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Trial · Interventional

CompletedPhase 2Results postedRegistry data

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

Short name OraGrowtH210

Overview

Status
Completed
Phase
Phase 2
Enrollment
104 participants (actual)
Sponsor
Lumos Pharma · Industry
Design
Randomized · Open label (no masking)
Countries
6 countries

United States, Australia, Israel, New Zealand, Poland, Ukraine

Start
31 Dec 2020
Primary completion
4 Sept 2024
Completion
4 Sept 2024
First posted
4 Nov 2020
Last update posted
17 Jun 2026
Conditions
Growth Hormone Deficiency

Timeline

1 trial · 1 completed · 1 with posted results

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
202020212022202320242025
  1. Ph 2

    OraGrowtH210

    NCT04614337

    31 Dec 2020 to 4 Sept 2024

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

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.

Interventions

  • LUM-201Drug
  • rhGH Norditropin® pen (34 µg/kg)Drug

Arms4

  • Experimental

    LUM-201 (0.8 mg/kg/day)

  • Experimental

    LUM-201 (1.6 mg/kg/day)

  • Experimental

    LUM-201 (3.2 mg/kg/day)

  • Active comparator

    rhGH (34 µg/kg/day)

Primary outcomes2

Outcomes the sponsor listed as primary.

  1. Percentage of Participants With a Positive Growth Response From Day 1 to Month 6 (AHV >= 6.85 cm/yr)

    Time frame · Day 1 to Month 6

    Registry description

    Annualized height velocity (AHV); Height is measured in triplicate, by a calibrated stadiometer and taking the mean value AVH equation is (h2-h1/t2-t1)\*365.25; h1 = height measured at day 1 h2 = height measured at month 6 t1 = day 1 t2 = month 6

  2. AHV After 6 Months on LUM-201 Compared to rhGH

    Time frame · Day 1 to Month 6

    Registry description

    Annualized height velocity to be measured.

Secondary outcomes(18)
  1. Percentage of Participants With a Positive Result on Both PEM Tests (at Screening and on Day 1)

    Time frame · Screening to Day 1

    Registry description

    PEM Test Reproducibility Safety Population

  2. Change in Height Standard Deviation Score (SDS)

    Time frame · Day 1 to Month 6

    Registry description

    Full Analysis Set Population month 6

  3. Change in Height Standard Deviation Score (SDS)

    Time frame · Day 1 to Month 12

    Registry description

    Full Analysis Set Population month 12

  4. Change in Weight From Baseline

    Time frame · Day 1 to Month 6

    Registry description

    Change in Weight from baseline

  5. Change in Weight From Baseline

    Time frame · Day 1 to Month 12

    Registry description

    Change in Weight from baseline

  6. Change in Weight SDS

    Time frame · Day 1 to Month 6

    Registry description

    Change in Weight-SDS (Standard Deviation Score)

  7. Change in Weight SDS

    Time frame · Day 1 to Month 12

    Registry description

    Change in Weight-SDS (Standard Deviation Score)

  8. Change in Body Mass Index (BMI)

    Time frame · Day 1 to Month 6

    Registry description

    Change in BMI from baseline

  9. Change in BMI

    Time frame · Day 1 to Month 12

    Registry description

    Change in BMI (Body Mass Index) from baseline

  10. Change in BMI SDS

    Time frame · Day 1 to Month 6

    Registry description

    Change in BMI SDS

  11. Change in BMI SDS

    Time frame · Day 1 to Month 12

    Registry description

    Change in BMI SDS This is not a Z-Score analysis. Standard deviation score of 0 is the population mean for the age/sex. Normal range is typically -2 to +2 SDS. A positive score is an improvement and a negative score a decrease.

  12. Bone Age

    Time frame · Day 1 to Month 6

    Registry description

    Change in bone age, measured by X-ray of left hand and wrist using Greulich \& Pyle atlas

  13. Bone Age

    Time frame · Day 1 to Month 18

    Registry description

    Change in bone age, measured by X-ray of left hand and wrist using Greulich \& Pyle atlas

  14. Pharmacokinetics of LUM-201

    Time frame · Day 1 to Month 6

    Registry description

    Serum concentrations at 30 minutes (Cmax/Steady State)

  15. Growth Hormone (GH) Concentration on Maintenance Treatment

    Time frame · Month 6

    Registry description

    Serum GH concentration

  16. Growth Hormone (GH) Concentration on Maintenance Treatment

    Time frame · Month 12

    Registry description

    Serum GH concentration

  17. Insulin-like Growth Factor 1 SDS

    Time frame · Month 6

    Registry description

    Serum concentrations of insulin-like growth factor 1 This is not a Z-Score analysis. Standard deviation score of 0 is the population mean for the age/sex. Normal range is typically -2 to +2 SDS. A positive score is an improvement and a negative score a decrease.

  18. Insulin-like Growth Factor 1 SDS

    Time frame · Month 12

    Registry description

    Serum concentrations of insulin-like growth factor 1 This is not a Z-Score analysis. Standard deviation score of 0 is the population mean for the age/sex. Normal range is typically -2 to +2 SDS. A positive score is an improvement and a negative score a decrease.

