- Company to Host Conference Call and Webcast Today at 8:30 a.m. EDT -
EXTON, Pa., March 19, 2018 (GLOBE NEWSWIRE) -- Fibrocell Science, Inc. (NASDAQ:FCSC), a gene therapy company focused on transformational autologous cell-based therapies for skin and connective tissue diseases, today reported financial results for the year ended December 31, 2017 and recent operational highlights. Fibrocell will host a conference call and webcast today at 8:30 a.m. EDT.
“We are pleased with the substantial progress of our gene therapy candidates that continues to advance and positions us to achieve important milestones in 2018,” said John Maslowski, President and Chief Executive Officer of Fibrocell. “In January 2018, the U.S. Food and Drug Administration granted us allowance to enroll pediatric patients in the Phase 2 portion of our Phase 1/2 clinical trial of FCX-007 for the treatment of recessive dystrophic epidermolysis bullosa, a key milestone for the program.”
“In addition, we completed necessary pre-clinical studies for FCX-013, our product candidate for the treatment of moderate to severe localized scleroderma. We used the data to support our submission of an Investigational New Drug Application to the FDA in January 2018, and in March, the FDA allowed the IND for FCX-013 to progress to clinical trials,” said Mr. Maslowski.
Recent program highlights and new updates are as follows:
FCX-007
FCX-013
Corporate
Financial Results for the Twelve Months Ended December 31, 2017
For the twelve months ended December 31, 2017, Fibrocell reported a diluted net loss of $1.33 per share, compared to a diluted net loss of $1.18 per share for the same period in 2016.
The 2017 period included approximately $4.9 million of non-cash warrant revaluation income, as compared to approximately $11.9 million of non-cash warrant revaluation income for the same period in 2016. Additionally, the 2017 period included non-cash deemed dividends on Series A preferred stock of approximately $4.1 million increasing net loss attributable to common stockholders. No non-cash deemed dividends were recorded in the same period in 2016.
Research and development expenses increased 1% to approximately $12.2 million for the twelve months ended December 31, 2017, as compared to approximately $12.1 million for the same twelve-month period in 2016. This increase was due primarily to increased costs related to the Phase 1/2 clinical trial of FCX-007 and increased pre-clinical development costs related to FCX-013. These increases were partially offset by reduced compensation and employee related expenses in the 2017 period as a result of our restructuring related initiatives implemented in June 2016.
Selling, general and administrative expenses decreased 30.9% to approximately $6.7 million for the twelve months ended December 31, 2017, as compared to approximately $9.8 million for the same twelve-month period in 2016. This decrease was due primarily to reduced compensation and employee related expenses, all due to reductions in management staffing made in the last half of 2016 and in early 2017.
As of December 31, 2017, the Company had cash and cash equivalents of approximately $17.4 million and working capital of approximately $13.5 million. Fibrocell used approximately $17.0 million in cash for operations during the twelve months ended December 31, 2017, as compared to approximately $29.4 million used for the same twelve-month period in 2016.
The Company believes that its cash and cash equivalents will be sufficient to fund operations into the first quarter of 2019.
Conference Call and Webcast
To participate on the live call, please dial 800-239-9838 (domestic) or +1-323-794-2551 (international), and provide the conference code 6756079 five to ten minutes before the start of the call. The conference call will also be webcast live under the investor relations section of Fibrocell's website at www.fibrocell.com/investors/events and will be archived there for 30 days following the call.
About Fibrocell
Fibrocell is an autologous cell and gene therapy company translating personalized biologics into medical breakthroughs for diseases affecting the skin and connective tissue. Fibrocell’s most advanced product candidate, FCX-007, is the subject of a Phase 1/2 clinical trial for the treatment of recessive dystrophic epidermolysis bullosa. Fibrocell is also developing FCX-013, the Company’s product candidate for the treatment of moderate to severe localized scleroderma. Fibrocell’s gene therapy portfolio is being developed in collaboration with Intrexon Corporation (NYSE:XON), a leader in synthetic biology. For more information, visit www.fibrocell.com or follow Fibrocell on Twitter at @Fibrocell.
Trademarks
Fibrocell, the Fibrocell logo, and Fibrocell Science are trademarks of Fibrocell Science, Inc. and/or its affiliates. All other names may be trademarks of their respective owners.
