Expanded Access to Telisotuzumab Vedotin

Last updated: September 30, 2025
Sponsor: AbbVie
Overall Status: Planned

Phase

N/A

Condition

N/A

Treatment

Telisotuzumab vedotin

Clinical Study ID

NCT04830202
C20-503
  • Ages > 18
  • All Genders

Study 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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

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

Study Design

Treatment Group(s): 1
Primary Treatment: Telisotuzumab vedotin
Phase:
Study Start date:
Estimated Completion Date:

Connect with a study center

  • Western Heamatology and Oncology Clinics /ID# 243364

    West Perth, Western Australia 6005
    Australia

    Site Not Available

  • University Hospital Cologne /ID# 254773

    Cologne, 50937
    Germany

    Site Not Available

  • Asklepios Fachkliniken Muenchen-Gauting /ID# 259196

    Gauting, 82131
    Germany

    Site Not Available

  • Hong Kong United Oncology Centre /ID# 241857

    Yau Ma Tei,
    Hong Kong

    Site Not Available

  • The Chaim Sheba Medical Center /ID# 256530

    Ramat Gan, Tel-Aviv 5265601
    Israel

    Site Not Available

  • Shaare Zedek Medical Center /ID# 252374

    Jerusalem, 91031
    Israel

    Site Not Available

  • Rabin Medical Center /ID# 228611

    Petakh Tikva, 4941492
    Israel

    Site Not Available

  • Sutter Medical Group /ID# 254816

    Sacramento, California 95816
    United States

    Site Not Available

  • Oncology & Hematology Specialist /ID# 248083

    Mountain Lakes, New Jersey 07046-1743
    United States

    Site Not Available

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