A Study to Evaluating the Efficacy and Safety of Recombinant Long-acting Human Growth Hormone (TJ101) in Children With Growth Hormone Deficiency
Primary Purpose
Pediatric Growth Hormone Deficiency
Status
Completed
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
TJ101
NordiFlex
Sponsored by
About this trial
This is an interventional treatment trial for Pediatric Growth Hormone Deficiency
Eligibility Criteria
Inclusion Criteria:
- Boys: 3 years ≤ boy's age ≤ 10 years;Girls: 3 years ≤ girl's age ≤ 9 years
- Pre-pubertal children(Tanner stage I)
- GHD confirmed by 2 different GH provocation tests with peak GH concentration below 10 ng/mL in screening or one month
- Height (HT) of at least 2.0 standard deviations (SD) below the mean height for chronological age (CA) and gender according to Table of standard deviation unit values of age and height of Chinese children aged 3-12 years , (HT SDS ≤ -2.0)
- Height velocity≤5.0cm/years (Including height records before at least three months);
- IGF-1 SDS≤-1.0
- Bone age (BA) is no more than two chronological age
- Body mass Index (BMI) must be within ±2 SD of mean BMI for the chronological age and sex according to Table of standard deviation unit values of Age and BMI of Chinese children aged 3-12 years
- Without prior exposure to any rhGH therapy
- For children with growth hormone deficiency that is one of its multiple pituitary hormone deficiencies, alternative therapies targeting the hypothalamus-pituitary-target gland axis must be used for at least 3 months before screening
- Written informed consent of the parent or legal guardian of the subject and assent of the subject (if the subject can read)
Exclusion Criteria:
- beyond physiological dosage of glucocorticoid therapy
- Evidence of closed epiphyses
- Any other chronic condition that can cause short stature and cannot be treated with hormone replacement therapy(Including but not limited Chronic kidney disease, malnutrition, absorption disorders, uncontrolled hypothyroidism, celiac disease, rickets and social-psychological dwarfism)
- Abnormal liver and renal function (ALT>1.5 times the upper limit of normal range and Cr exceeding the upper limit of normal range)
- Presence of anti-hGH antibodies at screening
- Concomitant administration of other treatments that may have an effect on growth such as anabolic steroids, with the exception of ADHD(attention deficit hyperactivity disorder) drug hormone replacement therapies [thyroxine, hydrocortisone, desmopressin (DDAVP)]
- Mutations in growth hormone receptors are suspected, or any syndrome that causes insensitivity to growth hormone
- At screening, ophthalmologic examination (including fundus microscopy) indicated increased intracranial pressure and/or retinopathy.
- At screening, previous or existing intracranial tumor growth was confirmed by cranial magnetic resonance imaging (MRI) scan (using contrast agent) (MRI results up to 1 year prior to screening were acceptable)
- Diseases such as severe cardiopulmonary, blood system, malignant tumor or potential tumor (family history), or systemic infection, low immune function and mental diseases
- Significant spinal abnormalities, including scoliosis (Cobb Angle & GT;60 ˚), kyphosis and spina bifida.
- Subjects diagnosed with type 2 or type 1 diabetes who were considered to have received no standard treatment, did not follow their prescribed treatment, or exhibited poor metabolic control, or had fasting glucose > 5.6 mmol/L twice in a row
- Chromosomal abnormalities and medical syndromes (Turner's syndrome, Laron syndrome, Noonan syndrome, Prader-Willi syndrome, Russell-Silver Syndrome, SHOX mutations/deletions and skeletal dysplasias), with the exception of septo-optic dysplasia
- Children with low birth weight (birth weight and/or body length are 2 SD below average according to the standard of the general Chinese population of the same gestational age and sex)
- The subject and/or the parent/legal guardian are likely to be non-compliant in respect to study conduct
- Subject who has received an investigational product or has participated in a clinical study within 30 days before screening or during the clinical trials.