Forward-Looking Statements
This press release contains, and our officers and representatives may from time to time make, statements that are “forward-looking statements” within the meaning of the safe harbor provisions of the U.S. Private Securities Litigation Reform Act of 1995. All statements that are not historical facts are hereby identified as forward-looking statements for this purpose and include, among others, statements relating to: Fibrocell’s expectations regarding the timing of dosing and reporting of results for its Phase 1/2 clinical trial of FCX-007; Fibrocell’s expectations regarding the enrollment of pediatric patients in the Phase 2 portion of its Phase 1/2 clinical trial of FCX-007 and the Phase 1 portion of its Phase 1/2 clinical trial for FCX-013; the potential advantages of Fibrocell’s product candidates; the sufficiency of the Company’s cash and cash equivalents to fund operations into the first quarter of 2019 and other statements regarding Fibrocell’s future operations, financial performance and financial position, prospects, strategies, objectives and other future events.
Forward-looking statements are based upon management’s current expectations and assumptions and are subject to a number of risks, uncertainties and other factors that could cause actual results and events to differ materially and adversely from those indicated herein including, among others: that interim clinical trial results are not necessarily indicative of final clinical results and final clinical trial results may not be positive with regard to safety or efficacy of FCX-007 or FCX-013; uncertainties and delays relating to the initiation, enrollment and completion of pre-clinical studies and clinical trials; whether pre-clinical study and clinical trial results will validate and support the safety and efficacy of Fibrocell’s product candidates; unanticipated or excess costs relating to the development of Fibrocell’s gene therapy product candidates; Fibrocell’s ability to obtain additional capital to continue to fund operations; Fibrocell’s ability to maintain its collaboration with Intrexon Corporation; and the risks, uncertainties and other factors discussed under the caption “Item 1A. Risk Factors” in Fibrocell’s most recent Form 10-K filing and Form 10-Q filings. As a result, you are cautioned not to place undue reliance on any forward-looking statements. While Fibrocell may update certain forward-looking statements from time to time, Fibrocell specifically disclaims any obligation to do so, whether as a result of new information, future developments or otherwise.
Investor & Media Relations Contact:
Karen Casey
484.713.6133
kcasey@fibrocell.com
Fibrocell Science, Inc.
Selected Financial Information
($ in thousands, except per share and share data)
Year Ended December 31, | ||||||||||
2017 | 2016 | |||||||||
Revenue from product sales | $ | — | $ | 337 | ||||||
Collaboration revenue | — | 18 | ||||||||
Total revenue | — | 355 | ||||||||
Cost of product sales | — | 696 | ||||||||
Cost of collaboration revenue | — | 1 | ||||||||
Total cost of revenue | — | 697 | ||||||||
Gross loss | — | (342 | ) | |||||||
Research and development expense | 6,512 | 8,400 | ||||||||
Research and development expense - related party | 5,720 | 3,724 | ||||||||
Selling, general and administrative expense | 6,749 | 9,773 | ||||||||
Intangible asset impairment expense | — | 3,905 | ||||||||
Restructuring costs | — | 335 | ||||||||
Operating loss | (18,981 | ) | (26,479 | ) | ||||||
Other income (expense): | ||||||||||
Warrant revaluation income (expense) | 4,920 | 11,884 | ||||||||
Derivative revaluation income | (1,407 | ) | (462 | ) | ||||||
Interest expense | (828 | ) | (228 | ) | ||||||
Other income (expense), net | 56 | (7 | ) | |||||||
Loss before income taxes | (16,240 | ) | (15,292 | ) | ||||||
Income taxes | — | — | ||||||||
Net loss | (16,240 | ) | (15,292 | ) | ||||||
Dividend paid in-kind to preferred stockholders | (264 | ) | — | |||||||
Deemed dividend on preferred stock | (4,099 | ) | — | |||||||
Net loss attributable to common stockholders | $ | (20,603 | ) | $ | (15,292 | ) | ||||
Per Share Information: | ||||||||||
Net loss: | ||||||||||
Basic | $ | (1.33 | ) | $ | (1.04 | ) | ||||
Diluted | $ | (1.33 | ) | $ | (1.18 | ) | ||||
Weighted average number of common shares outstanding: | ||||||||||
Basic | 15,454,199 | 14,641,528 | ||||||||
Diluted | 15,460,118 | 14,647,534 |
Condensed Consolidated Balance Sheets Data: | December 31, | December 31, | ||||
2017 | 2016 | |||||
Cash and cash equivalents | $ | 17,417 | $ | 17,515 | ||
Working capital | 13,477 | 15,041 | ||||
Total assets | 19,411 | 19,582 | ||||
Warrant liability, current and long term | 1,073 | 6,034 | ||||
Total liabilities | 10,404 | 11,721 | ||||
Total stockholders’ equity | 9,007 | 7,861 | ||||