Somatuline Depot (lanreotide prolonged-release subcutaneous) / Ipsen 
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 41 Diseases   16 Trials   16 Trials   501 News 


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  • ||||||||||  Somatuline Depot (lanreotide prolonged-release subcutaneous) / Ipsen
    Enrollment change:  Comparison of Lanreotide Autogel (clinicaltrials.gov) -  Apr 30, 2020   
    P3,  N=4, Terminated, 
    Recruiting --> Active, not recruiting | N=40 --> 13 N=196 --> 4
  • ||||||||||  Somatuline Depot (lanreotide prolonged-release subcutaneous) / Ipsen, Teijin
    Review, Journal:  Medical Treatment with Somatostatin Analogues in Acromegaly: Position Statement. (Pubmed Central) -  Apr 10, 2020   
    This position statement includes the characteristics, indications, dose, interval (including extended dose interval in case of lanreotide autogel), switching and preoperative use of somatostatin analogues in medical treatment of acromegaly. The recommended approach is based on the expert opinions in case of insufficient clinical evidence, and where discrepancies among the expert opinions were found, the experts voted to determine the recommended approach.
  • ||||||||||  Keytruda (pembrolizumab) / Merck (MSD), Somatuline Depot (lanreotide prolonged-release subcutaneous) / Ipsen
    Enrollment closed:  PLANET: Study of Pembrolizumab With Lanreotide Depot for Gastroenteropancreatic Neuroendocrine Tumors (clinicaltrials.gov) -  Apr 7, 2020   
    P1/2,  N=22, Active, not recruiting, 
    The recommended approach is based on the expert opinions in case of insufficient clinical evidence, and where discrepancies among the expert opinions were found, the experts voted to determine the recommended approach. Suspended --> Active, not recruiting
  • ||||||||||  Somavert (pegvisomant) / Pfizer, Somatuline Depot (lanreotide prolonged-release subcutaneous) / Ipsen, Teijin, Signifor LAR (pasireotide) / Novartis
    [VIRTUAL] MEDICATIONS FOR ACROMEGALY- COST-UTILITY AND VALUE OF INFORMATION ANALYSIS () -  Mar 8, 2020 - Abstract #ISPOR2020ISPOR_1148;    
    No second-line treatment is recommended. Significant uncertainty of parameters impairs optimal decision-making, and this conclusion can be generalized to other countries.
  • ||||||||||  Somatuline Depot (lanreotide prolonged-release subcutaneous) / Ipsen, Teijin
    Retrospective data, Journal:  Efficacy and safety of lanreotide in Korean patients with metastatic, well-differentiated gastroenteropancreatic-neuroendocrine tumors: a retrospective analysis. (Pubmed Central) -  Feb 9, 2020   
    Lanreotide autogel is a long-acting somatostatin analogue with proven efficacy and safety in patients with well-differentiated (WD) gastroenteropancreatic-neuroendocrine tumors (GEP-NETs) in a prior randomized phase III trial (CLARINET)...Hepatic tumor volume > 25% and prior systemic therapy were significantly associated with poorer PFS in the multivariate analysis. Lanreotide is well-tolerated and effective for Korean patients with GEP-NETs in the daily practice setting.
  • ||||||||||  Somatuline Depot (lanreotide prolonged-release subcutaneous) / Ipsen, Teijin
    Clinical, Journal:  A Patient-Reported Outcomes Analysis Of Lanreotide In The Treatment Of NETs Patients With Carcinoid Syndrome: Evidence From The ELECT Trial. (Pubmed Central) -  Nov 24, 2019   
    P3
    The purpose of this analysis of patient-reported outcomes from the ELECT (Evaluation of Lanreotide Depot/Autogel Efficacy and Safety as a Carcinoid Syndrome Treatment) trial (NCT00774930) was to explore the effect of lanreotide on symptoms of carcinoid syndrome...The higher response rates in the diarrhea burden are consistent with the previously reported effects of lanreotide on octreotide rescue medication use, while the findings of a greater efficacy of lanreotide vs placebo in the quality-of-life domains represent a novel aspect in the benefits of lanreotide. ClinicalTrials.gov identifier: NCT00774930.
  • ||||||||||  Somatuline Depot (lanreotide prolonged-release subcutaneous) / Ipsen
    Trial termination, HEOR, Combination therapy:  QoL in IMBO: Quality of Life in Patients With Inoperable Malignant Bowel Obstruction (clinicaltrials.gov) -  Oct 1, 2019   
    P2,  N=43, Terminated, 
    Some patients treated with octreotide were unaware of an SSA with the flexibility of self-injection. Completed --> Terminated; The study was terminated early due to insufficient recruitment.
