Safety and Efficacy Phase 3 Study of Long-acting hGH (MOD-4023) in Growth Hormone Deficient Children
Primary Purpose
Pediatric Growth Hormone Deficiency
Status
Active
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
MOD-4023
Somatropin
Sponsored by
About this trial
This is an interventional treatment trial for Pediatric Growth Hormone Deficiency
Eligibility Criteria
Main Study Inclusion Criteria:
- Pre-pubertal children aged ≥3 years , and not yet 11 years for girls or not yet 12 years for boys with either isolated GHD, or GH insufficiency as part of multiple pituitary hormone deficiency.
- Confirmed diagnosis of GHD by two different GH provocation tests defined as a peak plasma GH level of ≤10 ng/mL.
- Bone age (BA) is not older than chronological age and should be less than 10 for girls and less than 11 for boys.
- Without prior exposure to any r-hGH therapy (naïve patients).
Impaired height and height velocity defined as:
- Annualized height velocity (HV) below the 25th percentile for CA (HV < -0.7 SDS) and gender according to sponsor calculator
- The interval between 2 height measurements should be at least 6 months, but should not exceed 18 months prior to inclusion
- Baseline IGF-I level of at least 1 SD below the mean IGF-1 level standardized for age and sex (IGF-1 SDS ≤-1)
- Normal calculated GFR per updated bedside Schwartz formula for pediatric patients
- Children with multiple hormonal deficiencies must be on stable replacement therapies (no change in dose) for other hypothalamo-pituitary-organ axes for at least 3 months prior ICF signing
- Normal 46XX karyotype for girls.
Willing and able to provide written informed consent of the parent or legal guardian and written assent from patient
LT-OLE Inclusion Criteria:
- Completion of the main study (12 months of treatment) with adequate compliance.
- Willing and able to provide written informed consent of the parent or legal guardian and written assent from patient
- Agree to refrain from sexual activity
Main Study Exclusion Criteria:
- Children with prior history of leukemia, lymphoma, sarcoma or any other forms of cancer.
- History of radiation therapy or chemotherapy
- Malnourished children defined as BMI < -2 SDS for age and sex
- Children with psychosocial dwarfism
- Children born small for gestational age (SGA - birth weight and/or birth length <-2 SDS for gestational age)
- Presence of anti-hGH antibodies at screening
- Any clinically significant abnormality likely to affect growth or the ability to evaluate growth, such as, but not limited to, chronic diseases like renal insufficiency, spinal cord irradiation, etc.
- T2 and T1 diabetic patients, who in the opinion of the investigator are not receiving standard of care treatment or are non-compliant with their prescribed treatment or who are in poor metabolic control.
- Chromosomal abnormalities including Turner's syndrome, Laron syndrome, Noonan syndrome, Prader-Willi syndrome, Russell-Silver syndrome, SHOX mutations/deletions and skeletal dysplasias.
- Concomitant administration of other treatments that may have an effect on growth such as anabolic steroids, or sex steroids, with the exception of ADHD drugs or hormone replacement therapies (thyroxin, hydrocortisone, desmopressin)
- Children requiring glucocorticoid therapy (e.g. for asthma) that are taking chronically a dose greater than 400 μg/d of inhaled budesonide or equivalent
- Major medical conditions and/or presence of contraindication to r-hGH treatment.
- More than one closed epiphyses
- Known or suspected HIV-positive patient, or patient with advanced diseases such as AIDS or tuberculosis.
- Drug, substance, or alcohol abuse.
- Known hypersensitivity to the components of study medication.
- Other causes of short stature such as celiac disease, uncontrolled primary hypothyroidism and rickets.
- Likely non-compliance in respect to study conduct
- Participation in any other trial of an investigational agent within 30 days prior to consent
Study enrollment has been met or study is closed by sponsor prior to completion of screening process.
