For Healthcare Professionals

Phase 2 Study of LUM-201 in Children With Growth Hormone Deficiency (OraGrowtH210 Trial)

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About the study

This is a multi-national trial. The goals of the trial are to study LUM-201 as a possible treatment for Pediatric Growth Hormone Deficiency (PGHD) and investigate a predictive enrichment marker (PEM) strategy to select subjects likely to respond to therapy with LUM-201.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:


  1. Have an established diagnosis of idiopathic PGHD as determined by standard diagnostic criteria. Eligible subjects must be naïve-to-treatment and be prepubertal.
  2. Morning cortisol ≥ 7 µg/dL or stimulated cortisol ≥ 14 µg/dL.
  3. At Screening, be ≥ 3.0 years and ≤ 11.0 years for girls and ≤ 12.0 years for boys.
  4. Have HT-SDS ≤ -2.0 or HT-SDS ≥ 2 SD below mean parental HT-SDS.
  5. Have a baseline height velocity < 5.5 cm/year based on at least 6 months of growth.
  6. Have a bone age delayed by ≥ 6 months with respect to chronological age.
  7. Have prepubertal status as evidenced by Tanner Stage I breast development in girls and testicular volume < 4.0 mL in boys.
  8. In girls, have genetic testing results to rule out Turner syndrome. If SHOX genetic testing results are available, they need to be negative.
  9. Have normal thyroid function. Subjects diagnosed with hypothyroidism must have documented successful treatment for at least 30 days prior to Day 1.

EXCLUSION CRITERIA

Exclusion Criteria:


  1. 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. (Examples: diabetes, idiopathic short stature).
  2. A medical or genetic condition that, in the opinion of the Investigator and/or MM, adds unwarranted risk to use of LUM-201 or rhGH.
  3. 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 (Example: glucocorticoids).
  4. Evidence or history of an intracranial mass (e.g., pituitary tumor, craniopharyngioma).
  5. Suspicion of absent pituitary function as evidenced by a maximal stimulated GH ≤ 3 ng/mL on two prior standard of care GH stimulation tests, or pituitary deficiencies beyond GH and thyroid function.
  6. Malnutrition as evidenced by medical history or a body weight < 3rdth percentile for current height.
  7. BMI > 95th percentile.
  8. Gestational age-adjusted birth weight < 5th percentile (small for gestational age).
  9. History of spinal, cranial, or total body irradiation.
  10. Treatment with medications known to act as moderate or strong inhibitors or strong inducers of CYP3A/4, or with medications known to act as strong inhibitors of P-glycoprotein (P-gp) or potent substrates of P-gp or Multidrug and toxin extrusion protein 1 (MATE1).

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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.

Study’s details


Contition

Growth Hormone Deficiency

Age (in years)

3 - 12

Phase

Phase 2

Participants needed

80

Est. Completion Date

Apr 30, 2025

Treatment type

Interventional


Sponsor

Lumos Pharma

ClinicalTrials.gov identifier

NCT04614337

Study number

LUM201-01

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