- |||||||||| Inpefa (sotagliflozin) / Lexicon Pharma, YG1699 / Youngene Therap
Effects of YG1699 and Sotagliflozin on Intestinal Glucose Absorption and GLP-1 in Mice (Poster Halls B-C; [Board No. 882]) - Apr 10, 2023 - Abstract #ADA2023ADA_1456; Background and Aims: YG1699, a dual inhibitor of SGLT1 and SGLT2, recently showed greater glucose reduction than dapagliflozin in patients with type 1 diabetes. YG1699 delays intestinal glucose absorption and induces an incretin response in BALB/c mice, indicating significant gastrointestinal SGLT1 inhibition.
- |||||||||| YG1699 / Youngene Therap
Trial completion, Enrollment change, Trial completion date, Trial primary completion date: To Evaluate the Safety, Tolerability, and Pharmacokinetics of YG1699?Antidiabetic? in Healthy Chinese Sbjects (clinicaltrials.gov) - Jan 31, 2023 P1, N=31, Completed, YG1699 delays intestinal glucose absorption and induces an incretin response in BALB/c mice, indicating significant gastrointestinal SGLT1 inhibition. Recruiting --> Completed | N=20 --> 31 | Trial completion date: May 2022 --> Aug 2022 | Trial primary completion date: Mar 2022 --> Aug 2022
- |||||||||| YG1699 / Youngene Therap, Farxiga (dapagliflozin) / Ono Pharma, AstraZeneca
Post-prandial glucose reduction with YG1699 compared to dapagliflozin in subjects with type 1 diabetes (Short Oral Discussion Area) - Jul 9, 2022 - Abstract #EASD2022EASD_970; P2 YG1699 reduced post-prandial glucose significantly more than dapagliflozin in subjects with T1D and was well-tolerated in this study. The pattern of lower post-prandial glucose, a greater GLP-1 response, and similar urinary glucose excretion compared to dapagliflozin in the MMTT indicate that YG1699 provided dual inhibition of SGLT1 and SGLT2.
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