CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 185 enrolled
Drug / intervention
Nivolumab +1 moredrug
Likely dose
Nivolumab 3 mg/kgfrom 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/NCT03591731
NCT03591731Phase 2Completed

A GCO Trial Exploring the Efficacy and Safety of Nivolumab Monotherapy or Nivolumab Plus Ipilimumab in Pre-treated Patients With Advanced, Refractory Pulmonary or Gastroenteropancreatic Poorly Differentiated Neuroendocrine Tumors (NECs)

Intergroupe Francophone de Cancerologie Thoracique·interventional·Posted Jul 19, 2018·Updated Apr 1, 2025

In Brief

A Phase 2 clinical trial evaluating Nivolumab and Ipilimumab for Neuroendocrine Carcinoma. Completed, enrolled 185 participants across 7 sites.

Detailed Summary

Neuroendocrine tumors of the lung include the small cell carcinoma (SCLC), and large cell neuroendocrine carcinoma (LCNEC) and represent 20% of lung cancer. One of the only studies reported to date is reporting on a progression-free survival (PFS) and overall survival (OS) of 5.2 months and 7.7 months, respectively. Poorly differentiated gastroentero-pancreatic neuroendocrine carcinomas (GEP-NEC) represent a small sub-group of digestive NENs, according to the studies, 7 to 21% of patients. However, their prognosis is more negative, with the 5-year survival at less than 20%. Many Phase III trials showed superiority in terms of efficacy and tolerance of nivolumab+/-ipilimumab versus standard chemotherapy in second-line treatment in metastatic solid tumors. Neuroendocrine tumors are considered as rare disease without therapeutic guidelines in this setting. The French academic oncology groups (IFCT, FFCD and GERCOR) have the opportunity to recruit a sufficient number of patients, in a reasonable period of time, to provide a proof-of-concept of the safety and efficacy of nivolumab+/-ipilimumab in this population.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesFrance

Timeline

Phase 2CompletedFinished
20192020202120222023202420252026
First PostedJul 19, 2018
Enrollment StartJan 2, 2019
Primary CompletionJul 9, 2021
Study CompletionDec 15, 2024
TodayJul 2, 2026
Enrollment to primary: 2.5 yearsPosted 8.0 years ago

Interventions

Nivolumabdrug

Nivolumab 3 mg/kg every 2 weeks

Ipilimumabdrug

Ipilimumab 1 mg/kg every 6 weeks