Clinical Trials · NCT01278342

Study to Evaluate the Efficacy and Safety of Sandostatin LAR at High Dose or in Combination Either With GH-receptor Antagonist or Dopamine-agonist in Acromegalic Patients

CompletedPhase 4Octreotide (Approved)
Phase
Phase 4
Recruitment status
Completed
Sponsor
Novartis Pharmaceuticals
Enrollment
70
Start date
Sep 2006
Locations
20 sites, 5 countries
Primary endpoint
The Percentage of Participants With Complete Response (CR) at 8 Months
View Octreotide compound reference