DRUG
pasireotide LAR
Investigational drug pasireotide LAR was supplied in vials with 20 mg or 40 mg powder and 2 mL vehicle was supplied in ampoules for reconstitution.
Status
Terminated
Phase
Phase 2
Enrollment
118
Locations
42
Results
Posted
Publications
0
Study summary
This study will assess the effectiveness and safety of pasireotide long-acting release in patients who have rare tumors of neuroendocrine origin.
Interventions
DRUG
Investigational drug pasireotide LAR was supplied in vials with 20 mg or 40 mg powder and 2 mL vehicle was supplied in ampoules for reconstitution.
Timeline
First posted
Aug 13, 2009
Study start
Sep 2009
Primary completion
Jun 2015
Study completion
Jun 2015
Results posted
Jul 26, 2016
Registry updated
Jul 26, 2016
Outcomes
Percentage of Responders at Month 6 - Pooled Pancreatic NETs (PNETs)
Time frame · 6 months
The primary efficacy endpoint was defined as the percentage of responders at Month 6 among pooled PNET patients (insulinoma, gastrinoma, VIPoma, and glucagonoma). A responder was defined as a patient who either attained normalization or had a greater than 50% reduction from baseline of the level of the primary biochemical tumor marker at Month 6 (M6). Four insulinoma pts were excluded from analysis because of unavailability of normal ranges for the associated primary biochemical tumor marker (insulin-to-glucose ratio). One patient with VIPoma with a normal baseline was also excluded. As a result, only 20 out of 25 patients with PNET were included in the assessment of the primary endpoint, which was less than the planned sample size of 34. Therefore, the primary objective could not be assessed with sufficient power. Patients with missing Month 6 assessment were considered as non-responders. Responder analyses are reported only for indications with minimum of 6 patients.
Percentage of Responders at Month 6 - Individual NETs
Time frame · 6 months
Percentage of responders for each of the 10 NET indications considered in the study. Responder analyses were performed for an indication only if there were at least 6 patients in the efficacy analyzable set. For all other individual indications, the numbers of patients in the efficacy analyzable sets were less than 6 and therefore no responder analyses were carried out for these indications.
Percentage of Responders With Probability of Success at Month 6 - Individual NETs
Time frame · 6 months
Percentage of responders for each of the 10 NET indications considered in the study. Responder analyses were performed for an indication only if there were at least 6 patients in the efficacy analyzable set. For all other individual indications, the numbers of patients in the efficacy analyzable sets were less than 6 and therefore no responder analyses were carried out for these indications. The probability of success was a chance that the true responder rate was greater than 15%) for the indications gastrinoma, prolactinoma, and Nelson's syndrome.
PNETs: Number of Patients Attaining Normalization or a More Than 50% Reduction in Primary Biochemical Tumor Marker
Time frame · Baseline, month 6
Specific primary biochemical tumor markers were used to assess the efficacy of pasireotide in PNETs. A Month 6 responder was defined as the patients who either attained normalization or greater than 50% reduction from baseline in the level of the primary biochemical tumor marker at Month 6. One gastrinoma patient had a missing primary tumor marker value at Month 6, but had a Month 5 assessment done on Day 141, which fell within the allowed window period for Month 6.
PiNETs: Number of Patients Attaining Normalization or a More Than 50% Reduction in Primary Biochemical Tumor Marker
Time frame · Baseline, month 6
Specific primary biochemical tumor markers were used to assess the efficacy of pasireotide in PNETs. A Month 6 responder was defined as the patients who either attained normalization or greater than 50% reduction from baseline in the level of the primary biochemical tumor marker at Month 6.
Nelson's Syndrome: Number of Patients Attaining Normalization or a More Than 50% Reduction in Primary Biochemical Tumor Marker
Time frame · Baseline, month 6
Six patients with Nelson's syndrome met the responder's criteria of attaining normalization or a reduction of more than 50% in primary tumor marker at Month 6.
Eligibility
Inclusion Criteria: * Male and Female Patients at least 18 years old * Patient who have rare tumors of neuroendocrine origin, such as tumors of the: 1. pancreas 2. pituitary glands 3. Nelson syndrome 4. ectopic-ACTH secreting tumor * Patients who have failed standard of care treatment or for whom no standard of care treatment exist * Signed Informed Consent Exclusion Criteria: * Patients with active gallbladder disease * Patients with any ongoing or planned anti-neoplastic or interferon therapy * Poorly controlled diabetes mellitus * Female patients who are pregnant or lactating, or are of childbearing potential and not practicing a medically acceptable method of birth control Other protocol-defined inclusion/exclusion criteria may apply.
Study locations
Argentina · Australia · Brazil · Canada · France · Germany · Italy · Mexico · Russia · Spain · Thailand · United States. Showing up to 24 locations stored in the fast local snapshot.
Cedars Sinai Medical Center Cedars Sinai 4
Los Angeles, California, United States
Cedars Sinai Medical Center The Pituitary Center (3)
Los Angeles, California, United States
Stanford University Medical Center SC
Stanford, California, United States
Dana Farber Cancer Institute Deptof DanaFarberCancerInst(5)
Boston, Massachusetts, United States
Mount Sinai School of Medicine Study Coordinator
New York, New York, United States
Swedish Medical Center Dept.ofSwedishMedicalCtr.(2)
Seattle, Washington, United States
Novartis Investigative Site
Buenos Aires, Buenos Aires, Argentina
Novartis Investigative Site
Westmead, New South Wales, Australia
Novartis Investigative Site
Fitzroy, Victoria, Australia
Novartis Investigative Site
Fortaleza, Ceará, Brazil
Novartis Investigative Site
Belo Horizonte, Minas Gerais, Brazil
Novartis Investigative Site
Botucatu, São Paulo, Brazil
Novartis Investigative Site
Halifax, Nova Scotia, Canada
Novartis Investigative Site
Montreal, Quebec, Canada
Novartis Investigative Site
Strasbourg, France, France
Novartis Investigative Site
Angers, France
Novartis Investigative Site
Bron, France
Novartis Investigative Site
Le Kremlin-Bicêtre, France
Novartis Investigative Site
Lille, France
Novartis Investigative Site
Marseille, France
Novartis Investigative Site
Pessac, France
Novartis Investigative Site
Reims, France
Novartis Investigative Site
Berlin, Germany
Novartis Investigative Site
Berlin, Germany
Publications
No PMID-linked publications were present in this registry snapshot.
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