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Clinical Trial Summary

A Phase Ib trial to evaluate the safety and efficacy of Fecal Microbial Transplantation (FMT) in combination with Nivolumab in subjects with metastatic or inoperable melanoma, microsatellite instability-high (MSI-H) or mismatch-repair deficient (dMMR) cancer, or Non-Small Cell Lung Cancer (NSCLC)


Clinical Trial Description

This study is a Phase I single-center adaptive design study to evaluate the safety and efficacy of FMT in combination with Nivolumab for adult subjects with treatment-refractory or inoperable melanoma, MSH-H, dMMr or NSCLC. FMT will be conducted with fecal capsules, originating from patients that have achieved a durable complete response with immune checkpoint inhibitors. The study will evaluate the safety and efficacy of the combination of FMT with Nivolumab, a human immunoglobulin G4 (IgG4) monoclonal antibody that blocks PD-1 (anti PD-1) treatment and explore different biomarkers. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04521075
Study type Interventional
Source Ella Therapeutics Ltd
Contact Elizbeth Tarshish, Msc
Phone +972-504048559
Email elizabeth@ellatherapeutics.com
Status Recruiting
Phase Phase 1/Phase 2
Start date November 1, 2020
Completion date July 1, 2023

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