LT-OLE Exclusion Criteria:
- Concomitant administration of other treatments that may have an effect on growth such as anabolic steroids, or sex steroids, with the exception of ADHD drugs or HRT (thyroxin, hydrocortisone, desmopressin)
- Change in medical condition during the treatment period (such as, but not limited to, development of a serious inter-current critical illness, a severe adverse drug reaction, etc.)
- Positive pregnancy test
- Unresolved drug related (Genotropin or MOD-4023) SAE from the treatment period as per medical monitor judgement.
Sites / Locations
- Children's Hospital of Orange County- Children's Clinic
- Children's Hospital- Colorado
- Rocky Mountain Pediatrics
- Nemours Children's Health System
- University of Miami Medical Center
- St Luke's Children's Specialty Center
- Children's Hospital of Iowa
- Tufts Medical Center
- University of Massachusettes
- University of Minnesota
- The Diabetes & Obesity Clinical Specialist
- Goryeb Children's Hospital
- Buffalo Children's Hospital
- Albert Einstein College of Medicine at Yeshiva University
- Children's Hospital of Cincinnati / Cincinnati Center for Growth Disorders
- Children's Hospital of Pittsburgh
- Cook Children's Medical Center
- Mary Bridge Children's Hospital & Health Center
- Hospital Materno Infantil San Roque
- Hospital de Ninos de la Santisima Trinidad Cordoba
- John Hunter Children's Hospital
- Children's Hospital at Westmead
- PM Hospital for Children
- Health Institution- 2nd City Pediatric Hospital
- MHAT Sveta Marina
- Centre de recherche du CHU Sainte-Justine
- Dexa Diab
- Uniendo
- Hospital Pablo Tobon Uribe
- Maritime Hospital JSC
- Vere XXI JSC
- Aghia Sophia Children's Hospital
- General Children's Hospital of Athens P&A Kyriakou
- Manipal Hospital
- Getwell Health & Research Institute
- Jehangir Clinical Development Centre
- Postgraduate Institute of Medical Education and Research
- Care Hospital
- Meditrina Institute of Medical Sciences
- All India Institute of Medical Sciences
- Sir Gangaram Hospital
- Haemek Medical Center
- Soroka Medical Center
- Assaf Harofeh Medical Center
- Bnei Zion Medical Center
- Shaare Zedek Medical Center
- Scheider Children's Medical Center
- Tel Hashomer Medical Center
- Kaplan Medical Center
- Sourasky Medical Center
- Bundang Cha Hospital
- Inje University Busan Paik Hospital
- KyungPook National University Hospital
- Chosun University Hospital
- Severance Hospital
- Hospital Angeles de Puebla
- The Liggins Institute
- Wellington Children's Hospital
- Uniwersyteckie Centrum Kliniczne in Gdansk
- Centrum Zdrowia Matki Polki
- Bashkirian State Medical University
- Kazan State Medical Univeristy/Pediatric Republic Clinical Hospital
- Endocrinology Scientific Center
- Pediatric City Clinical Hospital/Russian Medical Academy of Continuous Education
- Saint Petersburg State Pediatric Medical University
- Voronezh State Medical University
- Hospital Miguel Servet
- Hospital Josep Trueta
- Hospital de Navarra
- Hospital Universitario Central de Asturias
- Parc Tauli
- Hospital Universitario de Santiago de Compostela
- Taipei Veterans General Hospital
- Tri-Service General Hospital
- Ukrainian Research and Practical Centre of Endocrine Surgery, Transplantation of Endocrine Organs and Tissues of the Ministry of Health of Ukraine
- Institute of Endocrinology and Metabolism/VP Komisarenko of Academy of Medical Science of Ukraine
- Odesa Regional Clinical Children's Hospital
- Vinnitsa Regional Clinical Highly Specialized Endocrinology Centre
- Zaporizhzhya Regional Clinical Child Hospital
- Royal Hospital for Children
- St. George's University Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
MOD-4023
Genotropin
Arm Description
Once weekly subcutaneous injection of long acting r-hGH (MOD-4023)
Once daily subcutaneous injection of Somatropin (r-hGH; Genotropin)
Outcomes
Primary Outcome Measures
Annual Height Velocity
Annual Height Velocity in cm. Annual Height Velocity at 12 months is based on the difference between the heights at 12 months and baseline.
