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68Ga-NOTA-Aca-BBN(7-14) PET/CT in Patients With Primary Gliomas

Primary Purpose

Glioma

Status
Unknown status
Phase
Early Phase 1
Locations
China
Study Type
Interventional
Intervention
68Ga-NOTA-Aca-BBN
PET/CT
Sponsored by
Peking Union Medical College Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Glioma focused on measuring PET/CT, Bombesin, gastrin-releasing peptide receptor, 68Gallium labeling

Eligibility Criteria

3 Years - 70 Years (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Must be able to provide a written informed consent
  • Clinically based and magnetic resonance imaging (MRI)-based suspected newly diagnosed primary glioma.
  • The tumor will be surgically removed and histological diagnosis will be available.

Exclusion Criteria:

  • Females planning to bear a child recently or with childbearing potential;
  • Known severe allergy or hypersensitivity to IV radiographic contrast;
  • Inability to lie still for the entire imaging time because of cough, pain, etc.
  • Inability to complete the needed examinations due to severe claustrophobia, radiation phobia, etc.
  • Concurrent severe and/or uncontrolled and/or unstable other medical disease that, in the opinion of the investigator, may significantly interfere with study compliance.

Sites / Locations

  • Peking Union Medical College HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

68Ga-NOTA-Aca-BBN(7-14) PET/CT

Arm Description

The patients were injected with 111-148 MBq of 68Ga-NOTA-Aca-BBN(7-14) in one dose intravenously and underwent PET/CT scan 30 min later.

Outcomes

Primary Outcome Measures

Standardized uptake value of 68Ga-NOTA-Aca-BBN(7-14) in primary glioma
The semiquantitative analysis will be performed by the same person for all the cases, and the standardized uptake value (SUV) of the tracer in primary glioma will be measured.

Secondary Outcome Measures

Adverse events collection
Adverse events within 1 week after the injection and scanning of patients and patients will be followed and assessed.

Full Information

First Posted
August 2, 2015
Last Updated
April 5, 2017
Sponsor
Peking Union Medical College Hospital
Collaborators
National Institute for Biomedical Imaging and Bioengineering (NIBIB)
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1. Study Identification

Unique Protocol Identification Number
NCT02520882
Brief Title
68Ga-NOTA-Aca-BBN(7-14) PET/CT in Patients With Primary Gliomas
Official Title
Safety and Diagnostic Performance of 68Gallium-labeled NOTA-Aca-BBN(7-14) PET/CT in Patients With Primary Gliomas
Study Type
Interventional

2. Study Status

Record Verification Date
March 2015
Overall Recruitment Status
Unknown status
Study Start Date
January 2015 (undefined)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Peking Union Medical College Hospital
Collaborators
National Institute for Biomedical Imaging and Bioengineering (NIBIB)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is an open-label positron emission tomography/computed tomography (PET/CT) study to investigate the diagnostic performance and evaluation efficacy of 68Ga-NOTA-Aca-BBN(7-14) in glioma patients. A single dose of 111-148 Mega-Becquerel (MBq) 68Ga-NOTA-Aca-BBN(7-14) will be injected intravenously. Visual and semiquantitative method will be used to assess the PET/CT images.
Detailed Description
Non-invasive imaging evaluation of GRPR expression would be of great help in drug development, patient stratification and therapeutic response monitoring. Various GRPR targeting imaging probes have been develop to meet the purpose. Bombesin (BBN) is an amphibian homolog of mammalian gastrin-releasing peptide (GRP). BBN(7-14), with the amino acid sequence of Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2, has been extensively used for the development of molecular probes for the imaging of gastrin-releasing peptide receptor (GRPR), after being labeled with various radionuclides. Multiple preclinical studies have demonstrated receptor-specific accumulation of the tracers in GRPR positive tumors. For interests in clinical translation of 68Ga-NOTA-Aca-BBN(7-14), an open-label dynamic whole-body PET/ CT study was designed to investigate the safety and diagnostic performance of 68Ga-NOTA-Aca-BBN(7-14) in patients with glioma.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioma
Keywords
PET/CT, Bombesin, gastrin-releasing peptide receptor, 68Gallium labeling

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
68Ga-NOTA-Aca-BBN(7-14) PET/CT
Arm Type
Experimental
Arm Description
The patients were injected with 111-148 MBq of 68Ga-NOTA-Aca-BBN(7-14) in one dose intravenously and underwent PET/CT scan 30 min later.
Intervention Type
Drug
Intervention Name(s)
68Ga-NOTA-Aca-BBN
Other Intervention Name(s)
68Ga-NOTA-Aca-BBN(7-14)
Intervention Description
68Ga-NOTA-Aca-BBN(7-14) were injected into the patients before the PET/CT scans
Intervention Type
Device
Intervention Name(s)
PET/CT
Primary Outcome Measure Information:
Title
Standardized uptake value of 68Ga-NOTA-Aca-BBN(7-14) in primary glioma
Description
The semiquantitative analysis will be performed by the same person for all the cases, and the standardized uptake value (SUV) of the tracer in primary glioma will be measured.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Adverse events collection
Description
Adverse events within 1 week after the injection and scanning of patients and patients will be followed and assessed.
Time Frame
1 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Must be able to provide a written informed consent Clinically based and magnetic resonance imaging (MRI)-based suspected newly diagnosed primary glioma. The tumor will be surgically removed and histological diagnosis will be available. Exclusion Criteria: Females planning to bear a child recently or with childbearing potential; Known severe allergy or hypersensitivity to IV radiographic contrast; Inability to lie still for the entire imaging time because of cough, pain, etc. Inability to complete the needed examinations due to severe claustrophobia, radiation phobia, etc. Concurrent severe and/or uncontrolled and/or unstable other medical disease that, in the opinion of the investigator, may significantly interfere with study compliance.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zhaohui Zhu, Dr.
Phone
+86 10 69154196
Email
13611093752@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Jingjing Zhang, Dr.
Phone
+86 15101033017
Email
zhangjingjingtag@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fang Li, Dr.
Organizational Affiliation
Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College
Official's Role
Study Chair
Facility Information:
Facility Name
Peking Union Medical College Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100730
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jingjing Zhang, Dr.
Phone
+86 15101033017
Email
zhangjingjingtag@163.com
First Name & Middle Initial & Last Name & Degree
Fang Li, Dr.

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

68Ga-NOTA-Aca-BBN(7-14) PET/CT in Patients With Primary Gliomas

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