jRCT ロゴ

臨床研究等提出・公開システム

Top

Japanese

Mar. 09, 2023

Mar. 06, 2025

jRCTs051220187

Amelioration of beta cell function in drug-naive type 2 diabetes with tofogliflozin, oral semaglutide or imeglimin: A multicenter randomized trial ((ABCD-TO-SEIZE trial))

A multicenter trial on the effects of oral hypoglycemic agents on beta-cell function in drug-naive type 2 diabetes ((ABCD-TO-SEIZE trial))

Furukawa Yasushi

Wakayama Medical University Hospital

811-1 Kimiidera, Wakayama City, Wakayama, Japan

+81-73-441-0625

y-furuka@wakayama-med.ac.jp

Furukawa Yasushi

Wakayama Medical University Hospital

811-1 Kimiidera, Wakayama City, Wakayama, Japan

+81-73-441-0625

y-furuka@wakayama-med.acj.jp

Recruiting

Mar. 09, 2023

May. 26, 2023
87

Interventional

randomized controlled trial

open(masking not used)

active control

parallel assignment

treatment purpose

1) Patients aged at least 18 years at the time of consent acquisition.
2) Patients with type 2 diabetes requiring medication.
3) Patients who have never been treated with medication for type 2 diabetes.
4) Patients with HbA1c less than 9.0%.
5) Patients who have the capacity to consent and have provided written informed consent.

(1) Patients with type 1 diabetes.
(2) Patients requiring insulin therapy (e.g., insulin-dependent, insulin-independent but requiring insulin therapy to correct hyperglycemia, severe ketosis, diabetic coma or pre-coma, severe infection, pre- or postoperative, severe pancreatic disease, severe trauma).
(3) Patients with a history of taking alpha glucosidase inhibitors or SGLT2 inhibitors.
(4) Patients who are pregnant or lactating or may be pregnant or wish to become pregnant during the research period.
(5) Patients with inadequately treated endocrine disorders (e.g., pituitary, adrenal or thyroid disease).
(6) Patients with heart failure symptoms of NYHA functional class III or IV.
(7) Patients with diagnosed or suspected malignancy.
(8) Patients treated with oral or injectable corticosteroids.
(9) Patients with eGFR <45 mL/min/1.72 m^2.
(10) Patients with severe liver disease (AST or ALT > 100 IU/L).
(11) Patients with poorly controlled dysuria due to neurogenic bladder, benign prostatic hyperplasia, etc.
(12) Patients with symptomatic urinary tract infection or genital infection.
(13) Patients with a history of cerebral infarction.
(14) Patients with a history of renal disease, such as nephrectomy, renal transplantation, etc.
(15) Patients who underwent gastrectomy.
(16) Patients who cannot avoid eating, drinking, or taking other medications for at least 30 minutes after waking up.
(17) Patients currently participating in other interventional trials (including clinical trials).
(18) Patients judged as ineligible for participation in this study by the Principal Investigator, Site Principal Investigator or Sub-Investigator.

18age old over
No limit

Both

Type 2 Diabetes

The subjects are randomly assigned to one of three groups and treated for 24 weeks: T) Tofogliflozin 20 mg/day, S) oral semaglutide 3, 7 or 14 mg/day and I) imeglimin 2000 mg/day. Randomization will be performed using a dynamic randomization algorithm designed to minimize imbalance in BMI and 75-g oral glucose tolerance test derived disposition index (DI) before treatment. The subjects will undergo a 75-g oral glucose tolerance test at week 25 (after a 1-week wash-out period).

Change in Disposition Index (DI: Insulinogenic Index(II)120 min * Matsuda index) at week 25 (after 1-week wash-out period) from baseline

(1) Change in the following other DIs from baseline at week 25:
1.DI2: II 30 min * Matsuda index
2.DI3: II 30 min * 1/Ins0
3.DI4: delta AUCIns0-120 / delta AUCGlu0-120 *
Matsuda index

(2) Change in II 30 min and II 120 min from baseline at week 25

(3) Percentage change in the following DIs from baseline at week 25:
1.DI: II 120 min * Matsuda index
2.DI2: II 30 min * Matsuda index
3.DI3: II 30 min * 1/Ins0
4.DI4: delta AUCIns0-120 / delta AUCGlu0-120 * Matsuda index

(4) Percentage change in II 30 min and II 120 min from baseline at week 25

(5) Change in the following parameters at week 25 from baseline:
1.HbA1C
2.Fasting glucose
3.HOMA-Beta*
*HOMA-beta = (0-min insulin levels*360) / (0-min glucose levels-63)
4. BMI, blood pressure, pulse rate, Hb, TG, LDL-C, HDL-C, UN, Cr, UA, GFR, Na, K, Cl, AST, ALT, gamma-GTP, ALP

Kowa Company, Ltd.
Not applicable
Wakayama Medical University Certified Review Board
811-1 Kimiidera, Wakayama, Wakayama

+81-73-441-0896

wa-rinri@wakayama-med.ac.jp
Approval

Dec. 23, 2022

No

none

History of Changes

No Publication date
10 Mar. 06, 2025 (this page) Changes
9 June. 03, 2024 Detail Changes
8 May. 31, 2024 Detail Changes
7 May. 07, 2024 Detail Changes
6 July. 03, 2023 Detail Changes
5 June. 30, 2023 Detail Changes
4 June. 28, 2023 Detail Changes
3 May. 29, 2023 Detail Changes
2 April. 06, 2023 Detail Changes
1 Mar. 09, 2023 Detail