Secondary Outcome Measures
Height Velocity at 6 Months
Height velocity in cm measured after 6 months of treatment. Annualized Height velocity after 6 months is calculated based on the difference between the heights at 6 months and baseline.
Change in Height Standard Deviation Score (SDS)
Change in height Standard Deviation Score (SDS) after 6 and 12 months is calculated based on the difference between the heights at 6 and 12 months and baseline.
Change in Bone Maturation (BM)
Annual change in bone age measurements as per Gruelich-Pyle method
Insulin-like Growth Factor-1 (IGF-1) Standard Deviation Score (SDS)
Via central lab analysis
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02968004
Brief Title
Safety and Efficacy Phase 3 Study of Long-acting hGH (MOD-4023) in Growth Hormone Deficient Children
Official Title
A Phase 3, Open-label, Randomized, Multicenter, 12 Months, Efficacy and Safety Study of Weekly MOD-4023 Compared to Daily Genotropin - Therapy in Pre-pubertal Children With Growth Hormone Deficiency
Study Type
Interventional
2. Study Status
Record Verification Date
January 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
December 2016 (undefined)
Primary Completion Date
August 2019 (Actual)
Study Completion Date
December 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
OPKO Health, Inc.
4. Oversight
5. Study Description
Brief Summary
This will be an open-label, randomized, multicenter, efficacy and safety study of weekly MOD-4023 compared to daily Genotropin therapy in pre-pubertal children with growth hormone deficiency.
Detailed Description
The study will consist of a 12 month, open-label, randomized, active controlled, parallel group study comparing the efficacy and safety of weekly MOD-4023 to daily growth hormone (GH), Genotropin. After 12 months, subjects will have the option to enter the long term open-label extension.
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
224 (Actual)
8. Arms, Groups, and Interventions
Arm Title
MOD-4023
Arm Type
Experimental
Arm Description
Once weekly subcutaneous injection of long acting r-hGH (MOD-4023)
Arm Title
Genotropin
Arm Type
Active Comparator
Arm Description
Once daily subcutaneous injection of Somatropin (r-hGH; Genotropin)
Intervention Type
Drug
Intervention Name(s)
MOD-4023
Other Intervention Name(s)
Somatrogon
Intervention Description
Once weekly subcutaneous injection using pre-filled pen device.
Intervention Type
Drug
Intervention Name(s)
Somatropin
Other Intervention Name(s)
Genotropin
Intervention Description
Once daily subcutaneous injection of Genotropin using pre-filled pen device.
Primary Outcome Measure Information:
Title
Annual Height Velocity
Description
Annual Height Velocity in cm. Annual Height Velocity at 12 months is based on the difference between the heights at 12 months and baseline.
Time Frame
52 weeks
Secondary Outcome Measure Information:
Title
Height Velocity at 6 Months
Description
Height velocity in cm measured after 6 months of treatment. Annualized Height velocity after 6 months is calculated based on the difference between the heights at 6 months and baseline.
Time Frame
After 6 months of treatment
Title
Change in Height Standard Deviation Score (SDS)
Description
Change in height Standard Deviation Score (SDS) after 6 and 12 months is calculated based on the difference between the heights at 6 and 12 months and baseline.
Time Frame
After 6 and 12 months
Title
Change in Bone Maturation (BM)
Description
Annual change in bone age measurements as per Gruelich-Pyle method
Time Frame
52 weeks
Title
Insulin-like Growth Factor-1 (IGF-1) Standard Deviation Score (SDS)
Description
Via central lab analysis
Time Frame
Baseline and at 12 months
Other Pre-specified Outcome Measures:
Title
Device
Description
Proportion of successful single injections out of total number of single injections using the MOD-4023 Pen in the USA
Time Frame
6 weeks
Title
Device
Description
Proportion of successful single injections out of total number of single injections using the MOD-4023 Pen in the USA at Week 1 based on the Observer Assessment Tool (OAT)
Time Frame
1 week
10. Eligibility
Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
11 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Main Study Inclusion Criteria:
Pre-pubertal children aged ≥3 years , and not yet 11 years for girls or not yet 12 years for boys with either isolated GHD, or GH insufficiency as part of multiple pituitary hormone deficiency.
