Fibrocell Reports Third Quarter 2016 Financial Results And Recent Operational Highlights

EXTON, Pa., Nov. 03, 2016 (GLOBE NEWSWIRE) -- Fibrocell Science, Inc. (NASDAQ:FCSC) today reported financial results for the third quarter ended September 30, 2016 and recent operational highlights. Fibrocell will host a conference call and webcast today at 8:30 a.m. EDT.

"Fibrocell is focused on advancing our innovative gene therapy candidates that use genetically-modified autologous fibroblast cells to target the underlying cause of debilitating skin and connective tissue diseases and have the potential to offer hope and relief to patients," said David Pernock, Chairman and Chief Executive Officer of Fibrocell. "We are pleased with the progress of the Phase I/II clinical trial of FCX-007 for the treatment of Recessive Dystrophic Epidermolysis Bullosa (RDEB), and continue to expect to dose the first subject in the Phase I portion of the trial at the end of 2016.  Furthermore, development of FCX-013—our product candidate for the treatment of linear scleroderma—will be proceeding into a pre-clinical dose-ranging study this month, with a toxicology/biodistribution study to follow."

Recent Operational Highlights

FCX-007
  • During the third quarter, Fibrocell completed enrollment of three adult subjects in the NC1+ cohort of the Phase I portion of its Phase I/II clinical trial of FCX-007 for the treatment of RDEB. One adult subject is enrolled in the NC1- cohort and two more subjects are required to complete enrollment in this cohort.  The primary objective of this open-label clinical trial is to evaluate the safety of FCX-007 in RDEB subjects. 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. 
  • The manufacture of FCX-007 for all four enrolled patients in the Phase I portion of the trial is underway and the Company expects to dose the first subject at the end of 2016. Additional adult subjects will be dosed after a required 90-day waiting period is complete to ensure there are no safety concerns for the first dose of the new gene-therapy product. Three-month post-treatment data for safety, mechanism of action and efficacy for the adult subjects in the Phase I portion of this trial are expected in the third quarter of 2017.

FCX-013
  • In November, Fibrocell plans to initiate 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 FDA in the fourth quarter of 2017. 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.

Corporate
  • In September, Fibrocell completed a private placement in which the Company sold convertible promissory notes having an aggregate principal amount of $18.1 million and warrants to purchase an aggregate of 18.1 million shares of the Company's common stock. Fibrocell intends to use the $17.9 million of net proceeds from the financing for the continued pre-clinical and clinical development of its product candidates and for other general corporate purposes.

Financial Results for the Nine Months Ended September 30, 2016 and 2015

For the nine months ended September 30, 2016, Fibrocell reported a diluted net loss of $0.31 per share, compared to a diluted net loss of $0.44 per share for the same period in 2015.

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