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Phase 2, Open-Label, Imaging Trial of I-124-CLR1404 in Patients With Newly Diagnosed or Recurrent Glioblastoma
The primary objective of this trial is to determine the optimal dose and imaging time point(s) of I-124-CLR1404 in subjects with newly diagnosed and recurrent glioma to be used in future trials.
Details
| Lead sponsor | Cellectar Biosciences, Inc. |
|---|---|
| Phase | Phase 2 |
| Status | TERMINATED |
| Enrolment | 7 |
| Start date | 2014-02 |
| Completion | 2015-12 |
Conditions
- Glioblastoma
Interventions
- I-124-CLR1404
Primary outcomes
- Optimal Imaging Parameters - Dose — 8 days
Up to two dose levels (5 mCi and 7.5 mCi) will be evaluated in conjunction with multiple imaging time points to determine the optimal parameters for PET/CT brain imaging. Dosing will begin at 5 mCi and if the images are deemed inadequate, as assessed by count statistics and image quality, the 7.5 mCi dose level will be evaluated.
Countries
United States