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68Ga-NY104 PET/CT Imaging in Renal Cell Carcinoma

Primary Purpose

Renal Cell Carcinoma

Status
Recruiting
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
68Ga-NY104 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 Renal Cell Carcinoma focused on measuring 68Ga-NY104, carbonic anhydrase IX

Eligibility Criteria

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

Inclusion Criteria: Written informed consent provided for participation in the trial Age ≥ 18 y at least one of the following indications should be applied Scheduled for surgical resection of renal mass confirmed recurrent/metastatic clear cell renal cell carcinoma suspicion for recurrent/metastatic clear cell renal cell carcinoma Exclusion Criteria: On VEGF TKI treatment less than 1 week before 68Ga-NY104 PET/CT. Pregnancy or lactation Severe claustrophobia.

Sites / Locations

  • Peking Union Medical College HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

68Ga-NY104 PET/CT

Arm Description

Each patient will receive one dose of 68Ga-NY104 by intravenous route. Dedicated whole-body PET/CT imaging will be performed.

Outcomes

Primary Outcome Measures

Binary reading of focal lesions identified on 68Ga-NY104 PET/CT
Define lesion as PET positive or PET negative lesion.

Secondary Outcome Measures

SUVmax of focal lesions identified on 68Ga-NY104 PET/CT
the tracer uptake is quantified using maximal standard uptake value (SUVmax) by drawing a 3-dimensional region of interest (ROI) over the lesion using a threshold of 40% SUVmax.

Full Information

First Posted
June 5, 2023
Last Updated
June 5, 2023
Sponsor
Peking Union Medical College Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05902377
Brief Title
68Ga-NY104 PET/CT Imaging in Renal Cell Carcinoma
Official Title
68Ga-NY104 PET/CT Imaging in Patients With Confirmed or Suspicious Renal Cell Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 1, 2021 (Actual)
Primary Completion Date
July 1, 2023 (Anticipated)
Study Completion Date
July 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Peking Union Medical College 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
This is a prospective, single-center study in patients with renal cell carcinoma. The goal is to determine the sensitivity and specificity of 68Ga-NY104 PET/CT in the detection of clear cell renal cell carcinoma.
Detailed Description
Two types of patients will be recruited in this study. Type 1, patients with renal masses scheduled for surgery, type 2, patients with confirmed or suspicious recurrent/metastatic ccRCC. Each patient will receive one dose of 68Ga-NY104 by intravenous route. Dedicated whole-body PET/CT imaging will be performed. Imaging interpretations and reference standards will be used to estimate the sensitivity and specificity of 68G-NY104 PET/CT. 46 patients will be recruited in Peking Union Medical College Hospital. This study will be conducted according to local regulations and laws, the ethical principles that have their origin in the Declaration of Helsinki, and the principles of Good Clinical Practice.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Cell Carcinoma
Keywords
68Ga-NY104, carbonic anhydrase IX

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
46 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
68Ga-NY104 PET/CT
Arm Type
Experimental
Arm Description
Each patient will receive one dose of 68Ga-NY104 by intravenous route. Dedicated whole-body PET/CT imaging will be performed.
Intervention Type
Diagnostic Test
Intervention Name(s)
68Ga-NY104 PET/CT
Other Intervention Name(s)
68Ga-NYM005 PET/CT
Intervention Description
Participants will be administered a single, intravenous bolus of 68Ga-NY104 The recommended administered activity of 68Ga-NY104 is 1.8-2.2 MBq per kilogram bodyweight, subject to variation that may be required owing to variable elution efficiencies obtained during the lifetime of the 68Ga / 68Ga generator. The CT and PET imaging session will begin approximately 45 to 75 minutes after 68Ga-NY104 administration.
Primary Outcome Measure Information:
Title
Binary reading of focal lesions identified on 68Ga-NY104 PET/CT
Description
Define lesion as PET positive or PET negative lesion.
Time Frame
From study completion to 1 month after completion
Secondary Outcome Measure Information:
Title
SUVmax of focal lesions identified on 68Ga-NY104 PET/CT
Description
the tracer uptake is quantified using maximal standard uptake value (SUVmax) by drawing a 3-dimensional region of interest (ROI) over the lesion using a threshold of 40% SUVmax.
Time Frame
From study completion to 1 month after completion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Written informed consent provided for participation in the trial Age ≥ 18 y at least one of the following indications should be applied Scheduled for surgical resection of renal mass confirmed recurrent/metastatic clear cell renal cell carcinoma suspicion for recurrent/metastatic clear cell renal cell carcinoma Exclusion Criteria: On VEGF TKI treatment less than 1 week before 68Ga-NY104 PET/CT. Pregnancy or lactation Severe claustrophobia.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Huo Li, MD
Phone
18612672038
Email
huoli@pumch.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Wenjia Zhu, MD
Phone
18614080164
Email
zhuwenjia_pumc@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Huo Li, MD
Organizational Affiliation
Peking Uion Medical College Hospital
Official's Role
Principal Investigator
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
Wenjia Zhu
Phone
18614080164
Email
zhuwenjia_pumc@163.com

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

68Ga-NY104 PET/CT Imaging in Renal Cell Carcinoma

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