REDWOOD CITY, Calif., June  04, 2026  (GLOBE NEWSWIRE) -- Rezolute, Inc. (NASDAQ:RZLT) (&#34;Rezolute&#34; or the &#34;Company&#34;), a late-stage ultra-rare disease company focused on treating refractory hypoglycemia caused by a

RZLT

Rezolute Announces Four Presentations at the Upcoming Annual Meeting of the Endocrine Society

Rezolute to present sunRIZE results at ENDO 2026; potential data catalyst for RZLT

<section class="insight" data-version="1">
 <section data-block="information">
 <h3>Information</h3>
 REDWOOD CITY, Calif., June 04, 2026 (GLOBE NEWSWIRE) -- Rezolute, Inc. (NASDAQ:RZLT) (&amp;#34;Rezolute&amp;#34; or the &amp;#34;Company&amp;#34;), a late-stage ultra-rare disease company focused on treating refractory hypoglycemia caused by a
 </section>

 <section data-block="ai-summary-paragraph">
 <h3>AI Summary</h3>
 Rezolute announced four ENDO 2026 presentations on ersodetug (RZ358) in congenital hyperinsulinism, including an oral sunRIZE result and posters on natural history and compassionate-use data. Although the December 2025 sunRIZE readout missed primary endpoints, the company cites CGM signals and FDA review, which could refresh sentiment if new analyses show meaningful improvements.
 </section>

 <section data-block="ai-summary-bullets">
 <h3>Key Points</h3>
 <ul><li>Rezolute to present four ENDO 2026 abstracts on ersodetug (RZ358) in HI.</li><li>SunRIZE Phase 3 results previously missed primary and key secondary endpoints.</li><li>FDA encouraged submission of comprehensive analysis datasets for independent review.</li><li>Compassionate-use case series in tumor HI and other HI-focused posters.</li></ul>
 </section>

 <section data-block="companies-mentioned">
 <h3>Companies Mentioned</h3>
 <ul><li>Rezolute, Inc. (RZLT): Primary subject; ENDO abstracts highlight sunRIZE results and compassionate-use data.</li><li>Hacettepe University (N/A): Institution of the oral presentation; potential regulatory/data impact remains indirect.</li><li>Endocrine Society (N/A): Host organization of ENDO 2026; event timing influences market attention.</li><li>U.S. Food and Drug Administration (N/A): Encouraged comprehensive analyses; independent review could affect program trajectory.</li></ul>
 </section>

 <section data-block="category">
 <h3>Corporate Developments</h3>
 Category: Corporate Developments. The news describes scheduled company-presented data at a major conference and related regulatory interactions, which can affect near-term sentiment and valuation without new definitive efficacy results.
 </section>

 <section data-block="market-moving">
 <h3>Market-Moving</h3>
 <ul><li>Endo 2026 presentations could shift sentiment near-term for RZLT.</li><li>FDA independent evaluation update could influence near-term regulatory trajectory.</li><li>SunRIZE prior miss may limit upside; data may validate secondary endpoints.</li><li>Event timing: June 13-16; potential trading catalysts over next few sessions.</li></ul>
 </section>

 <section data-block="key-facts">
 <h3>Key Facts</h3>
 <ul><li>SunRIZE enrolled 63 participants across 12+ countries.</li><li>Arms: 5 mg/kg, 10 mg/kg, placebo; 6 months pivotal phase.</li><li>Study endpoints: change in hypoglycemia events/week; CGM time in hypoglycemia.</li><li>December 2025: sunRIZE did not meet primary or key secondary endpoints.</li><li>ENDO 2026 dates: June 13-16, 2026; four presentations.</li></ul>
 </section>

 <section data-block="trading-thesis">
 <h3>Trading Thesis</h3>
 Near-term volatility around ENDO 2026 data is likely; outcomes hinge on FDA review of sunRIZE analyses and any new efficacy signals.
 </section>
</section>


