At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 9 enrolled
Drug / intervention
Mizagliflozindrug
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.
Phase 2 Randomized Single Ascending Dose Study in Post-Bariatric Hypoglycemia Subjects to Determine the Effect of Mizagliflozin Formulations on Postprandial Glucose and Insulin Levels
In Brief
A Phase 2 clinical trial evaluating Mizagliflozin for Postbariatric Hypoglycemia. Completed, enrolled 9 participants across 2 sites.
Detailed Summary
This clinical study will examine the safety and tolerability, as well as the effects of orally administered mizagliflozin on post prandial glucose and insulin levels in subjects diagnosed with post-bariatric hypoglycemia (PBH).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPostbariatric Hypoglycemia
CountriesUnited States
Collaborators--
Timeline
Phase 2CompletedFinished
2023202420252026
Enrollment StartSep 2022
First PostedSep 2022
Primary CompletionFeb 2023
TodayJul 2026
First PostedSep 15, 2022
Enrollment StartSep 13, 2022
Primary CompletionFeb 17, 2023
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 3.8 years ago
Interventions
Mizagliflozindrug
Encapsulated or Liquid Formulation