Condition: Crohn Disease · Sponsor: Weizmann Institute of Science
In this study, the investigators will explore our protein-based platform assessing commensals potentially contributing to features of CD, while assessing the global composition and abundance of AMPs expressed in the GI tract under specific CD-relevant clinical contexts. This would enable us to (a) identify new commensals contributing to features of CD spectrum and various sub-types; (b) uncover the mechanistic basis of dysbiosis in CD (c) utilize the pipeline to develop new theranostic for disease exacerbation, complication and treatment responses; and (d) potentially enable future exploitation of novel AMP combinations, and their respective antimicrobial capacity to counteract dysbiosis in CD. Uncovering the proteomic manifestations of perturbed host-microbiome communications in CD will eventually enable the development and validation of clinical non-invasive surrogate markers, mechanistically determine causative drivers of CD, and potentially facilitate the development of novel therapeutic interventions.
This description comes directly from the study's public registry record.
Eran Elinav, Prof · +97289524014 · Eran.Elinav@weizmann.ac.il
shimrit eliyahu miller · +97289524014 · Shimrit.miller@weizmann.ac.il
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| Emek medical center | Afula, Israel | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06494826