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18F-Labeled Picolinamide PET Imaging of Melanoma Diagnosis

Primary Purpose

Melanoma

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
18F-P3BZA
Sponsored by
Xijing Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Melanoma focused on measuring Picolinamide, PET/CT, Diagnosis, Melanoma

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients with melanoma: diagnosed by pathology and ready for surgery

Exclusion Criteria:

  • patients with melanoma: refuse or cannot endure surgery
  • pregnant women

Sites / Locations

  • Xijing Hospital Nuclear Medicine Department

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Melanoma patients

Arm Description

Melanoma patients enrolled for the clinical diagnosis study are performed with both 18F-P3BZA PET/CT and18F-FDG PET/CT scans before surgery.

Outcomes

Primary Outcome Measures

SUV of organs and melanoma
The maximum standardized uptake values (SUVmax) with unit of g/mL of 18F-P3BZA and 18F-FDG in melanoma tissues.

Secondary Outcome Measures

Full Information

First Posted
December 13, 2016
Last Updated
January 24, 2017
Sponsor
Xijing Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03033485
Brief Title
18F-Labeled Picolinamide PET Imaging of Melanoma Diagnosis
Official Title
18F-Labeled Picolinamide PET-CT in the Management of Patients With Melanoma: The Radiation Dosimetry and Diagnostic Applications in Melanoma Patients
Study Type
Interventional

2. Study Status

Record Verification Date
January 2017
Overall Recruitment Status
Unknown status
Study Start Date
December 2017 (Anticipated)
Primary Completion Date
August 2018 (Anticipated)
Study Completion Date
December 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Xijing Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to assess the dosimetric properties of the positron emission tomography (PET) imaging probe 18F labeled Picolinamide (18F-P3BZA) and preliminarily evaluate its diagnosis value in melanoma patients.
Detailed Description
50 patients with pathology diagnosed melanoma will be enrolled for the clinical study. If agree to take part in this study, the patient will be performed with 18F-P3BZA PET/CT scan and 18F-FDG PET/CT scan in the other day before and after surgery. Next, all of the resected tissues from the patients will be checked with pathology. 6 of 50 patients are performed for whole-body PET scans at 0, 15, 30, 45, 60, and 120 minutes and a CT scan at 60 minutes after tracer injection (mean dose, 5.0 ± 0.5 mCi in 2.0 ± 0.5ml) will be performed. During the imaging period, 1 mL blood samples will be obtained for time-activity curve calculations at 1, 5, 10, 30,60, 90, 120, and 180 minutes after injection. The estimated radiation doses will be calculated by using OLINDA/EXM software. The images produced by these scans will be compared to see the diagnosis value of 18F-P3BZA. Screening Tests: Women who decide to take part in this study will be asked if they think they might be pregnant at the start of the study. All of them must have a negative blood pregnancy test (Human chorionic gonadotropin, HCG). PET-CT Scan Procedure: Before the PET-CT scan is performed, patient will be asked to remove any metallic objects when she/he arrive at the PET-CT Center. After a property rest, he/she will be injected with about 5mCi 18F-P3BZA. The first scan will take at 60 minutes after injection and a delay scan will take at 120 minutes after injection. Each PET/CT scan will take about 20 minutes. After 18F-P3BZA scan, the patient will be asked to avoid stressful exercise. Starting about 12 hours before 18F-FDG scan, he/she will be asked to limit the amount of carbohydrates until the scans are done. Follow-Up Visits: Patients' primary care physician will follow-up them for next 24 hours. After then, they may order additional imaging or surgical results after this study for follow-up purposes. The study doctor will review these results to compare them with the PET-CT images. The study doctors will also review the results of any biopsies you may have had as a result of PET-CT findings. This is an investigational study. PET-CT and CT scans are FDA approved and commercially available.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Melanoma
Keywords
Picolinamide, PET/CT, Diagnosis, Melanoma

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Melanoma patients
Arm Type
Experimental
Arm Description
Melanoma patients enrolled for the clinical diagnosis study are performed with both 18F-P3BZA PET/CT and18F-FDG PET/CT scans before surgery.
Intervention Type
Radiation
Intervention Name(s)
18F-P3BZA
Other Intervention Name(s)
18F labeled Picolinamide
Intervention Description
18F-P3BZA is a type of 18F labeled Picolinamide targeting melanin which is highly secreted in Melanoma. The toxicity of P3BZA was evaluated by SoBran Bioscience. The final report showed that there no signs of toxicity during the conduct of the toxicity study. No treatment-related differences were noted in mean body weight and body weight changes, clinical chemistry, haematology, or coagulation parameter after a single intravenous dose of P3BZA at 0.0589mg/kg.
Primary Outcome Measure Information:
Title
SUV of organs and melanoma
Description
The maximum standardized uptake values (SUVmax) with unit of g/mL of 18F-P3BZA and 18F-FDG in melanoma tissues.
Time Frame
1 hour after injection

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients with melanoma: diagnosed by pathology and ready for surgery Exclusion Criteria: patients with melanoma: refuse or cannot endure surgery pregnant women
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jing Wang, M.D, Ph.D
Phone
86-29-84775449
Email
wangjing@fmmu.edu.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaowei Ma, M.D
Phone
86-29-84771048
Email
mxw_cn@hotmail.com
Facility Information:
Facility Name
Xijing Hospital Nuclear Medicine Department
City
Xi'an
State/Province
Shaanxi
ZIP/Postal Code
710032
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

18F-Labeled Picolinamide PET Imaging of Melanoma Diagnosis

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