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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06049368
Other study ID # PUMCH-PSS093
Secondary ID
Status Not yet recruiting
Phase Phase 1/Phase 2
First received
Last updated
Start date October 1, 2023
Est. completion date March 31, 2024

Study information

Verified date September 2023
Source Peking Union Medical College Hospital
Contact Zhaohui Zhu, MD
Phone 86-13611093752
Email 13611093752@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Prostate specific membrane antigen (PSMA) is a type II transmembrane protein and acts as a glutamate carboxypeptidase enzyme. It is first described in prostate cancer cell lines and later identified in various tissues, include salivary gland. This pilot study was designed to evaluate the diagnostic performance of 68Ga-P16-093 in primary sjogren's syndrome patients.


Description:

Primary sjogren's syndrome (pSS) is a systemic autoimmune disease mainly presented hyperglobulinemia and exocrine gland involvement,and lack of diagnostic gold standard.Prostate-specific membrane antigen (PSMA), as known as folate hydrolase I or glutamate carboxypeptidase II, is overexpressed on the cells of prostatic adenocarcinoma. However, PSMA is also expressed by various solid organs , such as salivary gland,which is often observed damage in primary Sjogren's syndrome patients.Therefore, PSMA may be an ideal target for evaluating salivary gland injury.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date March 31, 2024
Est. primary completion date December 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - pathological diagnosis confirmed by operation or biopsy. - Obtain written informed consent and accepted follow-up. Exclusion Criteria: - Pregnant, lactating women or having parenting plans during the study - Head and neck radiotherapy history ; - Active hepatitis C infection (PCR positive), include immunodeficiency syndrome, sarcoidosis, amyloidosis, graft versus host disease, IgG4 related diseases. - Other situaition researchers considered it was not appropriate to participate in trials.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
68Ga-P16-093
Intravenous injection of 68Ga-P16-093 with the dosage of 1.5-1.8 MBq (0.04-0.05 mCi)/kg. Tracer doses of 68Ga-P16-093 will be used to image lesions of glioma by PET/CT.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Peking Union Medical College Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Diagnostic performance evaluating the number of regions in damaged salivary glands detected by 68Ga-P16-093 through study completion, an average of 1 year
Secondary standardized uptake value (SUV) of lesion comparing the SUVmax of different grades in salivary gland lesion, derived from 68Ga-P16-093 through study completion, an average of 1 year]
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