- Known or suspected to be HIV positive, serologically positive for syphilis, or other chronic infectious diseases, such as AIDS, tuberculosis, hepatitis, etc
- The history of drug, drug or alcohol abuse
- Other conditions not considered suitable for inclusion by the researchers
Sites / Locations
- Second Affiliated Hospital of Anhui Medical University
- Beijing Children's Hospital,Capital Medical University
- Children's Hospital, Capital Institute of Paediatrics
- Chongqing Three Gorges Central Hospital
- Sun Yat-sen Memorial Hospital, Sun Yat-sen University
- The Third Affiliated Hospital of Sun Yet-sen University
- Liuzhou Maternity and Children Healthcare Hospital
- Hainan Third People's Hospital
- Tangshan Women and Children's Hospital
- Henan Children's Hospital
- Tongji Hospital affiliated to Tongji Medical College of Huazhong University of Science and Technology
- Wuhan Children's Hospital
- Hunan Children's Hospital
- The First Affiliated Hospital of Nanhua University
- Children's Hospital of Nanjing Medical University
- Jiangsu Provincial Maternal and Child Health Hospital
- Children's Hospital affiliated to Soochow University
- Jiangxi Provincial Children's Hospital
- Pingxiang Maternity and Child Care Hospital
- The First Bethune Hospital of Jilin University
- Shengjing Hospital of China Medical University
- General Hospital of Ningxia Medical University
- Affiliated Hospital of Jining Medical College
- Linyi Women and Children's Hospital
- Shanghai Children's Medical Center
- Shanghai Jiaotong University School of Medicine Ruijin Hospital
- Chengdu Women's and Children's Central Hospital
- West China Second Hospital of Sichuan University
- Taizhou First People's Hospital
- Ningbo Women & Children's Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
TJ101
NordiFlex
Arm Description
TJ101 1.2 mg/kg once a week for 52weeks
NordiFlex Injection 0.034 mg/kg once a day for 52 weeks
Outcomes
Primary Outcome Measures
The Annualized Height velocity at 52 week
The Annualized Height velocity at 52 week
Secondary Outcome Measures
change in Annualized Height velocity at 26 week (compared to Baseline value)
change in Annualized Height velocity at 52 week (compared to Baseline value)
Full Information
NCT ID
NCT04633057
First Posted
November 12, 2020
Last Updated
September 10, 2023
Sponsor
I-Mab Biopharma Co. Ltd.
1. Study Identification
Unique Protocol Identification Number
NCT04633057
Brief Title
A Study to Evaluating the Efficacy and Safety of Recombinant Long-acting Human Growth Hormone (TJ101) in Children With Growth Hormone Deficiency
Official Title
A Phase III, Randomized, Open-label, Positive-controlled, Multi-center Study to Evaluating the Efficacy and Safety of Recombinant Long-acting Human Growth Hormone (TJ101) in Children With Growth Hormone Deficiency
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
January 25, 2021 (Actual)
Primary Completion Date
July 31, 2023 (Actual)
Study Completion Date
July 31, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
I-Mab Biopharma Co. Ltd.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
A Phase III, Randomized, open-label, positive-drug parallel control, Study to Evaluate the Efficacy and Safety of TJ101 in Child subject with growth hormone deficieney.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pediatric Growth Hormone Deficiency
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
168 (Actual)
8. Arms, Groups, and Interventions
Arm Title
TJ101
Arm Type
Experimental
Arm Description
TJ101 1.2 mg/kg once a week for 52weeks
Arm Title
NordiFlex
Arm Type
Active Comparator
Arm Description
NordiFlex Injection 0.034 mg/kg once a day for 52 weeks
Intervention Type
Drug
Intervention Name(s)
TJ101
Intervention Description
TJ101/ Recombinant Human Somatropin Injection treatment: after screening, subjects will be randomized to receive TJ101 1.2 mg/kg once a week until 52 weeks back site, investigator evaluate effectiveness and safety.
Intervention Type
Drug
Intervention Name(s)
NordiFlex
Intervention Description
TJ101/ Recombinant Human Somatropin Injection treatment: after screening, subjects will be randomized to receive Recombinant Human Somatropin Injection 0.034 mg/kg once a day, until 52 weeks back site, investigator evaluate effectiveness and safety.
