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Clinical Trial Details — Status: Available

Administrative data

NCT number NCT04830202
Other study ID # C20-503
Secondary ID
Status Available
Phase
First received
Last updated

Study information

Verified date April 2024
Source AbbVie
Contact ABBVIE CALL CENTER
Phone 844-663-3742
Email abbvieclinicaltrials@abbvie.com
Is FDA regulated No
Health authority
Study type Expanded Access

Clinical Trial 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.


Recruitment information / eligibility

Status Available
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - The participant must not be eligible for a telisotuzumab vedotin clinical trial.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Telisotuzumab vedotin
Intravenous Infusion

Locations

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

Sponsors (1)

Lead Sponsor Collaborator
AbbVie

Countries where clinical trial is conducted

United States,  Australia,  Germany,  Hong Kong,  Israel, 

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