A Long-Term Safety Study of Somavaratan in Japanese Children With Growth Hormone Deficiency

Phase 3

Terminated

• Conditions: Growth Hormone Deficiency
• Interventions: Drug: Somavaratan

• Registration Number: NCT03145831
• Lead Sponsor: Versartis Inc.

Brief Summary

This study is a multi-center, open-label safety study assessing long-term somavaratan administration.

Detailed Description

This study is a multi-center, open-label safety study assessing long-term somavaratan administration. It is open to subjects completing a somavaratan Japanese Phase 2/3 study (Protocol J14VR5) in children with growth hormone deficiency (GHD), as well as approximately 20 new children currently receiving daily rhGH therapy for GHD (switch subjects). For switch subjects, the first dose of somavaratan will be administered approximately 48 hours after the last dose of the daily rhGH. All subjects will receive somavaratan 3.5mg/kg twice-monthly. The study will be conducted at approximately 40 medical institutions in Japan.

Study Timeline

• Study Start: 2017-03-31
• Study First Submitted: 2017-04-05
• Study First Submitted QC: 2017-05-04
• Study First Posted: 2017-05-09
• Primary Completion: 2017-11-30
• Study Completion: 2017-11-30
• Status Verified: 2018-03
• Last Update Submitted: 2018-03-07
• Last Update Posted: 2018-03-09

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 21

Inclusion Criteria

1. Chronological Age ≥ 3.0 years.
2. Pre-pubertal status: Absent breast development in girls, testicular volume < 4.0 mL in boys.
3. Subjects with GHD (diagnosed according to the current diagnostic guidelines) who are receiving treatment with daily rhGH.
4. Normal thyroid function at screening visit in subjects not being treated for hypothyroidism. Subjects requiring thyroxine replacement must be considered adequately treated by the PI and Medical Monitor.
5. Normal adrenal function (morning cortisol and/or local stimulation test) at screening visit or within 6 months of the screening visit, in subjects not being treated for adrenal insufficiency. Subjects with adrenal insufficiency must receive glucocorticoid treatment for a minimum of 4 weeks before study drug administration.
6. Pathology relating to cause of GHD must be stable for at least 6 months prior to screening.
7. Willingness to discontinue daily rhGH therapy.
8. Legally authorized representatives must be willing and able to give informed consent

Exclusion Criteria

• 1. Prior (in the last 12 months) or concomitant treatment with a growth promoting agent other than rhGH [e.g., IGF-I, GH releasing hormone (GHRH), sex steroids (except when used as primer for GH stimulation test), aromatase inhibitors and/or GnRH agonist].

  2. Current significant disease (e.g., diabetes, cystic fibrosis, renal insufficiency). In all cases of concurrent disease, screening must be approved in writing by the medical monitor.

  3. Chromosomal aneuploidy, significant gene mutations (other than those that cause GHD) or confirmed diagnosis of a named syndrome (e.g., Russell Silver, Prader Willi, Turner, etc.).

  4. Birth weight and/or birth length less than 5th percentile for gestational age using local gestational age growth charts.

  5. Prolonged daily (> 14 days) use of anti-inflammatory doses of oral glucocorticoids.

  6. Prior history of malignancy. 7. Treatment with an investigational drug in the 30 days prior to screening. 8. Known allergy to constituents of the study drug formulation. 9. Ocular findings suggestive of increased intracranial pressure and/or retinopathy at screening.

  7. Significant spinal abnormalities including scoliosis, kyphosis, Chiari malformation, and spina bifida variants.

  8. Significant abnormality in screening laboratory studies (as assessed by PI and medical monitor).

  9. Current social conditions which would prevent completion of study activities (e.g., planned family move to a distant location).

  10. History of pancreatitis or undiagnosed chronic abdominal pain. 14. History of spinal or total body irradiation. 15. Presence of other pituitary hormone deficiencies that are not properly treated.

  11. Unwillingness to provide consent for participation in all trial activities

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Somavaratan	Somavaratan	fusion protein, subcutaneous bolus injection, 3.5 mg/kg twice monthly

Primary Outcome Measures

Name	Time	Method
Adverse Events	12 months	Incidence and severity of adverse events

Secondary Outcome Measures

Name	Time	Method
Height velocity	12 months	Comparison of Height Velocity (HV) and HV-SDS before and after switching therapy
IGF-I expression	12 months	Change from Day 1
Immunogenicity	12 months	Evaluated by anti-drug antibody response

Trial Locations

Locations (1)

Eric Humphriss; 🇺🇸 Menlo Park, California, United States