Status:
UNKNOWN
A Study of Recombinant Human Growth Hormone Injection for Short Children With Small for Small for Gestational Age(SGA)
Lead Sponsor:
Changchun GeneScience Pharmaceutical Co., Ltd.
Collaborating Sponsors:
Tongji Hospital
Beijing Children's Hospital
Conditions:
Small for Gestational Age Infant
Eligibility:
All Genders
24-90 years
Phase:
PHASE3
Brief Summary
According to the results of the phase II study, choose the best dose of JINTOPIN AQ for short SGA children, further to evaluate the efficacy and safety of the treatment of short SGA children.
Eligibility Criteria
Inclusion
- Clinical diagnosis of full-term small for gestational age, SGA.
- Chronological age between 2-6.5 years in girls and 2-7.5 years in boys. Both genders.
- Prepubertal stage (Tanner I).
- Height was lower than the mean -2SD of the values of normal children of the same age and gender when participating in the study.
- A GH peak concentration \>10µg/L in a provocative test within a year before participating in the study.
- Bone age\<Chronological age+1.
- Normal glucose regulation：Fasting blood-glucose \< 5.6mmol/L, and 2 hours postprandial blood-glucose \< 7.8mmol/L.
- Gestational age was 37 to 42 weeks.
- The subjects and their guardians signed informed consent.
Exclusion
- Subjects with Liver and renal insufficiency (ALT \> 1.5 times of upper limit of normal value, Cr\> upper limit of normal value).
- Patients are positive for antibodies to hepatitis B core (HBc), hepatitis B surface antigen (HBsAg) or hepatitis B e antigen (HBeAg).
- Known Highly allergic constitution or allergic to the test drug.
- Subjects with diabetes, severe cardiopulmonary and pulmonary disease, and hematological diseases, malignant tumors, or systemic infection, immunocompromised patients and patients with psychosis.
- Subjects with other growth disorders, such as Turner syndrome, constitutional delay of growth and puberty, and Laron syndrome and growth hormone receptor deficiency.
- Subjects who have received the treatment of GH.
- Subjects took part in other clinical trial study within 3 months.
- Children who have treated with other hormone (such as gonadal hormone and glucocorticoids etc, continuous administration of more than a month) and that may affect growth hormone secretion or action including oxygen male dragon, growth hormone releasing hormone, etc. within 3 months.
- Other conditions which in the opinion of the investigator preclude enrollment into the study.
Key Trial Info
Start Date :
December 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT03245333
Start Date
December 1 2014
Last Update
December 12 2017
Active Locations (5)
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1
Tongji Hospital of Tongji Medical College of Huazhong University of Science and Technology
Wuhan, Hubei, China
2
The first affiliated Hospital with Nanjing Medical University
Nanjing, Jiangsu, China
3
The Children's Hospital of Zhejiang University School of Medicine
Hangzhou, Zhejiang, China
4
Beijing Children's Hospital, Capital Medical University
Beijing, China