CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 577 enrolled
Drug / intervention
Nivolumab +2 morebiological
Likely dose
Not stated in 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/NCT03906071
NCT03906071Phase 3Completed

A Randomized Phase 3 Study of Sitravatinib in Combination With Nivolumab Versus Docetaxel in Patients With Advanced Non-Squamous Non-Small Cell Lung Cancer With Disease Progression On or After Platinum-Based Chemotherapy and Checkpoint Inhibitor Therapy SAPPHIRE

Mirati Therapeutics Inc.·interventional·Posted Apr 8, 2019·Updated Oct 21, 2025

In Brief

A Phase 3 clinical trial evaluating Nivolumab, Sitravatinib, and 1 other intervention for Metastatic Non-Squamous Non-Small Cell Lung Cancer. Completed, enrolled 577 participants across 261 sites in 12 countries.

Detailed Summary

This study will compare the efficacy of the investigational agent sitravatinib in combination with nivolumab versus docetaxel in patients with advanced non-squamous NSCLC who have previously experienced disease progression on or after platinum-based chemotherapy and checkpoint inhibitor therapy.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBelgium, Canada, France, Germany, Hungary, Israel, Italy, Netherlands, Spain, Switzerland, United Kingdom, United States

Timeline

Phase 3CompletedFinished
2020202120222023202420252026
First PostedApr 8, 2019
Enrollment StartJul 15, 2019
Primary CompletionMar 20, 2023
Study CompletionSep 30, 2025
TodayJul 2, 2026
Enrollment to primary: 3.7 yearsPosted 7.2 years ago

Interventions

Nivolumabbiological

Nivolumab is an antibody directed at the programmed death receptor-1 (PD-1), blocking its interaction with PD-L1 and PD-L2.

Sitravatinibdrug

Sitravatinib is a small molecule inhibitor of receptor tyrosine kinases.

Docetaxeldrug

Docetaxel is an anti-neoplastic agent that acts by disrupting the microtubular network in cells.