ZETAMET™ BONE GRAFT IN THE REPAIR OF BONE DEFECTS FROM METASTATIC BREAST CANCER IN VERTEBRAL BONES

Last updated: June 27, 2025
Sponsor: Zetagen Therapeutics, Inc
Overall Status: Active - Not Recruiting

Phase

2

Condition

N/A

Treatment

ZetaFuse™ Bone Graft

ZetaMet™ (ZetaFuse™ Bone Graft)

Clinical Study ID

NCT05280067
ZG-2021-002
  • Ages 22-75
  • Female

Study Summary

ZetaMet™ (ZetaFuse™ Bone Graft) is indicated for patients with destructive, lytic lesions due to metastatic breast cancer to bone, with or without involvement of other sites, with at least one metastatic lesion located in a vertebral body of the spine, and a Spinal Instability Neoplastic Score (SINS) ≥3 and ≤9. ZetaMet™ (ZetaFuse™ Bone Graft) is percutaneously implanted into the bone defect created by the metastatic tumor in a spinal vertebral body. ZetaMet™ (ZetaFuse™ Bone Graft) is only for implantation into the vertebral body.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Age between 22 (inclusive) and 75 years (inclusive) at the time of enrollment.

  • Life expectancy of 12 months or more.

  • Female patient with histologically confirmed diagnosis of primary breast cancer.

  • Metastatic breast cancer to bone, with or without involvement of other sites (patients with single metastasis qualify)

  • At least one lytic metastatic lesion located in the vertebral body of the spine.

  • Normal spinal alignment.

  • SINS ≥3 and ≤9.

  • Signed and dated Informed Consent Form (ICF).

  • Patient is willing and able to participate in required follow-up visits at theInvestigational Site and to complete study procedures and questionnaires.

Exclusion

Exclusion Criteria:

  • Vertebral body collapse.

  • Spinal cord compression.

  • Known allergy to Investigational Device materials.

  • Using medications or any drug known to potentially interfere with bone/soft tissuehealing (e.g., chronic systemic steroids).

  • Current tobacco smoker or stopped smoking in past 6 months.

  • Uncontrolled diabetes mellitus, HbAIC cutoff.

  • An active systemic infection (e.g., hepatitis, acquired immunodeficiency syndrome (AIDS), AIDS-related complex (ARC).

  • Currently participating in any investigational trial not related to this trial.

  • Any other severe acute or chronic medical condition that may interfere with theinterpretation of the trial results, in the judgment of the PI, which would make thepatient inappropriate for entry into this trial.

  • Pregnant or planning to become pregnant during the trial.

Study Design

Total Participants: 10
Treatment Group(s): 2
Primary Treatment: ZetaFuse™ Bone Graft
Phase: 2
Study Start date:
September 01, 2022
Estimated Completion Date:
October 31, 2025

Study Description

This is an open-label single-arm study. Subjects (N=10) will be recruited from up to 4 Investigational Sites in Canada. Key inclusion criteria are metastatic breast cancer to bone with at least one lytic metastatic lesion located in a vertebral body of the spine and a SINS ≥3 and ≤9. ZetaMet™ (ZetaFuse™ Bone Graft) will be percutaneously implanted into the vertebral body defect(s) created by the lytic metastatic tumor. Post-operative care will be per standard of care (SOC) at the Investigational Site. Subjects will be followed for 180 days post-treatment. If post-surgical radiation treatment is planned, it should not occur for at least 84 days post-surgery to allow for bone formation.

Connect with a study center

  • Vancouver Coastal Health Research Institute

    Vancouver, British Columbia V5Z 1M9
    Canada

    Site Not Available

  • McGill University Health Center

    Montréal, Quebec H3G1A4
    Canada

    Site Not Available

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