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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT02438007
Registration number
NCT02438007
Ethics application status
Date submitted
19/03/2015
Date registered
8/05/2015
Date last updated
15/03/2023
Titles & IDs
Public title
A Study of Galeterone Compared to Enzalutamide In Men Expressing Androgen Receptor Splice Variant-7 mRNA (AR-V7) Metastatic CRPC
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Scientific title
ARMOR3-SV: A Phase 3, Randomized, Open Label, Multi-Center, Controlled Study of Galeterone Compared to Enzalutamide in Men Expressing Androgen Receptor Splice Variant-7 mRNA (AR-V7) Metastatic (M1) Castrate Resistant Prostate Cancer (CRPC)
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Secondary ID [1]
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ARMOR3-SV
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Universal Trial Number (UTN)
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Trial acronym
ARMOR3-SV
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Prostate Cancer
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Condition category
Condition code
Cancer
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Prostate
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - Galeterone
Treatment: Drugs - Enzalutamide
Experimental: Galeterone -
Active comparator: Enzalutamide -
Treatment: Drugs: Galeterone
2550 mg galeterone tablets once daily PO
Treatment: Drugs: Enzalutamide
160 mg enzalutamide capsules once daily PO
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Intervention code [1]
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Treatment: Drugs
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Radiographic Progression-free survival
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Assessment method [1]
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Timepoint [1]
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= 8 months
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Secondary outcome [1]
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Overall Survival
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Assessment method [1]
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Timepoint [1]
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= 8 months
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Secondary outcome [2]
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Time to Initiation of Cytotoxic Chemotherapy
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Assessment method [2]
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Timepoint [2]
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= 8 months
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Eligibility
Key inclusion criteria
* Progressive metastatic (M1) disease on androgen deprivation therapy
* Detectable AR-V7 from circulating tumors (CTCs)
* ECOG performance status 0 or 1
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Minimum age
18
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Maximum age
No limit
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Sex
Males
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Can healthy volunteers participate?
No
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Key exclusion criteria
* Prior treatment with second generation anti-androgens (e.g. abiraterone, enzalutamide)
* Prior treatment with chemotherapy for CRPC
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 3
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Stopped early
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/06/2015
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
1/11/2016
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Sample size
Target
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Accrual to date
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Final
953
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA,VIC
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Recruitment hospital [1]
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St. George Private Hospital, Oncology Day Care Centre - Kogarah
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Recruitment hospital [2]
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Ashford Cancer Centre/Adelaide Cancer Centre Research - Kurralta Park
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North Coast Cancer Institute - Port Macquarie
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Prince of Wales Hospital - Randwick
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Macquarie University - Sydney
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Peninsula Specialist Centre - Kippa-Ring
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ICON Cancer Care - Southport
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Princess Alexandra Hospital - Woolloongabba
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Box Hill Hospital - Box Hill
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Monash Medical Centre - East Bentleigh
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Peter MacCallum Cancer Centre - East Melbourne
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Cabrini Hospital - Malvern
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2217 - Kogarah
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5037 - Kurralta Park
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2444 - Port Macquarie
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2031 - Randwick
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2109 - Sydney
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4102 - Kippa-Ring
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4215 - Southport
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4102 - Woolloongabba
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3128 - Box Hill
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3165 - East Bentleigh
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3002 - East Melbourne
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3144 - Malvern
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
LTN PHARMACEUTICALS, INC.
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Address
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Ethics approval
Ethics application status
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Summary
Brief summary
The purpose of this study is to compare galeterone to enzalutamide in men expressing androgen receptor spice variant-7 mRNA (AR-V7) in metastatic (M1) castrate resistant prostate cancer (CRPC).
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Trial website
https://clinicaltrials.gov/study/NCT02438007
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Trial related presentations / publications
Aragon-Ching JB. The promising role of poly(ADP-ribose) polymerase inhibitors in prostate cancer. Asian J Androl. 2016 Jul-Aug;18(4):592-3. doi: 10.4103/1008-682X.172821.
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Public notes
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Contacts
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT02438007
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