Confirmed diagnosis of GHD by two different GH provocation tests defined as a peak plasma GH level of ≤10 ng/mL.
Bone age (BA) is not older than chronological age and should be less than 10 for girls and less than 11 for boys.
Without prior exposure to any r-hGH therapy (naïve patients).
Impaired height and height velocity defined as:
Annualized height velocity (HV) below the 25th percentile for CA (HV < -0.7 SDS) and gender according to sponsor calculator
The interval between 2 height measurements should be at least 6 months, but should not exceed 18 months prior to inclusion
Baseline IGF-I level of at least 1 SD below the mean IGF-1 level standardized for age and sex (IGF-1 SDS ≤-1)
Normal calculated GFR per updated bedside Schwartz formula for pediatric patients
Children with multiple hormonal deficiencies must be on stable replacement therapies (no change in dose) for other hypothalamo-pituitary-organ axes for at least 3 months prior ICF signing
Normal 46XX karyotype for girls.
Willing and able to provide written informed consent of the parent or legal guardian and written assent from patient
LT-OLE Inclusion Criteria:
Completion of the main study (12 months of treatment) with adequate compliance.
Willing and able to provide written informed consent of the parent or legal guardian and written assent from patient
Agree to refrain from sexual activity
Main Study Exclusion Criteria:
Children with prior history of leukemia, lymphoma, sarcoma or any other forms of cancer.
History of radiation therapy or chemotherapy
Malnourished children defined as BMI < -2 SDS for age and sex
Children with psychosocial dwarfism
Children born small for gestational age (SGA - birth weight and/or birth length <-2 SDS for gestational age)
Presence of anti-hGH antibodies at screening
Any clinically significant abnormality likely to affect growth or the ability to evaluate growth, such as, but not limited to, chronic diseases like renal insufficiency, spinal cord irradiation, etc.
T2 and T1 diabetic patients, who in the opinion of the investigator are not receiving standard of care treatment or are non-compliant with their prescribed treatment or who are in poor metabolic control.
Chromosomal abnormalities including Turner's syndrome, Laron syndrome, Noonan syndrome, Prader-Willi syndrome, Russell-Silver syndrome, SHOX mutations/deletions and skeletal dysplasias.
Concomitant administration of other treatments that may have an effect on growth such as anabolic steroids, or sex steroids, with the exception of ADHD drugs or hormone replacement therapies (thyroxin, hydrocortisone, desmopressin)
Children requiring glucocorticoid therapy (e.g. for asthma) that are taking chronically a dose greater than 400 μg/d of inhaled budesonide or equivalent
Major medical conditions and/or presence of contraindication to r-hGH treatment.
More than one closed epiphyses
Known or suspected HIV-positive patient, or patient with advanced diseases such as AIDS or tuberculosis.
Drug, substance, or alcohol abuse.
Known hypersensitivity to the components of study medication.
Other causes of short stature such as celiac disease, uncontrolled primary hypothyroidism and rickets.
Likely non-compliance in respect to study conduct
Participation in any other trial of an investigational agent within 30 days prior to consent
Study enrollment has been met or study is closed by sponsor prior to completion of screening process.
LT-OLE Exclusion Criteria:
Concomitant administration of other treatments that may have an effect on growth such as anabolic steroids, or sex steroids, with the exception of ADHD drugs or HRT (thyroxin, hydrocortisone, desmopressin)
Change in medical condition during the treatment period (such as, but not limited to, development of a serious inter-current critical illness, a severe adverse drug reaction, etc.)
