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Recruiting NCT05736367

NCT05736367 Investigating the Metabolic Pathways in Hormone Receptor Positive/HER2 Negative Breast Cancer

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Clinical Trial Summary
NCT ID NCT05736367
Status Recruiting
Phase —
Sponsor Rutgers, The State University of New Jersey
Condition Breast Cancer
Study Type INTERVENTIONAL
Enrollment 16 participants
Start Date 2024-11-15
Primary Completion 2026-06-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
U-13C-glucose

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 16 participants in total. It began in 2024-11-15 with a primary completion date of 2026-06-30.

⚠ 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

To analyze the metabolic activity of Hormone Receptor Positive (HR+)/Her 2 Negative (Her2-) Breast cancer.

Eligibility Criteria

Inclusion Criteria: * Have hormone receptor (HR) positive \[estrogen receptor( ER)+/progesterone receptor (PR)+, ER+/PR- or ER-/PR+)/Her2 negative breast cancer previously diagnosed by biopsy. * Have early stage, clinical or anatomic stage I, II or III breast cancer (cT1cN0, cT1cN1, cT2N0, cT2N1, cT3N0) * Candidates for intended curative primary resection who have not had neoadjuvant therapy (endocrine/hormonal therapy, chemotherapy with or without immunotherapy). * Willing to undergo mandatory intraoperative small excisional and core biopsies (4-6 passes) of tumor and normal tissue for research purposes at the time of proposed surgical resection. Exclusion Criteria: * Is currently enrolled, or will enroll in, a different clinical study in which investigational therapeutic procedures are performed or investigational therapies are administered while participating in this study. * Has triple negative (ER-/PR-/Her2-) or HER2+ breast cancer. * Concomitant active malignancy * Is of child-bearing potential who has not had a recent negative pregnancy test done outside of this clinical trial (i.e., as part of standard preparation for diagnosis and treatment for her cancer)

Contact & Investigator

Central Contact

Coral Omene, MD, PhD

✉ co273@cinj.rutgers.edu

📞 732-235-3374

Principal Investigator

Coral Omene, MD, PhD

PRINCIPAL INVESTIGATOR

Cancer Institute of New Jersey Rutgers

Frequently Asked Questions

Who can join the NCT05736367 clinical trial?

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

Is NCT05736367 currently recruiting?

Yes, NCT05736367 is actively recruiting participants. Contact the research team at co273@cinj.rutgers.edu for enrollment information.

Where is the NCT05736367 trial being conducted?

This trial is being conducted at New Brunswick, United States, New Brunswick, United States.

Who is sponsoring the NCT05736367 clinical trial?

NCT05736367 is sponsored by Rutgers, The State University of New Jersey. The principal investigator is Coral Omene, MD, PhD at Cancer Institute of New Jersey Rutgers. The trial plans to enroll 16 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: November 2026  ·  Data Methodology