CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 272 enrolled
Drug / intervention
LY2963016 +2 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/NCT03338023
NCT03338023Phase 3Completed

A Prospective, Randomized, Open-Label Comparison of a Long-Acting Basal Insulin Analog, LY2963016, to Lantus® in Combination With Mealtime Insulin Lispro in Adult Chinese Patients With Type 1 Diabetes Mellitus

Eli Lilly and Company·interventional·Posted Nov 9, 2017·Updated Mar 29, 2021

In Brief

A Phase 3 clinical trial evaluating LY2963016, Lantus®, and 1 other intervention for Type 1 Diabetes. Completed, enrolled 272 participants across 20 sites.

Detailed Summary

The purpose of this study is to compare long-acting basal insulin analog LY2963016 to Lantus® in combination with mealtime insulin lispro in adult Chinese participants with Type 1 Diabetes Mellitus (T1DM).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsType 1 Diabetes
CountriesChina
Collaborators--

Timeline

Phase 3CompletedFinished
201820192020202120222023202420252026
First PostedNov 9, 2017
Enrollment StartMar 23, 2018
Primary CompletionMar 5, 2020
TodayJul 2, 2026
Enrollment to primary: 1.9 yearsPosted 8.6 years ago

Interventions

LY2963016drug

Administered SC

Lantus®drug

Administered SC

Insulin Lisprodrug

Administered SC