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8-K - 8-K - OSIRIS THERAPEUTICS, INC.a12-17190_18k.htm

Exhibit 99.1

 

GRAPHIC

 

Osiris Therapeutics Reports Second Quarter 2012 Financial Results

 

Biosurgery sales rise 43% over prior quarter, Prochymal® becomes first approved stem cell drug and company ends the first half with $40 million in cash and no debt

 

COLUMBIA, Md. — July 30, 2012 - Osiris Therapeutics, Inc. (NASDAQ: OSIR), the leading stem cell company focused on developing and marketing products to treat medical conditions in inflammatory, cardiovascular, orthopedic and wound healing markets, announced today its results for the second quarter ended June 30, 2012.

 

Highlights and Recent Developments

 

·                  Achieved an historic, first approval from Health Canada to market its stem cell drug, Prochymal (remestemcel-L), for the treatment of acute graft-vs-host disease (GvHD) in children.

 

·                  Obtained a second approval for Prochymal in New Zealand, through its medical regulatory agency, Medsafe.

 

·                  Attained a transitional pass-through status from the Center for Medicare & Medicaid Services (CMS), with C-Codes being designated for Grafix®.    Also, CMS also issued a preliminary positive decision for the assignment of permanent Healthcare Common Procedure Coding System (HCPCS) Q-codes.

 

·                  In the largest study of allogeneic or “off-the-shelf” stem cells ever conducted in heart attack patients, reported interim one-year results showing that treatment with Prochymal resulted in a statistically significant reduction in heart failure in patients experiencing first-time acute myocardial infarction.

 

·                  Selected by the Biomedical Advanced Research and Development Authority (BARDA) to submit a full proposal for a Broad Agency Announcement (BAA) to fund advanced research and development of countermeasures, specifically for the use of Grafix in mass casualty thermal burn injuries.

 

·                  Reported $1.6 million of revenue from the distribution of our Biosurgery products during the second quarter — a 43% increase over the previous quarter.

 

·                  Reported cash, receivables and short-term investments of $40.1 million as of June 30, 2012.

 

“This past quarter was not only memorable, but monumental, for Osiris,” stated C. Randal Mills, Ph.D., President and Chief Executive Officer of Osiris Therapeutics.  “We have set a new benchmark to measure our success, and remain as committed as ever to extending the reach of this remarkable technology.  Whether through our Biosurgery or Therapeutics units, we will continue to develop innovative cell therapy solutions for patients in need.”

 

Second Quarter Financial Results

 

Biosurgery product revenue rose 43% from the previous quarter to $1.63 million.  As of June 30, 2012, Osiris had $40.1 million of cash, receivables and short-term investments.

 

Research and development expenses for the second quarter of 2012 were $4.1 million, compared to $5.2 million incurred in the second quarter of 2011.  General and administrative (G&A) expenses were $1.4 million for the second quarter of 2012 compared to $3.3 million for the same period of the prior year. The 2011 G&A expense included a non-cash charge of $1.7 million related to the extension of the expiration date of a warrant. Net cash used in operations for the three months ended June 30, 2012 was $4.4 million.

 

7015 Albert Einstein Drive  ·  Columbia, Maryland  21046  · Ph 443.545.1800  ·  Fax 443.545.1701  ·  www.Osiris.com

 



 

Webcast and Conference Call

 

A webcast and conference call to discuss the financial results is scheduled for today, July 30, 2012 at 9:00 a.m. ET.  To access the webcast, visit the Investor Relations section of the company’s website at http://investor.osiris.com/events.cfm.  Alternatively, callers may participate in the conference call by dialing (877) 303-6133 (U.S. participants) or (970) 315-0493 (international participants).

 

A replay of the conference call will be available approximately two hours after the completion of the call through August 05, 2012. Callers can access the replay by dialing (855) 859-2056 (U.S. participants) or (404) 537-3406 (international participants). The audio replay confirmation code is 99408506. To access a replay of the webcast, visit the Investor Relations section of the company’s website at http://investor.osiris.com/events.cfm.

 

About Osiris Therapeutics

 

Osiris Therapeutics, Inc., having developed the world’s first approved stem cell drug, Prochymal®, is the leading stem cell company. The company is focused on developing and marketing products to treat medical conditions in inflammatory, cardiovascular, orthopedic and wound healing markets.  In Biosurgery, Osiris currently markets Grafix® for burns and chronic wounds, and Ovation® for orthopedic applications. Osiris is a fully integrated company with capabilities in research, development, manufacturing and distribution of stem cell products.  Osiris has developed an extensive intellectual property portfolio to protect the company’s technology, including 48 U.S. and 144 foreign patents.

