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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT04340193
Registration number
NCT04340193
Ethics application status
Date submitted
7/04/2020
Date registered
9/04/2020
Date last updated
11/01/2024
Titles & IDs
Public title
A Study of Nivolumab and Ipilimumab and Nivolumab Alone in Combination With Trans-arterial ChemoEmbolization (TACE) in Participants With Intermediate Stage Liver Cancer
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Scientific title
A Randomized, Multi-center, Double-blinded, Placebo-controlled Phase 3 Study of Nivolumab and Ipilimumab, Nivolumab Monotherapy, or Placebo in Combination With Trans-arterial ChemoEmbolization (TACE) in Patients With Intermediate-stage Hepatocellular Carcinoma (HCC)
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Secondary ID [1]
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CA209-74W
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Universal Trial Number (UTN)
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Trial acronym
CheckMate 74W
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Cancer, Hepatocellular
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Condition category
Condition code
Cancer
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Liver
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Oral and Gastrointestinal
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Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
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Intervention/exposure
Study type
Interventional(has expanded access)
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Description of intervention(s) / exposure
Treatment: Drugs - nivolumab
Treatment: Drugs - ipilimumab
Treatment: Surgery - TACE
Experimental: Nivolumab + Ipilimumab + TACE - TACE (Trans-arterial ChemoEmbolization)
Experimental: Nivolumab + TACE -
Active comparator: TACE -
Treatment: Drugs: nivolumab
Specified dose on specified days
Treatment: Drugs: ipilimumab
Specified dose on specified days
Treatment: Surgery: TACE
TACE (Trans-arterial ChemoEmbolization)
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Intervention code [1]
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Treatment: Drugs
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Intervention code [2]
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Treatment: Surgery
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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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Number of treated participants with adverse events (AEs)
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Assessment method [1]
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Timepoint [1]
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Up to 2 years and 4 months
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Primary outcome [2]
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Number of deaths in all treated patients
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Assessment method [2]
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Timepoint [2]
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Up to 2 years and 4 months
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Primary outcome [3]
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Number of treated participants with laboratory abnormalities
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Assessment method [3]
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Timepoint [3]
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Up to 2 years and 4 months
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Eligibility
Key inclusion criteria
* Participant has intermediate-stage hepatocellular carcinoma (HCC) whose tumor characteristics exceed the Beyond Milan and Up-to-7 (BMU7) criteria and is eligible for trans-arterial ChemoEmbolization (TACE)
* Participant has no extrahepatic spreading (EHS), no regional lymph node involvement, no main, left main, or right main portal vein thrombosis, and no macrovascular invasion (MVI)
* Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 or 1
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* Known fibrolamellar HCC, sarcomatoid HCC, or mixed cholangiocarcinoma and HCC
* Prior liver transplant or participants who are on the waiting list for liver transplantation
* Active, known, or suspected autoimmune disease
Other protocol defined inclusion/exclusion criteria apply
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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
15/09/2020
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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
12/12/2023
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Sample size
Target
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Accrual to date
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Final
26
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA,VIC,WA
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Recruitment hospital [1]
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Local Institution - Wollongong
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Local Institution - 0037 - Birtinya
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Local Institution - 0010 - Adelaide
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Local Institution - 0001 - Melbourne
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Local Institution - 0139 - Murdoch
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2500 - Wollongong
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4560 - Birtinya
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5000 - Adelaide
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3065 - Melbourne
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Recruitment postcode(s) [5]
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6150 - Murdoch
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Bristol-Myers Squibb
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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 evaluate the safety and tolerability of nivolumab with and without ipilimumab in combination with Trans-arterial ChemoEmbolization (TACE) to TACE alone in participants with intermediate liver cancer.
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Trial website
https://clinicaltrials.gov/study/NCT04340193
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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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Bristol-Myers Squibb
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Address
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Bristol-Myers Squibb
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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/NCT04340193
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