Carcinoid SyndromePhase 3ELECTNCT00774930
An Efficacy and Safety Study of Somatuline Depot (Lanreotide) Injection to Treat Carcinoid Syndrome
A Phase 3 study testing Lanreotide in people with Carcinoid Syndrome, run by Ipsen at 54 sites in 11 countries.
Trial summary
The purpose of this study was to determine whether monthly deep subcutaneous (s.c.) injections of lanreotide Autogel (Somatuline Depot) were effective and safe in controlling diarrhoea and flushing by reducing the usage of s.c. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Carcinoid Syndrome
- What is being tested?
- Lanreotide
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 115 participants
- Where
- 54 sitesin 11 countries
- Study dates
- May 2009to Dec 2015
- Phase
- Phase 3
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Subjects were eligible for participation in the study if they met the following criteria:
- At least 18 years of age at the time of first dosing.
- Subjects must have given signed informed consent before any study related activities were conducted.
- Subjects in the United States of America (USA) must have given written authorisation for the release of protected health information in compliance with the Health Insurance Portability and Accountability Act (HIPAA) regulations; subjects in other countries must have provided appropriate authorisation as needed by regulatory authorities in each country.
- Subjects must have been willing to receive s.c. octreotide injections as rescue medication, as needed to control their symptoms, if any.
- If female, the subject must not have been pregnant (confirmed by negative pregnancy test) and must have had the following documented via verbally given history:
- At least 1 year postmenopausal (natural cessation of menses), or
- Surgically sterile (if by tubal ligation, surgery must have been performed more than 3 months prior to entry into the study), or
- If the subject was of childbearing potential and sexually active, she must have been using an acceptable form of contraception (oral, injected, transdermal or implanted contraceptives, diaphragm or barrier method with spermicidal and/or intrauterine device); local methods such as condoms or sponges/vaginal tablets were not acceptable forms of contraception.
- Subjects with a histopathologically confirmed diagnosis of carcinoid tumour or, a carcinoid tumour of unknown location with liver metastases (documented biopsy), and a history of carcinoid syndrome (flushing and/or diarrhoea) who were either naïve to treatment with a somatostatin analogue (SSTa) or responsive (according to the opinion of the principal investigator) to conventional doses of Sandostatin LAR® Depot (LAR; ≤30 mg every 4 weeks) or to daily doses of ≤600 μg of s.c. octreotide.
- Confirmation of positive somatostatin receptor (SSTR) status by somatostatin receptor scintigraphy (SRS; up to 6 months prior to study entry at the Screening Visit).
- Absence of tumour progression documented by two sequential computed tomography (CT) scans or two sequential magnetic resonance imaging (MRI) scans (≥3 months apart); the last CT or MRI scan must have been performed within 6 months of study entry (Screening Visit).
- Subjects previously treated with LAR, must have received their last dose of LAR at least 4 weeks prior to first dose of study treatment (no later than at the Screening Visit).
- Be able to communicate and cooperate with the principal investigator and the staff and willing to comply with the study instructions.
Subjects were excluded from entering the study for the following reasons:
- History of known allergy or hypersensitivity to investigational drug or any components of its formulation, or octreotide.
- History of carcinoid syndrome refractory to treatment with conventional doses of SSTa.
- Treatment with any other investigational drug within 30 days prior to study entry (Screening Visit) and/or at any time during the subject's participation in the study.
- Treatment with interferon, chemotherapy and/or radiotherapy (a radiolabelled SSTa) and/or tumour debulking <3 months prior to study entry (Screening Visit).
- History of hepatic arterial embolisation, hepatic arterial chemoembolisation and/or selective internal radiation therapy (selective internal radiation [SIR] therapy [SIRT]; e.g. SIR Spheres) <6 months prior to study entry (Screening Visit).
- Short bowel syndrome.
- Uncontrolled diabetes and/or hypertension.
- Severe renal impairment (glomerular filtration rate <30 mL/min/1.73 m2) and/or severe liver impairment as evidenced by serum total bilirubin >1.5 mg/dL associated with bile duct blockage or with alkaline phosphatase (ALP), aspartate aminotransferase (AST) or alanine aminotransferase (ALT) >5.0 upper limit of normal (ULN).
