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Drug Interaction Potential of Pro-Inflammatory Conditions

NCT07360938

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

Pro-inflammatory cytokines, which are elevated in pro-inflammatory disease states (e.g., type II diabetes mellitus [T2DM], irritable bowel diseases [IBD], and end stage renal disease [ESRD]) have been shown to inhibit hepatic drug-metabolizing enzymes, including members of the cytochrome P450 (CYP) family, and drug transporters; resultantly, pro-inflammatory diseases have been demonstrated to increase the exposure and potential for adverse drug events with co-administered CYP and drug transporter substrates.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Diabetes Mellitus, Type 2
  • End Stage Renal Disease
  • Irritable Bowel Syndrome

Eligibility basics and study details

Study type
Observational
Phase
Not applicable
Ages
12 to 99 years
Sex
All
Healthy volunteers
Not accepted
Sponsor
Indiana University
Last updated on ClinicalTrials.gov
January 22, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Indiana · 1

  • Indiana University Hospital · Indianapolis, IN

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.