Zydus Cadila completes patient enrolment for 2 Phase III trials of Desidustat

Ahmedabad: Zydus Cadila, global pharmaceutical company, has recently announced that the company has completed patient enrolment in DREAM-ND and DREAM-D Phase III trials of Desidustat, an oral small molecule hypoxia-inducible factor prolyl hydroxylase (HIF-PH) inhibitor for treatment of anaemia in patients with Chronic Kidney Disease (CKD).

The DREAM-ND Phase III trial has now enrolled 588 CKD patients not-on-dialysis. This Phase II study is a multicentre (68 sites), randomized, active-controlled clinical trial to evaluate the efficacy and safety of Desidustat versus Darbepoetin for the treatment of anaemia in patients with chronic kidney disease (CKD) who are not on dialysis.

The DREAM-D Phase III trial is being conducted in 392 CKD patients on Dialysis. The primary end-point in Phase III DREAM-D multicentre study (44 sites) will be the efficacy of Desidustat tablet versus Epoetin alfa injection based on the change of hemoglobin (Hb) levels. The secondary end-points will include number of hemoglobin (Hb) responders, time to achieve target range Hb level, percentage of time spent in target Hb range, serum hepcidin levels, serum potassium (K+) levels, vascular endothelial growth factor (VEGF) levels, lipid profile and lipoproteins.