- Diagnosis of cardiac disease New York Heart Association (NYHA) functional classification >Class I. (Subject has limitation of physical activity. Ordinary physical activity causes undue fatigue, palpitation, or dyspnoea).
- Life expectancy less than 1 year.
- Any malignancies except carcinoid tumour, basocellular carcinoma of the skin, in situ carcinoma of the cervix and ≥5 years disease free after curative cancer treatment.
- Any serious medical condition that could jeopardise the safety of the subject and/or the efficacy assessments of the study.
- Subject is being treated with a proton pump inhibitor (PPI) and has been at a stable dose (no change in dose or frequency of administration) for less than 4 weeks at study entry (Screening Visit).
Trial locations and contacts
54 sites in 11 countries.
54 sites in 11 countries
United States16 sites
University of New Mexico Cancer Care Center
Albuquerque, New Mexico, 97239
University of Michigan
Ann Arbor, Michigan, 48109
Penn State Milton S. Hershey Medical Center
Hershey, Pennsylvania, 17033
University of Mississippi Medical Center
Jackson, Mississippi, 39216
Louisiana State University Health Science Center
Kenner, Louisiana, 70065
VA Greater Los Angeles Health Care System
Los Angeles, California, 90073
David Geffen School of Medicine at UCLA
Los Angeles, California, 90095
Kentuckiana Cancer Institute
Louisville, Kentucky, 40202
Froedtert & Medical College of Wisconsin
Milwaukee, Wisconsin, 53226
Eastern Virginia Medical School
Norfolk, Virginia, 23510
University of Pennsylvania
Philadelphia, Pennsylvania, 19104
UPMC Liver Cancer Center
Pittsburgh, Pennsylvania, 15213
Providence Portland Medical Center
Portland, Oregon, 97213
Oregon Health Science University
Portland, Oregon, 97239
Stanford Cancer Center
Stanford, California, 94305
Cedars Sinai Outpatient Cancer Center
West Hollywood, California, 90048
Ukraine11 sites
Cherkassy Regional Oncology Dispensary
Cherkassy
Chernivtsi Regional Oncology Center
Chernivtsi, 58013
Oncology and Medical Radiology Chair of Dnepropetrovsk State Medical Academy
Dnipro
Regional Anticancer Center, Department of oncoproctology
Donetsk
Municipal Clinical Hospital #2, Proctology department
Kharkiv
Kyiv City Oncological Hospital, Thoracic department
Kyiv
Medical Centre "Mriya"
Kyiv
National Cancer Institute
Kyiv
Odessa Regional Clinical Hospital
Odesa, 65117
Uzhgorods'ka Tsentral'na Mis'ka Klinichna Likarnya, Mis'kyy Onkologichnyy Tsentr
Uzhhorod
Vinnytsya Regional Clinical Oncological Center, Vinnytsya State Medical University
Vinnytsia
Brazil7 sites
Biocancer - Centro de Pesquisa e Tratamento do Câncer
Belo Horizonte
Hospital LifeCenter
Belo Horizonte
Oxion Medicina Oncológica
Belo Horizonte
Hospital Universitário de Brasilia
Brasília
Hospital Erasto Gaertner
Curitiba
Irmandade da Santa Casa de Misericórdia de Porto Alegre
Porto Alegre
Hospital de Base de São José do Rio Preto
São José do Rio Preto
India7 sites
Sir Gangaram Hospital
Delhi
Indo-American Cancer Institute & Research Centre
Hyderabad
Omega Hospitals
Hyderabad
Santokaba Durlabhji Memorial Hospital and Research Institute
Jaipur, 302015
Bhagwan Mahaveer cancer hospital and research centre
Jaipur
Shatabdi Super Speciality hospital
Mumbai, 422005
Tata Memorial Hospital
Mumbai
South Africa4 sites
Rondebosch Oncology Unit
Cape Town, 7700
Groote Schuur Hospital
Cape Town
Westridge Medical Centre
Durban
GVI Oncology Clinical Trial Unit
Port Elizabeth, 7570
Russia3 sites
Non-Federal Institution of Healthcare "Central Clinical Hospital # 1 of the LLC "Russian Railways (RZD)"
