drugset / Trial / NCT02698410

Efficacy and Safety of Lanreotide Autogel (ATG) in Combination With Temozolomide in Subjects With Thoracic Neuroendocrine Tumors.

NCT02698410

Phase 2 Completed 40 enrolled Ipsen
NaSingle-groupOpen-labelTreatment

Summary

The purpose of the protocol is to evaluate the efficacy and safety of Lanreotide ATG 120 mg in combination with Temozolomide in subjects with unresectable advanced neuroendocrine tumours of the lung or thymus as Disease Control Rate at 9 months.

Timeline

Start
2016-07
Primary completion
2019-02-08
Completion
2019-06-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Lanreotide Other / unclassified 120 mg Subcutaneous
Subject Temozolomide Small molecule 250 mg Oral