ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Efficacy and Safety of Pasireotide Long Acting Release vs. Octreotide Long Acting Release in Patients With Metastatic Carcinoid Disease

ClinicalTrials.gov ID: NCT00690430

Public ClinicalTrials.gov record NCT00690430. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 5, 2026, 4:24 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Blinded Efficacy and Safety Study of Pasireotide LAR vs Octreotide LAR in Patients With Metastatic Carcinoid Tumors Whose Disease-related Symptoms Are Inadequately Controlled by Somatostatin Analogues.

Study identification

NCT ID
NCT00690430
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
186 participants

Conditions and interventions

Interventions

  • Octreotide Drug
  • Pasireotide Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 31, 2008
Primary completion
Mar 31, 2012
Completion
Mar 31, 2012
Last update posted
Jul 29, 2013

2008 – 2012

United States locations

U.S. sites
10
U.S. states
7
U.S. cities
10
Facility City State ZIP Site status
Scottsdale Healthcare/TGen Clinical Research Service TGen Clinical Research Service Scottsdale Arizona 85258
University of Arizona / Arizona Cancer Center Tucson Arizona 85724
Loma Linda University Dept. of Loma Linda CancerCent Loma Linda California 92354
Cedars Sinai Medical Center Cedars Sinai 4 Los Angeles California 90048
H. Lee Moffitt Cancer Center/University of South Florida Dept of H. Lee Moffit Tampa Florida 33612
Mount Sinai School of Medicine Study Coordinator New York New York 10029
Montefiore Medical Center MMC The Bronx New York 10467
Duke University Medical Center Dept. of Duke Cancer Center(2) Durham North Carolina 27710
St. Luke's Hospital and Health Network St. Luke's Cancer Network Bethlehem Pennsylvania
MD Anderson Cancer Center/University of Texas Dept. of MD Anderson (9) Houston Texas 77030-4009

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 52 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00690430, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 29, 2013 · Synced May 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00690430 live on ClinicalTrials.gov.

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