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NCT06632860

A Dual-targeting Tracer TATE-RGD for the Diagnosis of SSTR- and RGD- Positive Tumors

Recruiting now EARLY_PHASE1 Last updated 9 July 2025
What this trial tests

EARLY_PHASE1 trial testing 68Ga-TATE-RGD in Iodine-resistant Thyroid Cancer in 40 participants. Currently enrolling.

Timeline
1 August 2024
Primary endpoint
20 December 2025
30 December 2025

Quick facts

Lead sponsorPeking Union Medical College Hospital
PhaseEARLY_PHASE1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment40
Start date1 August 2024
Primary completion20 December 2025
Estimated completion30 December 2025
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Peking Union Medical College Hospital

Who can join

Adults 18 to 90, any sex, with Iodine-resistant Thyroid Cancer or Meningioma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The US FDA approved a targeted somatostatin receptor 2 imaging agent, 68Ga-DOTATATE, in 2016. It has higher uptake in small cell lung cancer, pulmonary carcinoid, and medullary thyroid cancer. Integrin αvβ3 is highly expressed in some tumor cells and new blood vessels, making it an ideal target for targeted diagnosis and treatment of tumors and tumor vessels.68Ga-labeled DOTA-TATE-RGD is a new type of tumor-specific imaging agent developed by researchers based on the above foundation, which is used for targeted diagnosis and internal radiation therapy for patients with SSTR2 and αvβ3 positive tumors.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Emerging PET Imaging Agents and Targeted Radioligand Therapy: A Review of Clinical Applications and Trials.
    Palihati M, Das JP, Yeh R, Capaccione K. · · 2025 · cited 5× · PMID 40863874 · DOI 10.3390/tomography11080083

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06632860.

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