Drug intelligence / Profile preview

revita

Development stage
Unknown
Lead developer
Tides Medical
Administration
Topical
01

Overview

Revita is a dehydrated human amnion-chorion membrane (dHACM) allograft developed by **Tides Medical**. It is uniquely available in two primary multi-layer configurations: **Amnion-Intermediate-Chorion (AIC)** and **Amnion-Chorion-Amnion (ACA)**. These grafts are derived from the human placenta and processed to preserve the natural extracellular matrix (ECM), growth factors, and cytokines essential for tissue regeneration. Revita acts as a biological scaffold that promotes cellular migration, proliferation, and angiogenesis while providing a protective barrier and reducing inflammation. It is primarily indicated for the treatment of chronic wounds, such as **diabetic foot ulcers (DFU)** and **venous leg ulcers (VLU)**, where it serves to accelerate the healing process in patients who have failed standard wound care therapies.

Brand names
Revita
Other names
Amnion-Intermediate-Chorion + Amnion-Chorion-AmnionAmnion-Intermediate-ChorionAmnion-Chorion-AmnionAICACAdehydrated human amnion-chorion membranedHACM
02

Targets

PDGFR (PDGFR family)EGFR (Epidermal growth factor receptor)VEGFR (VEGFR family)TGFBR (TGF-beta receptor)MET (Mesenchymal-epithelial transition factor receptor)FGFR (FGFR family)

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