At a glance
ClinicalIndex Comparison RecordPhase 3Completed· 20 enrolled
Drug / intervention
Xeris glucagon +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.
Equivalence of A Stable Liquid Glucagon Formulation With Freshly Reconstituted Lyophilized Glucagon
In Brief
A Phase 3 clinical trial evaluating Xeris glucagon and Lilly glucagon for Type 1 Diabetes. Completed, enrolled 20 participants across 1 site.
Detailed Summary
This study will test the hypothesis that micro-doses of Xerisol Glucagon (Xeris Pharmaceuticals) will be non-inferior by pharmacokinetic and pharmacodynamic criteria vs. micro-doses of Glucagon for Injection (Eli Lilly).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsType 1 Diabetes
CountriesUnited States
Collaborators--
Timeline
Phase 3CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedDec 2013
Enrollment StartApr 2014
Primary CompletionAug 2018
TodayJul 2026
First PostedDec 23, 2013
Enrollment StartApr 1, 2014
Primary CompletionAug 2, 2018
TodayJul 2, 2026
Enrollment to primary: 4.3 yearsPosted 12.5 years ago
Interventions
Xeris glucagondrug
The subject is given an injection of xeris glucagon
Lilly glucagondrug
The subject is given an injection of lilly glucagon