PD-L2 Targeting Nanobody Radiotracer for PET Imaging of Solid Tumor

Sponsor
Peking University Cancer Hospital & Institute (Other)
Overall Status
Recruiting
CT.gov ID
NCT05803746
Collaborator
(none)
20
1
1
24
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Study Details

Study Description

Brief Summary

The objective of this study is to construct a noninvasive approach using 68Ga- Mirc415 PET/CT to detect the PD-L2 expression of tumor lesion in patients with colorectal cancer, lung cancer and other solid tumor to identify patients benefiting from anti-PD-(L)1 treatment.

Condition or Disease Intervention/Treatment Phase
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
PD-L2 Targeting Nanobody Radiotracer for PET Imaging of Solid Tumor
Actual Study Start Date :
Jul 15, 2022
Anticipated Primary Completion Date :
Jul 15, 2024
Anticipated Study Completion Date :
Jul 15, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Imaging cohort

All enrolled participants will be allocated to this arm (single-arm study). Study participants will undergo 68Ga-Mirc415 PET/CT scan.

Drug: 18F-FDG
All study participants will undergo one 18F-FDG PET/ CT scan.

Outcome Measures

Primary Outcome Measures

  1. MPR [[Time Frame: After 2-4 cycles of immunotherapy (each cycle is 28 days)]]

    In the surgical pathology after neo-adjuvant immunotherapy, the proportion of active tumors was less than 10%.

Secondary Outcome Measures

  1. PFS [2 years]

    progression free survival

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Aged 18-75, male and female, with ECOG score of 0 or 1;

  2. Subjects with head and neck tumors, lung cancer, esophageal cancer, breast cancer, ovarian cancer, cholangiocarcinoma, colorectal cancer, gastric cancer, pancreatic cancer, melanoma, bone or soft tissue sarcoma, solid tumors or suspected tumor subjects who intend to undergo pathological tissue biopsy or receive tumor surgical treatment in the near future (within 2 months);

  3. The expected survival was more than 26 weeks;

  4. Blood routine test, liver and kidney function meet the following standards: blood routine: WBC >= 4.0 x 109/L or neutrophil >= 1.5 x 109/:, PLT >= 100 x 10^9 / L, Hb

= 90g / L; Pt or APTT <= 1.5 upper limit of normal value; liver and kidney function: total bilirubin <= 1.5 x ULT (upper limit of normal value), ALT / AST <= 2.5 upper limit of normal value or <= 5 x ULT (subject with liver metastasis), ALP <= 2.5 upper limit of normal value (if bone metastasis or liver metastasis exists, ALP <= 4.5 upper limit of normal value); BUN <= 1.5 x ULT, SCR <= 1.5 x ULT;

  1. According to RECIST1.1, there was at least one measurable target lesion;

  2. Women must take effective contraceptive measures during the study period and within 6 months after the end of the study; men should agree to use contraceptive measures during the study period and within 6 months after the end of the study period;

  3. Understand and sign informed consent voluntarily with good compliance.

Exclusion Criteria:
  1. The function of liver and kidney was seriously abnormal;

  2. Preparation for pregnant, pregnant and lactating women;

  3. Inability to lie flat for half an hour;

  4. Suffering from claustrophobia or other mental disorders; 5) Other researchers considered it unsuitable to participate in the trial. -

Contacts and Locations

Locations

Site City State Country Postal Code
1 Beijing Cancer Hospital Beijing China

Sponsors and Collaborators

  • Peking University Cancer Hospital & Institute

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hua Zhu, Professor, Peking University Cancer Hospital & Institute
ClinicalTrials.gov Identifier:
NCT05803746
Other Study ID Numbers:
  • 2022KT114
First Posted:
Apr 7, 2023
Last Update Posted:
Apr 7, 2023
Last Verified:
Mar 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 7, 2023