Safety and Efficacy of Y-shape Pegylated Somatropin in Growth Hormone Deficiency Children

Xiamen Amoytop Biotech

Status and phase: Completed; Phase 3; Phase 2

Conditions: Growth Hormone Deficiency

Treatments: Drug: Y-shape pegylated somatropin; Drug: Norditropin®; Drug: Norditropin

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT04513171

TB1805GH

Details and patient eligibility

About

This is a multicenter, randomized, open-labeled, positive controlled phase 2&3 combined study to evaluate the safety and efficacy of weekly Y-shape pegylated somatropin, compared to daily somatropin (Norditropin®), in prepubertal, treatment-naive children with growth hormone deficiency.

Full description

This multicenter, randomized, open-labeled, positive controlled study is divided into two stages. The first one is aimed to exploit the optimal dose of Y-shape pegylated somatropin, while the second one is aimed to confirm the efficacy and safety of the study drug. A total of 400 prepubertal children with growth hormone deficiency were expected to enrolled. Subjects will firstly undergo a 52 weeks treatment, and then followed for 5 weeks.

Enrollment: 434 patients

Sex: All

Ages: 3 to 11 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Diagnosis of GHD confirmed by two different GH stimulation tests, defined as a peak of GH level of <10.0 ng/ml, determined with a validated assay. Bone age (BA) at least 2 years less than the chronological age. Growth velocity less than 5.0 cm/year. Impaired HT defined as at least 2.0 standard deviations (SD) below of the mean height for chronological age and sex (HT SDS<-2.0).
• Prepubertal (Tanner Ⅰ) males and females by physical examination, aged older than 3 years and younger than10 years for girls and 11 years for boys.
• Short stature with normal intelligence.
• Baseline IGF-1 level below the median IGF-1 level standardized for age and sex.
• Written, signed informed consent of the parent(s) or legal guardian(s) of the subject and written assent of the subject (if the subject is 8 years old or above).

Exclusion criteria

• Prior exposure to growth promotion treatment, such as recombinant human growth hormone or gonadal hormones, for more than 1 month.
• Known hypersensitivity to somatropin or excipients, such as mannitol, lysine, sodium chloride.
• Children with closed epiphyses.
• Short stature etiologies other than GHD, such as idiopathic short stature, Turner syndrome, Prader-Willi syndrome, Russell-Silver syndrome, born small for gestational age regardless of GH status.
• Other causes of short stature such as hypothyroidism, adrenocortical hormone deficiency, antidiuretic hormone deficiency.
• Any medical conditions and/or presence that may affect growth velocity such as liver dysfunction, kidney dysfunction, malnutrition, diabetes mellitus, severe dysfunction in major organ such as heart, sever systemic infections, severe immune dysfunction, mental disorders, and other congenital malformations.
• Suffering from chronic infectious diseases such as chronic hepatitis B, AIDS or tuberculosis.
• Receiving non-physiological adrenal corticosteroids.
• Confirmed pituitary and/or hypothalamic malignance by MRI within one year prior to screening. History or presence of any other malignance disease, any evidence of present tumor growth.
• Evidence of congenital intracranial hypertension.
• Evidence of slipped capital femoral epiphysis.
• Evidence of scoliosis over 15°.
• Participation in any other trial of an investigational agent within 3 months prior to screening.
• Any other conditions which in the opinion of the investigator precluded enrollment into the study.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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434 participants in 6 patient groups

Y-shape pegylated somatropin low dose

Experimental group

Treatment:

Drug: Y-shape pegylated somatropin

Drug: Y-shape pegylated somatropin

Drug: Y-shape pegylated somatropin

Drug: Y-shape pegylated somatropin

Y-shape pegylated somatropin middle dose

Experimental group

Treatment:

Drug: Y-shape pegylated somatropin

Drug: Y-shape pegylated somatropin

Drug: Y-shape pegylated somatropin

Drug: Y-shape pegylated somatropin

Y-shape pegylated somatropin high dose

Experimental group

Treatment:

Drug: Y-shape pegylated somatropin

Drug: Y-shape pegylated somatropin

Drug: Y-shape pegylated somatropin

Drug: Y-shape pegylated somatropin

Norditropin-1

Active Comparator group

Treatment:

Drug: Norditropin®

Y-shape pegylated somatropin optimal dose

Experimental group

Treatment:

Drug: Y-shape pegylated somatropin

Drug: Y-shape pegylated somatropin

Drug: Y-shape pegylated somatropin

Drug: Y-shape pegylated somatropin

Norditropin-2

Active Comparator group

Treatment:

Drug: Norditropin