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A Long-term Follow-up Study of Patients Who Received VOR33 Summary VOR33 long-term follow-up (LTFU) study
View Full Description Full Description VBP201 study is the VOR33 long-term follow-up (LTFU) study focusing on assessing long term safety and efficacy of VOR33. This study may last up to 15 years (counted from the date of VOR33 infusion completion). All patients who have participated in a study involving the drug product VOR33 and have completed the applicable study or prematurely discontinued, but have at least received the VOR33 infusion, will be asked to participate in the LTFU study.
View Eligibility Criteria Eligibility Criteria Inclusion Criteria: A patient is included in this study if he/she: Has received any part of or all of a VOR33 infusion Exclusion Criteria: There are no exclusion criteria.
Check Your Eligibility
Let’s see if you might be eligible for this study.
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There are 9 Locations for this study
University of California San Diego Moores Cancer Center La Jolla California, 92037, United States
More Info
Miami Cancer Institute Miami Florida, 33176, United States
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Washington University School of Medicine Siteman Cancer Center Saint Louis Missouri, 63110, United States
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John Theurer Cancer Center at Hackensack University Medical Center Hackensack New Jersey, 07601, United States
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Columbia University Medical Center - Herbert Irving Comprehensive Cancer Center New York New York, 10032, United States
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Memorial Sloan Kettering Cancer Center New York New York, 10065, United States
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University Hospitals Seidman Cancer Center Cleveland Ohio, 44106, United States
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Fred Hutchinson Cancer Research Center Seattle Washington, 98109, United States
More Info
Hôpital Maisonneuve-Rosemont Montréal Quebec, H1T 2, Canada
More Info How clear is this clinincal trial information?
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