Primary Outcome Measure Information:
Title
The Annualized Height velocity at 52 week
Description
The Annualized Height velocity at 52 week
Time Frame
52weeks after first dose
Secondary Outcome Measure Information:
Title
change in Annualized Height velocity at 26 week (compared to Baseline value)
Time Frame
26weeks after first dose
Title
change in Annualized Height velocity at 52 week (compared to Baseline value)
Time Frame
52weeks after first dose
10. Eligibility
Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Boys: 3 years ≤ boy's age ≤ 10 years;Girls: 3 years ≤ girl's age ≤ 9 years
Pre-pubertal children(Tanner stage I)
GHD confirmed by 2 different GH provocation tests with peak GH concentration below 10 ng/mL in screening or one month
Height (HT) of at least 2.0 standard deviations (SD) below the mean height for chronological age (CA) and gender according to Table of standard deviation unit values of age and height of Chinese children aged 3-12 years , (HT SDS ≤ -2.0)
Height velocity≤5.0cm/years (Including height records before at least three months);
IGF-1 SDS≤-1.0
Bone age (BA) is no more than two chronological age
Body mass Index (BMI) must be within ±2 SD of mean BMI for the chronological age and sex according to Table of standard deviation unit values of Age and BMI of Chinese children aged 3-12 years
Without prior exposure to any rhGH therapy
For children with growth hormone deficiency that is one of its multiple pituitary hormone deficiencies, alternative therapies targeting the hypothalamus-pituitary-target gland axis must be used for at least 3 months before screening
Written informed consent of the parent or legal guardian of the subject and assent of the subject (if the subject can read)
Exclusion Criteria:
beyond physiological dosage of glucocorticoid therapy
Evidence of closed epiphyses
Any other chronic condition that can cause short stature and cannot be treated with hormone replacement therapy(Including but not limited Chronic kidney disease, malnutrition, absorption disorders, uncontrolled hypothyroidism, celiac disease, rickets and social-psychological dwarfism)
Abnormal liver and renal function (ALT>1.5 times the upper limit of normal range and Cr exceeding the upper limit of normal range)
Presence of anti-hGH antibodies at screening
Concomitant administration of other treatments that may have an effect on growth such as anabolic steroids, with the exception of ADHD(attention deficit hyperactivity disorder) drug hormone replacement therapies [thyroxine, hydrocortisone, desmopressin (DDAVP)]
Mutations in growth hormone receptors are suspected, or any syndrome that causes insensitivity to growth hormone
At screening, ophthalmologic examination (including fundus microscopy) indicated increased intracranial pressure and/or retinopathy.
At screening, previous or existing intracranial tumor growth was confirmed by cranial magnetic resonance imaging (MRI) scan (using contrast agent) (MRI results up to 1 year prior to screening were acceptable)
Diseases such as severe cardiopulmonary, blood system, malignant tumor or potential tumor (family history), or systemic infection, low immune function and mental diseases
Significant spinal abnormalities, including scoliosis (Cobb Angle & GT;60 ˚), kyphosis and spina bifida.
Subjects diagnosed with type 2 or type 1 diabetes who were considered to have received no standard treatment, did not follow their prescribed treatment, or exhibited poor metabolic control, or had fasting glucose > 5.6 mmol/L twice in a row
Chromosomal abnormalities and medical syndromes (Turner's syndrome, Laron syndrome, Noonan syndrome, Prader-Willi syndrome, Russell-Silver Syndrome, SHOX mutations/deletions and skeletal dysplasias), with the exception of septo-optic dysplasia
Children with low birth weight (birth weight and/or body length are 2 SD below average according to the standard of the general Chinese population of the same gestational age and sex)
The subject and/or the parent/legal guardian are likely to be non-compliant in respect to study conduct
Subject who has received an investigational product or has participated in a clinical study within 30 days before screening or during the clinical trials.
