Trial Investigating the Efficacy and Safety of Weekly Lonapegsomatropin Compared to Daily Somatropin in Children and Adolescents With Short Stature or Growth Failure Due to Growth Hormone Sufficient Disorders

NCT ID: NCT07221851

Last Updated: 2025-11-10

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE3
• Total Enrollment: 186 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-11-30
• Study Completion Date: 2029-03-31

Brief Summary

This basket trial will enroll prepubertal children and adolescents with clinically diagnosed and genetically confirmed (if applicable) TS, SHOX-D, SGA, or ISS between ages of ≥2 and <18 years with open growth plates. The purpose of the study is to see how well treatment with once-weekly lonapegsomatropin works compared to treatment with daily somatropin. Approximately 186 participants will be distributed equally (1:1), to receive either lonapegsomatropin for 2 years or somatropin for 1 year followed by lonapegsomatropin for 1 year. This trial will be conducted in the United States, France, Germany, Italy, Romania, Spain and South Korea.

Conditions

Turner Syndrome; Short Stature Homeobox Gene Mutation; Idiopathic Short Stature; Small for Gestational Age at Delivery

Keywords

Turner Syndrome; Noonan Syndrome; Growth Hormone; Short Stature; Growth Failure; Sex Chromosome Disorders; Chromosome Disorders; Endocrine System Diseases; Pituitary Hormones, Anterior; Pituitary Hormones; Hormones; Hormone Substitutes; Human Growth Hormone; Lonapegsomatropin; Sex Chromosome Disorders of Sex Development; Impaired Growth; somatropin; Growth Hormone Sufficiency; Short Stature Homeobox Gene Mutation; Short Stature Children Born Small for Gestational Age; Idiopathic Short Stature

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Lonapegsomatropin, once daily

Participants will receive Lonapegsomatropin by subcutaneous injection for 2 years (104 weeks)

Group Type: EXPERIMENTAL

Lonapegsomatropin [SKYTROFA®]

Intervention Type: COMBINATION_PRODUCT

Subcutaneous injection once weekly

somatropin, once daily

Participants will receive somatropin by subcutaneous injection for 1 year (52 weeks) followed by lonapegsomatropin for 1 year (52 weeks)

Group Type: ACTIVE_COMPARATOR

Somatropin Pen Injector

Intervention Type: COMBINATION_PRODUCT

Subcutaneous injection once daily

Interventions

Lonapegsomatropin [SKYTROFA®]

Subcutaneous injection once weekly

Intervention Type: COMBINATION_PRODUCT

Somatropin Pen Injector

Subcutaneous injection once daily

Intervention Type: COMBINATION_PRODUCT

Eligibility Criteria

Inclusion Criteria

1. Chronological age between ≥2 and <18 years, at start of screening.

2. Naïve to growth hormone and growth hormone promoting therapies.

3. Prepubertal.

4. Able to stand without assistance.

5. Diagnosis of TS, SHOX-D, SGA, or ISS with impaired growth or short stature, according to the following disease-specific criteria:

TS or SHOX-D (Léri-Weill dyschondrosteosis):

1. Diagnosis confirmed by a genetic test. NOTE: Historical test results are acceptable for proof of diagnosis. For karyotypes, a minimum of 20 cells must be counted.

2. Impaired growth or short stature defined as:

(i.) AHV <25th percentile over a time span of 6-16 months prior to screening utilizing a historical height properly documented in a health care setting (self-measurement record is not accepted) OR (ii.) Height <5th percentile for sex and age according to the Centers for Disease Control Growth Charts for the United States

SGA without catch-up growth:

c. Birth weight and/or birth length < -2.0 SDS for gestational age according to the 2006 World Health Organization Child Growth Standards. For infants born premature, the Fenton Preterm Infant Growth Chart (Fenton 2013) should be used.

d. Impaired growth or short stature defined as: (i.) AHV <25th percentile over a time span of 6-16 months prior to screening properly documented in a health care setting (self-measurement record is not accepted) OR (ii.) Height < -2.0 SDS for age and sex according to the 2000 Centers for Disease Control Growth Charts for the United States for children ≥ 3 years or height < -2.5 SDS for age and sex according to the for children ≥ 2 years and < 3 years

ISS:

e. Height < -2.25 SDS for sex and age according to the Centers for Disease Control Growth Charts for the United States with no identifiable cause for short stature.

f. Documented normal GH-IGF-1 axis, defined as either: (i.)IGF-1 SDS >0 at screening based on central laboratory OR (ii.)Historical documentation of normal peak GH upon stimulation test (as defined by local institution) g. 46,XX chromosome as determined by karyotype or microarray if female. For karyotypes, a minimum of 30 cells must be counted.

