Inactive Instrument

Fibrocell Science, Inc.

Equities

US3157214079

Biotechnology & Medical Research

Fibrocell Science, Inc. Announces Resignation of Robert Sheroff as Vice President, Technical Operations

May 02, 2015 at 01:44 am IST

Fibrocell Science, Inc. announced that on April 30, 2015, Robert Sheroff, its Vice President, Technical Operations and one of named executive officers, informed the company of his decision to resign effective June 1, 2015. Mr. Sheroff's resignation did not result from any disagreement with the Company on any matter relating to the company's operations, policies or practices. The Company and Mr. Sheroff may enter into a consulting agreement in the future.

Latest news about Fibrocell Science, Inc.

Fibrocell Science, Inc.(NasdaqGM:FCSC) dropped from S&P TMI Index	16/19/16	CI
Fibrocell Science, Inc.(NasdaqGM:FCSC) dropped from NASDAQ Composite Index	13/19/13	CI
Castle Creek Pharmaceutical Holdings, Inc. completed the acquisition of Fibrocell Science, Inc..	13/19/13	CI
Fibrocell Science, Inc. Reports Earnings Results for the Third Quarter Ended September 30, 2019	15/19/15	CI
Castle Creek Pharmaceutical Holdings, Inc. entered into a definitive agreement to acquire Fibrocell Science, Inc. for $63.3 million.	12/19/12	CI
Fibrocell Science, Inc Appoints Sean D. Buckley as Chief Financial Officer	23/19/23	CI
Fibrocell Science, Inc. Reports Earnings Results for the Second Quarter Ended June 30, 2019	15/19/15	CI
Fibrocell Science, Inc. Receives FDA Regenerative Medicine Advanced Therapy Designation for FCX-007 Gene Therapy for the Treatment of RDEB	29/19/29	CI
Fibrocell Science, Inc. Reports Earnings Results for the First Quarter Ended March 31, 2019	16/19/16	CI
Fibrocell Announces Collaboration with Castle Creek Pharmaceuticals to Develop and Commercialize FCX-007 Gene Therapy	15/19/15	CI
Fibrocell Science, Inc. Reports Earnings Results for the Full Year Ended December 31, 2018	28/19/28	CI
Fibrocell Announces Positive Feedback from Type B End-of-Phase 2 Meeting with FDA on Phase 3 Clinical Trial Design for FCX-007	27/19/27	CI
Fibrocell Science, Inc. Auditor Raises 'Going Concern' Doubt	27/19/27	CI
Fibrocell Science, Inc. announced that it has received $0.9 million in funding from EB Research Partnership, Inc., Endowment Arm, Epidermolysis Bullosa Medical Research Foundation, Endowment Arm	11/18/11	CI
Fibrocell Science, Inc. announced that it expects to receive $0.9 million in funding from EB Research Partnership, Inc., Endowment Arm, Epidermolysis Bullosa Medical Research Foundation, Endowment Arm	07/18/07	CI
Fibrocell Science, Inc. Reports Consolidated Unaudited Earnings Results for the Nine Months Ended September 30, 2018	13/18/13	CI
Fibrocell Science, Inc. Receives Guidance from FDA on Phase 3 Clinical Trial Design for FCX-007	25/18/25	CI
Fibrocell Science, Inc. Announces U.S. Food and Drug Administration Granted Fast Track Designation to FCX-013	05/18/05	CI
Fibrocell Science, Inc. Announces Unaudited Consolidated Earnings Results for the Six Months Ended June 30, 2018; Expects to Enroll A Total of Six Patients Ages Seven and Older by the End of the Third Quarter of 2018	09/18/09	CI
Fibrocell Science, Inc. announced that it has received $0.119769 million in funding	05/18/05	CI
Fibrocell Science, Inc. announced that it expects to receive $0.119769 million in funding	02/18/02	CI
Fibrocell Science, Inc. Appoints Sean D. Buckley as Vice President of Business Administration and Corporate Secretary	23/18/23	CI
Fibrocell Science, Inc. announced that it has received $0.191084 million in funding	31/18/31	CI
Fibrocell Science, Inc. announced that it expects to receive $0.191084 million in funding	29/18/29	CI
Fibrocell Science, Inc. Provides an Update on Interim Results and Progress of its Phase 1/2 Clinical Trial of FCX-007 for the Treatment of Recessive Dystrophic Epidermolysis Bullosa	21/18/21	CI

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Fibrocell Science, Inc. is an autologous cell and gene therapy company. The Company is focused on discovering and developing localized therapies for diseases affecting the skin, connective tissue and joints. Its product candidate, azficel-T, is in development to treat patients suffering from vocal cord scarring that is either idiopathic or age-related. It is investigating the indication in a Phase II clinical trial. Its gene-therapy product candidate, FCX-007, is in pre-clinical development for the treatment of recessive dystrophic epidermolysis bullosa. Its gene-therapy product candidate, FCX-013, is in pre-clinical development for the treatment of linear scleroderma. Its product, LAVIV (azficel-T), is indicated for the improvement of the appearance of moderate to severe nasolabial fold wrinkles in adults. A third gene-therapy program is focused on the treatment of arthritis. Its product, LAVIV (azficel-T), is focused on improving the appearance of nasolabial fold wrinkles in adults.

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