Registry Study for Talimogene Laherparepvec



Status:Enrolling by invitation
Conditions:Skin Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - 99
Updated:3/16/2019
Start Date:April 27, 2010
End Date:March 23, 2023

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A Registry Study to Evaluate the Survival and Long-Term Safety of Subjects Who Previously Received Talimogene Laherparepvec in Amgen or BioVEX-Sponsored Clinical Trials

A Registry Study to Evaluate the Survival and Long-Term Safety of Subjects Who Previously
Received Talimogene Laherparepvec in Amgen or BioVEX-Sponsored Clinical Trials

A registry study is to evaluate the overall survival, use of subsequent anti-cancer therapy,
and the long-term safety of subjects who have received at least one dose of talimogene
laherparepvec on an Amgen or BioVEX-sponsored clinical trial for any tumor type. Follow-Up
will occur every 3 months.

Inclusion Criteria:

All subjects must provide informed consent prior to initiation of any study activities.

All subjects must have received at least one dose of talimogene laherparepvec on an Amgen
or BioVEX-sponsored clinical trial for any tumor type and must have discontinued treatment
and participation, including long-term follow-up (if applicable) in that trial.

Exclusion Criteria:

Subjects currently receiving talimogene laherparepvec in Amgen or BioVEX-sponsored clinical
trial.

Subject currently participating, including for long-term follow-up (if applicable), in
other Amgen-sponsored talimogene laherparepvec clinical trial.
We found this trial at
27
sites
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Mobile, AL
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Aurora, CO
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Canton, OH
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Chapel Hill, NC
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Dallas, TX
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Franklin, WI
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Germantown, TN
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Greenville, South Carolina 29605
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Houston, TX
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Indianapolis, IN
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Jacksonville, FL
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Little Rock, AR
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Miami Beach, FL
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Minneapolis, MN
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Morristown, NJ
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Murray, UT
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Nashville, TN
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New Brunswick, New Jersey 08901
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New Brunswick, NJ
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Park Ridge, IL
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Portland, OR
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Saint Louis, MO
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Salt Lake City, UT
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Salzburg,
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Santa Rosa, CA
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Tampa, FL
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Winston-Salem, NC
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