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A Postmarketing Prospective Cohort Study of Melanoma Patients Treated With IMLYGIC® in Clinical Practice to Characterize Risk of Herpetic Infection Among Patients, Close Contacts, Health Care Providers & Long-term Safety in Treated Patients
A postmarketing Cohort study of Melanoma patients treated with IMLYGIC (Talimogene Laherparepvec) in clinical Practice to Characterize the risk of herpetic infection with detection of Talimogene Laherparepvec DNA among patients, close contacts, and health care providers; and long term safety in treated patients for up to 5 years after the first IMLYGIC dose.
Age
All ages
Sex
ALL
Healthy Volunteers
No
Corazon United States of America, LLC doing business as Life Clinical Trials
Coral Springs, Florida, United States
Mercy Medical Center
Baltimore, Maryland, United States
Jefferson City Medical Group PC
Jefferson City, Missouri, United States
TriHealth Cancer Institute - Kenwood
Cincinnati, Ohio, United States
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania, United States
Allegheny Health Network
Pittsburgh, Pennsylvania, United States
University of Tennessee Medical Center
Knoxville, Tennessee, United States
Intermountain Medical Center
Murray, Utah, United States
University of Wisconsin Hospital and Clinics
Madison, Wisconsin, United States
Medizinische Universitaet Graz
Graz, Austria
Start Date
August 10, 2017
Primary Completion Date
January 30, 2026
Completion Date
January 30, 2026
Last Updated
February 5, 2026
187
ACTUAL participants
Lead Sponsor
Amgen
NCT05039801
NCT06066138
Data Source & Attribution
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