Drug Interaction Potential of Pro-Inflammatory Conditions

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age12-99
SponsorIndiana University

About this trial

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. However, the clinical relevance of pro-inflammatory disease-drug interactions has not been systematically evaluated. The long-term goal of this research is to establish clinical strategies to mitigate pro-inflammatory disease-drug interactions and associated adverse drug events. The specific objective of this study is to determine the clinical relevance of pro-inflammatory disease-drug interactions, including establishment of the effect of pro-inflammatory diseases on drug disposition throughout disease trajectories (i.e., determining the differential effects on drug disposition based on the severity of disease). Towards this objective, this study will investigate the extent of increases in inflammation in patients with varying severities of pro-inflammatory diseases and estimate the resulting effects on drug disposition. Cytokine/chemokine concentrations and immune cell profiles will be assayed from blood samples of adult and pediatric patients with differing severities of pro-inflammatory diseases, using established disease monitoring parameters (e.g., glycosylated hemoglobin \[HbA1C\] for T2DM, C-reactive protein \[CRP\] for IBD, proteinuria for ESRD). The effect of changes in inflammation during differing severities of these pro-inflammatory diseases on drug disposition will then be estimated using established pharmacokinetic modeling approaches (e.g., physiologically-based pharmacokinetic modeling \[PBPK\]).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosed with a pro-inflammatory disease, including T2DM, IBD, and ESRD

Ability to provide written informed consent and HIPAA authorization

Disqualifiers

Diagnosis or past medical history of non-IBD autoimmune disorder, including systemic lupus erythematosus, Sjogren's syndrome, multiple sclerosis, type 1 diabetes mellitus, Behcet's disease, and ankylosing spondylitis

Current infection requiring medical treatment (note: if a prospective patient's infection resolves, they can be re-screened for trial inclusion)

Concomitant treatment with systemic immunosuppressant drugs

Trial population

This is a prospective observational study that will collect blood samples at 1-3 timepoints per patient. The study will not include any therapeutic intervention, and no study visits will involve patient interaction with the health system solely for study participation. The study will enroll up to 150 patients. All enrolled patients will undergo the study procedures, which will enable quantification of plasma cytokine concentrations and immune cell profiles at 1-3 timepoints.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • None (Observational)

    Other intervention

    This observational study will not involve any interventions. Instead, the study will collect blood samples at one or multiple time points.

Treatment groups

150 Participants
are divided into 3 treatment groups
Group A: Type 2 Diabetes Mellitus1 intervention
Group B: End Stage Renal Disease1 intervention
Group C: Irritable Bowel Syndrome1 intervention

Trial outcomes

Primary outcomes

1

Quantification of Plasma Cytokine Concentrations

The first primary objective will involve quantification of plasma cytokine concentrations from patient blood samples.

Time frame
Through study completion, up to 2 years post enrollment
2

Phenotyping of Patient Immune Cells

The second primary objective will involve phenotyping of patient immune cells from patient blood samples.

Time frame
Through study completion, up to 2 years post enrollment
3

Quantification of the Plasma Concentrations of Endogenous Biomarkers of Drug Metabolism and Transport

The third primary objective will involve quantification of the plasma concentrations of endogenous biomarkers of drug metabolism and transport from patient blood samples

Time frame
Through study completion, up to 2 years post enrollment
4

Measures of Inflammatory Disease Severity

The fourth primary objective will involve collecting measures of inflammatory disease severity based on information collected from patients' electronic health records.

Time frame
Through study completion, up to 2 years post enrollment

Secondary outcomes

1

Patient Genomic Markers

The secondary objective will involve determining patient genomic markers (using whole genome sequencing).

Time frame
Through study completion, up to 2 years post enrollment

Other outcomes

Sponsors and contacts

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