AD-233A
DrugPO, Once daily(QD), 24 weeks
NCT Number: NCT07816198
The purpose of this study is to evaluate the efficacy and safety of AD-233A, AD-233B, AD-233C and/or AD-233D combination therapy
Trial opening soon.
Get Notified19 year and older
All sexes
Interventional
Phase 3
Condition or disease: Type 2 Diabetes Mellitus
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
PO, Once daily(QD), 24 weeks
PO, Once daily(QD), 24 weeks
PO, Once daily(QD), 24 weeks
PO, Once daily(QD), 24 weeks
PO, Once daily(QD), 24 weeks
PO, Once daily(QD), 24 weeks
Time frame: Baseline, Week 24
Contact information is provided by the study sponsor or research team.
Addpharma Inc.
Industry
A Multicenter, Randomized, Double-blind, Active-controlled, Phase III Study to Evaluate the Efficacy and Safety of AD-233A, AD-233B, AD-233C and/or AD-233D Combination Therapy in Patients With Type 2 Diabetes Mellitus
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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