Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07300007

PK and Relative Bioavailability of Liquid Metformin vs Tablets in Healthy Adults

An Open-Label, Randomized, Crossover Study to Characterize the Pharmacokinetics and Relative Bioavailability of Liquid Metformin at 100 mg/mL and 250 mg/mL Compared With Standard Metformin Tablets

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
24 (estimated)
Sponsor
Aspargo Labs, Inc · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

The study will evaluate the pharmacokinetics and relative bioavailability of two liquid metformin formulations (100 mg/mL and 250 mg/mL)

Detailed description

The study will compare the pharmacokinetic profiles of two liquid metformin formulations (100 mg/mL and 250 mg/mL) with a standard metformin immediate-release tablet.

Conditions

Interventions

TypeNameDescription
DRUGLiquid Metformin 100 mg/mLA single oral dose of liquid metformin at a concentration of 100 mg/mL will be administered under fasting conditions in one treatment period of the crossover.
DRUGLiquid Metformin 250 mg/mLA single oral dose of liquid metformin at a concentration of 250 mg/mL will be administered under fasting conditions in one treatment period of the crossover.

Timeline

Start date
2026-03-15
Primary completion
2026-05-15
Completion
2026-05-28
First posted
2025-12-23
Last updated
2025-12-23

Regulatory

Source: ClinicalTrials.gov record NCT07300007. Inclusion in this directory is not an endorsement.