Positive pregnancy test
Unresolved drug related (Genotropin or MOD-4023) SAE from the treatment period as per medical monitor judgement.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tony Cruz
Organizational Affiliation
Sponsor GmbH
Official's Role
Study Director
Facility Information:
Facility Name
Children's Hospital of Orange County- Children's Clinic
City
Orange
State/Province
California
ZIP/Postal Code
92868
Country
United States
Facility Name
Children's Hospital- Colorado
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80045
Country
United States
Facility Name
Rocky Mountain Pediatrics
City
Centennial
State/Province
Colorado
ZIP/Postal Code
80112
Country
United States
Facility Name
Nemours Children's Health System
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32207
Country
United States
Facility Name
University of Miami Medical Center
City
Miami
State/Province
Florida
ZIP/Postal Code
33136
Country
United States
Facility Name
St Luke's Children's Specialty Center
City
Boise
State/Province
Idaho
ZIP/Postal Code
83712
Country
United States
Facility Name
Children's Hospital of Iowa
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52242
Country
United States
Facility Name
Tufts Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02111
Country
United States
Facility Name
University of Massachusettes
City
Worcester
State/Province
Massachusetts
ZIP/Postal Code
01655
Country
United States
Facility Name
University of Minnesota
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55454
Country
United States
Facility Name
The Diabetes & Obesity Clinical Specialist
City
Las Vegas
State/Province
Nevada
ZIP/Postal Code
89148
Country
United States
Facility Name
Goryeb Children's Hospital
City
Morristown
State/Province
New Jersey
ZIP/Postal Code
07962
Country
United States
Facility Name
Buffalo Children's Hospital
City
Buffalo
State/Province
New York
ZIP/Postal Code
14222
Country
United States
Facility Name
Albert Einstein College of Medicine at Yeshiva University
City
Mineola
State/Province
New York
ZIP/Postal Code
11501
Country
United States
Facility Name
Children's Hospital of Cincinnati / Cincinnati Center for Growth Disorders
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45229
Country
United States
Facility Name
Children's Hospital of Pittsburgh
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15224
Country
United States
Facility Name
Cook Children's Medical Center
City
Fort Worth
State/Province
Texas
ZIP/Postal Code
76104
Country
United States
Facility Name
Mary Bridge Children's Hospital & Health Center
City
Tacoma
State/Province
Washington
ZIP/Postal Code
98405
Country
United States
Facility Name
Hospital Materno Infantil San Roque
City
Paraná
State/Province
Entre Rios
ZIP/Postal Code
3100
Country
Argentina
Facility Name
Hospital de Ninos de la Santisima Trinidad Cordoba
City
Córdoba
ZIP/Postal Code
5000
Country
Argentina
Facility Name
John Hunter Children's Hospital
City
New Lambton Heights
State/Province
New South Wales
ZIP/Postal Code
2305
Country
Australia
Facility Name
Children's Hospital at Westmead
City
Westmead
State/Province
New South Wales
ZIP/Postal Code
2145
Country
Australia
Facility Name
PM Hospital for Children
City
Subiaco
State/Province
Western Australia
ZIP/Postal Code
6008
Country
Australia
Facility Name
Health Institution- 2nd City Pediatric Hospital
City
Minsk
ZIP/Postal Code
220020
Country
Belarus
Facility Name
MHAT Sveta Marina
City
Varna
