Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
FCX-013 is an autologous gene therapy candidate designed for the treatment of localized scleroderma (morphea). It consists of autologous dermal fibroblasts that are genetically modified to express matrix metalloproteinase 1 (MMP-1), an enzyme responsible for breaking down Type I and Type III collagen. The expression of MMP-1 is regulated by Precigen's proprietary RheoSwitch Therapeutic System (RTS), a gene switch that allows for precise, dose-dependent control of protein expression through the administration of an oral activator ligand. By targeting the excessive collagen deposition characteristic of scleroderma lesions, FCX-013 aims to reduce skin thickening and improve joint mobility. The therapy was originally developed by Fibrocell Science in collaboration with Precigen and is currently under development by Castle Creek Biosciences following its acquisition of Fibrocell.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on FCX-013.