Moscow
Russian Academy of Medical Sciences "Russian Oncological Research Centre named after N.N. Blokhin RAMS"
Moscow
Federal Institution of Healthcare "Leningradsky Regional Oncological Dispensary"
Saint Petersburg
Serbia2 sites
Clinic of Endocrinology, diabetes and metabolic diseases, Clinical Center of Serbia
Belgrade, 11000
Oncology Institute of Vojvodina, Sremska Kamenica
Kamenitz, 21 204
Poland1 site
Klinika Endokrynologii, Diabetologii i Leczenia Izotopami
Wroclaw, 50-367
Turkey (Türkiye)1 site
Erciyes University Medical Faculty
Kayseri, 38039
About this study
Official title: A Double Blind, Randomized Placebo Controlled Clinical Trial Investigating the Efficacy and Safety of Somatuline Depot (Lanreotide) Injection in the Treatment of Carcinoid Syndrome
The purpose of this study was to determine whether monthly deep subcutaneous (s.c.) injections of lanreotide Autogel (Somatuline Depot) were effective and safe in controlling diarrhoea and flushing by reducing the usage of s.c. short-acting octreotide as a rescue medication to control symptoms in subjects with carcinoid syndrome.
Read the detailed description
This study consisted of a Screening period, conducted up to 4 months before randomisation, followed by three phases: a 16-week, double blind (DB), randomised, placebo-controlled phase; a 32-week initial open label (IOL) phase; and a long term open label extension (LTOLE) phase.
The DB phase evaluated lanreotide Autogel versus placebo in subjects with a history of carcinoid syndrome (flushing and/or diarrhoea). This was followed by a 32-week IOL phase in which all subjects received lanreotide Autogel 120 mg every 4 weeks. Subjects in countries where lanreotide Autogel had not been approved for the treatment of carcinoid syndrome, who were well-controlled at the end of the 32-week IOL phase and chose to continue to receive lanreotide Autogel, were given the option of participating in a LTOLE phase. The LTOLE phase of the study was planned to end at least 2 years after the last subject had completed his/her participation in the 32-week IOL phase or when marketing approval for the treatment of symptoms of carcinoid syndrome had been obtained in the respective countries (whichever occurred first) or at any time the study was terminated by the Sponsor. The actual overall duration of the study was 6.5 years. During the LTOLE phase all subjects continued to be treated with lanreotide Autogel 120 mg every 4 weeks.
The study planned to enrol approximately 100 adult subjects worldwide. Screening continued until 115 subjects were enrolled in the study.
- Conditions
- Carcinoid Syndrome
- Being tested
- Lanreotide, Placebo
- Keywords
- Carcinoid tumor, Somatuline Depot, Lanreotide Autogel, Neuroendocrine tumor, NET, Diarrhea, Flushing, Carcinoid tumour, Neuroendocrine tumour, Diarrhoea
- Medical subject headings
- Serotonin Syndrome, Carcinoid Tumor, Neuroendocrine Tumors, Diarrhea, Flushing
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
LanreotideDrug
Also called Somatuline, Somatuline Depot, Somatuline Autogel, Lanreotide Autogel
deep s.c. injection, 120 mg, every 4 weeks (±3 days).
PlaceboDrug
deep s.c. injection of placebo (0.9% saline solution) every 4 weeks (±3 days) for 16 weeks, then deep s.c. injection of lanreotide 120 mg, every 4 weeks (±3 days).
| Study group | Role | What they receive |
|---|---|---|
| Lanreotide Autogel (Somatuline Depot) 120 mg | Experimental | Subjects received deep s.c. lanreotide Autogel 120 mg every 4 weeks (±3 days) for 16 weeks (DB phase).
