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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/ct2/show/NCT01605227
Registration number
NCT01605227
Ethics application status
Date submitted
22/05/2012
Date registered
24/05/2012
Date last updated
14/03/2018
Titles & IDs
Public title
Study of Cabozantinib (XL184) Versus Prednisone in Men With Metastatic Castration-resistant Prostate Cancer Previously Treated With Docetaxel and Abiraterone or MDV3100
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Scientific title
A Phase 3, Randomized, Double-blind, Controlled Study of Cabozantinib (XL184) Versus Prednisone in Metastatic Castration-resistant Prostate Cancer Patients Who Have Received Prior Docetaxel and Prior Abiraterone or MDV3100
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Secondary ID [1]
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0
2012-001834-33
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Secondary ID [2]
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XL184-307
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Universal Trial Number (UTN)
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Trial acronym
COMET-1
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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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Castration Resistant Prostate Cancer
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Pain
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Prostatic Neoplasms
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Condition category
Condition code
Cancer
0
0
0
0
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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 - cabozantinib
Treatment: Drugs - prednisone
Experimental: cabozantinib - Subjects randomized to the cabozantinib arm will also receive placebo-matched prednisone capsules.
Active Comparator: prednisone - Subjects randomized to the prednisone arm will also receive placebo-matched cabozantinib.
Treatment: Drugs: cabozantinib
Tablets taken orally once-daily
Treatment: Drugs: prednisone
Taken twice a day orally. Commercially-obtained prednisone tablets will be over-encapsulated in order to blind identity.
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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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Overall Survival (OS)
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Assessment method [1]
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The primary analysis of OS is defined as the time from randomization to death due to any cause. Participants that had not died or were permanently lost to follow-up were censored at the last known date alive. Median OS was calculated using Kaplan-Meier estimates. Analysis for OS was performed after 614 events had occurred.
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Timepoint [1]
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OS was measured from the time of randomization until 614 events, approximately 24 months after study start
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Secondary outcome [1]
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Bone Scan Response (BSR)
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Assessment method [1]
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BSR is defined as >=30% reduction in the bone scan lesion area (BSLA) compared with baseline. Confirmation of bone scan was not required for response or progression. Bone scans were evaluated by an independent radiology facility (IRF) for response.
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Timepoint [1]
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BSR was measured at the end of Week 12 as determined by the IRF
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Eligibility
Key inclusion criteria
- Histological or cytological diagnosis of castration resistant prostate cancer (serum
testosterone less than 50 ng/dL).
- Evidence of bone metastasis related to prostate cancer on bone scans.
- Received prior docetaxel (minimum cumulative dose of 225 mg/m2) and either abiraterone
or MDV3100 treatment and has evidence of prostate cancer progression on each agent
independently.
- Maintenance of LHRH agonist or antagonist unless treated with orchiectomy.
- Recovered from toxicities related to any prior treatments, unless the toxicities are
clinically non significant or easily manageable.
- Adequate organ and marrow function.
- Capable of understanding and complying with the protocol requirements and signed the
informed consent form.
- Sexually active fertile patients and their partners must agree to use medically
accepted methods of contraception (eg, barrier methods, including male condom, female
condom, or diaphragm with spermicidal gel) during the course of the study and for 4
months after the last dose of study treatment.
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Minimum age
18
Years
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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 cabozantinib.
- Treatment with docetaxel, abiraterone, or MDV3100 in the last 2 weeks; or with any
other type of cytotoxic or investigational anticancer agent in the last 2 weeks.
- Radiation within 4 weeks (excluded if to mediastinum) or radionuclide treatment within
6 weeks of randomization.
- Known brain metastases or cranial epidural disease.
- Requires concomitant treatment, in therapeutic doses, with anticoagulants.
- Requires chronic concomitant treatment of strong CYP3A4 inducers (eg, dexamethasone,
phenytoin, carbamazepine, rifampin, rifabutin, rifapentin, phenobarbital, and St.
John's Wort).
- Uncontrolled, significant intercurrent illness including, but not limited to,
cardiovascular disorders, gastrointestinal disorders, active infections, non-healing
wounds, recent surgery.
- Clinically significant hematemesis or hemoptysis, or other signs indicative of
pulmonary hemorrhage in the last 3 months, or history of other significant bleeding in
the past 6 months.
- Cavitating pulmonary lesion(s) or a lesion invading or encasing a major blood vessel.
