Clinical Trial · NCT04168528

Phase I/IIa Study of 68GaNOTA-Anti-MMR-VHH2 for PET/CT

Overview

Phase I study to evaluate the human safety and tolerability, biodistribution and dosimetry of 68GaNOTA-Anti-MMR-VHH2 Phase IIa study to evaluate tumour uptake of 68Ga-NOTA-anti-MMR-VHH2 in patients with breast cancer or melanoma. To correlate uptake of 68Ga-NOTA-anti-MMR-VHH2 in cancer lesions to immunohistological MMR staining after resection or biopsy of the same lesion.

Sponsor

Unknown Organization

Phase

Phase 1/2

Contacts

Tony LAHOUTTE, MD (PRINCIPAL_INVESTIGATOR)

ClinicalTrials.gov

NCT04168528

Drug / Compound

NOTA-Anti-MMR-VHH2

Isotope(s):
Target(s):
  • Mannose Receptor (CD206/MRC1)
Ligand Class: Small Proteins and Antibody Fragments
Chelator: NOTA

NOTA-Anti-MMR-VHH2

Isotope(s):
Target(s):
  • Mannose Receptor (CD206/MRC1)
Ligand Class: Small Proteins and Antibody Fragments
Chelator: NOTA

Eligibility

Inclusion

  • Patients who have given informed consent
  • Patients with local, locally advanced or metastatic disease of a malignant solid tumor. In order to minimize partial volume effect the diameter of at least 1 tumor lesion should be ≥ 10 mm in short axis for invaded adenopathies and ≥ 10 mm in long axis for all other types of lesions.
  • Patients will only be included in the study if they meet all of the following criteria:
  • Patients at least 18 years old

Exclusion

  • Eastern Cooperative Oncology Group (ECOG) performance status 3 or higher
  • Pregnant patients
  • Patients with abnormal liver (Bilirubin ≥1.5 x ULN, ALT (SGPT) ≥3 x ULN) or kidney function (Serum creatinine clearance ≤50 ml/min as calculated with Cockcroft-Gault formula)
  • Breast feeding patients
  • Patients will not be included in the study if one of the following criteria applies: