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Phase 3 Study of LUM-201 in Children With Growth Hormone Deficiency

RecruitingPhase 3

A Multicenter, 12-Month, Randomized, Double Blind, Placebo-Controlled Phase 3 Efficacy and Safety Study of Daily Oral LUM-201 in Naïve-to-Treatment, Prepubertal Children With Growth Hormone Deficiency (GHD)

Who can join

Ages 3 to 11 · All sexes

Full eligibility criteria
Inclusion Criteria:

* Subjects must be naïve to treatment and prepubertal
* Subjects must have a maximal GH response of \< 10 ng/mL from 2 prior GH stimulation tests conducted within the preceding 12 months
* Impaired height defined as ≥ 2.0 standard deviations (SDs) below the mean height for chronological age and sex
* Morning or random cortisol level of ≥ 7.0 μg/dL
* ≥ 3.0 years and age ≤ 10.0 years for girls and ≤ 11.0 years for boys
* Baseline height velocity (HV) based on ≥ 6 months of growth assessments \< 25th percentile for age and sex
* Bone Age delay of ≥ 12 months compared to the chronological age
* In girls, have genetic testing results to rule out Turner syndrome. If SHOX genetic testing results are available, they need to be negative.
* Have normal thyroid function. Subjects diagnosed with hypothyroidism must have documented successful treatment for at least 3 months prior to Day 1
* Baseline IGF-1 standard deviation score (SDS) ≤ -1.0

Exclusion Criteria:

* Any medical or genetic condition which, in the opinion of the Investigator or Medical Monitor (MM), can be an independent cause of short stature and/or limit the response to exogenous growth factor treatment.
* Arm span to height ratio \> 2 SDs below the mean for age and sex
* A medical or genetic condition that, in the opinion of the Investigator and/or MM, adds unwarranted risk to use of LUM-201
* Use of any medication that, in the opinion of the Investigator and/or MM, can independently cause short stature or limit the response to exogenous growth factors
* Current inflammatory diseases requiring systemic corticosteroid treatment for \> 2 consecutive weeks within the last 3 months prior to the Screening Visit
* Use of hormone replacement therapy for any hormone deficiency other than thyroid deficiency
* Any ECG at the Screening Visit noted to have a clinically significant abnormality, as confirmed by the MM
* Any subjects suspected of having past or present intracranial tumor growth as confirmed by brain imaging prior to the Screening or Day 1 Visit
* Any subject suspected of having intracranial hypertension (IH) as confirmed by fundoscopy and other assessments
* Any subject with serum alanine transaminase (ALT), aspartate transaminase (AST), or total bilirubin \> upper limit of normal (ULN)
* Suspicion of absent pituitary function as evidenced by a maximal stimulated GH ≤ 3.0 ng/mL on any prior standard of care GH stimulation test completed within 12 months
* Body weight ≤ 14.0 kg
* BMI \< -2 or \> +2 SDs for age and sex based on WHO standards
* Birth weight for gestational age \< 3rd percentile based on WHO standards
* Treatment with medications known to be moderate or strong inhibitors or strong inducers of cytochrome P450 (CYP) 3A/4
* History of spinal, cranial, or total body irradiation
* Attention deficit hyperactivity disorder (ADHD) diagnosis

About the study

The OraGrowtH Phase 3 Trial is a multi-national trial. The goals of the trial are to study LUM-201 as a treatment for Pediatric Growth Hormone Deficiency (PGHD) in naive to treatment children and validate the LUM-201 predictive enrichment marker (LUM-201 PEM) strategy to select subjects likely to respond to therapy with daily oral LUM-201.

What is being tested

Sponsor: Lumos Pharma · Participants: 150 · Started: May 20, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT06948214

Locations in the U.S.

AlabamaLumos Pharma Investigational Site, Birmingham
CaliforniaLumos Pharma Investigational Site, Madera
Lumos Pharma Investigational Site, Orange
Lumos Pharma Investigational Site, Sacramento
Lumos Pharma Investigational Site, San Diego
ColoradoLumos Pharma Investigational Site, Centennial
Lumos Pharma Investigational Site, Greenwood Village
District of ColumbiaLumos Pharma Investigational Site, Washington D.C.
FloridaLumos Pharma Investigational Site, Hollywood
Lumos Pharma Investigational Site, Jacksonville
Lumos Pharma Investigational Site, Miami
Lumos Pharma Investigational Site, Orlando
Lumos Pharma Investigational Site, Tallahassee
IndianaLumos Pharma Investigational Site, Indianapolis
IowaLumos Pharma Investigational Site, Iowa City
LouisianaLumos Pharma Investigational Site, New Orleans
MinnesotaLumos Pharma Investigational Site, Minneapolis
MissouriLumos Pharma Investigational Site, Kansas City
NevadaLumos Pharma Investigational Site, Las Vegas
New JerseyLumos Pharma Investigational Site, New Brunswick
New YorkLumos Pharma Investigational Site, Staten Island
OhioLumos Pharma Investigational Site, Columbus
OklahomaLumos Pharma Investigational Site, Oklahoma City
South CarolinaLumos Pharma Investigational Site, Columbia
TexasLumos Pharma Investigational Site, Amarillo
Lumos Pharma Investigational Site, Corpus Christi
Lumos Pharma Investigational Site, Fort Worth
Lumos Pharma Investigational Site, San Antonio
VirginiaLumos Pharma Investigational Site, Charlottesville
WashingtonLumos Pharma Investigational Site, Seattle

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.