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A Multicenter, Randomized, Double-blind Study of the Safety and Efficacy of REAMBERIN®, 1.5% Solution for Infusions, in Addition to Standard Rehydration Therapy in Patients With Diabetic Ketoacidosis
A number of scientific papers have been published on the efficacy and safety of adding REAMBERIN® (meglumin sodium succinate), a 1.5% infusion solution, to standard therapy for patients with diabetic ketoacidosis (DKA), which showed that the addition of the medication to DKA therapy at a dose of 10 ml/kg/day or an average of 800.68±151.59 ml on the first day of infusion, leads to a more rapid and successful resolution of DKA, achieving a state of compensation, a more rapid transfer of the patient from the intensive care unit (ICU) and discharge from the hospital. A combined, two-stage, multicenter, randomized, double-blind, phase II/III study with an adaptive design is planned. Stage 1 (phase II) will be a sequential evaluation of 2 doses of the study medication (750 ml and 1500 ml) versus placebo. At the 2nd stage of the study (phase III), additional recruitment of patients will be carried out in two groups in a 1:1 ratio to the experimental group or placebo group, to receive the optimal dose in accordance with the result obtained at stage 1.
Age
18 - 75 years
Sex
ALL
Healthy Volunteers
No
State Budgetary Institution of Healthcare of the Arkhangelsk Region "First City Clinical Hospital named after E.E. Volosevich"
Arkhangelsk, Russia
Regional budgetary healthcare institution "Ivanovo regional clinical hospital"
Ivanovo, Russia
Kuzbass Clinical Hospital of Emergency Medical Care named after M.A. Podgorbunsky
Kemerovo, Russia
Start Date
May 1, 2025
Primary Completion Date
December 1, 2027
Completion Date
December 31, 2027
Last Updated
June 24, 2025
312
ESTIMATED participants
Reamberin
DRUG
Placebo
DRUG
Lead Sponsor
POLYSAN Scientific & Technological Pharmaceutical Company
NCT06693115
NCT07423559
Data Source & Attribution
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