Study on 225Ac-DOTATATE (RYZ101) Alone and with Pembrolizumab for Advanced or Metastatic Breast Cancer with SSTRs

Sponsor: RayzeBio, Inc.

Sponsor score: 0
Inactive

ClinicalTrials ID:NCT06590857

This clinical trial is testing a new treatment using 225Ac-DOTATATE (RYZ101) alone and in combination with pembrolizumab for patients with advanced or metastatic breast cancer that is ER+, HER2-negative, and expresses SSTRs.

Patient Parameters

Program Overview

The purpose of this study is to evaluate the safety and effectiveness of a new treatment, 225Ac-DOTATATE (RYZ101), both alone and combined with pembrolizumab, in patients with advanced or metastatic breast cancer that is ER+ (estrogen receptor positive), HER2-negative, and shows specific markers called SSTRs (somatostatin receptors).

Eligibility Criteria

Inclusion Criteria

Subjects must meet all the following criteria for enrollment in the study:

  • Eastern Cooperative Oncology Group performance status ≤2.
  • Histologically confirmed, ER+, HER2-negative, locally advanced and unresectable or metastatic breast cancer not amenable to treatment with curative intent.
  • At least one RECIST v1.1-measurable tumor lesion that is SSTR-PET positive (defined as maximum standard uptake value (SUVmax) higher than liver mean standard uptake value (SUVmean) on SSTR-PET imaging) and at least 80% of RECIST v1.1measurable tumor lesions are SSTR-PET positive
  • Sufficient renal function, as evidenced by eGFR ≥60 mL/min/1.73m2 calculated using the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation
  • Adequate hematologic and hepatic function

Exclusion Criteria

Subjects who meet any of the following criteria will be excluded from the study:

  • Prior radiopharmaceutical therapy, including radioembolization.
  • Any toxicities from prior treatments that have not recovered to CTCAE Grade ≤1, except for alopecia.
  • Significant cardiovascular disease
  • Known active uncontrolled or symptomatic central nervous system (CNS) metastases, carcinomatous meningitis, spinal cord compression, or leptomeningeal disease.
  • History of hypersensitivity or allergy to 225Ac, 68Ga, 64Cu, octreotate, or any of the excipients of DOTATATE imaging agents.
  • Prior or concurrent malignancy whose natural history or treatment has the potential to interfere with the study safety or efficacy assessments.
  • Pregnancy or lactation.

Inclusion Criteria

  • Have a performance status score of 0, 1, or 2, indicating full activity or some restriction in strenuous activities.
  • Have a confirmed diagnosis of ER+ (estrogen receptor positive) and HER2-negative breast cancer that is advanced, cannot be surgically removed, or has spread to other parts of the body.
  • Have at least one tumor that can be measured and shows specific markers (SSTRs) on a PET scan.
  • Have good kidney function, as shown by a creatinine clearance of 60 mL/min or higher.
  • Have adequate blood, liver, and blood clotting function.

Exclusion Criteria

  • Have a history of severe allergic reactions to any of the study drugs or imaging agents.
  • Have had previous treatments involving radioactive particles.
  • Have received certain types of immune therapy targeting specific proteins on T-cells.
  • Have not fully recovered from side effects of previous treatments, except for hair loss.
  • Have significant heart disease.
  • Have known cancer spread to the brain, spinal cord, or surrounding areas, unless treated and stable for at least 6 months.
  • Have allergies to pembrolizumab or any components of the study drugs.
  • Have another cancer that could interfere with the study.

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