Press ReleaseView printer-friendly version Back
Fibrocell Reports 2016 Financial Results and Recent Operational Highlights
“We are pleased with the significant progress of our distinctive gene therapy candidates that have the potential to be transformative for patients suffering from rare and devastating genetic diseases of the skin and connective tissue,” said
“Furthermore, we expanded our
Recent Operational Highlights
November 2016, Fibrocell appointed Alfred Lane, MD, as Chief Medical Advisor. Dr. Lane’s medical career spans four decades with more than 25 years at the Stanford University School of Medicine. A board certified dermatologist and pediatrician, Dr. Laneis a Professor of Dermatology and Pediatrics (Emeritus) at Stanford University School of Medicineand the former Chair of the Department of Dermatologywhere he led a research team focused on developing gene therapy for Epidermolysis Bullosa and other genetic skin diseases. In addition, Dr. Laneis affiliated with Lucile Packard Children’s Hospital at Stanford.
January 2017, FCX-007 was granted Fast Track Designation by the U. S. Food and Drug Administration( FDA) for the treatment of RDEB. The Fast Track program is designed to facilitate development and expedite review of new therapies that address unmet medical needs of patients with serious conditions. Previously, FCX-007 was granted both Orphan Drug and Pediatric Rare Disease Designations by the FDA. FCX-007 is being developed in collaboration with Intrexon Corporation(NYSE: XON), a leader in synthetic biology.
February 2017, the first patient was dosed in the Phase I portion of the Phase I/II clinical trial of FCX-007 for the treatment of RDEB. The primary objective of this open-label clinical trial is to evaluate the safety of FCX-007 in RDEB patients. Additionally, the trial will assess the mechanism of action of FCX-007 through the evaluation of type VII collagen expression and the presence of anchoring fibrils, as well as the efficacy of FCX-007 through evidence of wound healing. Six adult patients are targeted for the Phase I portion of the trial.
- Additional patients are expected to be dosed with FCX-007 after a required four-week waiting period and subsequent health assessment of the first patient. Twelve-week post-treatment data for safety, mechanism of action and efficacy for multiple patients in the Phase I portion of this trial are expected in the third quarter of 2017.
November 2016, Fibrocell initiated a pre-clinical dose-ranging study for FCX-013, its product candidate for the treatment of linear scleroderma. The Company plans to follow this study with a toxicology/biodistribution study, and expects to submit an Investigational New Drug (IND) application to the FDAin the fourth quarter of 2017. The design of both pre-clinical studies was based on feedback from the FDAafter pre-IND review. Linear scleroderma is a form of localized scleroderma, a chronic autoimmune disease characterized by thickening of the skin and connective tissue that can be debilitating and painful. FCX-013 is being developed in collaboration with Intrexon.
December 2016, Fibrocell appointed John Maslowskias Chief Executive Officer and Douglas Swirskyas Chairman of the Company’s Board of Directors, succeeding David Pernock. In addition, Mr. Maslowski was appointed to the Company’s Board. Mr. Maslowski joined Fibrocell in 2005 and most recently served as the Company’s Senior Vice President of Scientific Affairs with oversight of research and development, clinical and regulatory affairs.
March 8, 2017, Fibrocell closed a public offering with certain of its existing investors for the sale of $8.0 millionof the Company’s Series A Convertible Preferred Stock and accompanying common stock warrants. Fibrocell intends to use the net proceeds of approximately $7.65 millionfrom the financing for the continued clinical and pre-clinical development of its product candidates and for other general corporate purposes.
Financial Results for the Twelve Months Ended
For the twelve months ended
The 2016 period included
Research and development expenses decreased to
Selling, general and administrative expenses decreased to
The Company believes that its cash and cash equivalents at
Conference Call and Webcast
To participate on the live call, please dial 877-780-3379 (domestic) or +1-719-325-2472 (international), and provide the conference code 8114421 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 http://www.fibrocell.com/investors/events and will be archived there for 30 days following the call. Please visit Fibrocell's website several minutes prior to the start of the broadcast to ensure adequate time for any software download that may be necessary.
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, has begun a Phase I/II trial for the treatment of recessive dystrophic epidermolysis bullosa (RDEB). Fibrocell is in pre-clinical development of FCX-013, its product candidate for the treatment of linear scleroderma. In addition, Fibrocell has a third program in the research phase for the treatment of arthritis and related conditions. Fibrocell’s gene therapy portfolio is being developed in collaboration with
Fibrocell, the Fibrocell logo,
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 the completion of adult patient enrollment, dosing and reporting of results for the Phase I portion of its Phase I/II clinical trial of FCX-007; the expected initiation of a toxicology/biodistribution study and submission of an IND for FCX-013 in 2017; the potential advantages of Fibrocell’s product candidates; the sufficiency of the Company’s cash and cash equivalents to fund operations into the second quarter of 2018 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: 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 and wind-down of azficel-T (including LAVIV) operations; Fibrocell’s ability to regain compliance with The NASDAQ Capital Market’s continued listing requirements; Fibrocell’s ability to obtain additional capital to continue to fund operations; Fibrocell’s ability to maintain its collaboration with
|Fibrocell Science, Inc.|
|Selected Financial Information|
|($ in thousands, except per share and share data)|
|Consolidated Statements of Operations Data:||Year Ended
|Revenue from product sales||$||337||$||270|
|Cost of product sales||696||426|
|Cost of collaboration revenue||1||296|
|Total cost of revenue||697||722|
|Gross profit (loss)||(342||)||(230||)|
|Research and development expenses||8,400||9,968|
|Research and development expenses – related party||3,724||15,924|
|Selling, general and administrative expenses||9,773||11,285|
|Intangible asset impairment expense||3,905||-|
|Other income (expense):|
|Warrant revaluation income||11,884||2,929|
|Derivative revaluation expense||(462||)||-|
|Other income (expense), net||(7||)||25|
|Loss before income taxes||(15,292||)||(34,453||)|
|Income tax benefit||-||-|
|Per share information:|
|Weighted average number of common shares outstanding|
|Consolidated Balance Sheets Data:||As of December 31,|
|Cash and cash equivalents||$||17,515||$||29,268|
|Warrant liability, current and long term||6,034||8,275|
|Total stockholders’ equity||7,861||14,203|
Investor & Media Relations Contact:
Karen Casey484.713.6133 firstname.lastname@example.org