 

Osiris, Prochymal, Grafix and Ovation are registered trademarks of Osiris Therapeutics, Inc. More information can be found on the company’s website, www.Osiris.com. (OSIR-G)

 

Forward-Looking Statements

 

This press release contains forward-looking statements.  Forward-looking statements include statements about our expectations, beliefs, plans, objectives, intentions, assumptions and other statements that are not historical facts. Words or phrases such as “anticipate,” “believe,” “continue,” “ongoing,” “estimate,” “expect,” “intend,” “may,” “plan,” “potential,” “predict,” “project” or similar words or phrases, or the negatives of those words or phrases, may identify forward-looking statements, but the absence of these words does not necessarily mean that a statement is not forward-looking.  Examples of forward-looking statements may include, without limitation, statements regarding any of the following: our product development efforts; our clinical trials and anticipated regulatory requirements, and our ability to successfully navigate these requirements; the success of our product candidates in development; status of the regulatory process for our biologic drug candidates; implementation of our corporate strategy; our financial performance; our product research and development activities and projected expenditures, including our anticipated timeline and clinical strategy for mesenchymal stem cells and biologic drug candidates and marketed Biosurgery products (including Prochymal®, Chondrogen®, Grafix® and Ovation®); our cash needs; patents, trademarks and other proprietary rights; the safety and ability of our products and potential products to treat disease; our ability to supply a sufficient amount of our marketed products or product candidates and, if approved or otherwise commercially available, products to meet demand; our costs to comply with governmental regulations; our relationship with collaborating partners; our ability to maintain and benefit from our collaborative arrangements; our ability to benefit from government contracts; our plans for sales and marketing; our plans regarding facilities; types of regulatory frameworks we expect will be applicable to our products and potential products; and results of our scientific research. Forward-looking statements are subject to known and unknown risks and uncertainties and are based on potentially inaccurate assumptions that could cause actual results to differ materially from those expected or implied by the forward-looking statements.  Our actual results could differ materially from those anticipated in forward-looking

 



 

statements for many reasons, including the factors described in the section entitled “Risk Factors” in our Annual Report on Form 10-K and other Periodic Reports filed on Form 10-Q, with the United States Securities and Exchange Commission.  Accordingly, you should not unduly rely on these forward-looking statements. We undertake no obligation to publicly revise any forward-looking statement to reflect circumstances or events after the date of this press release or to reflect the occurrence of unanticipated events.

 

For additional information, please contact:

 

Erica Elchin

Osiris Therapeutics, Inc.

(443) 545-1834

OsirisPR@Osiris.com

 



 

OSIRIS THERAPEUTICS, INC.

Condensed Balance Sheets

Amounts in thousands, except per share data

 

 

 

June 30, 2012

 

December 31, 2011

 

 

 

(Unaudited)

 

 

 

Assets

 

 

 

 

 

Current assets:

 

 

 

 

 

Cash

 

$

1,109

 

$

1,661

 

Investments available for sale

 

37,637

 

45,604

 

Accounts receivable

 

1,393

 

728

 

Inventory

 

475

 

767

 

Deferred tax asset

 

 

2,188

 

Prepaid expenses and other current assets

 

3,371

 

470

 

Total current assets

 

43,985

 

51,418

 

 

 

 

 

 

 

Property and equipment, net

 

2,153

 

2,463

 

Restricted cash

 

392

 

392

 

Total assets

 

$

46,530

 

$

54,273

 

 

 

 

 

 

 

Liabilities and Stockholders’ Equity

 

 

 

 

 

 

 

 

 

 

 

Current liabilities:

 

 

 

 

 

Accounts payable and accrued expenses

 

$

5,166

 

$

4,692

 

Deferred revenue, current portion

 

 

3,333

 

Total current liabilities

 

5,166

 

8,025

 

 

 

 

 

 

 

Other long-term liabilities

 

405

 

430

 

Total liabilities

 

5,571

 

8,455

 

 

 

 

 

 

 

Stockholders’ equity

 

 

 

 

 

Common stock, $.001 par value, 90,000 shares authorized, 32,868 shares outstanding - 2012, 32,828 shares outstanding - 2011

 

33

 

33

 

Additional paid-in-capital

 

278,785

 

278,092

 

Accumulated other comprehensive income

 

5

 

20

 

Accumulated deficit

 

(237,864

)

(232,327

)

Total stockholders’ equity

 

40,959

 

45,818

 

Total liabilities and stockholders’ equity

 

$

46,530

 

$

54,273

 

 



 

OSIRIS THERAPEUTICS, INC.

