CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 49 enrolled
Drug / intervention
LY900014-U200 +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/NCT03334448
NCT03334448Phase 1Completed

Bioequivalence Study Comparing the Pharmacokinetics and Glucodynamics of LY900014 U-200 Formulation With LY900014 U-100 Formulation in Healthy Subjects

Eli Lilly and Company·interventional·Posted Nov 7, 2017·Updated May 1, 2020

In Brief

A Phase 1 clinical trial evaluating LY900014-U200 and LY900014-U100 for Healthy. Completed, enrolled 49 participants across 1 site.

Detailed Summary

The study involves a comparison of a LY900014 U-200 formulation with a LY900014 U-100 formulation. LY900014 is a type of fast acting insulin. Study participants will be administered LY900014 U-100 two times and LY900014 U-200 two times, over 4 study periods, by injection under the skin. Blood samples will be taken to compare how the body handles the study drugs and how they affect the blood sugar levels. Side effects and tolerability will be documented. The study will last about 4 weeks, not including screening and follow up. Screening is required within 28 days prior to the start of the study and follow up is required at least 2 weeks after the last dose of study drug.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy
CountriesSingapore
Collaborators--

Timeline

Phase 1CompletedFinished
201820192020202120222023202420252026
First PostedNov 7, 2017
Enrollment StartDec 4, 2017
Primary CompletionMar 15, 2018
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 8.7 years ago

Interventions

LY900014-U200drug

Administered SC

LY900014-U100drug

Administered SC