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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04689893
Other study ID # PUMCHTIOJR11
Secondary ID
Status Recruiting
Phase Phase 1
First received
Last updated
Start date March 15, 2020
Est. completion date March 15, 2022

Study information

Verified date December 2020
Source Peking Union Medical College Hospital
Contact Guozhu Hou, MD
Phone 15611145656
Email 15611145656@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is an open-label whole-body PET/CT study for investigating the value of 68Ga-DOTA-TATE and 68Ga-DOTA-JR11 PET/CT in patients with Tumor-induced osteomalacia.


Description:

Tumor-induced osteomalacia (TIO), also known as oncogenic osteomalacia, is a rare paraneoplastic syndrome. The key to the cure of TIO is surgical resection of the culprit tumor. Over the last decade, 68Ga-labeled SSTR-based imaging has made a significant impact in detecting the culprit tumor of TIO 68Ga-DOTA-TATE is the most used SSTR PET tracer for the detection of TIO and it was recommended as first-line imaging method for localization of the causative tumor. However, false positive, including fracture and/or inflammation, in 68Ga-DOTA-TATE PET/CT is a challenge in image interpretation, which may make the causative tumor indistinguishable in multiple suspicious lesions. There is no effective way to identify multiple suspicious lesions with intensive increased uptake on 68Ga-DOTA-TATE PET/CT. 68Ga-DOTA-JR11 is a SSTR2 specific antagonist used for PET tracer. However, the SSTR2 affinity of 68Ga-DOTA-JR11 is lower than 68Ga-DOTA-TATE, which means that the uptake of 68Ga-DOTA-JR11 by suspected lesions may be lower than that of 68Ga-DOTA-TATE. The purpose of this prospective study is to compare the sensitivity of 68Ga-DOTA-JR11 and 68Ga-DOTA-TATE PET/CT for detecting the responsible tumor of TIO and investigate if 68Ga-DOTA-JR11 PET/CT can identify the culprit tumor of TIO in multiple suspicious lesions.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date March 15, 2022
Est. primary completion date March 15, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - suspected or confirmed untreated TIO patients; - 68Ga-DOTA-TATE and 68Ga-DOTA-JR11 PET/CT within two weeks; - signed written consent. Exclusion Criteria: - pregnancy; - breastfeeding; - any medical condition that in the opinion of the investigator may significantly interfere with study compliance.

Study Design


Intervention

Drug:
68Ga-Dotatate
68Ga-Dotatate was injected into the patients before the PET/CT scans
68Ga-DOTA-JR11
68Ga-DOTA-JR11 was injected into the patients before the PET/CT scans

Locations

Country Name City State
China Peking union medical college hospital Beijing Dongcheng

Sponsors (1)

Lead Sponsor Collaborator
Peking Union Medical College Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Diagnostic value Sensitivity and Specificity of 68Ga-DOTA-JR11 PET/CT for TIO in comparison with 68Ga-DOTATATE PET/CT through study completion, an average of 1 year
See also
  Status Clinical Trial Phase
Terminated NCT03510455 - BGJ398 for the Treatment of Tumor-Induced Osteomalacia Phase 2
Available NCT03775187 - Expanded Access to Burosumab