Phase III Clinical Study of Pegylated Somatropin (PEG Somatropin) to Treat Growth Hormone Deficiency Children

GeneScience Pharmaceuticals (GenSci)

Status and phase

Completed

Phase 3

Conditions

Growth Hormone Deficiency

Treatments

Biological: PEG-somatropin

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT01495468

GenSci-004-CT

Details and patient eligibility

About

This was a multicenter, randomized, open-label, parallel controlled phase III study, compared pegylated somatropin with Jintropin AQ (somatropin liquid injection, daily administration formulation).

All the subjects were randomized into two groups, test group (PEG somatorpin) and control group (Jintropin AQ), 200 children were enrolled in test group and 100 children were enrolled in control group. Considering the case loss during the clinical study, 20% of the patients were added in each of the group, that is 240 children were in test group and 120 children were in control group, totally 360 children were enrolled in the phase III clinical study.

Whole treatment were lasted for 6 months, 4 times of follow-up were carried out at the point of baseline, 1 month, 3 month and 6 month after treatment. The evaluation of the primary time point was 3 month and 6 month after treatment, if the treatment was less than 6 months, the evaluation would be made when the treatment is finished.

Enrollment

343 patients

Sex

All

Ages

8 to 15 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

1. Subjects have a height less than two standard deviations (SD) below the median height for individuals of he same age or height,the growth velocity (CV≤4.0 cm/yr),GH peak concentration <7.0ng/ml in two difference provocative tests, Bone age (BA) ≤9 years in girls and ≤10 years in boys, at least 2 year less than his/her chronological age (CA)
be in preadolescence (Tanner stage 1) and have a CA > 3 years
have a height value recorded 3 months before the start of GH treatment to calculate pre-treatment GV.
receive no prior GH treatment.
sign informed consent

Exclusion criteria

1. patients positive for hepatitis B e-antibody (HBeAb), hepatitis B surface antigen (HBsAg) or hepatitis B e antigen (HBeAg)
2.Known hypersensitivity to Somatropin or any other components of the study product.
1. severe cardiopulmonary or hematological diseases, a current or past history of malignant tumors, immunodeficiency diseases, or mental diseases
1. with other growth disorders, such as Turner syndrome, constitutional delay of growth and puberty, and Laron syndrome
1. Subjects took part in other clinical trial study during 3 months.
1. Other conditions which in the opinion of the investigator preclude enrollment into the study.