RecruitingPhase 2NCT04732416

HM15136 (Efpegerglucagon) Treatment for 8 Weeks in Subjects Aged ≥2 Years With Congenital Hyperinsulinism (CHI)

A Phase 2, Multiple Ascending Dose, Open-label, Proof-of-concept Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of HM15136 (Efpegerglucagon) Treatment for 8 Weeks in Subjects Aged ≥2 Years With Congenital Hyperinsulinism (CHI)


Sponsor

Hanmi Pharmaceutical Company Limited

Enrollment

16 participants

Start Date

May 5, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

This study is designed to evaluate the safety, tolerability, pharmacokinetics (PK), and efficacy of HM15136 when used as add-on therapy in subjects with CHI with persistent hypoglycemia while on standard of care treatment (SoC). HM15136 will be administered once weekly in multiple doses to subjects in multiple age including pediatric to find appropriate exposure-response data.


Eligibility

Min Age: 2 Years

Inclusion Criteria4

  • Male and female subjects aged ≥2 years with CHI with persistent hypoglycemia despite current SoC treatment according to the investigator's evaluation or documentation
  • Stable therapy with SoC medications with or without nutritional supplementation
  • Previously undergone near-total pancreatectomy or being treated with a nonsurgical approach, having been evaluated as not eligible for pancreatic surgery
  • HbA1c <7%

Exclusion Criteria5

  • Subjects with type 1 or type 2 diabetes mellitus
  • Other reasons for hypoglycemia, including but not limited to drug-induced hyperinsulinemic hypoglycemia, etc
  • Treatment of CHI with continuous intravenous glucose or glucagon infusion within 3 months prior to screening
  • Subjects with current use of any drugs that are known to interfere with the study drug, glucose metabolism, or study procedures (eg, use of systemic glucocorticoids \[excluding topical, intra-articular or ophthalmic application, nasal spray, or inhaled forms\] or insulin)
  • Have conditions that could affect glucose levels such as pheochromocytoma, insulinoma, and glucagonoma

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Interventions

DRUGHM15136

Low dose of HM15136/ High dose of HM15136, SC injection, weekly


Locations(7)

University of California Los Angeles

Los Angeles, California, United States

The Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, United States

Otto-von-Guericke-Universitaet Magdeburg

Magdeburg, Germany

Hadassah Medical Center (HMC)

Jerusalem, Israel

Asan Medical Center

Seoul, South Korea

Great Ormond Street Hospital (GOSH) for Children NHS Foundation Trust

London, United Kingdom

Central Manchester University Hospitals NHS Foundation Trust - Royal Manchester Children's Hospital - Centre for Paediatrics and Child Health

Manchester, United Kingdom

View Full Details on ClinicalTrials.gov

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NCT04732416


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