After completing the DB phase (or if they met criteria for early roll over [ERO]) the subjects entered the IOL phase during which they received lanreotide Autogel 120 mg deep s.c. every 4 weeks for 32 weeks. During the LTOLE phase, subjects continued treatment with lanreotide Autogel 120 mg deep s.c. every 4 weeks until at least 2 years after the last subject completed the IOL phase or when marketing approval for the treatment of symptoms of carcinoid syndrome was obtained [whichever occurred first]). Receives: Drug: Lanreotide |
| Placebo (DB) and lanreotide Autogel 120 mg in IOL and LTOLE | Placebo comparator | Subjects received deep s.c. placebo every 4 weeks (±3 days) for 16 weeks (DB phase).
After completing the DB phase (or if they met criteria for ERO) the subjects entered the IOL phase during which they received lanreotide Autogel 120 mg deep s.c. every 4 weeks for 32 weeks. During the LTOLE phase, subjects continued treatment with lanreotide Autogel 120 mg deep s.c. every 4 weeks until at least 2 years after the last subject completed the IOL phase or when marketing approval for the treatment of symptoms of carcinoid syndrome was obtained [whichever occurred first]). Receives: Drug: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage of Days With Subcutaneous Octreotide as Rescue Medication
Use of s.c. octreotide required to control symptoms associated with carcinoid syndrome, measured as the percentage of days that s.c. octreotide was used as rescue medication, based on subject Interactive Voice Response System (IVRS) or Interactive Web Response System (IWRS) diary records.
Measured: 16-week DB phase
Secondary outcomes (9)
Average Frequency of Diarrhoea Events (Per Day) Based on Subject Diary Records.
Measured: 16-week DB phase
Average Frequency of Flushing Events (Per Day) Based on Subject Diary Records.
Measured: 16-week DB phase
Percentage of Days of Use of Other Rescue Medication
Usage of other concomitant rescue medications for diarrhoea and/or flushing events, measured as the percentage of days that the medications were used as rescue medication based on subject IVRS/IWRS diary records. Subjects were required to record the use and dose of s.c. octreotide, if any, as well as the use of other concomitant rescue medications (e.g. loperamide 2 mg tabs, and/or tincture of opium).
Measured: 16-week DB phase
Proportion of Subjects Who Rolled Over Into the IOL Phase Before Completing the DB Phase of the Study
Subjects who rolled over early were those who received less than four DB injections before receiving the first IOL injection.
Measured: 16-week DB phase
Changes From Baseline in "Global Health Status/Quality of Life (QoL)" Score (Based on Items 29 and 30 of the European Organisation for the Research and Treatment of Cancer Quality of Life Questionnaire [EORTC-QLQ] C30)
Baseline is defined as the last non-missing observation obtained prior to the initiation of study treatment.
Q29 and Q30 range from 1 (Very poor) to 7 (Excellent) with 1 being worst case and 7 the most favourable answer. Scores were derived according to the rules contained within the EORTC scoring manual. All of the scores range in score from 0 to 100. A high score for global health status/QoL represents high QoL. The principle for scoring the scale is: Estimate the average of the items (I1, I2, ..., In) that contribute to the scale; this is the raw score. Raw score = RS = (I1 + I2 +…+ In)/n.
For global health status/QoL: Score = {(RS - 1)/range} x 100, where range is the difference between the maximum possible value of RS and the minimum possible value of RS.
Measured: Baseline and Week 12 of DB phase
Changes From Baseline in "Gastrointestinal (G.I). Symptoms" Subscore (Based on Items Q34, Q35, Q36, Q37 and Q38 of EORTC G.I. Neuroendocrine Tumour [NET] 21]
Baseline is defined as the last non-missing observation obtained prior to the initiation of study treatment.
The QLQ-G.I.NET21 questionnaire contains 21 single items (Q31 to Q51) which are supplemental items to the EORTC QLQ-C30 questionnaire. Q31 to Q51 range from 1 to 4 with 1 being the most favourable answer and 4 the worst case (1 = Not at all, 2 = A little, 3 = Quite a bit, 4 = Very much). Based on these items the scores were generated. All of the scores range in score from 0 to 100. A high score for a symptom scale represents a high level of symptomatology. The principle for scoring the scale is: Estimate the average of the items (I1, I2, ..., In) that contribute to the scale; this is the raw score. RS = (I1 + I2 +…+ In)/n.
