drugset / Trial / NCT00884715

Pharmacokinetics, Efficacy and Safety of an Octreotide Implant in Patients With Carcinoid Syndrome

NCT00884715

Phase 1/2 Terminated 10 enrolled Endo USA Inc., a Keenova Therapeutics Company
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Evaluate the pharmacokinetics, safety and efficacy of an octreotide implant for the treatment of the symptoms of carcinoid syndrome.

Timeline

Start
2009-07
Primary completion
2011-11
Completion
2011-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Octreotide Peptide 117 mg Subcutaneous
Subject Octreotide Peptide 234 mg Subcutaneous

Indications