CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 97 enrolled
Drug / intervention
Emibetuzumab +1 moredrug
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/NCT02082210
NCT02082210Phase 2Completed

A Phase 1b/2 Study of Ramucirumab in Combination With LY2875358 in Patients With Advanced Cancer

Eli Lilly and Company·interventional·Posted Mar 10, 2014·Updated Dec 19, 2020

In Brief

A Phase 2 clinical trial evaluating Emibetuzumab and Ramucirumab for Advanced Cancer and 5 related conditions. Completed, enrolled 97 participants across 4 sites.

Detailed Summary

The purpose of this study is to find a recommended schedule and dose range for Emibetuzumab when given with ramucirumab that may be safely given to participants with cancer. In Part A of this study, escalating doses of Emibetuzumab will be given in combination with a fixed dose of ramucirumab to evaluate the safety of the combination. After a recommended schedule and dose range of Emibetuzumab and ramucirumab has been established, Part B of the study will confirm safety and to see how well certain tumors respond to the combination of study drugs. The average amount of time on study is expected to be about 6 months.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedMar 10, 2014
Enrollment StartMar 7, 2014
Primary CompletionDec 5, 2017
Study CompletionJan 24, 2018
TodayJul 2, 2026
Enrollment to primary: 3.7 yearsPosted 12.3 years ago

Interventions

Emibetuzumabdrug

Administered Intravenously (IV)

Ramucirumabdrug

Administered Intravenously (IV)