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Trial registered on ANZCTR


Registration number
ACTRN12623001157662
Ethics application status
Approved
Date submitted
29/09/2023
Date registered
8/11/2023
Date last updated
29/09/2024
Date data sharing statement initially provided
8/11/2023
Type of registration
Prospectively registered

Titles & IDs
Public title
68Ga-NTA-476 Imaging in Prostate Cancer
Scientific title
Uptake, Safety and Tolerability of 68Ga-NTA-476 Imaging of Prostate Cancer Tumours
Secondary ID [1] 310709 0
none
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Prostate Cancer 331631 0
Condition category
Condition code
Cancer 328359 328359 0 0
Prostate

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
The novel Prostate Specific Membrane Antigen (PSMA) targeting molecule, NTA-476, is comprised of a small peptide targeting moiety that is attached to a linker and dodecane tetraacetic acid (DOTA) cage which enables chelation of the radionuclide 68Ga for Positron Emission Tomography (PET) imaging.

A single dose of 68Ga-NTA-476 will be administered on Day 1 of the study as an intravenous bolus injection under the supervision of the study Investigator or appropriately qualified delegate. The planned injected activity (IA) of 68Ga-NTA-476 is 1-1.5 MBq/kg.

Following administration of 68Ga-NTA-476 participants will complete PET imaging at 60 minutes and 2-3 hours. Each PET scan will take approximately 30-40 minutes.

As there is only a single intravenous injection of 68Ga-NTA-476 administered in this study, there are no strategies required to monitor adherence.
Intervention code [1] 327108 0
Diagnosis / Prognosis
Comparator / control treatment
68Ga-NTA-476 will be compared to 68Ga-PSMA-11 imaging. Standard of care 68Ga-PSMA-11 imaging will be obtained prior to participation in the trial as part of standard clinical care or during the screening period if not completed within the past 6 weeks.
Control group
Active

Outcomes
Primary outcome [1] 336207 0
Tumour uptake of 68Ga-NTA-476 as compared to 68Ga-PSMA-11 in participants with prostate cancer
Timepoint [1] 336207 0
PET/CT scans completed at 60 minutes and 2-3 hours following 68Ga-NTA-476 administration
Primary outcome [2] 336208 0
Uptake and washout of 68Ga-NTA-476 in normal organs as compared to 68Ga-PSMA-11 in participants with prostate cancer. This will be assessed as a composite outcome.
Timepoint [2] 336208 0
PET/CT scans completed at 60 minutes and 2-3 hours following 68Ga-NTA-476 administration
Secondary outcome [1] 427337 0
Safety and tolerability of a single dose of 68Ga-NTA-476
Timepoint [1] 427337 0
Safety will be assessed on the Imaging Day in the clinic during observation for up to 4 hours post injection of 68Ga-NTA-476 and followed up for a total of 1 week following administration.
Secondary outcome [2] 427338 0
Dosimetry of 68Ga-NTA-476
Timepoint [2] 427338 0
PET/CT scans completed at 60 minutes and 2-3 hours following 68Ga-NTA-476 administration

