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NCT06322238 · ClinicalTrials.gov registry record · Phase 2

Pharmacogenetic Panel to Prevent Adverse Drug Reactions in Daily Primary Care Practice:

A Phase 2 study of Pharmacogenomic Drug Interaction and Drug Metabolism, Poor, CYP2D6-Related, sponsored by Mayo Clinic.

Recruiting
Registry status
Phase 2
Development phase
66
Enrollment target
1
Study location

NCT06322238 is a Phase 2 study of Pharmacogenomic Drug Interaction and Drug Metabolism, Poor, CYP2D6-Related that is actively recruiting participants, run by Mayo Clinic. The registered enrollment target is 66 participants, below the 735-participant average among 4 other Pharmacogenomic Drug Interaction trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06322238, a Phase 2 study of Pharmacogenomic Drug Interaction and Drug Metabolism, Poor, CYP2D6-Related, is actively recruiting participants, sponsored by Mayo Clinic.

RECRUITING
Registry status
Phase 2
Development phase
66 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to determine whether the implementation of pre-emptive pharmacogenomic (PGx) testing of a panel of clinically relevant PGx markers, to guide the dose and drug selection for 39 commonly prescribed drugs, will result in an overall reduction in the number of clinically relevant drug-genotype associated ADRs which are causally related to the initial drug of inclusion (referred to as 'index drug').

Interventions

  • DIAGNOSTIC_TEST PGx panel test

Study Locations (1)

Minnesota

  • Mayo Clinic - Rochester

Trial Details

FieldValue
Enrollment Target 66 participants
Start Date 2024-12-01
Est. Completion 2027-04
Phase Phase 2

Sponsor

Mayo Clinic

2,844 total trials

What the Registry Record Tells You About NCT06322238

The ClinicalTrials.gov registry entry for NCT06322238 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 66 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 735-participant average among 4 other Pharmacogenomic Drug Interaction trials with a reported enrollment target (91% lower). The listed sponsor is Mayo Clinic, which has 2,844 total studies on file at ClinicalTrials.gov.

The record links to 5 conditions, with Pharmacogenomic Drug Interaction appearing as the primary indexed condition, and to 1 intervention - of which PGx panel test is the first listed.

NCT06322238 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.

Frequently Asked Questions

What is clinical trial NCT06322238 about?

NCT06322238 is a clinical study titled "Pharmacogenetic Panel to Prevent Adverse Drug Reactions in Daily Primary Care Practice:". The purpose of this study is to determine whether the implementation of pre-emptive pharmacogenomic (PGx) testing of a panel of clinically relevant PGx markers, to guide the dose and drug selection for 39 commonly prescribed drugs, will result in an overall reduction in the number of clinically rele...

What is the current status of trial NCT06322238?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 66 participants. The study started on 2024-12-01. Estimated completion is 2027-04.

What conditions does trial NCT06322238 study?

This clinical trial studies the following conditions: Pharmacogenomic Drug Interaction, Drug Metabolism, Poor, CYP2D6-Related, Drug Metabolism, Poor, CYP2C19-Related, Side Effect of Drug, Ineffective Drug Action.

What interventions are being tested in trial NCT06322238?

The interventions under investigation include: PGx panel test (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT06322238?

This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06322238 being conducted?

This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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