem cells and regenerative medicine, including a wide array of proprietary PureStem™ cell lines, HyStem® hydrogels, culture media, and differentiation kits. BioTime is developing Renevia™ (formerly known as HyStem®-Rx), a biocompatible, implantable hyaluronan and collagen-based matrix for cell delivery in human clinical applications. BioTime's therapeutic product development strategy is pursued through subsidiaries that focus on specific organ systems and related diseases for which there is a high unmet medical need. BioTime's majority-owned subsidiary Cell Cure Neurosciences Ltd. is developing therapeutic products derived from stem cells for the treatment of retinal and neural degenerative diseases. BioTime's subsidiary OrthoCyte Corporation is developing therapeutic applications of stem cells to treat orthopedic diseases and injuries. Another subsidiary, OncoCyte Corporation, focuses on the diagnostic and therapeutic applications of stem cell technology in cancer, including the diagnostic product PanC-Dx™ currently being developed for the detection of cancer in blood samples. ReCyte Therapeutics, Inc. is developing applications of BioTime's proprietary induced pluripotent stem cell technology to reverse the developmental aging of human cells to treat cardiovascular and blood cell diseases. BioTime's subsidiary LifeMap Sciences, Inc. markets GeneCards®, the leading human gene database, as part of an integrated database suite that also includes the LifeMap Discovery™ database of embryonic development, stem cell research and regenerative medicine, and MalaCards, the human disease database. LifeMap Sciences also markets BioTime research products and PanDaTox, an innovative, recently developed, searchable database that can aid in the discovery of new antibiotics and biotechnologically beneficial products. BioTime Acquisition Corporation is a new subsidiary being used to acquire the stem cell assets of Geron Corporation, including patents and other intellectual property, biological materials, reagents, and equipment for the development of new therapeutic products for regenerative medicine. BioTime's lead product, Hextend®, is a blood plasma volume expander manufactured and distributed in the U.S. by Hospira, Inc. and in South Korea by CJ CheilJedang Corporation under exclusive licensing agreements. Additional information about BioTime can be obtained at www.biotimeinc.com.

Forward-Looking Statements

Statements pertaining to future financial and/or operating results, future growth in research, technology, clinical development, and potential opportunities for BioTime and its subsidiaries, along with other statements about the future expectations, beliefs, goals, plans, or prospects expressed by management constitute forward-looking statements. Any statements that are not historical fact (including, but not limited to statements that contain words such as "will," "may" "believes," "plans," "anticipates," "expects," "estimates") should also be considered to be forward-looking statements. Forward-looking statements involve risks and uncertainties, including, without limitation, risks inherent in the development and/or commercialization of potential products, uncertainty in the results of clinical trials or regulatory approvals, need and ability to obtain future capital, and maintenance of intellectual property rights. Actual results may differ materially from the results anticipated in these forward-looking statements and as such should be evaluated together with the many uncertainties that affect the business of BioTime and its subsidiaries, particularly those mentioned in the cautionary statements found in BioTime's Securities and Exchange Commission filings. BioTime disclaims any intent or obligation to update these forward-looking statements.

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BIOTIME, INC.

CONDENSED CONSOLIDATED BALANCE SHEETS

December 31,

December 31,

2012

2011

ASSETS

CURRENT ASSETS

Cash and cash equivalents

$

4,349,967

$

22,211,897

Inventory

55,316

51,174

Prepaid expenses and other current assets

2,774,196

2,692,303

Total current assets

7,179,479

24,955,374

Equipment, net

1,348,554

1,347,779

Deferred license and consulting fees

669,326

843,944

Deposits

64,442

63,082

Intangible assets, net

20,486,792

18,619,516

TOTAL ASSETS

$

29,748,593

$

45,829,695

LIABILITIES AND EQUITY

CURRENT LIABILITIES

Accounts payable and accrued liabilities

$

3,989,962

$

2,681,111

Deferred grant income

-

261,777

Deferred license revenue, current portion

400,870

203,767

Total current liabilities

4,390,832

3,146,655

LONG-TERM LIABILITIES

Deferred license revenue, net of current portion

768,678

899,551

Deferred rent, net of current portion

57,214

66,688

Other long term liabilities

237,496

258,620

Total long-term liabilities

1,063,388

1,224,859

Commitments and contingencies

EQUITY

Preferred Shares, no par value, authorized 1,000,000 shares; none issued

-

-

Common Shares, no par value, authorized 75,000,000 shares; issued and outstanding shares; 51,183,318 issued, and 49,383,209 outstanding as of December 31, 2012 and 50,321,962 issued, and 49,035,788 outstanding at December 31, 2011, respectively

