Current partner codePEPTIDESDE
NCT00958841·Phase 2·INTERVENTIONAL

Study of Pasireotide in Patients With Rare Tumors of Neuroendocrine Origin

Status

Terminated

Phase

Phase 2

Enrollment

118

Locations

42

Results

Posted

Publications

0

Study summary

What the protocol is testing.

This study will assess the effectiveness and safety of pasireotide long-acting release in patients who have rare tumors of neuroendocrine origin.

Interventions

Treatment arms and agents.

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.

Timeline

From registration to results.

  1. First posted

    Aug 13, 2009

  2. Study start

    Sep 2009

  3. Primary completion

    Jun 2015

  4. Study completion

    Jun 2015

  5. Results posted

    Jul 26, 2016

  6. Registry updated

    Jul 26, 2016

Outcomes

What the study measures.

Primary 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.

Secondary outcomes

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

Who can take part.

Minimum age
18 Years
Maximum age
Not reported
Sex
ALL
Healthy volunteers
No

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

42 registered sites.

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

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Pasireotide.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.