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Adding an Immunotherapy Drug to the Usual Chemotherapy Treatment for Stage II-III Breast Cancer

Short Title: S2206


Enrollment Status: Recruiting

NCT #: NCT06058377

Specialty Area: Oncology

Condition Studied: Early Stage Breast Cancer

Age Groups: Adult; Older Adult

Phase: III


Study Information

Summary / Purpose

To find out if adding durvalumab (an immunotherapy medication) to standard chemotherapy helps prevent breast cancer from returning in patients with MP2 stage II–III hormone receptor-positive, HER2-negative breast cancer.

Study Type: Interventional
Accepts Healthy Volunteers: No

Who Can Participate

Eligibility Criteria:
  • Adults 18+ years of age
  • Diagnosed with hormone receptor-positive (HR+) and HER2-negative breast cancer
  • Stage II or III
  • Must have a MammaPrint High 2 Risk (MP2) result

What's Involved

Participation in the study will include:
  • Chemotherapy (paclitaxel, doxorubicin, and cyclophosphamide) with our without durvalumab given intravenously (IV)
  • Genetic testing and biospecimen collection
  • Mammograms to monitor response to treatment
  • Quality-of-life (QOL) assessments
  • Blood and urine tests to monitor your health and treatment effects
  • Electrocardiogram (ECG) to monitor heart function
  • Questionnaires

Principal Investigator

Additional Information

Location: Renown Health, Office of Clinical Research
Address:

1500 E 2nd St. Reno, NV 89502

General Research: 775-982-3646
Oncology Research: 775-982-5050
Email: Renown-CRD@renown.org

Disclaimer: This listing gives you general information about the study and isn't part of the official consent process. If you decide to learn more, the research team will talk with you and check if you meet any additional requirements to join the study.

ER Wait Times

How are wait times calculated?

Our estimated ER wait times reflect the average time from check-in to being seen by a medical professional during triage, where patients are prioritized based on the severity of their condition.

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