Clinical trial · Interventional
Study of 111In-DAC as a Medical Imaging Agent for the Detection of Breast Cancer
NCT00040430CI-TRIAL-00000040unknownPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The purpose of this study is to investigate the safety and imaging ability of 111In-DAC when used with planar and SPECT imaging for the detection of breast cancer.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 111In-DAC | Drug | — | UNRESOLVED |
| Diagnostic | Procedure | — | UNRESOLVED |
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria Patients will be eligible for the study if they: * Are non-pregnant, non-lactating females 18 years of age or older(must agree to use an appropriate and effective method of birth control during the study and for 2 weeks after study) * Are being evaluated for a known or suspected breast tumor (must present with either a mammographic abnormality 10mm or larger or a mammographically occult but palpable abnormality of the breast) * Have been previously scheduled for biopsy or surgical excision of the known or suspected tumor of the breast * Have signed an informed consent form Exclusion Criteria Patients will not be eligible for this study if they: * Have a history or suspicion of significant allergic reaction or anaphylaxis to any of the 111In-DAC components * Have a clinically unstable medical condition or opportunistic infection, a life-threatening disease state, impaired renal or hepatic function or are immunosuppressed * Are taking or have taken part in any investigational study within 30 days of start of study * Have received an indium agent within 30 days of start of study * Are not able to remain immobile during scanning time * Have taken drugs that may damage the kidneys within 2 weeks of start of study * Have abnormal laboratory test results: hemoglobin \< 9.5 gms/dl, serum creatinine \> 1.5 mg/100ml, alkaline phosphatase 2X the upper limit of normal * Have undergone an excisional and/or needle localization biopsy within 4 days prior to start of study
References
Publications (0)
Data not yet available
No reference posted for this study.