119,821,243

115,144,787

Contributed capital

93,972

93,972

Accumulated other comprehensive income

(59,570

)

(122,749

)

Accumulated deficit

(101,895,712

)

(80,470,009

)

Treasury Stock: 1,800,109 and 1,286,174 outstanding at December 31, 2012 and at December 31, 2011, respectively

(8,375,397

)

(6,000,000

)

Total shareholders' equity

9,584,536

28,646,001

Noncontrolling interest

14,709,837

12,812,180

Total equity

24,294,373

41,458,181

TOTAL LIABILITIES AND EQUITY

$

29,748,593

$

45,829,695

BIOTIME INC

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS

Unaudited

Three Months Ended December 31,

Full Year Ended December 31,

2012

2011

2012

2011

REVENUES:

License fees

$350,477

$62,168

$899,998

$263,757

Royalties from product sales

133,878

187,693

541,681

756,950

Grant income

704,372

1,161,569

2,222,458

2,767,181

Sale of research products

33,810

240,290

251,190

646,271

Total revenues

1,222,537

1,651,720

3,915,327

4,434,159

Cost of Sales

(160,355

)

(20,589

)

(434,271

)

(79,397

)

Total net revenues

1,062,182

1,631,131

3,481,056

4,354,762

EXPENSES:

Research and development

(4,793,278

)

(3,943,248

)

(18,116,688

)

(13,699,691

)

General and administrative

(3,327,238

)

(3,148,119

)

(10,365,045

)

(9,341,502

)

Total expenses

(8,120,516

)

(7,091,367

)

(28,481,733

)

(23,041,193

)

Loss from operations

(7,058,334

)

(5,460,236

)

(25,000,677

)

(18,686,431

)

OTHER INCOME/(EXPENSES):

Interest income, net

2,062

10,022

19,383

29,727

Other income/(expense), net

(93,811

)

(4,877

)

(317,710

)

219,067

Loss on sale of fixed assets

(1,859

)

-

(6,856

)

(6,246

)

Total other income/(expenses), net

(93,608

)

5,145

(305,183

)

242,548

NET LOSS

(7,151,942

)

(5,455,091

)

(25,305,860

)

(18,443,883

)

Less: Net loss attributable to the noncontrolling interest

1,116,988

94,440

3,880,157

1,928,383

NET LOSS ATTRIBUTABLE TO BIOTIME, INC.(1)

$(6,034,954

)

$(5,360,651

)

$(21,425,703

)

$(16,515,500

)

Foreign currency translation gain/(loss)

137,814

(118,206

)

63,179

(1,020,087

)

TOTAL COMPREHENSIVE LOSS (2)

$(5,897,140

)

$(5,478,857

)

$(21,362,524

)

$(17,535,587

)

BASIC AND DILUTED LOSS PER COMMON SHARE (1)

$(0.12

)

$(0.11

)

$(0.44

)

$(0.35

)

WEIGHTED AVERAGE NUMBER OF COMMON SHARES OUTSTANDING: BASIC AND DILUTED

49,263,968

48,990,590

49,213,687

47,053,518

(1) Basic and diluted loss per common share is calculated using "Net loss attributable to BioTime, Inc."

(2) Comprehensive net loss includes foreign currency translation gain of $137,814 and $63,179 for the three months and year ended December 31, 2012, respectively and translation loss of $118,206 and loss of $1,020,087 for the same periods in the prior year, respectively arise entirely from the translation of foreign subsidiary financial information for consolidation purposes and therefore not used in the calculation of basic and diluted loss per common share.



BioTime, Inc.
Peter Garcia, 510-521-3390, ext 367
Chief Financial Officer
pgarcia@biotimemail.com
or
Judith Segall, 510-521-3390, ext 301
jsegall@biotimemail.com

KEYWORDS: United States North America California

INDUSTRY KEYWORDS:

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