6. If on hormone replacement therapies for any hormone deficiencies other than growth hormone (e.g., adrenal, thyroid), must be on adequate and stable doses for ≥4 weeks prior to and throughout screening.

7. Written, signed informed consent provided by parent(s) or legal guardian(s) of the participant. Assent should be signed by participant as required by IRB/HREC/IEC.

Exclusion Criteria

1. Advanced bone age X-ray by central reading defined as >20% above chronological age in months (Greulich 1959).

2. Closed epiphyses as defined as bone age of ≥14.0 years in females or ≥16.0 years in males.

3. Current clinical diagnosis of diabetic retinopathy

4. Any diagnosis or presence at screening of the following:

1. Untreated moderate or severe sleep apnea as determined by formal (local) read of an inpatient or at-home sleep study.

2. Prader Willi syndrome with severe obesity, history of severe upper airway obstruction, or severe respiratory impairment.

5. Signs/symptoms of intracranial hypertension, active proliferative retinopathy.

6. Uncontrolled hypo- or hyperthyroidism.

7. Uncontrolled diabetes mellitus (defined as: HbA1c >7.5% from central laboratory at screening).

8. Known history or diagnosis of any gastrointestinal inflammatory condition, HIV, radiation exposure, other skeletal dysplasias, growth hormone deficiency, and/or cardio-thoracic surgery due to their independent effects on growth.

9. Any significant hepatic or renal abnormality, such as abnormal renal function (defined as eGFR <60 mL/min/1.73m2).

10. Undiagnosed or uncontrolled hypertension.

11. Receiving treatment with any agent that might influence growth or interfere with GH secretion or action including any sex steroids and stimulants for attention-deficit/hyperactivity disorder (ADHD).

12. High dose inhaled glucocorticoid for more than 28 consecutive days total over the course of 12 months.

13. Female who is pregnant, plans to be pregnant, or breastfeeding.

14. Participation in another interventional clinical trial involving an investigational compound within 90 days prior to screening or in parallel to this trial.

15. Any disease or condition that, in the judgement of the investigator, may make the participant unlikely to comply with the requirements of the protocol or any condition that presents undue risk from the investigational product or trial procedures.

1. Presence of Y chromosome material on genetic testing without history of gonadectomy.

2. Less than 10% of 45,X mosaicism.

3. Any known, clinically significant, congenital or acquired cardiovascular dysfunction that might interfere with growth.

a. Any known clinically significant abnormality likely to affect growth or the ability to evaluate growth with standing height measurements: (i.)Chromosomal aneuploidy, significant gene mutations, or medical syndromes with short stature, including but not limited to Turner syndrome, Laron syndrome, Noonan syndrome, Prader-Willi syndrome, abnormal SHOX-1 gene analysis or absence of GH receptors.

(ii.)Congenital abnormalities (causing skeletal abnormalities), including but not limited to skeletal dysplasias.

1. Known history of any condition that causes disproportionate short stature (i.e. skeletal dysplasias), chromosomal aneuploidy, significant gene mutations, or medical syndromes with short stature, including but not limited to Turner syndrome, Laron syndrome, Noonan syndrome, Prader-Willi syndrome, abnormal SHOX-1 gene analysis or absence of gH receptors.

• Minimum Eligible Age: 2 Years
• Maximum Eligible Age: 17 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Ascendis Pharma A/S

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Claus Strange

Role: STUDY_DIRECTOR

Ascendis Pharma A/S

Central Contacts

Ascendis Registry Inquiries

Role: CONTACT

Phone: +4561161658

Email: asnd_registryinquiries@ascendispharma.com

Other Identifiers

ASND0047

Identifier Type: -

Identifier Source: org_study_id