Approximately 1 in 11 patients with kidney failure requiring replacement therapy have inherited kidney diseases or congenital anomalies of the kidney and urinary tract. Genetic testing is ...

Understanding kidney development is crucial to comprehending the molecular basis of CAKUT syndrome in humans, and to developing future therapeutic interventions, such as cell-replacement therapies ...

In addition, a phase 1 trial in adult patients with CKD due to congenital anomalies of the kidney and urinary tract (CAKUT) is currently enrolling in the USA and will be expanding to Mexico ...

In medical terms, these conditions are referred to as Congenital Anomalies of the Kidney and Urinary Tract (CAKUT). CAKUT is one of the most common causes of kidney failure in children," said Dr ...

which has completed Phase I clinical trial for REACT in patients with congenital anomalies of the Kidney and Urinary Tract (CAKUT), as well as in Phase III and Phase II clinical trials for the ...