drugset / Trial / NCT03740724

A Study of FCX-013 Plus Veledimex for the Treatment of Moderate to Severe Localized Scleroderma (Morphea)

NCT03740724

Phase 1/2 Terminated 1 enrolled Castle Creek Biosciences, LLC.
NaSingle-groupOpen-labelTreatment

Summary

A two-component therapeutic consisting of FCX-013 and veledimex for the treatment of localized scleroderma (or morphea). The first component, FCX-013, is autologous human fibroblasts genetically-modified using lentivirus and encoded for matrix metalloproteinase 1 (MMP-1), a protein responsible for breaking down collagen. FCX-013 is designed to be injected under the skin at the location of the fibrotic lesions where the genetically-modified fibroblast cells will produce MMP-1 to break down excess collagen accumulation. With the FCX-013 therapy, the patient will take an oral compound (Veledimex) to induce MMP-1 protein expression from the injected cells. Once the fibrosis is resolved, the patient will stop taking the oral compound which will stop further MMP-1 production from the injected cells. FCX-013 plus veledimex is being developed in anticipation of improving skin function in patients by resolving fibrotic lesions and normalizing dermal collagen production

Timeline

Start
2019-12-18
Primary completion
2020-09-23
Completion
2022-04-21

Drugs

EvaluationDrugModalityDoseRoute
Subject FCX-013 Cell therapy Other
Subject veledimex Small molecule Oral

Indications