Expanded Access to Telisotuzumab Vedotin

May 11, 2026 updated by: AbbVie
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.

Study Overview

Status

Temporarily not available

Conditions

Intervention / Treatment

Study Type

Expanded Access

Expanded Access Type

  • Individual Patients

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Australia
    • Western Australia
      • West Perth, Western Australia, Australia, 6005
        • Available
        • Western Heamatology and Oncology Clinics /ID# 243364
  • Germany
      • Cologne, Germany, 50937
        • Available
        • University Hospital Cologne /ID# 254773
      • Gauting, Germany, 82131
        • Available
        • Asklepios Fachkliniken Muenchen-Gauting /ID# 259196
  • Hong Kong
      • Yau Ma Tei, Hong Kong
        • Available
        • Hong Kong United Oncology Centre /ID# 241857
  • Israel
      • Jerusalem, Israel, 91031
        • Available
        • Shaare Zedek Medical Center /ID# 252374
      • Petakh Tikva, Israel, 4941492
        • Available
        • Rabin Medical Center /ID# 228611
    • Tel-Aviv
      • Ramat Gan, Tel-Aviv, Israel, 5265601
        • Available
        • The Chaim Sheba Medical Center /ID# 256530
  • United States
    • California
      • Sacramento, California, United States, 95816
        • Available
        • Sutter Medical Group /ID# 254816
    • New Jersey
      • Mountain Lakes, New Jersey, United States, 07046-1743
        • Available
        • Oncology & Hematology Specialist /ID# 248083

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Exclusion Criteria:

  • There are other suitable treatment options.
  • The participant qualifies for ongoing clinical trials.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

AbbVie

Investigators

  • Study Director: ABBVIE INC., AbbVie

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

December 7, 2022

Primary Completion

December 7, 2022

Study Completion

December 7, 2022

Study Registration Dates

First Submitted

March 31, 2021

First Submitted That Met QC Criteria

March 31, 2021

First Posted (Actual)

April 5, 2021

Study Record Updates

Last Update Posted (Actual)

May 13, 2026

Last Update Submitted That Met QC Criteria

May 11, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • C20-503

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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