drugset / Trial / NCT00765323

Efficacy and Safety Study of Octreotide Implant in Patients With Acromegaly

NCT00765323

Phase 3 Terminated 169 enrolled Endo USA Inc., a Keenova Therapeutics Company
RandomizedParallel-groupOpen-labelTreatment

Summary

Evaluate the efficacy, safety and tolerability of the octreotide implant in patients with acromegaly that were previously treated with octreotide depot.

Timeline

Start
2008-09
Primary completion
2011-02
Completion
2011-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator Octreotide Peptide 10 mg Subcutaneous
Comparator Octreotide Peptide 20 mg Subcutaneous
Comparator Octreotide Peptide 30 mg Subcutaneous
Comparator Octreotide Peptide 40 mg Subcutaneous
Comparator Octreotide Peptide 84 mg Subcutaneous

Indications