Rezolute (RZLT) announced outcomes from an independent Data Monitoring Committee, DMC, review of the open label arm, OLA, portion of the sunRIZE Phase 3 study of ersodetug for the treatment of hypoglycemia due to congenital hyperinsulinism and provided additional study updates including guidance on its upcoming interim analysis by the DMC. This IA will assess the adequacy of the sample size for the primary endpoint and may recommend adjustments if necessary. Findings from the DMC include the following: Ersodetug was generally safe and well-tolerated in participants 3 months to 1 year of age. Observed ersodetug drug levels at peak and trough were comparable to exposures in older pediatric participants in the Phase 2b RIZE study, which were demonstrated to be effective. Safety and exposures validate the chosen dose regimen of 5 and 10 mg/kg administered bi-weekly and monthly. Subsequent infant participants may now be enrolled into the double-blind, placebo-controlled study. sunRIZE enrollment completion expected in Q2 2025, subject to outcomes from upcoming interim analysis
Maximize Your Portfolio with Data Driven Insights:
- Leverage the power of TipRanks' Smart Score, a data-driven tool to help you uncover top performing stocks and make informed investment decisions.
- Monitor your stock picks and compare them to top Wall Street Analysts' recommendations with Your Smart Portfolio
Published first on TheFly – the ultimate source for real-time, market-moving breaking financial news. Try Now>>
Read More on RZLT:
- RZLT Earnings Report this Week: Is It a Buy, Ahead of Earnings?
- Rezolute Highlights Promising Phase 2 Ersodetug Results
- Rezolute Gains FDA Breakthrough Designation for Ersodetug
- Rezolute receives BTD from FDA for ersodetug in treatment of hypoglycemia
- Rezolute reports inducement award under Nasdaq listing rule