- QTcF > 500 ms within 7 days of randomization.
- Unable to swallow capsules or tablets.
- Previously-identified allergy or hypersensitivity to components of the study treatment
formulations.
- Another diagnosis of malignancy requiring systemic treatment within 2 years of
randomization.
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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
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
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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
Completed
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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
1/07/2012
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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
1/03/2015
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Sample size
Target
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Accrual to date
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Final
1028
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA,TAS,VIC,WA
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Recruitment hospital [1]
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- Albury
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- Concord
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- Darlinghurst
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2640 - Albury
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2193 - Concord
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2010 - Darlinghurst
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2217 - Kogarah
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2444 - Port Macquarie
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2031 - Randwick
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2076 - Wahroonga
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2145 - Westmead
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4101 - South Brisbane
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4215 - Southport
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4102 - Woolloongabba
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5000 - Adelaide
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5037 - Kurralta Park
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7000 - Hobart
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3165 - Bentleigh East
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3128 - Box Hill
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3690 - Wodonga
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6000 - Perth
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Recruitment outside Australia
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Italy
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State/province [116]
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Pavia
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Country [117]
0
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Italy
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Pisa
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Country [118]
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Italy
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Pordenone
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Italy
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Ravenna
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Italy
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Rimini
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0
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Italy
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Roma
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Italy
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Rozzano
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0
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Italy
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Terni
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Country [124]
0
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Italy
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Torino
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Country [125]
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Italy
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Verona
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Netherlands
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Amsterdam
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Country [127]
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Netherlands
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Groningen
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Country [128]
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Netherlands
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Hoofddorp
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Netherlands
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Nieuwegein
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Netherlands
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Nijmegen
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Netherlands
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Rotterdam
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Netherlands
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Tilburg
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0
Netherlands
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Zwolle
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0
Puerto Rico
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Ponce
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Country [135]
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Spain
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Andalucía
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Country [136]
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Spain
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Asturias
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Country [137]
0
0
Spain
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Baleares
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Country [138]
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Spain
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Canarias
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Country [139]
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Spain
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Cataluña
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Country [140]
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Spain
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State/province [140]
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Comunidad Valenciana
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Spain
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Galicia
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Country [142]
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Spain
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Madrid, Communidad De
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Country [143]
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Spain
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Navarra
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Country [144]
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Sweden
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Gotenborg
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Sweden
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Malmo
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Country [146]
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Sweden
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Orebro
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Country [147]
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Sweden
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Stockholm
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Country [148]
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Sweden
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State/province [148]
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Umea
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Country [149]
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Sweden
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State/province [149]
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Uppsala
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Country [150]
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Sweden
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State/province [150]
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Vaxjo
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Country [151]
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United Kingdom
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State/province [151]
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Aberdeen
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Country [152]
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United Kingdom
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Bath
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Country [153]
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United Kingdom
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Birmingham
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Country [154]
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United Kingdom
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Brighton
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Country [155]
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United Kingdom
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Bristol
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United Kingdom
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Cambridge
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Country [157]
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United Kingdom
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Cardiff
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Country [158]
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United Kingdom
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Cottingham
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Country [159]
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United Kingdom
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Edinburgh
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Country [160]
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United Kingdom
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State/province [160]
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Inverness
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Country [161]
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United Kingdom
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Lancaster
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Country [162]
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United Kingdom
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Leeds
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Country [163]
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United Kingdom
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London
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Country [164]
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United Kingdom
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Maidstone
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Country [165]
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United Kingdom
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Northwood
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Country [166]
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United Kingdom
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State/province [166]
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Plymouth
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Country [167]
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United Kingdom
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Sheffield
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Country [168]
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United Kingdom
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Southampton
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Country [169]
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United Kingdom
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Sutton
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Country [170]
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United Kingdom
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State/province [170]
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Wirral
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Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
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Name
Exelixis
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
This study will evaluate the effect of cabozantinib compared to prednisone on overall
survival in men with previously treated metastatic castration-resistant prostate cancer with
bone-dominant disease who have experienced disease progression on docetaxel-containing
chemotherapy and abiraterone or MDV3100.
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Trial website
https://clinicaltrials.gov/ct2/show/NCT01605227
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
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Contact person for scientific queries
Summary Results
For IPD and results data, please see
https://clinicaltrials.gov/ct2/show/NCT01605227
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