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

Primary outcome results

Primary outcomeNumber· Day 1 to Month 6

Percentage of Participants With a Positive Growth Response From Day 1 to Month 6 (AHV >= 6.85 cm/yr)

GroupValue (percentage of participants)
LUM-201 (0.8 mg/kg/Day)44.4
LUM-201 (1.6 mg/kg/Day)72.7
LUM-201 (3.2 mg/kg/Day)72.7
Recombinant Human Growth Hormone (rhGH) (34 µg/kg/Day)100
Primary outcomeMean· Day 1 to Month 6

AHV After 6 Months on LUM-201 Compared to rhGH

GroupValue (centimeters per year)Spread
LUM-201 (0.8 mg/kg/Day)6.75751.30141
LUM-201 (1.6 mg/kg/Day)8.21351.88092
LUM-201 (3.2 mg/kg/Day)7.73421.79706
rhGH (34 µg/kg/Day)10.57392.04380
Secondary and other outcome results(6)
Secondary outcomeNumber· Screening to Day 1

Percentage of Participants With a Positive Result on Both PEM Tests (at Screening and on Day 1)

GroupValue (percentage of participants)
Subjects With Positive Agreement on PEM Tests100
Secondary outcomeMean· Day 1 to Month 6

Change in Height Standard Deviation Score (SDS)

GroupValue (Standard Deviation Score)Spread
LUM-201 (0.8 mg/kg/Day)0.1080.1230
LUM-201 (1.6 mg/kg/Day)0.2380.1767
LUM-201 (3.2 mg/kg/Day)0.2150.1716
rhGH (34 µg/kg/Day)0.4440.1810
Secondary outcomeMean· Day 1 to Month 12

Change in Height Standard Deviation Score (SDS)

GroupValue (Standard Deviation Score)Spread
LUM-201 (0.8 mg/kg/Day)0.2070.2359
LUM-201 (1.6 mg/kg/Day)0.3700.2786
LUM-201 (3.2 mg/kg/Day)0.3690.2514
rhGH (34 µg/kg/Day)0.7320.2424
Secondary outcomeMean· Day 1 to Month 6

Change in Weight From Baseline

GroupValue (kg)Spread
LUM-201 (0.8 mg/kg/Day)2.3921.3859
LUM-201 (1.6 mg/kg/Day)2.6801.2710
LUM-201 (3.2 mg/kg/Day)2.5300.7133
rhGH (34 µg/kg/Day)1.7370.6940
Secondary outcomeMean· Day 1 to Month 12

Change in Weight From Baseline

GroupValue (kg)Spread
LUM-201 (0.8 mg/kg/Day)4.2672.5291
LUM-201 (1.6 mg/kg/Day)4.1981.9390
LUM-201 (3.2 mg/kg/Day)4.0090.9526
rhGH (34 µg/kg/Day)4.0311.6109
Secondary outcomeMean· Day 1 to Month 6

Change in Weight SDS

GroupValue (Standard Deviation Score)Spread
LUM-201 (0.8 mg/kg/Day)0.3220.3149
LUM-201 (1.6 mg/kg/Day)0.3700.2817
LUM-201 (3.2 mg/kg/Day)0.5580.2139
rhGH (34 µg/kg/Day)0.1710.1414

Adverse events, as posted

Adverse events as posted: participants affected out of participants at risk, by group
GroupDeathsSerious eventsOther events
PEM Dose LUM-201 (0.8 mg/kg/Day)LUM-201: Administered orally once daily0 / 1041 / 10422 / 104
LUM-201 (0.8 mg/kg/Day)LUM-201: Administered orally once daily0 / 181 / 1814 / 18
LUM-201 (1.6 mg/kg/Day)LUM-201: Administered orally once daily0 / 221 / 2221 / 22
LUM-201 (3.2 mg/kg/Day)LUM-201: Administered orally once daily0 / 220 / 2220 / 22
rhGH (34 µg/kg/Day)rhGH Norditropin® pen (34 µg/kg): Administered subcutaneously (s.c., under the skin) once daily.0 / 201 / 2017 / 20

Each cell reads participants affected / participants at risk, as the registry posted them.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies0

Studies that cite this trial.

No study cites this trial.

Eligibility

Who could join, as posted.

Sex
All
Age
from 3 Years up to 12 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: * Have an established diagnosis of idiopathic PGHD as determined by standard diagnostic criteria. Eligible subjects must be naïve-to-treatment and be prepubertal. * Morning cortisol ≥ 7 µg/dL or stimulated cortisol ≥ 14 µg/dL. * At Screening, be ≥ 3.0 years and ≤ 11.0 years for girls and ≤ 12.0 years for boys. * Have HT-SDS ≤ -2.0 or HT-SDS ≥ 2 SD below mean parental HT-SDS. * Have a baseline height velocity \< 5.5 cm/year based on at least 6 months of growth. * Have a bone age delayed by ≥ 6 months with respect to chronological age. * Have prepubertal status as evidenced by Tanner Stage I breast development in girls and testicular volume \< 4.0 mL in boys. * 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 30 days prior to Day 1. 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. (Examples: diabetes, idiopathic short stature). * 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. * 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). * Evidence or history of an intracranial mass (e.g., pituitary tumor, craniopharyngioma). * 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. * Malnutrition as evidenced by medical history or a body weight \< 3rdth percentile for current height. * BMI \> 95th percentile. * Gestational age-adjusted birth weight \< 5th percentile (small for gestational age). * History of spinal, cranial, or total body irradiation. * 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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