Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
dCELL Human Dermis is an acellular dermal matrix (ADM) produced using the proprietary dCELL technology. This process involves the removal of cells, DNA, and other immunogenic components from human donor skin while preserving the structural integrity of the extracellular matrix (ECM), including collagen and elastin fibers. By maintaining the natural scaffold, the product provides a biocompatible environment that supports cellular infiltration, revascularization, and tissue remodeling. It is primarily indicated for the treatment of chronic and acute wounds, such as diabetic foot ulcers (DFUs) and venous leg ulcers (VLUs), as well as for use in plastic and reconstructive surgery. The developer, Tissue Regenix, utilizes this technology to minimize the risk of graft rejection while promoting effective wound healing.
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 dCELL Human Dermis.