Shijiazhuang Sihua Pharmaceutical Group Has Been Approved to Conduct Bioequivalence Studies and Clinical Trials for Type 2 Diabetes Involving Trogliptin Succinate Tablets


发布时间:2023-11-23

【概要描述】 On November 23, Shijiazhuang Sihua Pharmaceutical Group received approval from the National Medical Products Administration to conduct bioequivalence studies and clinical trials for type 2 diabetes involving trigratine succinate tablets.
On November 23, Shijiazhuang Sihua Pharmaceutical Group received approval from the National Medical Products Administration to conduct bioequivalence studies and clinical trials for type 2 diabetes involving troglitazone succinate tablets.
According to available information, ambrisentan succinate tablets are a long-acting, selective dipeptidyl peptidase-4 (DPP-4) inhibitor that requires only once-weekly dosing to provide selective and sustained DPP-4 inhibition. Ambrisentan succinate tablets can be used as monotherapy or in combination with other oral antihyperglycemic agents, offering unique advantages such as a low risk of hypoglycemia, no weight gain, minimal adverse effects, and, notably, a low incidence of gastrointestinal adverse reactions.
Over the past two years, Shijiazhuang Sihua Pharmaceutical has steadfastly pursued an innovation-driven development strategy, concentrating its strengths on tackling key scientific and technological challenges in the areas of innovative drugs, shortage medications, and treatments for rare diseases. The company has continuously accelerated its strategic planning and deployment in complex formulations, improved new drugs, and innovative medicines, thereby powerfully advancing the enterprise’s value chain toward the mid- to high-end segment.

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