For symptom scales: Score = {(RS - 1)/range} x 100, where range is the difference between the maximum possible value of RS and the minimum possible value of RS.
Measured: Baseline and Week 12 of DB phase
Changes From Baseline in QoL in "Endocrine Symptoms" Subscore (Assessed Based on Items Q31, Q32 and Q33 Using EORTC QLQ-G.I.NET-21 Questionnaires)
Baseline is defined as the last non-missing observation obtained prior to the initiation of study treatment.
The QLQ-G.I.NET21 questionnaire contains 21 single items (Q31 to Q51) which are supplemental items to the EORTC QLQ-C30 questionnaire. Q31 to Q51 range from 1 to 4 with 1 being the most favourable answer and 4 the worst case (1 = Not at all, 2 = A little, 3 = Quite a bit, 4 = Very much). Based on these items the scores were generated. All of the scores range in score from 0 to 100. A high score for a symptom scale represents a high level of symptomatology. The principle for scoring the scale is: Estimate the average of the items (I1, I2, ..., In) that contribute to the scale; this is the raw score. RS = (I1 + I2 +…+ In)/n.
For symptom scales: Score = {(RS - 1)/range} x 100, where range is the difference between the maximum possible value of RS and the minimum possible value of RS.
Measured: Baseline and Week 12 of DB phase
Absolute Changes From Baseline in Biochemical Markers (Plasma Chromogranin A [CgA])
Baseline is defined as the last non-missing observation obtained prior to the initiation of study treatment.
Measured: Baseline and Week 12 of DB phase
Absolute Changes From Baseline in Biochemical Markers (Urinary 5-hydroxyindoleacetic Acid [5-HIAA])
Baseline is defined as the last non-missing observation obtained prior to the initiation of study treatment.
Measured: Baseline and Week 12 of DB phase
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Oct 2008 (estimated)
- Study startMay 2009
- Primary completionMay 2013
- Study completionDec 2015
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Carcinoid SyndromeStudies of the same condition, open and under way.
- More trials run by IpsenThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Investigator
- Enrolment
- 115 participants (actual)
Sponsor and investigators
- Lead sponsor
- Ipsen
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Ipsen Medical Director, Study director, Ipsen
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00774930
- Sponsor's protocol ID
- 2-55-52030-730
- Other IDs
- TR321, 2010-019066-92
- Acronym
- ELECT
- Status last verified
- Sep 2022
- First submitted
- 15 Oct 2008
- Last updated
- 14 Oct 2022
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- Individual data sharing
- Yes: Qualified researchers may request access to patient level data and related study documents including the clinical study report, study protocol with any amendments, annotated case report form, statistical analysis plan, and dataset specifications. Patient level data will be anonymized, and study documents will be redacted to protect the privacy of study participants. Any requests should be submitted to www.vivli.org for assessment by an independent scientific review board.
Publications
Vinik AI, Wolin EM, Liyanage N, Gomez-Panzani E, Fisher GA; ELECT Study Group *. EVALUATION OF LANREOTIDE DEPOT/AUTOGEL EFFICACY AND SAFETY AS A CARCINOID SYNDROME TREATMENT (ELECT): A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL. Endocr Pract. 2016 Sep;22(9):1068-80. doi: 10.4158/EP151172.OR. Epub 2016 May 23.
PubMed 27214300Blot K, Duchateau L, Lescrauwaet B, Liyanage N, Ray D, Mirakhur B, Vinik AI. A Patient-Reported Outcomes Analysis Of Lanreotide In The Treatment Of NETs Patients With Carcinoid Syndrome: Evidence From The ELECT Trial. Patient Relat Outcome Meas. 2019 Oct 29;10:335-343. doi: 10.2147/PROM.S219982. eCollection 2019.
PubMed 31754316
Study at a glance
From the registry record, last updated by the sponsor on 14 Oct 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Double Blind, Randomized Placebo Controlled Clinical Trial Investigating the Efficacy and Safety of Somatuline Depot (Lanreotide) Injection in the Treatment of Carcinoid Syndrome
- ClinicalTrials.gov ID
- NCT00774930
- Acronym / sponsor ID
- ELECT / 2-55-52030-730
- Conditions
- Carcinoid Syndrome
- Keywords
- Carcinoid tumor, Somatuline Depot, Lanreotide Autogel, Neuroendocrine tumor, NET, Diarrhea, Flushing, Carcinoid tumour
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 115 participants (actual)
- Lead sponsor
- IpsenIndustry (pharma, biotech, devices)
- Study start
- May 2009
- Primary completion
- May 2013 (actual)
- Study completion
- Dec 2015 (actual)
- First posted
- 17 Oct 2008 (estimated)
- Results
- Posted 9 Feb 2016
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study was to determine whether monthly deep subcutaneous (s.c.) injections of lanreotide Autogel (Somatuline Depot) were effective and safe in controlling diarrhoea and flushing by reducing the usage of s.c. short-acting octreotide as a rescue medication to control symptoms in subjects with carcinoid syndrome.
Detailed description
This study consisted of a Screening period, conducted up to 4 months before randomisation, followed by three phases: a 16-week, double blind (DB), randomised, placebo-controlled phase; a 32-week initial open label (IOL) phase; and a long term open label extension (LTOLE) phase.
The DB phase evaluated lanreotide Autogel versus placebo in subjects with a history of carcinoid syndrome (flushing and/or diarrhoea). This was followed by a 32-week IOL phase in which all subjects received lanreotide Autogel 120 mg every 4 weeks. Subjects in countries where lanreotide Autogel had not been approved for the treatment of carcinoid syndrome, who were well-controlled at the end of the 32-week IOL phase and chose to continue to receive lanreotide Autogel, were given the option of participating in a LTOLE phase. The LTOLE phase of the study was planned to end at least 2 years after the last subject had completed his/her participation in the 32-week IOL phase or when marketing approval for the treatment of symptoms of carcinoid syndrome had been obtained in the respective countries (whichever occurred first) or at any time the study was terminated by the Sponsor. The actual overall duration of the study was 6.5 years. During the LTOLE phase all subjects continued to be treated with lanreotide Autogel 120 mg every 4 weeks.
The study planned to enrol approximately 100 adult subjects worldwide. Screening continued until 115 subjects were enrolled in the study.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Lanreotide Autogel (Somatuline Depot) 120 mg | Experimental | Drug: LanreotideSubjects received deep s.c. lanreotide Autogel 120 mg every 4 weeks (±3 days) for 16 weeks (DB phase). After completing the DB phase (or if they met criteria for early roll over [ERO]) the subjects entered the IOL phase during which they received lanreotide Autogel 120 mg deep s.c. every 4 weeks for 32 weeks. During the LTOLE phase, subjects continued treatment with lanreotide Autogel 120 mg deep s.c. every 4 weeks until at least 2 years after the last subject completed the IOL phase or when marketing approval for the treatment of symptoms of carcinoid syndrome was obtained [whichever occurred first]). |
| Placebo (DB) and lanreotide Autogel 120 mg in IOL and LTOLE | Placebo comparator | Drug: PlaceboSubjects received deep s.c. placebo every 4 weeks (±3 days) for 16 weeks (DB phase). After completing the DB phase (or if they met criteria for ERO) the subjects entered the IOL phase during which they received lanreotide Autogel 120 mg deep s.c. every 4 weeks for 32 weeks. During the LTOLE phase, subjects continued treatment with lanreotide Autogel 120 mg deep s.c. every 4 weeks until at least 2 years after the last subject completed the IOL phase or when marketing approval for the treatment of symptoms of carcinoid syndrome was obtained [whichever occurred first]). |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| LanreotideAlso: Somatuline, Somatuline Depot, Somatuline Autogel, Lanreotide Autogeldeep s.c. injection, 120 mg, every 4 weeks (±3 days). | Drug | Lanreotide Autogel (Somatuline Depot) 120 mg |
| Placebodeep s.c. injection of placebo (0.9% saline solution) every 4 weeks (±3 days) for 16 weeks, then deep s.c. injection of lanreotide 120 mg, every 4 weeks (±3 days). | Drug | Placebo (DB) and lanreotide Autogel 120 mg in IOL and LTOLE |
Primary outcome
Percentage of Days With Subcutaneous Octreotide as Rescue Medication
Time frame: 16-week DB phase
Use of s.c. octreotide required to control symptoms associated with carcinoid syndrome, measured as the percentage of days that s.c. octreotide was used as rescue medication, based on subject Interactive Voice Response System (IVRS) or Interactive Web Response System (IWRS) diary records.
