An observational time and motion study in a clinical oncology setting is utilized in order to
measure and compare product attributes and overall product efficiency between lanreotide and
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Locations near you
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Full eligibility criteria for NCT03017690
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Men and women must be 18 years of age or older
A current diagnosis of advanced, unresectable GEP-NET
Provided written informed consent to participate in the study
Currently receiving lanreotide or octreotide LAR and has received at least one prior injection of current somatostatin analogues (SSA).
Receiving treatment with lanreotide or octreotide LAR as part of a clinical trial
Scheduled to receive a dose of lanreotide or octreotide LAR that would necessitate more than 1 injection on the same day
Scheduled to receive any other treatment in the infusion center/room on the same day and as part of the same appointment
Known hypersensitivity to somatostatin analogues
All locations for NCT03017690
United States (5)
Tucson, Arizona, United States, 85719
Ochsner Medical Center Kenner
Kenner, Louisiana, United States, 70065
Mercy Medical Center
Baltimore, Maryland, United States, 21202
National Translational Research Group
East Setauket, New York, United States, 11733
Oncology Specialists of Charlotte
Charlotte, North Carolina, United States, 28207
View full eligibility
Tris trial is registered with FDA with number: NCT03017690. The sponsor of the trial is Ipsen and it is looking for 22 volunteers for the current phase.
Official trial title: Lanreotide and Octreotide LAR for Patients With Advanced Gastroenteropancreatic Neuroendocrine Tumors (GEP-NETs): An Observational Time and Motion Analysis
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