Condensed Statements of Operations

(Unaudited)

Amounts in thousands, except per share data

 

 

 

Three Months Ended

 

Six Months Ended

 

 

 

June 30,

 

June 30, 

 

 

 

2012

 

2011

 

2012

 

2011

 

 

 

 

 

 

 

 

 

 

 

Product revenues

 

$

1,626

 

$

130

 

$

2,763

 

$

167

 

Cost of product revenues

 

552

 

55

 

939

 

70

 

Gross profit

 

1,074

 

75

 

1,824

 

97

 

 

 

 

 

 

 

 

 

 

 

Revenue from collaborative research agreements and royalties

 

98

 

10,224

 

3,544

 

20,619

 

 

 

 

 

 

 

 

 

 

 

Operating expenses:

 

 

 

 

 

 

 

 

 

Research and development

 

4,072

 

5,209

 

8,035

 

9,920

 

General and administrative

 

1,418

 

3,280

 

2,941

 

4,976

 

 

 

5,490

 

8,489

 

10,976

 

14,896

 

 

 

 

 

 

 

 

 

 

 

(Loss) income from operations

 

(4,318

)

1,810

 

(5,608

)

5,820

 

 

 

 

 

 

 

 

 

 

 

Other income, net

 

21

 

25

 

39

 

54

 

 

 

 

 

 

 

 

 

 

 

(Loss) income before income taxes

 

(4,297

)

1,835

 

(5,569

)

5,874

 

 

 

 

 

 

 

 

 

 

 

Income tax benefit (expense)

 

32

 

(43

)

32

 

(43

)

 

 

 

 

 

 

 

 

 

 

Net (loss) income

 

$

(4,265

)

$

1,792

 

$

(5,537

)

$

5,831

 

 

 

 

 

 

 

 

 

 

 

Basic (loss) earnings per share

 

$

(0.13

)

$

0.05

 

$

(0.17

)

$

0.18

 

 

 

 

 

 

 

 

 

 

 

Diluted (loss) earnings per share

 

$

(0.13

)

$

0.05

 

$

(0.17

)

$

0.18

 

 

 

 

 

 

 

 

 

 

 

Weighted average common shares (basic)

 

32,860

 

32,821

 

32,845

 

32,814

 

 

 

 

 

 

 

 

 

 

 

Weighted average common shares (diluted)

 

32,860

 

33,134

 

32,845

 

33,124

 

 



 

OSIRIS THERAPEUTICS, INC.

Statements of Cash Flows

(Unaudited)

Amounts in thousands

 

 

 

Six months ended ,

 

 

 

June 30,

 

 

 

2012

 

2011

 

Cash flows from operating activities:

 

 

 

 

 

Net (loss) income

 

$

(5,537

)

$

5,831

 

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

 

 

 

 

 

Depreciation and amortization

 

348

 

375

 

Non cash share-based payments

 

687

 

994

 

Provision for bad debts

 

11

 

 

Non cash expense- extension of expiration date of warrant to related party

 

 

1,740

 

Changes in operating assets and liabilities:

 

 

 

 

 

Accounts receivable

 

(676

)

1,263

 

Inventory, prepaid expenses, and other current assets

 

(421

)

(120

)

Other assets

 

 

149

 

Accounts payable and accrued expenses

 

449

 

(1,195

)

Deferred revenue

 

(3,333

)

(20,480

)

Net cash used in operating activities

 

(8,472

)

(11,443

)

 

 

 

 

 

 

Cash flows from investing activities:

 

 

 

 

 

Purchases of property and equipment

 

(38

)

(40

)

Proceeds from sale of investments available for sale

 

7,985

 

11,555

 

Purchases of investments available for sale

 

(33

)

(5

)

Net cash provided by investing activities

 

7,914

 

11,510

 

 

 

 

 

 

 

Cash flows from financing activities:

 

 

 

 

 

Proceeds from the issuance of common stock, net

 

6

 

1

 

Net cash provided by financing activities

 

6

 

1

 

 

 

 

 

 

 

Net (decrease) increase in cash

 

(552

)

68

 

Cash at beginning of period

 

1,661

 

1,442

 

 

 

 

 

 

 

Cash at end of period

 

$

1,109

 

$

1,510