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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/show/NCT02743494




Registration number
NCT02743494
Ethics application status
Date submitted
15/04/2016
Date registered
19/04/2016
Date last updated
22/05/2020

Titles & IDs
Public title
An Investigational Immuno-therapy Study of Nivolumab or Placebo in Participants With Resected Esophageal or Gastroesophageal Junction Cancer
Scientific title
A Randomized, Multicenter, Double Blind, Phase III Study of Adjuvant Nivolumab or Placebo in Subjects With Resected Esophageal, or Gastroesophageal Junction Cancer
Secondary ID [1] 0 0
2015-005556-10
Secondary ID [2] 0 0
CA209-577
Universal Trial Number (UTN)
Trial acronym
CheckMate 577
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Advanced Cancer 0 0
Condition category
Condition code

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - Nivolumab
Other interventions - Placebo

Experimental: Nivolumab -

Placebo Comparator: Placebo -


Treatment: Drugs: Nivolumab
Specified dose on specified days

Other interventions: Placebo
Specified dose on specified days

Intervention code [1] 0 0
Treatment: Drugs
Intervention code [2] 0 0
Other interventions
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Disease-Free Survival of adjuvant nivolumab in participants with resected esophageal cancer or gastroesophageal junction cancer who have received chemoradiotherapy followed by surgery
Timepoint [1] 0 0
Approximately 58 months after the first participant is randomized
Secondary outcome [1] 0 0
Overall Survival of adjuvant nivolumab in participants with resected esophageal cancer or gastroesophageal junction cancer who have received chemoradiotherapy followed by surgery
Timepoint [1] 0 0
Approximately 77 months after the participant is randomized
Secondary outcome [2] 0 0
Overall survival rate
Timepoint [2] 0 0
Overall survival rate at 1, 2, and 3 years

Eligibility
Key inclusion criteria
- Diagnosed with Stage II/III carcinoma of the esophagus or gastroesophageal junction

- Completed pre-operative chemo radiotherapy followed by surgery

- Diagnosed with residual pathologic disease after being surgically rendered free of
disease with negative margins following complete resection
Minimum age
18 Years
Maximum age
No limit
Gender
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
- Diagnosed with cervical esophageal carcinoma

- Diagnosed with Stage IV resectable disease

- Did not receive concurrent chemoradiotherapy prior to surgery

- Participants who have received a live/attenuated vaccine within 30 days of the first
treatment

Other protocol defined Inclusion/exclusion criteria could apply

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled 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
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s


The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 3
Type of endpoint(s)
Statistical methods / analysis

Recruitment
Recruitment status
Active, not recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA,TAS,VIC,WA
Recruitment hospital [1] 0 0
Local Institution - Blacktown
Recruitment hospital [2] 0 0
Local Institution - Gosford
Recruitment hospital [3] 0 0
Royal North Shore Hospital - St Leonards
Recruitment hospital [4] 0 0
Local Institution - Tamworth
Recruitment hospital [5] 0 0
Local Institution - Brisbane
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Royal Adelaide Hospital - Adelaide
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Royal Hobart Hospital - Hobart
Recruitment hospital [8] 0 0
Monash Medical Centre Clayton - Clayton
Recruitment hospital [9] 0 0
Local Institution - Perth
Recruitment postcode(s) [1] 0 0
2148 - Blacktown
Recruitment postcode(s) [2] 0 0
2250 - Gosford
Recruitment postcode(s) [3] 0 0
2065 - St Leonards
Recruitment postcode(s) [4] 0 0
2340 - Tamworth
Recruitment postcode(s) [5] 0 0
4102 - Brisbane
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5000 - Adelaide
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7000 - Hobart
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3168 - Clayton
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6150 - Perth
Recruitment outside Australia
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Argentina
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Buenos Aires
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Santa FE
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Bruxelles
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Edegem
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Switzerland
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Turkey
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Adana
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Erzurum
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Istanbul
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United Kingdom
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Greater London
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Hampshire
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Manchester
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Cardiff
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United Kingdom
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London

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
Bristol-Myers Squibb
Address
Country
Other collaborator category [1] 0 0
Commercial sector/Industry
Name [1] 0 0
Ono Pharmaceutical Co. Ltd
Address [1] 0 0
Country [1] 0 0

Ethics approval
Ethics application status

Summary
Brief summary
The primary purpose of this study is to determine whether Nivolumab will improve disease-free
survival compared with placebo.
Trial website
https://clinicaltrials.gov/show/NCT02743494
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Bristol-Myers Squibb
Address 0 0
Bristol-Myers Squibb
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

Summary results
Other publications