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Recruiting NCT06489041

NCT06489041 Evaluating Microarray Pharmacogenetic Testing in Cancer Patients

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Clinical Trial Summary
NCT ID NCT06489041
Status Recruiting
Phase
Sponsor Wake Forest University Health Sciences
Condition Cancer
Study Type INTERVENTIONAL
Enrollment 120 participants
Start Date 2025-07-18
Primary Completion 2026-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Pharmacogenomic Testing with the "Global Diversity Array with Enhanced PGx"

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 120 participants in total. It began in 2025-07-18 with a primary completion date of 2026-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The purpose of this research is to evaluate the impact of a microarray PGx test on prescribing/dosing of drugs and cancer treatments in patients with cancer who are currently eligible for single-gene DPYD testing.

Eligibility Criteria

Inclusion Criteria: * Written informed consent and HIPAA authorization for release of personal health information. * Age ≥ 18 years at the time of consent. * Eligible for standard of care single-gene DPYD testing (i.e., receiving or expected to receive a fluoropyrimidine-based chemotherapy regimen). The potential participant meets inclusion criteria if the standard of care single-gene DPYD test is planned or previously ordered. If previously ordered, consent must occur no later than 60 days from the date the DPYD results were available. * Willing to provide additional buccal swabs if residual DNA from previous DPYD testing is inadequate for microarray testing. Exclusion Criteria: • History of prior allogeneic hematopoietic cell transplantation or liver transplantation

Contact & Investigator

Central Contact

Megan Lattanze

✉ Megan.Lattanze@advocatehealth.org

📞 (980) 442-4239

Principal Investigator

Jai Patel, PharmD

PRINCIPAL INVESTIGATOR

Atrium Health Levine Cancer

Frequently Asked Questions

Who can join the NCT06489041 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06489041 currently recruiting?

Yes, NCT06489041 is actively recruiting participants. Contact the research team at Megan.Lattanze@advocatehealth.org for enrollment information.

Where is the NCT06489041 trial being conducted?

This trial is being conducted at Charlotte, United States.

Who is sponsoring the NCT06489041 clinical trial?

NCT06489041 is sponsored by Wake Forest University Health Sciences. The principal investigator is Jai Patel, PharmD at Atrium Health Levine Cancer. The trial plans to enroll 120 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology