Percentage of Days With Subcutaneous Octreotide as Rescue Medication
| Group | Value (Percentage of days) |
|---|---|
| Lanreotide Autogel (Somatuline Depot) 120 mg | 33.72 |
| Placebo | 48.49 |
Trial · Interventional
CompletedPhase 3Results postedRegistry dataShort name ELECT
United States, Brazil, Czechia, India, Latvia, Poland, Russia, Serbia, South Africa, Turkey (Türkiye), Ukraine
1 trial · 1 completed · 1 with posted results
Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.
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.
Experimental
Lanreotide Autogel (Somatuline Depot) 120 mg
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 \[whichever occurred first\]).
Placebo comparator
Placebo (DB) and lanreotide Autogel 120 mg in IOL and LTOLE
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 \[whichever occurred first\]).
Outcomes the sponsor listed as primary.
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.
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
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).
Proportion of Subjects Who Rolled Over Into the IOL Phase Before Completing the DB Phase of the Study
Time frame · 16-week DB phase
Subjects who rolled over early were those who received less than four DB injections before receiving the first IOL injection.
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
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.
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
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.
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
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.
Absolute Changes From Baseline in Biochemical Markers (Plasma Chromogranin A [CgA])
Time frame · Baseline and Week 12 of DB phase
Baseline is defined as the last non-missing observation obtained prior to the initiation of study treatment.
Absolute Changes From Baseline in Biochemical Markers (Urinary 5-hydroxyindoleacetic Acid [5-HIAA])
Time frame · Baseline and Week 12 of DB phase
Baseline is defined as the last non-missing observation obtained prior to the initiation of study treatment.
Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.
| Group | Value (Percentage of days) |
|---|---|
| Lanreotide Autogel (Somatuline Depot) 120 mg | 33.72 |
| Placebo | 48.49 |
| Group | Value (Number of events per day) | Spread |
|---|---|---|
| Lanreotide Autogel (Somatuline Depot) 120 mg | 1.56 | 1.83 |
| Placebo | 1.35 | 1.45 |
| Group | Value (Number of events per day) | Spread |
|---|---|---|
| Lanreotide Autogel (Somatuline Depot) 120 mg | 0.92 | 1.45 |
| Placebo | 1.75 | 2.26 |
| Group | Value (Percentage of days) | Spread |
|---|---|---|
| Lanreotide Autogel (Somatuline Depot) 120 mg | 8.86 | 19.34 |
| Placebo | 6.25 | 17.48 |
| Group | Value (Percentage of subjects) |
|---|---|
| Lanreotide Autogel (Somatuline Depot) 120 mg | 18.6 |
| Placebo | 21.4 |
| Group | Value (Units on a scale) | Spread |
|---|---|---|
| Lanreotide Autogel (Somatuline Depot) 120 mg | 4.17 | 14.18 |
| Placebo | -1.72 | 18.21 |
| Group | Value (Units on a scale) | Spread |
|---|---|---|
| Lanreotide Autogel (Somatuline Depot) 120 mg | -4.06 | 12.80 |
| Placebo | 0.10 | 13.83 |
| Group | Value (Units on a scale) | Spread |
|---|---|---|
| Lanreotide Autogel (Somatuline Depot) 120 mg | -6.83 | 18.98 |
| Placebo | -2.69 | 22.23 |
| Group | Deaths | Serious events | Other events |
|---|---|---|---|
| Lanreotide Autogel (Somatuline Depot) 120 mg (DB Phase)Deep s.c. injections of lanreotide Autogel 120 mg every 4 weeks (±3 days) for 16 weeks (DB phase). Subjects then received deep s.c. injections of lanreotide Autogel 120 mg every 4 weeks for 32 weeks in the IOL phase and further deep s.c. injections with lanreotide Autogel every 4 weeks in the LTOLE phase. | – | 2 / 58 | 31 / 58 |
| Placebo (DB Phase)Deep s.c. injections of placebo every 4 weeks (±3 days) for 16 weeks (DB phase). Subjects then received deep s.c. injections of lanreotide Autogel 120 mg every 4 weeks for 32 weeks in the IOL phase and further deep s.c. injections with lanreotide Autogel every 4 weeks in the LTOLE phase. | – | 5 / 57 | 34 / 57 |
| Lanreotide Autogel (Somatuline Depot) 120 mg (IOL Phase)All 101 subjects in the IOL phase received deep s.c. injections of lanreotide Autogel 120 mg every 4 weeks for 32 weeks (56 and 45 of these subjects received treatment with lanreotide Autogel and placebo, respectively, during the DB phase). | – | 8 / 101 | 71 / 101 |
| Lanreotide Autogel (Somatuline Depot) 120 mg (LTOLE Phase)All 57 subjects in the LTOLE phase received further deep s.c. injections of lanreotide Autogel 120 mg every 4 weeks (32 and 25 of these subjects received treatment with lanreotide Autogel and placebo, respectively, during the DB phase). | – | 15 / 57 | 46 / 57 |
Each cell reads participants affected / participants at risk, as the registry posted them.
Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works
Studies that cite this trial.
2 studies on this page
PubMed tag: none · 2019
Blot et al. 2019Patient related outcome measurescited by 2
PMID 31754316PMC6825468DOI 10.2147/prom.s219982PUB-31754316
Indexing hint: Randomized controlled trial · 2016
Vinik et al. 2016Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologistscited by 73
PMID 27214300DOI 10.4158/ep151172.orPUB-27214300
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