Trials / Completed
CompletedNCT00128232
Safety and Efficacy of Octreotide Long Acting Release (LAR) in Treatment Naïve Acromegalic Patients
Safety and Efficacy of Octreotide LAR in Treatment Naïve Acromegalic Patients
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 100 (planned)
- Sponsor
- Novartis · Industry
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- —
Summary
Currently, the first line treatment for acromegaly is surgery, in order to remove the adenoma causing overproduction of growth hormone which leads to acromegaly. Octreotide LAR is approved for treatment of acromegaly after surgery if the disease is not controlled. This study was aimed to test the safety and efficacy of octreotide LAR in acromegalic patients who did not have any previous treatment for acromegaly.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Octreotide LAR |
Timeline
- Start date
- 2002-12-01
- Primary completion
- 2004-08-01
- First posted
- 2005-08-09
- Last updated
- 2012-04-30
Source: ClinicalTrials.gov record NCT00128232. Inclusion in this directory is not an endorsement.