Chu Hsien-I Memorial Hospital, Tianjin Medical University
Tianjin, China
NCT Number: NCT06703268
To assess the effectiveness of HSK7653 tablets following the substitution of daily DPP-4 inhibitor (DPP-4i) over a 24-week treatment period.
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Notify Me18 year–75 year
All sexes
Interventional
Phase 2
Tianjin, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
HSK7653 10 mg Q2W
Daily DPP-4 inhibitor
Time frame: 24 weeks
The change in time in range (TIR) of continuous glucose monitoring (CGM) relative to the baseline after 24 weeks of treatment.
Time frame: 24 weeks
Change from baseline in HbA1c after 24 weeks
Time frame: 24 weeks
Change from baseline in fasting glucose after 24 weeks
Time frame: 24 weeks
Change from baseline in mean glucose after 24 weeks
Time frame: 24 weeks
The incidence of treatment-emergent adverse events.
Haisco Pharmaceutical Group Co., Ltd.
Industry
A Multicenter, Randomized, Open-label, Controlled Study on Evaluating the Efficacy and Safety of Switching From Daily DPP-4 Inhibitors to HSK7653 Tablets in Patients With Type 2 Diabetes Mellitus in China
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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