Global, multi-center, repeat-dose, phase 2 study of RZ358 (ersodetug), an insulin receptor antibody, for congenital hyperinsulinism

Other authors

Institut Català de la Salut

[Demirbilek H] Hacettepe University Faculty of Medicine, Department of Pediatrics, Ankara, Turkey. [Melikyan M] Yerevan State Medical University Mkhitar Heratsi, Department of Endocrinology, Yerevan, Armenia. [Iotova V, Galcheva S] Varna Medical University Department of Pediatrics, Varna, Bulgaria. [Ozbek MN] SBÜ Gazi Yasargil EAH, Diyarbakir, Turkey. [Dastamani A] Great Ormond Street Hospital for Children, Department of Paediatric Endocrinology, London, UK. [Clemente M] Unitat d’Endocrinologia Pediàtrica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. CIBERER, Barcelona, Spain

Vall d'Hebron Barcelona Hospital Campus

Publication date

2025-10-09T07:50:56Z

2025-10-09T07:50:56Z

2025-06-13



Abstract

Hyperinsulinism; Hypoglycemia; Insulin receptor


Hiperinsulinisme; Hipoglucèmia; Receptor d'insulina


Hiperinsulinismo; Hipoglucemia; Receptor de insulina


Background: Congenital hyperinsulinism (cHI) is a rare, primarily pediatric disease characterized by dysregulated insulin secretion resulting in severe, persistent hypoglycemia, frequently leading to lifelong neurologic impairments. The safety, pharmacokinetics, and glycemic efficacy of ersodetug, a fully human monoclonal antibody that allosterically and reversibly binds the insulin receptor (INSR) and reduces excess insulin action, are being evaluated for the treatment of cHI-related hypoglycemia. Methods: A global, open-label, phase 2b study (ClinicalTrials.gov: NCT04538989) was conducted in 23 patients with cHI with persistent hypoglycemia on standard-of-care (SOC) therapies. Eligible participants (age ≥2 years) received add-on ersodetug at dose levels between 3 and 9 mg/kg intravenously (i.v.) bi-weekly for 8 weeks in 4 sequential dose cohorts. Findings: Enrolled participants (average age = 6.7 years) on SOC (87% medications; 17% previous pancreatectomy) experienced 13 events/week and 23% time in hypoglycemia at baseline. Ersodetug resulted in predictable, dose-proportional pharmacokinetics. No deaths, adverse drug reactions, study withdrawals, or dose-limiting toxicities occurred. Hypoglycemia (<70 mg/dL) events (self-monitored blood glucose) and time (continuous glucose monitoring) improved from baseline by medians of 59% (p < 0.001) and 54% (p < 0.001), respectively, across pooled dose levels and by 48%-84% (events) and 61%-65% (time) at doses of 6 or 9 mg/kg (p < 0.05) with a nearly universal individual patient response rate. Additional hypoglycemia metrics, including overnight hypoglycemia, similarly improved. Conclusion: Ersodetug was generally well tolerated and significantly improved hypoglycemia in participants with cHI. Ersodetug represents a novel INSR-targeted mechanism of action with the potential to be an effective therapy for all forms of cHI, alone or in combination with other therapies.


Rezolute, Inc. (Redwood City, CA), provided funds.

Document Type

Article


Published version

Language

English

Subjects and keywords

Hipoglucèmia - Tractament; Posologia; Insulina - Receptors; Pàncrees - Malalties - Tractament; Anticossos monoclonals - Ús terapèutic; CHEMICALS AND DRUGS::Enzymes and Coenzymes::Enzymes::Transferases::Phosphotransferases::Phosphotransferases (Alcohol Group Acceptor)::Protein Kinases::Protein-Tyrosine Kinases::Receptor Protein-Tyrosine Kinases::Receptor, Insulin; CHEMICALS AND DRUGS::Amino Acids, Peptides, and Proteins::Proteins::Blood Proteins::Immunoproteins::Immunoglobulins::Antibodies::Antibodies, Monoclonal; Other subheadings::Other subheadings::Other subheadings::/administration & dosage; DISEASES::Digestive System Diseases::Pancreatic Diseases::Congenital Hyperinsulinism; Other subheadings::Other subheadings::Other subheadings::/drug therapy; DISEASES::Nutritional and Metabolic Diseases::Metabolic Diseases::Glucose Metabolism Disorders::Hypoglycemia; COMPUESTOS QUÍMICOS Y DROGAS::enzimas y coenzimas::enzimas::transferasas::fosfotransferasas::fosfotransferasas (grupo alcohol aceptor)::proteína cinasas::proteína-tirosina cinasas::receptores proteína-tirosina cinasas::receptor de insulina; COMPUESTOS QUÍMICOS Y DROGAS::aminoácidos, péptidos y proteínas::proteínas::proteínas sanguíneas::inmunoproteínas::inmunoglobulinas::anticuerpos::anticuerpos monoclonales; Otros calificadores::Otros calificadores::Otros calificadores::/administración & dosificación; ENFERMEDADES::enfermedades del sistema digestivo::enfermedades pancreáticas::hiperinsulinismo congénito; Otros calificadores::Otros calificadores::Otros calificadores::/farmacoterapia; ENFERMEDADES::enfermedades nutricionales y metabólicas::enfermedades metabólicas::trastornos del metabolismo de la glucosa::hipoglucemia

Publisher

Elsevier

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Attribution-NonCommercial-NoDerivatives 4.0 International

http://creativecommons.org/licenses/by-nc-nd/4.0/

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