Clinical Trial · NCT00918281

Reproducibility of 18F Uptake by Solid Tumors Using PET Imaging Following Intravenous Administration of (18F) Injection

Overview

Study aimed to assess the reproducibility of PET imaging using AH111585 (18F) Injection. Subjects are evaluable if they undergo 2 administrations of AH111585 (18F) Injection (3 to 8 days apart) and the corresponding PET acquisitions, and tumors demonstrate detectable levels of 18F uptake on PET.

Sponsor

GE Healthcare

Phase

Phase 2

Contacts

Jeffrey Winick, Ph.D. (PRINCIPAL_INVESTIGATOR)

ClinicalTrials.gov

NCT00918281

Eligibility

Inclusion

The subject has a clinically acceptable (as judged by the investigator) physical examination at screening and is capable of self-care.
The subject has been diagnosed with at least one solid primary or metastatic tumor greater than 2.0 cm in diameter, including but not limited to NSCLC, RCC, GBM, melanoma, sarcoma, breast and H\&N cancers.
The subject has received clinical routine imaging diagnostic work-up within 8 weeks prior to the first \[18F\]AH111585 PET scan.

Exclusion

The subject is scheduled to undergo chemotherapy, radiotherapy, surgery or any other treatment against cancer between the first and second \[18F\]AH111585 PET scans.
For the immuno-histochemistry group, the subject's target tumour has been biopsied less than or equal to 1 week prior to the first \[18F\]AH111585 PET scan.
The subject has received chemotherapy within 3 weeks, or received radiotherapy, surgery or any other treatment against cancer within 4 weeks prior to the first \[18F\]AH111585 PET scan.
The subject has known hyper- or hypo-coagulation syndromes.
The subject is scheduled to undergo biopsy for the target tumour between the first and second \[18F\]AH111585 PET scans.