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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT04830202
Registration number
NCT04830202
Ethics application status
Date submitted
31/03/2021
Date registered
5/04/2021
Date last updated
3/04/2024
Titles & IDs
Public title
Expanded Access to Telisotuzumab Vedotin
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Scientific title
Expanded Access to Telisotuzumab Vedotin
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Secondary ID [1]
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C20-503
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Non-Small Cell Lung Cancer (NSCLC)
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0
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Condition category
Condition code
Cancer
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0
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Lung - Non small cell
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Intervention/exposure
Study type
Expanded Access
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Description of intervention(s) / exposure
Treatment: Drugs - Telisotuzumab vedotin
Treatment: Drugs: Telisotuzumab vedotin
Intravenous Infusion
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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
Eligibility
Key inclusion criteria
- The participant must not be eligible for a telisotuzumab vedotin clinical trial.
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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
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Study design
Purpose of the study
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Allocation to intervention
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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?
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Intervention assignment
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Other design features
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Phase
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
AVAILABLE
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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
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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
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Sample size
Target
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
WA
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Recruitment hospital [1]
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Western Heamatology and Oncology Clinics /ID# 243364 - West Perth
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Recruitment postcode(s) [1]
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6005 - West Perth
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Recruitment outside Australia
Country [1]
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United States of America
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State/province [1]
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California
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Country [2]
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United States of America
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State/province [2]
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New Jersey
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Country [3]
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Germany
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State/province [3]
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Cologne
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Country [4]
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Germany
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State/province [4]
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Gauting
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Country [5]
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Hong Kong
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State/province [5]
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Yau Ma Tei
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Country [6]
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Israel
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State/province [6]
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Tel-Aviv
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Country [7]
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Israel
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State/province [7]
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Jerusalem
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Country [8]
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Israel
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State/province [8]
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Petakh Tikva
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
AbbVie
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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 is an expanded access program (EAP) for eligible participants. This program is designed to provide access to Telisotuzumab vedotin prior to approval by the local regulatory agency. Availability will depend on territory eligibility. A medical doctor must decide whether the potential benefit outweighs the risk of receiving an investigational therapy based on the individual patient's medical history and program eligibility criteria.
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Trial website
https://clinicaltrials.gov/study/NCT04830202
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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ABBVIE INC.
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Address
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AbbVie
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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ABBVIE CALL CENTER
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Address
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Country
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Phone
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844-663-3742
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Fax
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Email
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[email protected]
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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/NCT04830202
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