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NCT04480619Not yet recruitingPhase 1/2

Safety and Efficacy of Ga68-IAC PET/CT for Diagnosis and Clinical Management in Metastatic Breast Cancer Patients

Safety and Efficacy of Ga-68-IAC Positron Emission Tomography (PET/CT) for Diagnosis and Clinical Management in Metastatic Breast Cancer Patients.

Source: ClinicalTrials.gov · Last updated 16 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is a phase I/IIa, open label, multicenter interventional study of Gallium-68 radiolabeled Integrin Adhesion Complex antagonist conjugate (Ga-68-IAC) Positron Emission Tomography (PET/CT) imaging, intended for diagnosis, and clinical management of patients with Metastatic breast cancer.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
25 (estimated)
First submitted
30 Jun 2020
Start date
30 Oct 2025
Primary completion date
30 May 2027
Lead sponsor
Advanced Imaging Projects, LLC
NCT number
NCT04480619

What you commit to

  • Study type: Interventional · Phase 1/2
  • Planned participants: 25
  • From 30 Oct 2025 to the primary completion date, 30 May 2027
  • 3 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Lab values

  • • Serum creatinine \>3.0 mg/dL (270 μM/L)
    • Hepatic enzyme levels more than 5 times upper limit of normal.
    • Known severe allergy or hypersensitivity to IV radiographic contrast.
    • Use of any other investigational product or device within 30 days prior to dosing or known requirement for any other investigational agent prior to completion of all scheduled study assessments.
    • Patients with a body weight of 400 pounds or more or not able to enter the bore of the PET/CT scanner due to BMI, because of the compromise in image quality with CT, PET/CT and MRI that will result.
    • Inability to lie still for the entire imaging time (e.g. cough, severe arthritis, etc.).
    • Inability to complete the needed investigational and standard-of-care imaging examinations due to other reasons (severe claustrophobia, radiation phobia, etc.)
    • Recognized concurrent active infection (e.g., HIV)
    • Previous Grade 3 or higher allergic reaction to Trastuzumab that resulted in discontinuation of Trastuzumab therapy. Any additional medical condition, serious intercurrent illness, or other extenuating circumstance that, in the opinion of the Investigator, may significantly interfere with study compliance.
    • Adult patients who require monitored anesthesia for PET scanning

Who the study is looking for

  • Patients with solid tumors (either 3+ by immunohistochemistry or with evidence of gene amplification (\>2.0) by fluorescence in situ hybridization (FISH))
    • At least 18 years of age
    • Able to provide informed consent.
    • Karnofsky score greater than 50
  • Females of childbearing potential must have a negative pregnancy test at screening/baseline
  • AIP-301 Ga-68 positive scan define by SUV greater than 10.
  • Adequate organ function, defined as:
    • Absolute neutrophil count (ANC) ≥ 1.5 x 109/L.
    • Hemoglobin (Hb) ≥9 g/dl (transfusion or use of EPO is permitted).
    • Platelets \> 100,000/mm3
    • Creatinine ≤ 1.5 x normal value based on the Cock Gault (CG) equation.
    • AST or ALT ≤ 2.5 x ULN (or ≤5 x ULN in case of liver metastasis)
    • Alkaline phosphatase ≤2.5 x ULN. Alkaline phosphatase may be more than 2.5 x ULN only in the case of bone metastases, and AST and ALT less than 1.5 x ULN.
    • Total bilirubin ≤1.5 mg/dl (higher bilirubin levels are permitted if the patient has Gilbert's syndrome).
    • Baseline LVEF ≥50% measured using echocardiogram or equilibrium
    • isotopic ventriculography (MUGA).

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Postgraduate Institute of Medical and Research
Coordinator of this site? Confirm its status
ChandigarhIndiaUnknown status
All India Institute of Medical Sciences
Coordinator of this site? Confirm its status
New DelhiIndiaUnknown status
University of Witwatersrand
Coordinator of this site? Confirm its status
JohannesburgSouth AfricaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.