Urica Therapeutics has reported topline data from the Phase I clinical trial of dotinurad in healthy subjects in the US.

A new urate transporter (URAT1) inhibitor, dotinurad is being developed for treating gout and could be used for ailments linked to hyperuricemia such as chronic kidney disease.

Discover B2B Marketing That Performs

Combine business intelligence and editorial excellence to reach engaged professionals across 36 leading media platforms.

Find out more

The placebo-controlled, randomised trial assessed the tolerability, safety, pharmacokinetics (PK) and pharmacodynamics (PD) of varying doses of dotinurad in healthy participants in the region.

According to the trial findings, dotinurad was found to be safe and well tolerated without any severe adverse events reported.

Additionally, no adverse events linked to the drug were seen at 1mg, 2mg and 4mg dose levels, which are currently approved and sold in Japan.

The PK and PD profile in US participants were comparable to those of Japanese counterparts with all doses analysed.

GlobalData Strategic Intelligence

US Tariffs are shifting - will you react or anticipate?

Don’t let policy changes catch you off guard. Stay proactive with real-time data and expert analysis.

By GlobalData

In 2020, dotinurad (URECE Tablets) received approval in Japan for usage as a once-a-day oral treatment for hyperuricemia irrespective of gout status.

Urica chairman and CEO Jay Kranzler said: “We are encouraged that the data from our Phase I clinical trial in US healthy volunteers show comparable pharmacokinetic, pharmacodynamic and safety profiles between US and Japanese healthy subjects.

“We are initiating a Phase Ib clinical trial in gout patients in the US this summer and expect to begin pivotal clinical trials in 2024.”

Clinical Trials Arena Excellence Awards - Nominations Closed

Nominations are now closed for the Clinical Trials Arena Excellence Awards. A big thanks to all the organisations that entered – your response has been outstanding, showcasing exceptional innovation, leadership, and impact

Excellence in Action
Science 37 has won the Research and Development Award in the Site Innovation category for its FDA inspected Direct-to-Patient Site model, delivering nationwide access, faster enrollment and higher retention. Explore how its virtual-first, in home approach is reshaping trial operations and accelerating time to data-driven decisions..

Discover the Impact