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Expanded Access to Telisotuzumab Vedotin

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT04830202
Expanded Access Status : Available
First Posted : April 5, 2021
Last Update Posted : April 3, 2024
Information provided by (Responsible Party):

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.

Condition or disease Intervention/treatment
Non-Small Cell Lung Cancer (NSCLC) Drug: Telisotuzumab vedotin

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Study Type : Expanded Access
Expanded Access Type : Individual Patients
  See clinical trials of the intervention/treatment in this expanded access record.
Official Title: Expanded Access to Telisotuzumab Vedotin

Resource links provided by the National Library of Medicine

Intervention Details:
  • Drug: Telisotuzumab vedotin
    Intravenous Infusion
    Other Name: ABBV-399

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers:   No

Inclusion Criteria:

- The participant must not be eligible for a telisotuzumab vedotin clinical trial.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT04830202

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Contact: ABBVIE CALL CENTER 844-663-3742

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United States, California
Sutter Medical Group /ID# 254816 Available
Sacramento, California, United States, 95816
United States, New Jersey
Oncology & Hematology Specialist /ID# 248083 Available
Mountain Lakes, New Jersey, United States, 07046-1743
Australia, Western Australia
Western Heamatology and Oncology Clinics /ID# 243364 Available
West Perth, Western Australia, Australia, 6005
University Hospital Cologne /ID# 254773 Available
Cologne, Germany, 50937
Asklepios Fachkliniken Muenchen-Gauting /ID# 259196 Available
Gauting, Germany, 82131
Hong Kong
Hong Kong United Oncology Centre /ID# 241857 Available
Yau Ma Tei, Hong Kong
The Chaim Sheba Medical Center /ID# 256530 Available
Ramat Gan, Tel-Aviv, Israel, 5265601
Shaare Zedek Medical Center /ID# 252374 Available
Jerusalem, Israel, 91031
Rabin Medical Center /ID# 228611 Available
Petakh Tikva, Israel, 4941492
Sponsors and Collaborators
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Study Director: ABBVIE INC. AbbVie
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Responsible Party: AbbVie Identifier: NCT04830202    
Other Study ID Numbers: C20-503
First Posted: April 5, 2021    Key Record Dates
Last Update Posted: April 3, 2024
Last Verified: April 2024
Keywords provided by AbbVie:
Non-Small Cell Lung Cancer (NSCLC)
Telisotuzumab vedotin
Expanded Access
Pre-approval Access
Compassionate Use
Special Access Program
Named Patient Basis
Special Access Scheme
Additional relevant MeSH terms:
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Carcinoma, Non-Small-Cell Lung
Lung Neoplasms
Respiratory Tract Neoplasms
Thoracic Neoplasms
Neoplasms by Site
Lung Diseases
Respiratory Tract Diseases
Carcinoma, Bronchogenic
Bronchial Neoplasms