Total Body PET-CT Imaging of Prostate Cancer Using Illuccix
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ClinicalTrials.gov Identifier: NCT05558956 |
Recruitment Status :
Not yet recruiting
First Posted : September 28, 2022
Last Update Posted : September 28, 2022
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Metastatic Castration-resistant Prostate Cancer | Drug: illuccix 68Ga-PSMA-11 Total Body PET-CT | Early Phase 1 |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 100 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Diagnostic |
Official Title: | Total Body PET-CT Imaging of Prostate Cancer Using Illuccix (Kit for the Preparation of Ga-68 PSMA-11 Injection) |
Estimated Study Start Date : | October 2022 |
Estimated Primary Completion Date : | January 2023 |
Estimated Study Completion Date : | January 2023 |

Arm | Intervention/treatment |
---|---|
Experimental: Low Dose
5 mCi dose of 68Ga-PSMA-11 (Illuccix) and a total body PET-CT scan for 8 min scan time.
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Drug: illuccix 68Ga-PSMA-11 Total Body PET-CT
Illuccix (kit for the preparation of gallium Ga 68 gozetotide injection) 68Ga-PSMA-11 |
Experimental: High dose
5 mCi dose of 68Ga-PSMA-11 (Illuccix) and a total body PET-CT scan for 5 min scan time.
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Drug: illuccix 68Ga-PSMA-11 Total Body PET-CT
Illuccix (kit for the preparation of gallium Ga 68 gozetotide injection) 68Ga-PSMA-11 |
- Comparing the imaging quality using low dose and high dose Ga-68 PSMA-11 at various scan lengths. [ Time Frame: 3 months ]In modulating the dose and scan time, including reconstitution of the images, we will identify optimal protocol for use of Illuccix on total body PET/CT through evaluation of image quality at variable dose and scan length.

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | Male |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Provision of signed and dated informed consent form
- Male ≥ 18 years of age
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Patients meeting clinical need for Illuccix PET scan:
- Patients with suspected metastasis who are candidates for initial definitive therapy
- Patients with suspected recurrence based on elevated serum prostate-specific antigen (PSA) level
- Patient is physically able to lay flat for the PET-CT procedure
Exclusion Criteria:
1. Assessment by the Investigator as unable or unwilling to comply with the requirements of the protocol.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05558956
Contact: Dan Rogers | 616-330-3886 | clinical.research@bamfhealth.com |
United States, Michigan | |
BAMF Health | |
Grand Rapids, Michigan, United States, 49503 | |
Contact: Dan Rogers 616-330-3886 clinical.research@bamfhealth.com |
Responsible Party: | BAMF Health |
ClinicalTrials.gov Identifier: | NCT05558956 |
Other Study ID Numbers: |
BAMF-2022-03 |
First Posted: | September 28, 2022 Key Record Dates |
Last Update Posted: | September 28, 2022 |
Last Verified: | September 2022 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
Studies a U.S. FDA-regulated Drug Product: | Yes |
Studies a U.S. FDA-regulated Device Product: | No |
Product Manufactured in and Exported from the U.S.: | No |
Prostatic Neoplasms Genital Neoplasms, Male Urogenital Neoplasms Neoplasms by Site Neoplasms |
Prostatic Diseases Gallium 68 PSMA-11 Radiopharmaceuticals Molecular Mechanisms of Pharmacological Action |