Study of 68GaNOTA-Anti-MMR-VHH2 in Oncological Lesions, Cardiovascular Atherosclerosis, Syndrome With Abnormal Immune Activation and sarcoïdosis

PHASE2RecruitingINTERVENTIONAL
Enrollment

140

Participants

Timeline

Start Date

January 26, 2021

Primary Completion Date

January 26, 2025

Study Completion Date

January 26, 2025

Conditions
Solid Malignancy Located in the Head and NeckCancerCarotid StenosisAtherosclerosis of ArteryHodgkin Lymphoma, AdultNon Hodgkin LymphomaHLHCardiac SarcoidosisSarcoidosis
Interventions
DRUG

68GaNOTA-Anti-MMR-VHH2

"All subjects will receive at least one single intravenous injection of the IMP followed by a total body PET/CT prior to receiving standard-of-care therapy.~For patients in cohorts 1 and 2 : an optional injection of the IMP during or after therapy can be administered if a patient is treated with non-surgical modalities. Patients in cohorts 6 and 7 who receive standard-of-care treatment can receive an optional injection of the IMP."

Trial Locations (1)

1090

RECRUITING

Uz Brussel, Brussels

All Listed Sponsors
lead

Universitair Ziekenhuis Brussel

OTHER