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Specific Molecular Imaging of DX600 Labeled by PET Radionuclide Targeting ACE2 in Patients

Specific Molecular Imaging of DX600 Labeled by PET Radionuclide Targeting ACE2 in Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04422457
Enrollment
30
Registered
2020-06-09
Start date
2020-06-13
Completion date
2022-03-01
Last updated
2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Solid Tumor

Brief summary

Angiotensin-converting enzyme 2 (ACE2) plays an important role in renin-angiotensin system (RAS) and has been reported to relate with cancer. Recently, it has also been proved as the key target for COVID-19 infection. DX600 is a polypeptide that can specific binding to ACE2 specifically with nanomolar affinity reported in literature. This study constrcuted a radio-tracer, DX600 Labeled by PET Radionuclide, to monitoring biodistribution ACE2 in human beings, evaluate the detection ability of radio-tracer in ACE2 over-expression tumors and dynamic changes of ACE2 expression under therapy.

Interventions

OTHER68Ga-DX600 PET/CT

DX600, labeled with 68Ga will be used as a molecular imaging tracer for PET/CT scanning

Sponsors

Peking University Cancer Hospital & Institute
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 18-75 years old; both sex; * ECoG 0 or 1; * Patients that would undergo biopsy or surgical operation with high ACE2 expression tumors such as colorectal cancer, renal cancer, pancreatic cancer, gastric cancer, liver cancer, lung cancer, brain cancer or suspected tumor. * use 18F-FDG PET/CT as baseline evaluation

Exclusion criteria

* Significant hepatic or renal dysfunction; * Is Pregnant or ready to pregnant; * Cannot lie on their back for half an hour; * Suffering from claustrophobia or other mental diseases; * Refusal to join the clinical study;

Design outcomes

Primary

MeasureTime frameDescription
SUV2 yearsThe uptake of uptake of the tracer in the primary and metastatic tumor lesions by measuring standardized uptake value(SUV)

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026