Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Fofogliflozin (SHR0534) is an orally bioavailable, selective inhibitor of the sodium-glucose cotransporter 2 (SGLT2) developed by Shanghai Hengrui Pharmaceutical for the management of type 2 diabetes mellitus. By targeting SGLT2 in the proximal renal tubules, fofogliflozin prevents the reabsorption of filtered glucose, thereby promoting its excretion in the urine and reducing plasma glucose levels. This mechanism operates independently of insulin secretion or action, offering a complementary approach to traditional antidiabetic therapies. Fofogliflozin has undergone Phase 1 and Phase 2 clinical evaluations in China, where it demonstrated dose-dependent increases in urinary glucose excretion and significant reductions in HbA1c levels in patients with type 2 diabetes.
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 fofogliflozin.