ZIP/Postal Code
9010
Country
Bulgaria
Facility Name
Centre de recherche du CHU Sainte-Justine
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H3T 1C5
Country
Canada
Facility Name
Dexa Diab
City
Bogotá
ZIP/Postal Code
110221
Country
Colombia
Facility Name
Uniendo
City
Bogotá
ZIP/Postal Code
110221
Country
Colombia
Facility Name
Hospital Pablo Tobon Uribe
City
Medellín
ZIP/Postal Code
050034
Country
Colombia
Facility Name
Maritime Hospital JSC
City
Batumi
ZIP/Postal Code
6010
Country
Georgia
Facility Name
Vere XXI JSC
City
Tbilisi
ZIP/Postal Code
0108
Country
Georgia
Facility Name
Aghia Sophia Children's Hospital
City
Athens
ZIP/Postal Code
11527
Country
Greece
Facility Name
General Children's Hospital of Athens P&A Kyriakou
City
Athens
ZIP/Postal Code
11527
Country
Greece
Facility Name
Manipal Hospital
City
Bengaluru
State/Province
Karnataka
ZIP/Postal Code
560017
Country
India
Facility Name
Getwell Health & Research Institute
City
Nagpur
State/Province
Maharashtra
ZIP/Postal Code
440012
Country
India
Facility Name
Jehangir Clinical Development Centre
City
Pune
State/Province
Maharashtra
ZIP/Postal Code
411001
Country
India
Facility Name
Postgraduate Institute of Medical Education and Research
City
Chandigarh
State/Province
Punjab
ZIP/Postal Code
160012
Country
India
Facility Name
Care Hospital
City
Hyderabad
State/Province
Telangna
ZIP/Postal Code
500001
Country
India
Facility Name
Meditrina Institute of Medical Sciences
City
Nagpur
ZIP/Postal Code
440010
Country
India
Facility Name
All India Institute of Medical Sciences
City
New Delhi
ZIP/Postal Code
110029
Country
India
Facility Name
Sir Gangaram Hospital
City
New Delhi
ZIP/Postal Code
110060
Country
India
Facility Name
Haemek Medical Center
City
Afula
ZIP/Postal Code
1834111
Country
Israel
Facility Name
Soroka Medical Center
City
Be'er Sheva
ZIP/Postal Code
84101
Country
Israel
Facility Name
Assaf Harofeh Medical Center
City
Be'er Ya'aqov
ZIP/Postal Code
7030000
Country
Israel
Facility Name
Bnei Zion Medical Center
City
Haifa
ZIP/Postal Code
3339509
Country
Israel
Facility Name
Shaare Zedek Medical Center
City
Jerusalem
ZIP/Postal Code
9103102
Country
Israel
Facility Name
Scheider Children's Medical Center
City
Petach Tikva
ZIP/Postal Code
49202
Country
Israel
Facility Name
Tel Hashomer Medical Center
City
Ramat Gan
ZIP/Postal Code
5265601
Country
Israel
Facility Name
Kaplan Medical Center
City
Reẖovot
ZIP/Postal Code
76100
Country
Israel
Facility Name
Sourasky Medical Center
City
Tel Aviv
ZIP/Postal Code
6423906
Country
Israel
Facility Name
Bundang Cha Hospital
City
Seongnam
State/Province
Gyeonggi-do
ZIP/Postal Code
13497
Country
Korea, Republic of
Facility Name
Inje University Busan Paik Hospital
City
Busan
ZIP/Postal Code
47392
Country
Korea, Republic of
Facility Name
KyungPook National University Hospital
City
Daegu
ZIP/Postal Code
41944
Country
Korea, Republic of
Facility Name
Chosun University Hospital
City
Gwangju
ZIP/Postal Code
61453
Country
Korea, Republic of
Facility Name
Severance Hospital
City
Seoul
ZIP/Postal Code
03722
Country
Korea, Republic of
Facility Name
Hospital Angeles de Puebla
City
Puebla
State/Province
Reserva Territorial Atilxcayotl
ZIP/Postal Code
72190
Country
Mexico
Facility Name
The Liggins Institute
City
Grafton
State/Province
Auckland
ZIP/Postal Code
1023
Country
New Zealand
Facility Name
Wellington Children's Hospital
City
Newtown
State/Province
Wellington
ZIP/Postal Code
6021
Country
New Zealand
Facility Name