  • ||||||||||  Somatuline Depot (lanreotide prolonged-release subcutaneous) / Ipsen
    Enrollment change, Trial withdrawal, Metastases:  NETways: Study to Assess the Use of Lanreotide Autogel (clinicaltrials.gov) -  Aug 6, 2019   
    P=N/A,  N=0, Withdrawn, 
    Final analyses are expected in Q1 2020, which will provide efficacy and safety data on use of LAN 120 mg at an increased dosing frequency. N=271 --> 0 | Not yet recruiting --> Withdrawn
  • ||||||||||  Somatuline Depot (lanreotide prolonged-release subcutaneous) / Ipsen, Teijin
    Trial primary completion date, Metastases:  Study of Lanreotide in Metastatic or Recurrent Grade I-II Hindgut NET (clinicaltrials.gov) -  May 20, 2019   
    P4,  N=28, Recruiting, 
    Trial primary completion date: Apr 2019 --> Apr 2020 Trial primary completion date: Feb 2019 --> Feb 2020
  • ||||||||||  Somatuline Depot (lanreotide prolonged-release subcutaneous) / Ipsen
    Enrollment change, Trial completion date, Trial primary completion date, Metastases:  SPINET: Efficacy and Safety of Lanreotide Autogel/ Depot 120 mg vs. Placebo in Subjects With Lung Neuroendocrine Tumours (clinicaltrials.gov) -  Mar 4, 2019   
    P3,  N=77, Active, not recruiting, 
    Trial completion date: Oct 2019 --> Feb 2020 | Trial primary completion date: Oct 2019 --> Feb 2020 N=216 --> 77 | Trial completion date: Aug 2019 --> Feb 2020 | Trial primary completion date: Aug 2019 --> Feb 2020
  • ||||||||||  Somatuline Depot (lanreotide prolonged-release subcutaneous) / Ipsen
    Trial completion date, Trial primary completion date, Metastases:  Community-based Neuroendocrine Tumor (NET) Research Study (clinicaltrials.gov) -  Dec 24, 2018   
    P=N/A,  N=100, Active, not recruiting, 
    N=216 --> 77 | Trial completion date: Aug 2019 --> Feb 2020 | Trial primary completion date: Aug 2019 --> Feb 2020 Trial completion date: Dec 2019 --> May 2020 | Trial primary completion date: Dec 2019 --> May 2020
  • ||||||||||  Somatuline Depot (lanreotide prolonged-release subcutaneous) / Ipsen, Teijin
    Clinical, Review, Journal:  An update of lanreotide acetate for treatment of adults with carcinoid syndrome. (Pubmed Central) -  Nov 27, 2018   
    These compounds have shown dramatic responses in symptom control and reduction of serotonin metabolites including urinary 5-hydroxyindoleacetic acid (5-HIAA) levels. This review researches the origins of carcinoid tumors, the development of lanreotide as a treatment and future directions for the treatment of carcinoid syndrome.
  • ||||||||||  Somatuline Depot (lanreotide prolonged-release subcutaneous) / Ipsen, Teijin
    Enrollment open, Trial completion date, Trial initiation date, Trial primary completion date:  A Phase II Trial of Lanreotide for the Prevention of Postoperative Pancreatic Fistula (clinicaltrials.gov) -  Oct 12, 2018   
    P2,  N=123, Recruiting, 
    This review researches the origins of carcinoid tumors, the development of lanreotide as a treatment and future directions for the treatment of carcinoid syndrome. Not yet recruiting --> Recruiting | Trial completion date: Oct 2021 --> Apr 2021 | Initiation date: Oct 2017 --> Feb 2018 | Trial primary completion date: Oct 2020 --> Apr 2020
  • ||||||||||  Somatuline Depot (lanreotide prolonged-release subcutaneous) / Ipsen, Teijin
    Biomarker, P3 data, Retrospective data, Journal:  BIOCHEMICAL RESPONSES IN SYMPTOMATIC AND ASYMPTOMATIC PATIENTS WITH NEUROENDOCRINE TUMORS: POOLED ANALYSIS OF 2 PHASE 3 TRIALS. (Pubmed Central) -  Aug 8, 2018   
    This pooled analysis of 2 randomized, placebo-controlled trials demonstrated that 5-HIAA and CgA are secreted as biochemical biomarkers in many patients with NETs, regardless of clinical syndromes. Significant biochemical response was associated with improved clinical outcomes, as measured by improved PFS or improved CS symptom control.