drugset / Trial / NCT02698410
Efficacy and Safety of Lanreotide Autogel (ATG) in Combination With Temozolomide in Subjects With Thoracic Neuroendocrine Tumors.
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Lanreotide | Other / unclassified | 120 mg | Subcutaneous |
| Subject | Temozolomide | Small molecule | 250 mg | Oral |