CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 256 enrolled
Drug / intervention
Axitinib +2 moredrug
Likely dose
Axitinib 5mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01744249
NCT01744249Phase 3Completed

A Phase II/III Randomized Double-blind Study of Sandostatin LAR in Combination With Axitinib Versus Sandostatin LAR With Placebo in Patients With Advanced G1-G2 Neuroendocrine Tumours (WHO 2010) of Non-pancreatic Origin

Grupo Espanol de Tumores Neuroendocrinos·interventional·Posted Dec 6, 2012·Updated Apr 28, 2026

In Brief

A Phase 3 clinical trial evaluating Axitinib, Sandostatin LAR, and 1 other intervention for Neuroendocrine Tumors and Advanced Cancer. Completed, enrolled 256 participants across 26 sites in 4 countries.

Detailed Summary

Assess whether therapy with axitinib, a potent angiogenic inhibitor of the tyrosine kinase receptors of VEGF bioavailable by oral administration, is capable of improving PFS in patients with advanced G1-G2 NETs of nonpancreatic origin with progressive disease documented in the 12 months prior to entering the study.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesGermany, Italy, Spain, United Kingdom
CollaboratorsPfizer

Timeline

Phase 3CompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedDec 6, 2012
Enrollment StartNov 1, 2011
Primary CompletionDec 31, 2023
TodayJul 2, 2026
Enrollment to primary: 12.2 yearsPosted 13.6 years ago

Interventions

Axitinibdrug

Orally, 5mg, twice daily, until progression or until unacceptable toxicity, with or without food intake.

Sandostatin LARdrug

Intramuscular, 30mg, single injection every 28 days, until disease progression or unacceptable toxicity

Placebodrug

orally, twice daily, until disease progression or unacceptable toxicity, with or without food intake.