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MiMedx Group

09/24/2024
https://clinicaltrials.gov/study/NCT06600724

MiMedx initiated a 170-patient study to evaluate 2 human amnion/chorion membrane (ppLHACM) products, EPIEFFECT and EPIXPRESS and SoC vs SoC alone in the treatment of non-healing DFUs. Primary outcome measures complete healing in 12 wks. Estimated study completion is August 2026. clinicaltrials.gov

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