Clinical Trials Logo

Clinical Trial Summary

The purpose of the study is to evaluate the efficacy and tolerability of the combination of Lanreotide Autogel 120 mg and Temozolomide in patients with progressive gastro-entero-pancreatic neuroendocrine tumours (GEP-NET) graded as G1 or G2 (G1/G2). All progressive tumours classified according to Response Evaluation Criteria In Solid Tumours (RECIST, 1.1).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02231762
Study type Interventional
Source Ipsen
Contact
Status Completed
Phase Phase 2
Start date October 2014
Completion date June 2017

See also
  Status Clinical Trial Phase
Completed NCT02730104 - Community-based Neuroendocrine Tumor (NET) Research Study
Completed NCT02608203 - [68 Ga]-DOTANOC PET/CT in GEP-NETs Phase 2/Phase 3
Completed NCT01842165 - 177Lutetium-octreotate Treatment Prediction Using Multimodality Imaging in Refractory NETs Phase 3
Completed NCT02630654 - Study For Evaluating The Value Of A Multi Biomarker Approach In Metastatic GEP NETs
Terminated NCT02078843 - Diagnostic Accuracy of Gallium-68-DOTATATE PET/CT Compared to Indium-111-pentetreotide Scintigraphy (SPECT/CT) for Gastroenteropancreatic Neuroendocrine Tumors Phase 1/Phase 2
Completed NCT02162446 - 68Ga-OPS202 Study for Diagnostic Imaging of GEP NET Phase 1/Phase 2
Completed NCT03043664 - Study of Pembrolizumab With Lanreotide Depot for Gastroenteropancreatic Neuroendocrine Tumors Phase 1/Phase 2
Completed NCT04524442 - Post-Authorization Safety Study (PASS) of LysaKare® in Adult Gastroenteropancreatic Neuroendocrine Tumor (GEP-NET) Patients Phase 4
Active, not recruiting NCT04711135 - Study to Evaluate Safety and Dosimetry of Lutathera in Adolescent Patients With GEP-NETs and PPGLs Phase 2