Uniwersyteckie Centrum Kliniczne in Gdansk
City
Gdańsk
ZIP/Postal Code
80-211
Country
Poland
Facility Name
Centrum Zdrowia Matki Polki
City
Łódź
ZIP/Postal Code
93-338
Country
Poland
Facility Name
Bashkirian State Medical University
City
Ufa
State/Province
Bashlortostan Republic
ZIP/Postal Code
450008/450106
Country
Russian Federation
Facility Name
Kazan State Medical Univeristy/Pediatric Republic Clinical Hospital
City
Kazan
State/Province
Tatarstan Republic
ZIP/Postal Code
420012/420138
Country
Russian Federation
Facility Name
Endocrinology Scientific Center
City
Moscow
ZIP/Postal Code
117036
Country
Russian Federation
Facility Name
Pediatric City Clinical Hospital/Russian Medical Academy of Continuous Education
City
Moscow
ZIP/Postal Code
125373
Country
Russian Federation
Facility Name
Saint Petersburg State Pediatric Medical University
City
Saint Petersburg
ZIP/Postal Code
194100
Country
Russian Federation
Facility Name
Voronezh State Medical University
City
Voronezh
ZIP/Postal Code
394024
Country
Russian Federation
Facility Name
Hospital Miguel Servet
City
Zaragoza
State/Province
Aragon
ZIP/Postal Code
50009
Country
Spain
Facility Name
Hospital Josep Trueta
City
Girona
State/Province
Cataluna
ZIP/Postal Code
17007
Country
Spain
Facility Name
Hospital de Navarra
City
Pamplona
State/Province
Navarra
ZIP/Postal Code
31008
Country
Spain
Facility Name
Hospital Universitario Central de Asturias
City
Oviedo
ZIP/Postal Code
33011
Country
Spain
Facility Name
Parc Tauli
City
Sabadell
ZIP/Postal Code
15706
Country
Spain
Facility Name
Hospital Universitario de Santiago de Compostela
City
Santiago De Compostela
ZIP/Postal Code
08950
Country
Spain
Facility Name
Taipei Veterans General Hospital
City
Taipei
ZIP/Postal Code
11217
Country
Taiwan
Facility Name
Tri-Service General Hospital
City
Taipei
ZIP/Postal Code
114
Country
Taiwan
Facility Name
Ukrainian Research and Practical Centre of Endocrine Surgery, Transplantation of Endocrine Organs and Tissues of the Ministry of Health of Ukraine
City
Kyiv
ZIP/Postal Code
01021
Country
Ukraine
Facility Name
Institute of Endocrinology and Metabolism/VP Komisarenko of Academy of Medical Science of Ukraine
City
Kyiv
ZIP/Postal Code
04114
Country
Ukraine
Facility Name
Odesa Regional Clinical Children's Hospital
City
Odesa
ZIP/Postal Code
65031
Country
Ukraine
Facility Name
Vinnitsa Regional Clinical Highly Specialized Endocrinology Centre
City
Vinnitsa
ZIP/Postal Code
21010
Country
Ukraine
Facility Name
Zaporizhzhya Regional Clinical Child Hospital
City
Zaporizhzhya
ZIP/Postal Code
69063
Country
Ukraine
Facility Name
Royal Hospital for Children
City
Glasgow
ZIP/Postal Code
G514TF
Country
United Kingdom
Facility Name
St. George's University Hospital
City
London
ZIP/Postal Code
SW17 OQT
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
35405011
Citation
Deal CL, Steelman J, Vlachopapadopoulou E, Stawerska R, Silverman LA, Phillip M, Kim HS, Ko C, Malievskiy O, Cara JF, Roland CL, Taylor CT, Valluri SR, Wajnrajch MP, Pastrak A, Miller BS. Efficacy and Safety of Weekly Somatrogon vs Daily Somatropin in Children With Growth Hormone Deficiency: A Phase 3 Study. J Clin Endocrinol Metab. 2022 Jun 16;107(7):e2717-e2728. doi: 10.1210/clinem/dgac220.
Results Reference
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Safety and Efficacy Phase 3 Study of Long-acting hGH (MOD-4023) in Growth Hormone Deficient Children
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