Fibrocell Reports Interim Results of Phase 1/2 Clinical Trial of FCX-007

Fibrocell Science (NASDAQ:FCSC) reported interim results in its Phase 1/2 clinical trial of FCX-007 for the treatment of recessive dystrophic epidermolysis bullosa (RDEB).
As quoted in the press release:

Three adult non-collagenous (NC)1+ patients have been dosed with a single intradermal injection session of FCX-007 in the margins of and across targeted wounds, as well as in separate intact skin sites. Five wounds were treated on the three subjects, ranging in size from 4.4cm²to 13.1cm².

Data from these patients show FCX-007 was well-tolerated through 12 weeks post-administration. There were no serious adverse events and no product related adverse events reported.

Wounds were evaluated during a monitoring period prior to dosing and they were observed to be open for up to eight months.

Click here to read the full press release.

Source: globenewswire.com