Eligibility
Key inclusion criteria
1. Willing and able to provide informed consent prior to start of any study procedures and assessments and must be willing to comply with all study procedures.
2. Adult participants at least 18 years of age.
3. Participants with a documented history of histologically confirmed diagnosis of prostate cancer.
o Participants must have PSA more than 0.1ng/mL.
o Participants on chemotherapy may be approved on a case-by-case basis at the principal investigator's discretion if the last dose of chemotherapy is administered at least 3 weeks prior to receipt of 68Ga-NTA-476, and subsequent dose of chemotherapy are to resume following completion of End of Treatment Visit (EOTV), if it is determined not to put the patient at an increased risk of adverse drug effects and/or interfere with the integrity of study outcome.
o Participants on other anti-cancer therapy, such as novel anti-androgen therapy, may be allowed on a case-by-case basis at the principal investigator's discretion, with an agreement of a washout period prior to 68Ga-NTA-476 dosing, if it is determined not to put the patient at an increased risk of adverse drug effects and/or interfere with the integrity of study outcome.
4. Eastern Cooperative Oncology Group (ECOG) performance status equal to or less than 2
5. Participants must have a life expectancy of more than 3 months in the opinion of the Investigator.
6. Male participants who are able to father a child must agree to avoid impregnating a partner and to adhere to a highly effective method of contraception during the study and for 14 days after the last injection of 68Ga-NTA-476. Participants must agree to not donate sperm during the study and for 14 days after the injection of 68Ga-NTA-476.
Minimum age
18 Years
Maximum age
No limit
Sex
Males
Can healthy volunteers participate?
No
Key exclusion criteria
7. Have any medical condition that would, in the Investigator’s judgment, prevent the participant’s full participation in the clinical study due to safety concerns or compliance with clinical study procedures, including but not limited to participants with severe claustrophobia.
8. Residual toxicity greater than Grade 1 from prior anti-cancer therapy (except alopecia). Participants with greater than Grade 1 toxicity from prior anti-cancer therapy may be approved on a case-by-case basis at the principal investigator's discretion, if it is determined not to put the patient at an increased risk of adverse drug effects and/or interfere with the integrity of study outcome.
9. History of uncontrolled allergic reactions and/or known or expected hypersensitivity to peptide therapeutics, including 68Ga-NTA-476 or any of its excipients.
10. Inadequate organ functions as reflected in laboratory parameters:
o Creatinine clearance (calculated using Cockcroft-Gault formula, or measured) less than 60 mL/min or serum creatinine greater than 1.5 x upper limit of normal (ULN)
o Platelet count of less than 75 x 10^9/L
o Absolute neutrophil count (ANC) less than 1.0 x 10^9/L
o Haemoglobin less than 9 g/dL
o Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) more than 3 x ULN, or more than 5 x ULN for patients with known liver metastases
o Total bilirubin more than 1.5 x ULN, except for patients with documented Gilbert’s syndrome who are eligible if total bilirubin equal to or less than 3 x ULN
11. For participants not taking warfarin or other anticoagulants: international normalised ratio (INR) equal to or more than 1.5 or prothrombin time (PT) equal to or more than 1.5 x ULN; and either partial thromboplastin time or activated partial thromboplastin time (PTT or aPTT) equal to or more than 1.5 x ULN. Participants taking warfarin must be on a stable dose that results in a stable INR less than 3.5. Among participants receiving other anticoagulant therapy, PT or aPTT must be within the intended therapeutic range of the anticoagulant.
12. Major surgery within 28 days prior to the dose of 68Ga-NTA-476. Exceptions may be approved on a case-by-case basis at the principal investigator's discretion, if it is determined not to put the participant at an increased risk of adverse drug effects and/or interfere with the integrity of study outcome.
13. Any uncontrolled intercurrent illness or clinically significant uncontrolled condition(s), including but not limited to active bacterial, fungal, or viral infections requiring systemic therapy.

Study design
Purpose of the study
Diagnosis
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Phase 0
Type of endpoint/s
Pharmacokinetics
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Date of first participant enrolment
Anticipated
31/07/2024
Actual
16/08/2024
Date of last participant enrolment
Anticipated
22/01/2025
Actual
Date of last data collection
Anticipated
22/01/2025
Actual
Sample size
Target
10
Accrual to date
1
Final
Recruitment in Australia
Recruitment state(s)
WA
Recruitment hospital [1] 25603 0
GenesisCare - Murdoch - Murdoch
Recruitment postcode(s) [1] 41428 0
6150 - Murdoch

Funding & Sponsors
Funding source category [1] 314924 0
Commercial sector/Industry
Name [1] 314924 0
3B Pharmaceuticals
Country [1] 314924 0
Germany
Primary sponsor type
Commercial sector/Industry
Name
GenesisCare
Address
Building 7C & D, Level 1, The Mill, 41-43 Bourke Road Alexandria NSW 2015
Country
Australia
Secondary sponsor category [1] 316929 0
None
Name [1] 316929 0
Address [1] 316929 0
Country [1] 316929 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 313915 0
Bellberry Human Research Ethics Committee
Ethics committee address [1] 313915 0
Ethics committee country [1] 313915 0
Australia
Date submitted for ethics approval [1] 313915 0
30/10/2023
Approval date [1] 313915 0
21/11/2023
Ethics approval number [1] 313915 0

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 129778 0
Dr Aviral Singh
Address 129778 0
GenesisCare, 100 Murdoch Drive, Murdoch WA 6150 (access via St John of God Murdoch Hospital, Gate 3
Country 129778 0
Australia
Phone 129778 0
+61 499583667
Fax 129778 0
Email 129778 0
aviral.singh@genesiscare.com
Contact person for public queries
Name 129779 0
Rebecca Nathan
Address 129779 0
GenesisCare, Building 7C & D, Level 1, The Mill, 41-43 Bourke Road Alexandria NSW 2015
Country 129779 0
Australia
Phone 129779 0
+61 429777325
Fax 129779 0
Email 129779 0
rebecca.nathan@genesiscare.com
Contact person for scientific queries
Name 129780 0
Rebecca Nathan
Address 129780 0
GenesisCare, Building 7C & D, Level 1, The Mill, 41-43 Bourke Road Alexandria NSW 2015
Country 129780 0
Australia
Phone 129780 0
+61429777325
Fax 129780 0
Email 129780 0
rebecca.nathan@genesiscare.com

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment
PICF does not allow for sharing of IPD


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.