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

NCT00918281 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2014-06-09

Study results available
· View outcomes & findings →

Summary

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.

Conditions

Interventions

DRUG

Fluciclatide Injection

Fluciclatide Injection (AH111585 (18F) Injection)

Sponsors & Collaborators

  • BIAFFIN GmbH & Co. KG (Biomolecular Interaction Analyses)

    collaborator UNKNOWN
  • Quintiles, Inc.

    collaborator INDUSTRY
  • i3 Statprobe

    collaborator INDUSTRY
  • GE Healthcare

    lead INDUSTRY

Principal Investigators

  • Jeffrey Winick, Ph.D. · GE Healthcare

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-06-30
Primary Completion
2011-09-30
Completion
2011-10-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00918281 on ClinicalTrials.gov