Testing the Safety of the Anti-cancer Drug, Sn-117m-DTPA, for Advanced Cancers That Have Spread to Bones
NCT06982222 · Status: NOT_YET_RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 24
Last updated 2026-05-13
Summary
This phase I trial tests the safety, side effects and best dose of tin (Sn)-177m-diethylenetriaminepentaacetic acid (DTPA) and how well it works in treating prostate, breast or non-small cell lung cancer that has spread from where it first started (primary site) to the bones (bone metastases). Sn-117m-DTPA was originally tested in tumors that had spread to the bones to help reduce bone pain. The drug has been improved and is designed to send low-level radiation to tumors in the bone while being gentler on the bone marrow, where blood cells are made. Sn-117m-DTPA may be safe and tolerable, and may slow down or shrink tumors in patients with metastatic prostate, breast, or non-small cell lung cancer that has spread to the bones.
Conditions
- Anatomic Stage IV Breast Cancer AJCC v8
- Metastatic Breast Carcinoma
- Metastatic Lung Non-Small Cell Carcinoma
- Metastatic Malignant Neoplasm in the Bone
- Metastatic Prostate Adenocarcinoma
- Stage IV Lung Cancer AJCC v8
- Stage IVB Prostate Cancer AJCC v8
Interventions
- PROCEDURE
-
Biospecimen Collection
Undergo urine and blood sample collection
- PROCEDURE
-
Bone Scan
Undergo technetium TC-99m bone scan
- PROCEDURE
-
Computed Tomography
Undergo PET/CT, SPECT/CT and PSMA PET/CT
- PROCEDURE
-
Positron Emission Tomography
Undergo PET/CT
- PROCEDURE
-
PSMA PET Scan
Undergo PSMA PET/CT
- PROCEDURE
-
Single Photon Emission Computed Tomography
Undergo SPECT/CT
- RADIATION
-
Technetium TC-99m
Undergo technetium TC-99m bone scan
- RADIATION
-
Tin Sn 117m Pentetate
Given IV
Sponsors & Collaborators
-
National Cancer Institute (NCI)
lead NIH
Principal Investigators
-
Zin W Myint · Ohio State University Comprehensive Cancer Center LAO
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-10-01
- Primary Completion
- 2027-02-12
- Completion
- 2027-02-12
- FDA Drug
- Yes
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