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A Long-Term Safety Trial of LUM-201 in Children With Idiopathic Growth Hormone Deficiency Who Have Previously Completed a LUM-201 Clinical Trial (OraGrowtH211)
Sponsor: Lumos Pharma
Summary
This is a multi-national trial. The trial aims to study the long-term safety of LUM-201 in subjects with Idiopathic Pediatric Growth Hormone Deficiency (iPGHD). This study will also assess pharmacodynamics and efficacy response to therapy with LUM-201.
Official title: An Extension Study to Monitor Long-Term Safety of LUM-201 Treatment in Children With Idiopathic Growth Hormone Deficiency
Key Details
Gender
All
Age Range
5 Years - 14 Years
Study Type
INTERVENTIONAL
Enrollment
60
Start Date
2023-08-01
Completion Date
2028-04
Last Updated
2024-02-15
Healthy Volunteers
No
Conditions
Interventions
LUM-201
Administered orally once daily
Locations (7)
University of Iowa
Iowa City, Iowa, United States
UMass Memorial Medical Center
Worcester, Massachusetts, United States
Children's Mercy Hospital
Kansas City, Missouri, United States
University of South Carolina
Charleston, South Carolina, United States
Texas Tech University Health Sciences Center
Amarillo, Texas, United States
Seattle Children's Hospital
Seattle, Washington, United States
Canberra Hospital
Garran, Australian Capital Territory, Australia