Last updated: September 30, 2025
Sponsor: AbbVie
Overall Status: Planned
Phase
N/A
Condition
N/ATreatment
Telisotuzumab vedotin
Clinical Study ID
NCT04830202
C20-503
Ages > 18 All Genders
Study Summary
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
AustraliaSite Not Available
University Hospital Cologne /ID# 254773
Cologne, 50937
GermanySite Not Available
Asklepios Fachkliniken Muenchen-Gauting /ID# 259196
Gauting, 82131
GermanySite Not Available
Hong Kong United Oncology Centre /ID# 241857
Yau Ma Tei,
Hong KongSite Not Available
The Chaim Sheba Medical Center /ID# 256530
Ramat Gan, Tel-Aviv 5265601
IsraelSite Not Available
Shaare Zedek Medical Center /ID# 252374
Jerusalem, 91031
IsraelSite Not Available
Rabin Medical Center /ID# 228611
Petakh Tikva, 4941492
IsraelSite Not Available
Sutter Medical Group /ID# 254816
Sacramento, California 95816
United StatesSite Not Available
Oncology & Hematology Specialist /ID# 248083
Mountain Lakes, New Jersey 07046-1743
United StatesSite Not Available

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