drugset / Trial / NCT03635437

Evaluation of Safety and Diabetes Status Upon Oral Treatment With GABA in Patients With Longstanding Type-1 Diabetes

NCT03635437

Phase 1/2 Completed 35 enrolled Per-Ola Carlsson Diamyd Medical AB · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The main goal of this study is to find a reasonably safe and tolerable treatment for adult patients with type 1-diabetes and that regain some of the endogenous insulin secretion, improve the patients' quality of life (QoL) and reduce the risk of both short- and long-term complications. The hypothesis tested is that oral GABA treatment with the newly developed compound Remygen will be safe and induce regain of some endogenous insulin secretion in adult patients with type 1-diabetes diagnosis for more than five years. The first part of the study will include 6 patients and be performed as a Safety and Dose Escalation study in three steps. The main study is a three-arm, open label, single center, clinical trial. Eligible patients will be randomized into one of three active treatment arms to receive oral GABA treatment for 6 months.

Timeline

Start
2018-09-05
Primary completion
2022-09-27
Completion
2022-09-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Alprazolam Small molecule 0.5 mg Oral
Subject Gamma-Aminobutyric Acid Small molecule 200 mg Oral
Subject Gamma-Aminobutyric Acid Small molecule 600 mg Oral
Subject Gamma-Aminobutyric Acid Small molecule 1200 mg Oral