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Network formation in gluten-free bread with application of transglutaminase

Patients were randomly assigned 1:1 to rifaximin SSD-40IR or placebo twice daily for 72 weeks

In some embodiments, the pharmaceutical formulation may include one or more therapeutic agents at a concentration of from about 0.0001% (w/w) to about 0.001% (w/w), from about 0.001% (w/w) to about 0.01% (w/w), from about 0.01 % (w/w) to about 0.1 % (w/w), from about 0.1% (w/w) to about 1% (w/w), from about 0.1 % (w/w) to about 10% (w/w), from about 0.5% (w/w) to about 5% (w/w), from about 1% (w/w) to about 10% (w/w), from about 5% (w/w) to about 15% (w/w), from about 10% (w/w) to about 30% (w/w), from about 15% (w/w) to about 45% (w/w), from about 20% (w/w) to about 55% (w/w), from about 25% (w/w) to about 65% (w/w), from about 30% (w/w) to about 70% (w/w), from about 35% (w/w) to about 75% (w/w), from about 40% (w/w) to about 80% (w/w), from about 50% (w/w) to about 85% (w/w), from about 60% (w/w) to about 90% (w/w), from about 75% (w/w) to about 95% (w/w), from about 90% (w/w) to about 96% (w/w), from about 92% (w/w) to about 98% (w/w), from about 95% (w/w) to about 99% (w/w), from about 98% (w/w) to about 99.5% (w/w), or from about 99% (w/w) to about 99.9% (w/w)

For multiple comparisons in cellular models, one-way analysis of variance (ANOVA) was performed, followed by Dunnetts post-hoc test to compare each experimental group with the control group