<link type="text/css" rel="stylesheet" href="https://www.globenewswire.com/styles/gnw_nitf.css"></link>REDWOOD CITY, Calif., June 04, 2026 (GLOBE NEWSWIRE) -- Rezolute, Inc. (NASDAQ:<a class="ticker" href="https://www.benzinga.com/quote/RZLT">RZLT</a>) ("Rezolute" or the "Company"), a late-stage ultra-rare disease company focused on treating refractory hypoglycemia caused by a congenital or any acquired form of hyperinsulinism (HI), today announced four presentations at the upcoming Annual Meeting of the Endocrine Society (ENDO) being held June 13-16, 2026, in Chicago, IL. The Company's presentations at the meeting will include one oral presentation to be made by Huseyin Demirbilek, M.D., Professor, Department of Pediatric Endocrinology, Hacettepe University Faculty of Medicine, Ankara, Turkey, and Principal Investigator of the Phase 3 sunRIZE study in congenital HI. The oral presentation will highlight previously reported results from sunRIZE. Additionally, three poster presentations will cover the natural history and adverse outcomes associated with congenital HI, as well as results from the Company's ersodetug clinical development program, including a case series report on compassionate use of ersodetug in a cohort of patients with tumor HI. Presentation Details: Presentation Title: Ersodetug (RZ358) in Congenital Hyperinsulinism: Top-Line Results from a Global, Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase 3 Study (sunRIZE) Format: Oral presentation Presenter: Huseyin Demirbilek, M.D. Poster Number: SAT-10-06 Session Date and Time: Saturday, June 13, 2026, from 2:30 - 2:45 p.m. CDT Session Title: Pediatric and Adolescent Endocrinology: Diabetes and Insulin Presentation Title: A Case Series on the Compassionate Use of Ersodetug, an Insulin Receptor Modulating Antibody, in Patients with Refractory Hypoglycemia Due to Malignant Insulin-Secreting Tumors Format: Poster presentation Presenter: Gopal Saha, M.B.B.S. Poster Number: SAT-087 Session Date and Time: Saturday, June 13, 2026, from 12:15 - 1:45 p.m. CDT Session Title: Neuroendocrinology and Pituitary: Neuroendocrine Tumors I Presentation Title: Association of Early-Life Hypoglycemia with Later Neurological Outcomes in Congenital Hyperinsulinism: A US Claims-Based Study  Format: Poster presentation Presenter: Cody Akana Poster Number: SAT-221 Session Date and Time: Saturday, June 13, 2026, from 12:15 - 1:45 p.m. CDT Session Title: Pediatric and Adolescent Endocrinology: Pediatric Diabetes, Metabolic and Cardiovascular Disorders I Presentation Title: Outcomes in Congenital Hyperinsulinism: A Systematic Review Format: Poster presentation Presenter: Davelyn Eaves Hood, M.D., M.B.A. Poster Number: MON-215 Session Date and Time: Monday, June 15, 2026, from 12:00 - 1:30 p.m. CDT Session Title: Pediatric and Adolescent Endocrinology: Pediatric Diabetes, Metabolic and Cardiovascular Disorders III For more information on the conference presentation schedule, please visit the ENDO 2026 <a href="https://endo2026.endocrine.org/" rel="nofollow" target="_blank">website</a>. About sunRIZE The Phase 3 sunRIZE study (RZ358-301) was a multi-center, randomized, double-blind, placebo-controlled, parallel arm study designed to evaluate the efficacy and safety of ersodetug in patients with congenital hyperinsulinism (HI), ages 3 months to 45 years old, who were experiencing continued hypoglycemia on currently available standard of care (SOC). Eligible participants were randomized to one of three treatment arms to receive either ersodetug (5 or 10 mg/kg) or matched placebo-control as add on to existing SOC. Study drug was administered every other week during an initial loading phase, and then every 4 weeks during the 6-month controlled pivotal treatment period. Following the pivotal treatment phase of the study, participants could roll-over into an optional open-label extension phase to continue to receive ersodetug. The study enrolled 63 participants in more than a dozen countries around the world, inclusive of U.S. patients. The primary and key secondary efficacy endpoints in the study were the change from baseline in the average number of hypoglycemia events per week and the average percent time in hypoglycemia, respectively, over six months of treatment. In December 2025, the Company announced that the sunRIZE study did not meet its primary or key secondary endpoints. Although statistical significance for the secondary endpoint (% time in hypoglycemia by continuous glucose monitoring ["CGM"]) was not achieved at the Week 24/End of Treatment evaluation window, larger and often nominally statistically significant glycemic improvements compared to placebo were consistently observed throughout the maintenance dosing phase of the study, across time and numerous pre-specified and post-hoc CGM-based endpoints. As a next step for the program, the U.S. Food and Drug Administration (FDA) encouraged Rezolute to submit comprehensive analysis datasets and summary outcomes for the agency's independent evaluation. About Ersodetug  Ersodetug is a fully human monoclonal antibody that binds allosterically to the insulin receptor to decrease receptor over-activation by insulin and related substances (such as IGF-2) in the setting of hyperinsulinism (HI), thereby improving hypoglycemia. Because ersodetug acts downstream from glucose absorption, gastrointestinal incretin hormones, and pancreatic insulin secretion, it has the potential to be universally effective at treating refractory hypoglycemia due to a congenital or any acquired form of HI, including tumor HI (insulinoma, NICTH) or hypoglycemia as a complication of a variety of bariatric or non-bariatric gastrointestinal surgeries. About Rezolute, Inc.  