Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Hengagliflozin proline (SHR3824) is a selective sodium-glucose cotransporter 2 (SGLT2) inhibitor developed by Jiangsu Hengrui Pharmaceuticals. It is formulated as an L-proline cocrystal to enhance its physicochemical properties. The drug was approved by the China National Medical Products Administration (NMPA) in December 2021 for the treatment of type 2 diabetes mellitus, either as monotherapy or in combination with metformin. By inhibiting SGLT2 in the proximal renal tubules, it blocks the reabsorption of filtered glucose, leading to increased urinary glucose excretion and a subsequent reduction in plasma glucose levels. Beyond its primary indication for glycemic control, hengagliflozin proline is being investigated in Phase 4 clinical trials for weight management in obese adults without diabetes, as SGLT2 inhibition is associated with caloric loss and weight reduction.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on hengagliflozin proline.