NaF Positron Emission Tomography/Computed Tomography (PET/CT)Imaging to Assess Treatment Responsiveness to TAK-700 in Patients With Castrate Resistant Prostate Cancer (CRPC) With Bone Metastasis

NCT01816048 · Status: TERMINATED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 8

Last updated 2019-12-09

Study results available
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Summary

The purpose of this study is to assess whether NaF PET/CT scans can be used to evaluate treatment response in bone metastases in subjects with prostate cancer treated with the investigational drug, TAK-700.

Conditions

Interventions

DRUG

TAK-700

TAK-700 will be administered at 300mg twice per day on 28-day continuous cycles

RADIATION

Fluorine F 18 Sodium Fluoride

Undergo NaF F18 PET/CT scan

PROCEDURE

Positron Emission Tomography

Undergo 18F NaF PET/CT scan

PROCEDURE

Computed Tomography

Undergo 18F NaF PET/CT scan

Sponsors & Collaborators

  • Millennium Pharmaceuticals, Inc.

    collaborator INDUSTRY
  • University of Wisconsin, Madison

    lead OTHER

Principal Investigators

  • Justine Y Bruce, MD · University of Wisconsin, Madison

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-05-31
Primary Completion
2015-12-31
Completion
2016-11-30

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 NCT01816048 on ClinicalTrials.gov