Rezolute is a late-stage ultra-rare disease company focused on treating refractory hypoglycemia caused by a congenital or any acquired form of hyperinsulinism (HI). The Company's antibody therapy, ersodetug, has been studied in clinical trials and used in real-world cases for the treatment of refractory hypoglycemia due to a variety of causes of HI. For more information, visit <a href="https://www.rezolutebio.com/" rel="nofollow" target="_blank">www.rezolutebio.com</a>. Forward-Looking Statements This release, like many written and oral communications presented by Rezolute and our authorized officers, may contain certain forward-looking statements regarding our prospective performance and strategies within the meaning of Section 27A of the Securities Act and Section 21E of the Securities Exchange Act of 1934, as amended. We intend such forward-looking statements to be covered by the safe harbor provisions for forward-looking statements contained in the Private Securities Litigation Reform Act of 1995 and are including this statement for purposes of said safe harbor provisions. Forward-looking statements, which are based on certain assumptions and describe future plans, strategies, and expectations of Rezolute, are generally identified by use of words such as &#34;anticipate,&#34; &#34;believe,&#34; &#34;estimate,&#34; &#34;expect,&#34; &#34;intend,&#34; &#34;plan,&#34; &#34;project,&#34; &#34;seek,&#34; &#34;strive,&#34; &#34;try,&#34; or future or conditional verbs such as &#34;could,&#34; &#34;may,&#34; &#34;should,&#34; &#34;will,&#34; &#34;would,&#34; or similar expressions. These forward-looking statements include, but are not limited to, the potential efficacy of ersodetug in treating hypoglycemia. Our ability to predict results or the actual effects of our plans or strategies is inherently uncertain. Accordingly, actual results may differ materially from anticipated results. Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this release. Except as required by applicable law or regulation, Rezolute undertakes no obligation to update these forward-looking statements to reflect events or circumstances that occur after the date on which such statements were made. Important factors that may cause such a difference include any other factors discussed in our filings with the SEC, including the Risk Factors contained in Rezolute's Annual Report on Form 10-K and Quarterly Reports on Form 10-Q, which are available at the U.S. Securities and Exchange Commission's website at <a href="http://www.sec.gov" title="www.sec.gov">www.sec.gov</a>. You are urged to consider these factors carefully in evaluating the forward-looking statements in this release and are cautioned not to place undue reliance on such forward-looking statements, which are qualified in their entirety by this cautionary statement.  Rezolute Contacts: Christen Baglaneas <a href="mailto:cbaglaneas@rezolutebio.com" rel="nofollow" target="_blank">cbaglaneas@rezolutebio.com</a> 508-272-6717 Carrie McKim <a href="mailto:cmckim@rezolutebio.com" rel="nofollow" target="_blank">cmckim@rezolutebio.com</a> 336-608-9706 <img alt="" class="__GNW8366DE3E__IMG" src="https://www.globenewswire.com/newsroom/ti?nf=OTczMTgwOSM3NjM2NDY0IzIwOTA4MTQ="></img> <img alt="" src="https://ml.globenewswire.com/media/MGM3ZjExZWQtYmNkZS00NmMzLTkwNWYtZGE0MTA3MzE4ZTE0LTExMDIzODUtMjAyNi0wNi0wNC1lbg==/tiny/Rezolute-Inc-.png" referrerpolicy="no-referrer-when-downgrade"></img><a href="https://www.globenewswire.com/NewsRoom/AttachmentNg/bbe03de3-6870-4230-b875-d8965a3d1b97"><img src="https://ml.globenewswire.com/media/bbe03de3-6870-4230-b875-d8965a3d1b97/small/rezolute-jpg.jpg" border="0" width="150" height="28" alt="Primary Logo"></img></a>

Rezolute announced four ENDO 2026 presentations on ersodetug (RZ358) in congenital hyperinsulinism, including an oral sunRIZE result and posters on natural history and compassionate-use data. Although the December 2025 sunRIZE readout missed primary endpoints, the company cites CGM signals and FDA review, which could refresh sentiment if new analyses show meaningful improvements.

Rezolute Announces Four Presentations at the Upcoming Annual Meeting of the Endocrine Society

AI Summary

Sentiment Rationale

Trading Thesis

Market-Moving

Key Facts

Companies Mentioned

Corporate Developments

Related News