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NCT05721729

Effect of Mizagliflozin Repeat Dosing on Adverse Events and Postprandial Glucose Excursions

Completed Phase 2 Last updated 18 December 2025
What this trial tests

Phase 2 trial testing Mizagliflozin in Postbariatric Hypoglycemia in 15 participants. Completed in 1 June 2025.

Timeline
23 June 2023
Primary endpoint
1 May 2024
1 June 2025

Quick facts

Lead sponsorVogenx, Inc.
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingtriple
Primary purposetreatment
Enrollment15
Start date23 June 2023
Primary completion1 May 2024
Estimated completion1 June 2025
Sites2 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Vogenx, Inc.

Who can join

Adults 18 to 75, any sex, with Postbariatric Hypoglycemia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a phase 2 crossover, randomized, placebo-controlled, single-blind, repeat dose study in PBH subjects to determine the effect of mizagliflozin on adverse events and postprandial glucose excursions.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. OR08-04 Efficacy and Safety of the SGLT1 Inhibitor Mizagliflozin in Patients with Post-Bariatric Hypoglycemia
    · 2025
  2. Managing post-bariatric hypoglycemia: a systematic review of pharmacological therapies.
    Sridharan K, Sivaramakrishnan G. · · 2025 · PMID 41126373 · DOI 10.1186/s13098-025-01988-y

Verify or expand the search:

Other trials of Mizagliflozin

Trials testing the same drug.

Other recruiting trials for Postbariatric Hypoglycemia

Currently open trials in the same condition.

Other Vogenx, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05721729.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing