Type 2 Diabetes Mellitus Clinical Trial
— TETRISOfficial title:
Efficacy and Safety of Teneligliptin Versus Sitagliptin as add-on Therapy to Metformin Plus Glimepiride in T2DM Patinets With Inadequate Glycemic Control
NCT number | NCT02567994 |
Other study ID # | MP_C303 |
Secondary ID | |
Status | Completed |
Phase | Phase 3 |
First received | |
Last updated | |
Start date | April 2015 |
Est. completion date | December 2017 |
Verified date | April 2018 |
Source | Handok Pharmaceuticals Co., Ltd. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
After a screening, a 2-week, single-blind placebo run-in, 200 patients will be randomized in a 1 : 1 ratio to the addition of either once-daily Teneligliptin 20mg or sitagliptin 100mg to ongoing stable doses of glimepiride in combination with metformin for 24 weeks.
Status | Completed |
Enrollment | 201 |
Est. completion date | December 2017 |
Est. primary completion date | October 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 19 Years and older |
Eligibility |
Inclusion Criteria: 1. Patients with Type 2 Diabetes Mellitus 2. Adults aged = 19 years old 3. Patients with HbA1c 7%~11% at Screening and Run-in visit Exclusion Criteria: |
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Samsung Medical Center | Seoul |
Lead Sponsor | Collaborator |
---|---|
Handok Pharmaceuticals Co., Ltd. |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change of HbAlc from baseline at Week 24 | 24 weeks |
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