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

Sponsor: RayzeBio, Inc.

Sponsor score: 0

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.

Locations

FACILITYZIPCITYSTATE
Research Facility85054PhoenixArizona
Research Facility92618IrvineCalifornia
Research Facility90404Santa MonicaCalifornia
Research Facility80504LongmontColorado
Research Facility32224JacksonvilleFlorida
Research Facility30322AtlantaGeorgia
Research Facility46202IndianapolisIndiana
Research Facility02215BostonMassachusetts
Research Facility48202DetroitMichigan
Research Facility55905RochesterMinnesota

Get This Program In Your Inbox

Receive detailed information about this treatment opportunity to review with your healthcare provider.