Known or suspected to be HIV positive, serologically positive for syphilis, or other chronic infectious diseases, such as AIDS, tuberculosis, hepatitis, etc
The history of drug, drug or alcohol abuse
Other conditions not considered suitable for inclusion by the researchers
Facility Information:
Facility Name
Second Affiliated Hospital of Anhui Medical University
City
Hefei
State/Province
Anhui
Country
China
Facility Name
Beijing Children's Hospital,Capital Medical University
City
Beijing
State/Province
Beijing
Country
China
Facility Name
Children's Hospital, Capital Institute of Paediatrics
City
Beijing
State/Province
Beijing
Country
China
Facility Name
Chongqing Three Gorges Central Hospital
City
Wanzhou
State/Province
Chongqing
Country
China
Facility Name
Sun Yat-sen Memorial Hospital, Sun Yat-sen University
City
Guangzhou
State/Province
Guangdong
Country
China
Facility Name
The Third Affiliated Hospital of Sun Yet-sen University
City
Guangzhou
State/Province
Guangdong
Country
China
Facility Name
Liuzhou Maternity and Children Healthcare Hospital
City
Liuzhou
State/Province
Guangxi
Country
China
Facility Name
Hainan Third People's Hospital
City
Sanya
State/Province
Hainan
Country
China
Facility Name
Tangshan Women and Children's Hospital
City
Tangshan
State/Province
Hebei
Country
China
Facility Name
Henan Children's Hospital
City
Zhengzhou
State/Province
Henan
Country
China
Facility Name
Tongji Hospital affiliated to Tongji Medical College of Huazhong University of Science and Technology
City
Wuhan
State/Province
Hubei
ZIP/Postal Code
430030
Country
China
Facility Name
Wuhan Children's Hospital
City
Wuhan
State/Province
Hubei
Country
China
Facility Name
Hunan Children's Hospital
City
Changsha
State/Province
Hunan
Country
China
Facility Name
The First Affiliated Hospital of Nanhua University
City
Hengyang
State/Province
Hunan
Country
China
Facility Name
Children's Hospital of Nanjing Medical University
City
Nanjing
State/Province
Jiangsu
Country
China
Facility Name
Jiangsu Provincial Maternal and Child Health Hospital
City
Nanjing
State/Province
Jiangsu
Country
China
Facility Name
Children's Hospital affiliated to Soochow University
City
Suzhou
State/Province
Jiangsu
Country
China
Facility Name
Jiangxi Provincial Children's Hospital
City
Nanchang
State/Province
Jiangxi
Country
China
Facility Name
Pingxiang Maternity and Child Care Hospital
City
Pingxiang
State/Province
Jiangxi
Country
China
Facility Name
The First Bethune Hospital of Jilin University
City
Changchun
State/Province
Jilin
Country
China
Facility Name
Shengjing Hospital of China Medical University
City
Shenyang
State/Province
Liaoning
Country
China
Facility Name
General Hospital of Ningxia Medical University
City
Yinchuan
State/Province
Ningxia
Country
China
Facility Name
Affiliated Hospital of Jining Medical College
City
Jining
State/Province
Shandong
Country
China
Facility Name
Linyi Women and Children's Hospital
City
Linyi
State/Province
Shandong
Country
China
Facility Name
Shanghai Children's Medical Center
City
Shanghai
State/Province
Shanghai
Country
China
Facility Name
Shanghai Jiaotong University School of Medicine Ruijin Hospital
City
Shanghai
State/Province
Shanghai
Country
China
Facility Name
Chengdu Women's and Children's Central Hospital
City
Chengdu
State/Province
Sichuan
Country
China
Facility Name
West China Second Hospital of Sichuan University
City
Chengdu
State/Province
Sichuan
Country
China
Facility Name
Taizhou First People's Hospital
City
Liuzhou
State/Province
Zhejiang
Country
China
Facility Name
Ningbo Women & Children's Hospital
City
Ningbo
State/Province
Zhejiang
Country
China
12. IPD Sharing Statement
Learn more about this trial
A Study to Evaluating the Efficacy and Safety of Recombinant Long-acting Human Growth Hormone (TJ101) in Children With Growth Hormone Deficiency
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