Expanded Access to Telisotuzumab Vedotin

NCT ID: NCT04830202

Last Updated: 2025-10-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

AVAILABLE

Study Classification

EXPANDED_ACCESS

Brief Summary

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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.

Detailed Description

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Conditions

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Non-Small Cell Lung Cancer (NSCLC)

Interventions

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Telisotuzumab vedotin

Intravenous Infusion

Intervention Type DRUG

Other Intervention Names

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ABBV-399

Eligibility Criteria

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Inclusion Criteria

\- The participant must not be eligible for a telisotuzumab vedotin clinical trial.
Minimum Eligible Age

18 Years

Eligible Sex

Accepts Healthy Volunteers

No

Sponsors

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AbbVie

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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ABBVIE INC.

Role: STUDY_DIRECTOR

AbbVie

Central Contacts

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ABBVIE CALL CENTER

Role: CONTACT

844-663-3742

Other Identifiers

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C20-503

Identifier Type: -

Identifier Source: org_study_id

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