Exploratory, Phase 0 Study of Positron Emission Tomography (PET) Imaging Agent, F-18 RGD-K5
Completed · Early Phase 1
Conditions studied: Sarcoma, Melanoma, Lung Cancer, Breast Cancer, High Grade Gliomas
In brief
The purpose of this research study is to get information from volunteers without cancer and patients with cancer who have received a new investigational study agent called, "\[F-18\] RGDK5," to evaluate biodistribution and dosimetry for the study agent and determine F-18 RGD-K5 uptake in angiogenic tumor. the system.
Key facts
- Study ID
- NCT00743353
- Run by
- Siemens Molecular Imaging
- People needed
- 16
- Starts
- 2008-08-01
- Expected to finish
- 2009-01-01
- Last updated by the study team
- 2009-02-02
Who can join
Age: 0 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- For Normal Volunteers
- Subject is ≥ 18 years old at the time of investigational product administration (Subject is male or female of any race / ethnicity)
- Subject or subject's legally acceptable representative provides informed consent
- Subject is capable of complying with study procedures
- Subject is capable of communicating with study personnel
- For Cancer Subjects (same first four bullets as 'normals')
- Subject must have had a diagnostic imaging study and is suspected of having a primary or metastatic tumor(s) ( > 2 cm, except breast tumor)-sarcoma; melanoma; lung cancer [including small cell and non-small cell lung cancer (NSCL)]; high grade glioma (including glioblastoma multi-forms), anaplastic astrocytoma, and anaplastic oligodendroglioma; breast carcinomas, and head and neck tumors, including laryngeal squamous cell carcinoma
- Subject is scheduled to have a clinical [F-18]FDG PET scan within ± 7 days (with no interventions between the two PET scans) of the investigational, [F-18]RGD-K5 PET scan
- Subject is scheduled to undergo resection or biopsy of the target tumor as a result of routine clinical treatment
- Subject has not received any anti-angiogenic agents (e.g. bevacizumab, sorafenib, sunitinib) within 10 days prior to PET/CT imaging
- Subject has laboratory test results within the following ranges:
- AST(SGOT)/ALT(SGPT) ≤ 2.5 x institutional upper limits of normal
- Serum creatinine ≤ 1.5 institutional upper limits of normal
- Platelet count of > 75,000x106/L
- Hemoglobin value of > 9 g/dL
- ANC > 1.2 x 106 /mL
- Exclusion Criteria 'Normals':
- Subject is < 18 at the time of investigational product administration
- Female subject is pregnant or nursing:
- by testing on site at the institution (serum or urine ßHCG) within 24 hours prior to the investigational product administration
- Subject is unable to remain still for duration of imaging procedure
- Subject has a history of renal disease
- Subject has previously received [F-18]RGD-K5 at any time, or any other investigational product in the past 30 days or will receive any other investigational product within 48 hours after the [F-18]RGD-K5 injection
- Subject has not been involved in an investigative, radioactive research procedure or therapeutic procedure within the past 6 months
- Subject has any other condition or personal circumstance including severe claustrophobia, severe dyspnea, severe back pain etc, that, in the judgment of the investigator, might interfere with the collection of complete good quality data
Where it is running
- Fox Chase Cancer Center — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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