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Evaluation of 68GaNOTA-Anti-HER2 VHH1 uptake in brain metastasis of cancer patients

Phase 2
Recruiting
Conditions
Cancer patients with brain metastasis
Registration Number
2024-513997-23-00
Lead Sponsor
Universitair Ziekenhuis Brussel
Brief Summary

To compare the uptake of 68GaNOTA-Anti-HER2 VHH1 in brain metastasis lesions from HER2-positive and HER2-negative patients

Detailed Description

Not available

Recruitment & Eligibility

Status
Ongoing, recruiting
Sex
Not specified
Target Recruitment
30
Inclusion Criteria

Patients who have given informed consent

Age 18 years or older patients with brain metastasized cancer, with at least 1 brain lesion of at least 8 mm maximal diameter, as measured by CT or MRI

Patients with potentially HER2-positive cancer. Either a HER2 staining should have been done in standard of care, or sufficient tissue should be available for HER2-staining for study purpose

Exclusion Criteria

Pregnant patients

Breast feeding patients

Patients with recent (< 1 week) gastrointestinal disorders with diarrhea as major symptom

Patients with any serious active infection

Patients who have any other life-threatening illness or organ system dysfunction, which in the opinion of the investigator would either compromise patient safety or interfere with the evaluation of the test radiopharmaceutical

Patients who cannot communicate reliably with the investigator

Patients at increased risk of death from a pre-existing concurrent illness

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The tumor targeting potential in brain metastasis will be visually scored as positive or negative by an experienced nuclear medicine physician, unaware of the HER2-status

The tumor targeting potential in brain metastasis will be visually scored as positive or negative by an experienced nuclear medicine physician, unaware of the HER2-status

The tumor targeting potential in brain metastasis will be assessed quantitatively using Standard Uptake Values (SUV) by an experienced nuclear medicine physician, unaware of the HER2-status.

The tumor targeting potential in brain metastasis will be assessed quantitatively using Standard Uptake Values (SUV) by an experienced nuclear medicine physician, unaware of the HER2-status.

Secondary Outcome Measures
NameTimeMethod
If available, uptake will be evaluated during and after treatment and compared to baseline values. Results will be compared to information of patient's disease course.

If available, uptake will be evaluated during and after treatment and compared to baseline values. Results will be compared to information of patient's disease course.

Trial Locations

Locations (1)

UZ Brussel

🇧🇪

Jette, Belgium

UZ Brussel
🇧🇪Jette, Belgium
Tony Lahoutte
Site contact
024775020
nucg.clinicaltrials@uzbrussel.be

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