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Rezolute Announces The Data Monitoring Committee's Recommendation To Continue Phase 3 Sunrize Study As Planned in Patients With Congenital HI, Without An Increase In The Study Sample Size

Author: Benzinga Newsdesk | April 23, 2025 07:03am

Independent Data Monitoring Committee (the "DMC") recommends continuation of sunRIZE trial as planned with no need to increase sample size

Enrollment on track and expected to be completed in May 2025; topline data anticipated in December 2025

U.S. sites activated and enrolling patients

REDWOOD CITY, Calif., April 23, 2025 (GLOBE NEWSWIRE) --  Rezolute, Inc. (NASDAQ:RZLT) (the "Company or "Rezolute"), a late-stage biopharmaceutical company dedicated to developing transformative therapies for rare diseases with serious unmet needs, today announced the DMC's recommendation to continue the Phase 3 sunRIZE study as planned in patients with congenital HI, without an increase in the study sample size.

"We are thrilled with the DMC's favorable recommendation, which appears to validate our initial assumptions for the design and powering of the Phase 3 sunRIZE study," said Brian Roberts, M.D., Chief Medical Officer at Rezolute. "While we remain blinded to the partial study data and are not privy to any of the statistical outputs from the DMC, we are nevertheless encouraged by this recommendation considering past outcomes from the Phase 2 RIZE study with the same objectively measured glycemic primary endpoint, real-world observations from our Expanded Access Program, and previously announced pharmacokinetic data from the open-label arm of the sunRIZE study. With U.S. clinical sites now also enrolling patients as part of our global study, and the Company tracking to complete enrollment next month, we look forward to announcing topline results, anticipated in December of this year, and remain confident in the potential of ersodetug to be a best-in-class treatment option for people living with hyperinsulinism."

The interim analysis of the Phase 3 sunRIZE study was performed by an unblinded DMC and was based on a pre-specified analysis of the primary study endpoint (hypoglycemia events), after approximately half of enrolled patients completed the primary assessments. The analysis was intended to evaluate for study futility or otherwise to inform a potential sample size increase, for purposes of optimizing the study power and statistical confidence in the final analysis outcomes. The Company has remained blinded throughout the interim analysis and has not seen the information made available to the DMC to inform its decision making, nor received any other information from the DMC after their meeting, other than its recommendation to continue the study as planned.

 

Posted In: RZLT

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