A Study of FCX-013 Plus Veledimex for the Treatment of Moderate to Severe Localized Scleroderma (… (NCT03740724) | Clinical Trial Compass
TerminatedPhase 1/2
A Study of FCX-013 Plus Veledimex for the Treatment of Moderate to Severe Localized Scleroderma (Morphea)
Stopped: Sponsor decision
United States1 participantsStarted 2019-12-18
Plain-language 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
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* Subject is an adult, ≥ 18 years of age with moderate to severe localized scleroderma/morphea with sclerotic lesions which have been unresponsive to standard of care therapy.
* Subject has stable control of localized disease (clinically inactive) over the 3 months prior to Screening and through Baseline
* Subject has not participated in previous clinical research study in the 3 months prior to Screening and through Baseline
* Subject has provided informed written consent
* Female subjects of childbearing potential and male subjects engaging in sexual activity that could lead to pregnancy agree to use adequate birth control regimen
* Subject is able to understand the study, cooperate with the study procedures and willing to return to the clinic for the required follow-up visits
Exclusion Criteria:
* Subject has a clinically significant skin disorder other than localized scleroderma/morphea in the anatomical area of interest
* Subject has localized scleroderma/morphea only located on the face or over a joint, or lesions that can be successfully managed with topical medications or phototherapy
* Subject has symptoms consistent with systemic scleroderma that have not been stable, or that require treatment that has not been stable for 3 months prior to Screening and through Baseline
* Subject has been treated with UVA1 phototherapy within 2 months prior to Baseline
* Subject requires treatment with a non-stable regimen of systemic immunosuppressive therapy,…
What they're measuring
1
Evaluate the Safety of FCX-013 Plus Veledimex
Timeframe: Study initiation through study completion