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Evaluation of Fluciclovine Uptake in Patients With Cervical, Ovarian Epithelial or Endometrial Cancers.

Primary Purpose

Cervical Cancer, Endometrial Cancer, Ovarian Epithelial Cancer

Status
Unknown status
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Fluciclovine F18
Sponsored by
Bital Savir-Baruch
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Cervical Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • GYN cancer (ovarian, endometrial, or cervical) was biopsy-proven and/or schedule for subsequent surgery based on clinical presentation (imaging, markers)
  • Age ≥ 18 years.
  • Can tolerate 18F-fluciclovine PET/CT exam (can lie on her back for the duration of the scan).
  • Ability to understand and the willingness to sign a written informed consent.

Exclusion Criteria:

  • Ongoing systemic therapy for cancer
  • Systemic therapy for cancer in the past 3 months
  • Inability to tolerate 18F-fluciclovine PET/CT exam
  • Pregnant or lactating women

Sites / Locations

  • Loyola University Medical CenterRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

18F-Fluciclovine

Arm Description

Outcomes

Primary Outcome Measures

18F-Fluciclovine uptake in gynecologic neoplasms
PET/CT imaging

Secondary Outcome Measures

Full Information

First Posted
November 17, 2017
Last Updated
February 27, 2020
Sponsor
Bital Savir-Baruch
Collaborators
Blue Earth Diagnostics
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1. Study Identification

Unique Protocol Identification Number
NCT03349463
Brief Title
Evaluation of Fluciclovine Uptake in Patients With Cervical, Ovarian Epithelial or Endometrial Cancers.
Official Title
Evaluation of Fluciclovine Uptake in Patients With Cervical, Ovarian Epithelial or Endometrial Cancers. Pilot Study.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Unknown status
Study Start Date
November 14, 2018 (Actual)
Primary Completion Date
December 2020 (Anticipated)
Study Completion Date
December 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Bital Savir-Baruch
Collaborators
Blue Earth Diagnostics

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
An important part of staging and deciding the method of treatment is knowing areas of how cancer is involved. Diagnostic imaging is often used to determine the location of the cancer using techniques like nuclear medicine, MRI (magnetic resonance imaging), CT (computerized tomography), and ultrasound. Each technique looks for cancer in different ways and are often used together to make a better determination of the extent of disease. One of the techniques used in cancer imaging is PET/CT. This technique combines a nuclear medicine study (PET or positron emission tomography) with CT performing both scans at the same time. PET/CT most commonly uses a radioactive sugar (FDG or fluorodeoxyglucose) to detect the cancer. The problem with FDG is that it is excreted by the kidneys and collected in the bladder. Even though the bladder is emptied prior to the scan, the FDG activity present there may interfere with the detection of small areas of cancer involvement in lymph nodes or adjacent areas. It is because of this that PET/CT using FDG is infrequently used in gynecological cancers. This purpose of this study is to evaluate if 18F-fluciclovine can be used to help determine the extent of gynecological cancers. 18F-fluciclovine (also known as AXUMIN) is a radioactive tracer which has been approved by the FDAFood and Drug Administration (FDA) for use in patients with prostate cancer. 18F-fluciclovine has much less excretion through the kidneys which improves the PET/CT imaging of the pelvis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cervical Cancer, Endometrial Cancer, Ovarian Epithelial Cancer

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
18F-Fluciclovine
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Fluciclovine F18
Other Intervention Name(s)
Axumin, anti-3-[18F] FACBC
Intervention Description
All study participants will receive 10 mCi of 18F-Fluciclovine (Axumin) one time administered through injection through the catheter into participant's arm immediately before PET/CT scan.
Primary Outcome Measure Information:
Title
18F-Fluciclovine uptake in gynecologic neoplasms
Description
PET/CT imaging
Time Frame
Day 30

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: GYN cancer (ovarian, endometrial, or cervical) was biopsy-proven and/or schedule for subsequent surgery based on clinical presentation (imaging, markers) Age ≥ 18 years. Can tolerate 18F-fluciclovine PET/CT exam (can lie on her back for the duration of the scan). Ability to understand and the willingness to sign a written informed consent. Exclusion Criteria: Ongoing systemic therapy for cancer Systemic therapy for cancer in the past 3 months Inability to tolerate 18F-fluciclovine PET/CT exam Pregnant or lactating women
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rachel Ochoa, BA
Phone
708-327-3221
Email
raochoa@luc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bital Savir-Baruch, M.D
Organizational Affiliation
Nuclear Medicine Assistant Professor
Official's Role
Principal Investigator
Facility Information:
Facility Name
Loyola University Medical Center
City
Maywood
State/Province
Illinois
ZIP/Postal Code
60153
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bital Savir-Baruch, M.D
Phone
708-216-2508
Email
bital.savir-baruch@lumc.edu
First Name & Middle Initial & Last Name & Degree
Bital Savir-Baruch, M.D.
First Name & Middle Initial & Last Name & Degree
Robert H Wagner, M.D.
First Name & Middle Initial & Last Name & Degree
Ronald K Potkul, M.D.
First Name & Middle Initial & Last Name & Degree
Abigail Winder, M.D.
First Name & Middle Initial & Last Name & Degree
Margaret Liotta, DO

12. IPD Sharing Statement

Plan to Share IPD
No
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Evaluation of Fluciclovine Uptake in Patients With Cervical, Ovarian Epithelial or Endometrial Cancers.

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