9 secondary outcomes
Average Frequency of Diarrhoea Events (Per Day) Based on Subject Diary Records.
Time frame: 16-week DB phase
Average Frequency of Flushing Events (Per Day) Based on Subject Diary Records.
Time frame: 16-week DB phase
Percentage of Days of Use of Other Rescue Medication
Time frame: 16-week DB phase
Proportion of Subjects Who Rolled Over Into the IOL Phase Before Completing the DB Phase of the Study
Time frame: 16-week DB phase
Changes From Baseline in "Global Health Status/Quality of Life (QoL)" Score (Based on Items 29 and 30 of the European Organisation for the Research and Treatment of Cancer Quality of Life Questionnaire [EORTC-QLQ] C30)
Time frame: Baseline and Week 12 of DB phase
Changes From Baseline in "Gastrointestinal (G.I). Symptoms" Subscore (Based on Items Q34, Q35, Q36, Q37 and Q38 of EORTC G.I. Neuroendocrine Tumour [NET] 21]
Time frame: Baseline and Week 12 of DB phase
Changes From Baseline in QoL in "Endocrine Symptoms" Subscore (Assessed Based on Items Q31, Q32 and Q33 Using EORTC QLQ-G.I.NET-21 Questionnaires)
Time frame: Baseline and Week 12 of DB phase
Absolute Changes From Baseline in Biochemical Markers (Plasma Chromogranin A [CgA])
Time frame: Baseline and Week 12 of DB phase
Absolute Changes From Baseline in Biochemical Markers (Urinary 5-hydroxyindoleacetic Acid [5-HIAA])
Time frame: Baseline and Week 12 of DB phase
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Oct 2022.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Results publication: PubMed 27214300Vinik AI, Wolin EM, Liyanage N, Gomez-Panzani E, Fisher GA; ELECT Study Group *. EVALUATION OF LANREOTIDE DEPOT/AUTOGEL EFFICACY AND SAFETY AS A CARCINOID SYNDROME TREATMENT (ELECT): A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL. Endocr Pract. 2016 Sep;22(9):1068-80. doi: 10.4158/EP151172.OR. Epub 2016 May 23.
- Derived from this study: PubMed 31754316Blot K, Duchateau L, Lescrauwaet B, Liyanage N, Ray D, Mirakhur B, Vinik AI. A Patient-Reported Outcomes Analysis Of Lanreotide In The Treatment Of NETs Patients With Carcinoid Syndrome: Evidence From The ELECT Trial. Patient Relat Outcome Meas. 2019 Oct 29;10:335-343. doi: 10.2147/PROM.S219982. eCollection 2019.
- Individual participant dataSharing planned: Yes. Qualified researchers may request access to patient level data and related study documents including the clinical study report, study protocol with any amendments, annotated case report form, statistical analysis plan, and dataset specifications. Patient level data will be anonymized, and study documents will be redacted to protect the privacy of study participants. Any requests should be submitted to www.vivli.org for assessment by an independent scientific review board.
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An Investigational Scan (Dual Energy CT) in Detecting Gastrointestinal Carcinoid Tumors
Carcinoid Syndrome, Carcinoid Tumor
Active, not recruiting
Investigation of a Transcatheter Tricuspid Valved Stent Graft in Patients With Carcinoid Heart Disease
Tricuspid Regurgitation, Tricuspid Valve Disease
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Ipsen Medical Director study director
Ipsen
54 sites in 11 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Lanreotide in people with Carcinoid Syndrome, run by Ipsen at 54 sites in 11 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 14 Oct 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 54 sites in United States, Ukraine, Brazil, India, South Africa and 6 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 9 Feb 2016). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Percentage of Days With Subcutaneous Octreotide as Rescue Medication (time frame: 16-week DB phase). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT00774930, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Oct 2022.