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CompletedNCT01287845Updated Jan 21, 2013

PET/CT (Positron Emission Tomography/Computed Tomography) Imaging for Safety and Tolerability and Diagnostic Performance of BAY1075553 in Patients With Prostate Cancer and Healthy Volunteers

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

Phase
Phase 1
Study type
Interventional
Enrollment
14
Allocation
Non-randomized
Ages
18 Years and older
Sex
Male
01

Study summary

PET/CT imaging study for evaluation of safety and tolerability and diagnostic performance of BAY1075553 in patients with prostate cancer and in healthy volunteers

02

Conditions studied

  • Diagnostic Imaging

Keywords

  • Prostate cancer
  • Neoplasm
  • Diagnostic Imaging
  • PET (Positron Emission Tomography) -tracer
  • PET-diagnosis
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In context

Prostatic Neoplasms

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 →

Lead sponsor

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.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Male
Accepts healthy volunteers
Yes

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.

Inclusion criteria

  • Part 1: Healthy volunteers only

    -- Males ≥ 40 years of age

  • Part 2: Prostate cancer patients

    • Males ≥ 18 years of age
    • Serum PSA (Prostate-Specific Antigen) value above normal.
    • Patients had an MRI and/or a positive [11C] - or [18F] -choline PET/CT for primary diagnosis (Note: MRI and [11C]-or [18F]-choline PET/CT are optional for primary prostate cancer patients) or recurrence detection of prostate cancer and the primary cancer disease (adenocarcinoma) is histologically confirmed
    • Patients with primary prostate cancer have to be scheduled for prostatectomy
    • In patients with primary prostate cancer, histopathological evaluation has to show an adenocarcinoma with a Gleason score of 3 + 3 or higher in at least two biopsies at any location in the prostate
    • Patients with advanced primary or recurrent prostate cancer and a high likelihood to display lymph node metastasis, ideally scheduled for explorative pelvic lymphadenectomy, are to be preferably included
  • Part 3: Prostate cancer patients -- The criteria for eligibility of part 3 are identical to the ones of part 2. Except it is now no longer a preference but mandatory to only enrol patients with a presumably high likelihood of metastatic disease, especially lymph node metastasis.

Exclusion criteria

Exclusion Criteria:

  • Concurrent severe and/or uncontrolled and/or unstable medical disease other than prostate cancer (e.g. poorly controlled diabetes, congestive heart failure, myocardial infarction within 12 months prior to planned injection of BAY1075553, unstable and uncontrolled hypertension, chronic renal or hepatic disease, severe pulmonary disease) which could compromise participation in the study
  • Acute renal insufficiency of any intensity, either due to hepato-renal syndrome or occurring in the peri-operative liver transplantation period
  • Active inflammatory bowel disease within the last 6 months
  • Acute prostatitis requiring medical treatment within the last 6 months
  • A non-urologic bacterial infection requiring active treatment with antibiotics within 3 months
  • Active other malignancy (except basal cell or squamous cell skin cancer) within the last 2 years
  • Patients with primary prostate cancer only: androgen ablation within 3 months before planned treatment
  • Subject fulfils criteria which in the opinion of the investigator preclude participation for scientific reasons, for reasons of compliance, or for reasons of the subject's safety
05

Study design

Phase
Phase 1
Primary purpose
Diagnostic
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
14 participants (actual)

Study arms

  • Experimental
    Arm 1

    Drug: BAY1075553

  • Experimental
    Arm 2

    Drug: BAY1075553

Interventions

  • DrugBAY1075553

    Cancer patients, single intravenous bolus injection of 300 MBq BAY1075553 over 60 seconds on the treatment day 1

  • DrugBAY1075553

    Healthy volunteers for dosimetry, single intravenous bolus injection of 300 MBq BAY1075553 over 60 seconds on the treatment day 1

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What researchers measure

Primary outcomes

  1. Safety parameters, for example laboratory and electrocardiogram abnormalities

    Time frame: Day 2

  2. Effective radiation dose given in mSv (milliSievert) in healthy volunteers

    Time frame: Day 1

Secondary outcomes

  1. Overall lesion detection rate

    Time frame: Day 1

  2. Lesion detection rate in comparison to histology, where available (cancer lesion detection rate)

    Time frame: Day 1

  3. 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

  4. Accumulation score in all lesions identified with BAY1075553

    Time frame: Day 1

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Study locations

2 sites
  • Ann Arbor, Michigan 48109-0028, United States
  • Linz, 4010, Austria
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 21, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01287845
Responsible party
Sponsor
First posted
Feb 2, 2011
Start date
Feb 2011
Primary completion
Oct 2011
Completion
Nov 2011
Last update
Jan 21, 2013

Study contacts

Bayer Study Director
study director · Bayer

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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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