A Phase 1 interventional study of BAY1075553 and BAY1075553 in Diagnostic Imaging, sponsored by Lantheus Biosciences Ltd.. Completed at 2 sites in 2 countries. Open to male participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2013-01-21.
Sponsored by Lantheus Biosciences Ltd. (part of Lantheus Holdings, Inc.) · Phase 1, Interventional, and Diagnostic
PET/CT imaging study for evaluation of safety and tolerability and diagnostic performance of BAY1075553 in patients with prostate cancer and in healthy volunteers
6,484 studies on the registry are indexed under Prostatic Neoplasms; 1,415 are open to participants now.
This study's enrollment of 14 is below the median of 58 across 4,908 interventional studies indexed under Prostatic Neoplasms.
Browse Prostatic Neoplasms studies →Lantheus Biosciences Ltd. is the lead sponsor of 4 studies on the registry; 1 is open to participants now.
First submitted before Lantheus Biosciences Ltd. became part of Lantheus Holdings, Inc..
Counted across the registry records on this site, refreshed daily.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Part 1: Healthy volunteers only
-- Males ≥ 40 years of age
Part 2: Prostate cancer patients
Exclusion Criteria:
Drug: BAY1075553
Drug: BAY1075553
Cancer patients, single intravenous bolus injection of 300 MBq BAY1075553 over 60 seconds on the treatment day 1
Healthy volunteers for dosimetry, single intravenous bolus injection of 300 MBq BAY1075553 over 60 seconds on the treatment day 1
Safety parameters, for example laboratory and electrocardiogram abnormalities
Time frame: Day 2
Effective radiation dose given in mSv (milliSievert) in healthy volunteers
Time frame: Day 1
Overall lesion detection rate
Time frame: Day 1
Lesion detection rate in comparison to histology, where available (cancer lesion detection rate)
Time frame: Day 1
Lesion detection rate in comparison to MRI (Magnetic Resonance Imaging) and/or [11C] (11Carbon)- or [18F] (18Fluor)-choline PET/CT (whenever available)
Time frame: Day 1
Accumulation score in all lesions identified with BAY1075553
Time frame: Day 1
This study is completed, as verified in Jan 2013. You cannot join it, but the record below documents what was studied.
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