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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04692831
Other study ID # 20-275
Secondary ID
Status Recruiting
Phase Phase 1
First received
Last updated
Start date November 30, 2020
Est. completion date November 30, 2024

Study information

Verified date April 2024
Source Memorial Sloan Kettering Cancer Center
Contact Randy Yeh, MD
Phone 212-639-3776
Email yehr@mskcc.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to see whether 89Zr-ss-pertuzumab is safe in people with HER2+ cancer.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date November 30, 2024
Est. primary completion date November 30, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Biopsy proven HER2-positive or HER2-low primary malignancy or metastatic disease Note: HER2 positivity is defined according to American Society of Clinical Oncology guidelines or ERBB2 amplification on next generation sequencing Note: HER2-low is defined as low HER2 expression, with immunohistochemistry (IHC) 1+ or IHC 2+ and in situ hybridization [ISH]-negative, including FISH. - Biopsy proven primary malignancy or metastatic disease - At least one malignant lesion on CT, MR, or FDG PET/CT within 60 days of protocol enrollment - Age 18 years or greater - ECOG performance of 0-2 Exclusion Criteria: - Creatinine > 2 times normal limit (obtained with 8 weeks of enrollment) - AST/ALT > 2 times normal limit (obtained with 8 weeks of enrollment) - Life expectancy < 3 months - Pregnancy or lactation - Patients who cannot undergo PET/CT due to weight limits (over 450 pounds)

Study Design


Related Conditions & MeSH terms


Intervention

Combination Product:
89Zr-ss-pertuzumab PET/CT
Patients will receive 89Zr-ss-pertuzumab. 89Zr-ss-pertuzumab PET/CT images will be reconstructed using iterative reconstruction and displayed in multiplanar reconstruction. In the event that 89Zr-ss-pertuzumab is unavailable, randomly labelled 89Zr-pertuzumab PET will be allowed to make HER2 PET imaging available for our patients. Once 89Zr-ss-pertuzumab is available, then patients will be imaged with 89Zr-ss-pertuzumab and randomly labelled 89Zr-pertuzumab will no longer be used.

Locations

Country Name City State
United States Memorial Sloan Kettering at Basking Ridge (Limited Protocol Activities) Basking Ridge New Jersey
United States Memorial Sloan Kettering Suffolk-Commack (Limited protocol activity) Commack New York
United States Memorial Sloan Kettering Westchester (Limited Protocol Activities) Harrison New York
United States Memorial Sloan Kettering Monmouth (Limited protocol activities) Middletown New Jersey
United States Memorial Sloan Kettering Bergen (Limited Protocol Activities) Montvale New Jersey
United States Memorial Sloan Kettering Cancer Center (All Protocol Activities) New York New York
United States PATTY AND GEORGE HOAG CANCER CENTER (Data or Specimen Analysis Only) Newport Beach California
United States Memorial Sloan Kettering Nassau (Limited Protocol Activites) Rockville Centre New York

Sponsors (2)

Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluate clinical safety of 89Zr-ss-pertuzumab CTCAE Version 5 will be utilized for toxicity evaluation Up to 20 months
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