Efficacy and Safety of Lanreotide Microparticles as Palliative Treatment in Peritoneal Carcinomatosis

November 4, 2020 updated by: Ipsen

Phase III, Multicentre, Randomised, Double-blind, Comparative Study to Assess the Efficacy and Safety of Lanreotide 30 mg Versus Placebo as a Palliative Treatment of Clinical Symptoms Associated With Intestinal Obstruction Due to Peritoneal Carcinomatosis in Inoperable Patients.

The purpose of this study is to determine whether lanreotide 30mg microparticles are effective in the relief of clinical symptoms due to small bowel obstruction in inoperable patients with peritoneal carcinomatosis.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Completed

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment (Actual)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
80

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • Phase 3

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Belgium
      • Bruxelles, Belgium
        • Institut Jules Bordet
      • Bruxelles, Belgium
        • Clinique Universitaire St. Luc
      • Hermalle-sous-Huy, Belgium
        • Clinique Notre-Dame
      • La Louvière, Belgium
        • Centre Hospitalier de Jolimont-Lobbes
  • France
      • Amiens, France
        • Hôpital Nord
      • Angers, France
        • Clinique de l'Anjou
      • Angers, France
        • Hôtel-Dieu
      • Argenteuil, France, 95100
        • Ch Victor Dupouy
      • Bordeaux, France, 33075
        • Hopital Saint André
      • Brest, France, 29609
        • Hôpital de la Cavale blanche
      • Caen, France
        • Centre François Baclesse
      • Cebazat, France, 63118
        • Hôpital Nord
      • Chatenay-Malabry, France
        • Clinique de l'Amandier
      • Clermont-Ferrand, France
        • Hôpital Hôtel-Dieu
      • Clichy, France, 92118
        • Hopital Beaujon
      • Colmar, France
        • Hôpital Pasteur
      • Compiegne, France, 60321
        • Centre Hospitalier de Compiegne
      • Creteil, France, 94000
        • Hopital Henri Mondor
      • Dreux, France, 28102
        • Centre Hospitalier Victor Jousselin
      • Hyeres, France
        • Clinique Sainte Marguerite
      • La Roche sur Yon, France
        • Centre Hospitalier departemental
      • Le Chesnay, France, 78150
        • Hôpital André Mignot
      • Levallois-Perret, France, 92309
        • Hôpital Notre-Dame du Perpétuel Secours
      • Limoges, France, 87042
        • CHU Dupuytren
      • Lorient, France
        • Hôpital Site de Lorient
      • Lyon, France
        • Hôpital de La Croix Rousse
      • Nice, France
        • Hopital de l'Archet 2
      • Orléans, France
        • Hôpital de la Source
      • Osny, France
        • Centre de Radiothérapie et Oncologie Médicale
      • Paris, France, 75651
        • Hôpital Pitie Salpétrière
      • Paris, France, 75012
        • Hopital Saint Antoine
      • Paris, France, 75012
        • Hôpital des Diaconesses
      • Paris, France, 75181
        • Hôtel Dieu
      • Paris, France, 75005
        • Hôpital du Val de Grâce
      • Paris, France, 75005
        • Institue Curie
      • Paris, France
        • Hopital Georges Pompidou
      • Pierre Benite, France, 69495
        • Centre Hospitalier LYON SUD
      • Reims, France
        • Institut Jean Godinot
      • Rennes, France
        • Centre Eugene Marquis
      • Roanne, France
        • Centre hospitalier de Roanne
      • Rouen, France
        • Hôpital Charles Nicolle
      • Rouen, France, 76038
        • CAC Becquerel
      • Saint Etienne, France, 42020
        • Institut de Cancérologie de la Loire
      • Saint-Brieuc, France, 22015
        • Clinique Armoricaine de Radiologie
      • Saint-Doulchard, France
        • Clinique Guillaume De Varye
      • Sens, France, 89108
        • Centre Hospitalier Gaston Ramon
      • Strasbourg, France, 67091
        • Hôpital Civil
      • Strasbourg, France
        • Hopital Hautepierre
      • Thionville, France, 57126
        • C.H.R. de Metz-Thionville
      • Toulouse, France
        • Hôpital Joseph Ducuing
      • Toulouse, France
        • Hôpital de Rangueil
      • Villejuif, France
        • Institut Gustave Roussy
  • Netherlands
      • Amsterdam, Netherlands
        • Academisch Medisch Centrum

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • digestive obstruction located in the upper part of the gastro-intestinal tract
  • digestive obstruction of malignant origin
  • peritoneal carcinomatosis confirmed by a CT Scan
  • at least two vomiting episodes per day or a presence of a nasogastric suction tube
  • inoperable patients

Exclusion Criteria:

  • specific anticancer therapy within the previous 15 days
  • signs of bowel perforation
  • somatostatin or any analogue as treatment of the bowel obstruction

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm

Participant Group / Arm

A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment, or no intervention, according to the trial's protocol.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
Experimental: 1
Drug: Lanreotide (microparticle formulation)
A single 30 mg intra-muscular injection on day 0. The duration of the blinded phase is 10 days. Patients may enter the open phase where they receive 30 mg intra-muscular injections, every 10 days until investigator/or patient decide to stop treatment.
Placebo Comparator: 2
Other: Placebo
A single intra-muscular injection on day 0.

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Time Frame
Percentage of responder patients (patient with 1 or less vomiting episode per day during at least 3 consecutive days or in whom nasogastric tube (NGT) has been removed during at least three consecutive days without vomiting recurrence)
Time Frame: On day 7 (plus 1 day at the latest) after the first injection
On day 7 (plus 1 day at the latest) after the first injection

Secondary Outcome Measures

Secondary Outcome Measures

In a clinical study's protocol, a planned outcome measure that is not as important as the primary outcome measure for evaluating the effect of an intervention but is still of interest. Most clinical studies have more than one secondary outcome measure.
Outcome Measure
Time Frame
Number of daily vomiting episodes or measurement of the daily drainage by NGT
Time Frame: Daily for the duration of the study
Daily for the duration of the study
Number of days with no vomiting episodes
Time Frame: For the duration of the study
For the duration of the study
Number of daily nausea episodes
Time Frame: Daily for the duration of the study
Daily for the duration of the study
Intensity of abdominal pain
Time Frame: Daily for the duration of the study
Daily for the duration of the study
Well-being
Time Frame: Daily for the duration of the study
Daily for the duration of the study
Symptom relief duration
Time Frame: Between the first day of clinical response and the end of follow-up
Between the first day of clinical response and the end of follow-up

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Ipsen

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
September 1, 2003

Primary Completion (Actual)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
October 1, 2008

Study Completion (Actual)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
October 1, 2008

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
September 13, 2005

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
September 20, 2005

First Posted (Estimate)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
September 22, 2005

Study Record Updates

Last Update Posted (Actual)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
November 5, 2020

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
November 4, 2020

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
November 1, 2020

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • 2-54-52030-156 (408)
  • 2005-002349-38 (EudraCT Number)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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