Improved Glycemic Control with Minimal Systemic Metformin Exposure: Effects of Metformin Delayed-Release (Metformin DR) Targeting the Lower Bowel over 16 Weeks in a Randomized Trial in Subjects with Type 2 Diabetes
Overview
Authors
Affiliations
Objective: Metformin use is restricted in patients with renal impairment due to potential excess systemic accumulation. This study evaluated the glycemic effects and safety of metformin delayed-release (Metformin DR), which targets metformin delivery to the ileum to leverage its gut-based mechanisms of action while minimizing systemic exposure.
Research Designs And Methods: Participants (T2DM [HbA1c 7-10.5%], eGFR ≥60 mL/min/1.73m2, not taking metformin for ≥2 months) were randomized to QD placebo (PBO); QD Metformin DR 600, 900, 1200, or 1500 mg; or to single-blind BID Metformin immediate-release (IR) 1000 mg. The primary endpoint was change in HbA1c for Metformin DR vs. PBO at 16 weeks in the modified intent-to-treat (mITT) population (≥ 1 post-baseline HbA1c while on study drug), using a mixed-effects repeated measures model.
Results: 571 subjects were randomized (56 years, 53% male, 80% white; BMI 32.2±5.5 kg/m2; HbA1c 8.6±0.9%; 51% metformin naive); 542 were in the mITT population. Metformin DR 1200 and 1500 mg significantly reduced HbA1c (-0.49±0.13% and -0.62±0.12%, respectively, vs. PBO -0.06±0.13%; p<0.05) and FPG (Caverage Weeks 4-16: -22.3±4.2 mg/dL and -25.1±4.1 mg/dL, respectively vs. -2.5±4.2 mg/dL p<0.05). Metformin IR elicited greater HbA1c improvement (-1.10±0.13%; p<0.01 vs. Placebo and all doses of Metformin DR) but with ~3-fold greater plasma metformin exposure. Normalizing efficacy to systemic exposure, glycemic improvements with Metformin DR were 1.5-fold (HbA1c) and 2.1-fold (FPG) greater than Metformin IR. Adverse events were primarily gastrointestinal but these were less frequent with Metformin DR (<16% incidence) vs. Metformin IR (28%), particularly nausea (1-3% vs 10%).
Conclusion: Metformin DR exhibited greater efficacy per unit plasma exposure than Metformin IR. Future studies will evaluate the effects of Metformin DR in patients with type 2 diabetes and advanced renal disease.
Trial Registration: Clinicaltrials.gov NCT02526524.
Metformin for preventing the progression of chronic kidney disease.
El-Damanawi R, Stanley I, Staatz C, Pascoe E, Craig J, Johnson D Cochrane Database Syst Rev. 2024; 6:CD013414.
PMID: 38837240 PMC: 11152183. DOI: 10.1002/14651858.CD013414.pub2.
Bramante C, Beckman K, Mehta T, Karger A, Odde D, Tignanelli C Clin Infect Dis. 2024; 79(2):354-363.
PMID: 38690892 PMC: 11327787. DOI: 10.1093/cid/ciae159.
The gastrointestinal tract is a major source of the acute metformin-stimulated rise in GDF15.
Kincaid J, Rimmington D, Tadross J, Cimino I, Zvetkova I, Kaser A Sci Rep. 2024; 14(1):1899.
PMID: 38253650 PMC: 10803367. DOI: 10.1038/s41598-024-51866-2.
Metformin reduces SARS-CoV-2 in a Phase 3 Randomized Placebo Controlled Clinical Trial.
Bramante C, Beckman K, Mehta T, Karger A, Odde D, Tignanelli C medRxiv. 2023; .
PMID: 37333243 PMC: 10275003. DOI: 10.1101/2023.06.06.23290989.
Metformin acts in the gut and induces gut-liver crosstalk.
Tobar N, Rocha G, Santos A, Guadagnini D, Assalin H, Camargo J Proc Natl Acad Sci U S A. 2023; 120(4):e2211933120.
PMID: 36656866 PMC: 9942892. DOI: 10.1073/pnas.2211933120.